<?xml version="1.0" encoding="UTF-8"?>

<rdf:RDF
 xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
 xmlns="http://purl.org/rss/1.0/"
 xmlns:content="http://purl.org/rss/1.0/modules/content/"
 xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/"
 xmlns:dc="http://purl.org/dc/elements/1.1/"
 xmlns:syn="http://purl.org/rss/1.0/modules/syndication/"
 xmlns:admin="http://webns.net/mvcb/"
>

<channel rdf:about="http://intranet.wiley-vch.de/vch/journals/">
<title>Chemistry articles from Wiley-VCH/ChemPubSoc Europe</title>
<link>http://intranet.wiley-vch.de/vch/journals/</link>
<description>The latest chemistry from ChemPubSoc Europe and Wiley-VCH</description>
<dc:language>en-us</dc:language>
<dc:rights>Copyright 2010, Wiley-VCH</dc:rights>
<dc:date>2012-02-08T04:19:08Z</dc:date>
<dc:publisher>Wiley-VCH</dc:publisher>
<dc:creator>mmueller@wiley-vch.de</dc:creator>
<dc:subject>Chemistry, Materials Science</dc:subject>
<items>
 <rdf:Seq>
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/open.201100009" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/open.201100004" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/open.201100002" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101842" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101835" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101830" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101822" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101814" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101807" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101794" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101788" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101786" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101770" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101765" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101763" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101757" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101744" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101739" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101735" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101722" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101715" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101709" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101702" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101699" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101695" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101690" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101684" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101673" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101670" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101662" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101656" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101648" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101645" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101636" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101634" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101633" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101624" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101623" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101619" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101615" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101614" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101609" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101605" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101601" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101599" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101595" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101592" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101587" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101584" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101583" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101576" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101563" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101543" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101540" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101539" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101535" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101529" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101525" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101518" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101509" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101505" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101499" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101498" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101495" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101491" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101489" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101484" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101480" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101477" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101470" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101463" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101462" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101454" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101450" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101449" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101442" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101434" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101421" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101356" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101320" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101301" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101293" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101269" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101258" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101240" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101231" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101230" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101222" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101133" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201200024" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101385" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101364" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101342" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101339" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101329" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101326" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101315" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101296" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101294" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101292" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101291" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101277" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101263" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101257" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101254" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101253" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101249" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101244" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101230" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101227" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101223" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101220" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101219" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101202" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101197" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101191" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101187" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101183" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101181" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101178" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101169" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101167" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101164" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101162" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101159" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101158" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101142" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101137" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101136" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101121" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101119" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101110" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101103" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101099" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101096" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101088" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101075" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101073" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101066" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101064" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101060" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101058" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101057" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101056" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101054" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101050" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101048" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101040" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101038" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101036" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101033" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101026" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201101014" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100992" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100990" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100988" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100981" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100968" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100956" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100954" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100951" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100942" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100940" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100936" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100932" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100931" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100929" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100928" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100927" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100925" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100919" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100917" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100905" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100904" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100894" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100890" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100856" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100853" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100806" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100762" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100609" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100688" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100631" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100629" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100609" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100608" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100585" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100570" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100530" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100525" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100523" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100468" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100445" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100444" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100431" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100430" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100427" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100423" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100418" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100415" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100389" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100376" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100373" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100372" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100370" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100366" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100342" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100339" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100332" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100286" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100281" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100262" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100257" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201190001" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100083" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100080" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100076" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100074" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100070" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100069" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100068" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100066" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100055" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100051" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100044" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100040" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100039" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100036" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100035" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100021" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100008" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201101018" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100996" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100983" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100959" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100948" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100936" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100929" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100916" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100903" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100894" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100888" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100879" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100876" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100873" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100872" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100868" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100864" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100857" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100843" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100842" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100833" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100832" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100829" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100820" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100813" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100810" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100807" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100806" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100796" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100788" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100785" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100783" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100781" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100780" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100776" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100774" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100772" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100771" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100770" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100765" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100748" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100745" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100743" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100737" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100732" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100731" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100730" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100727" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100721" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100720" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100717" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100714" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100711" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100708" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100686" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100681" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100680" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100677" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100674" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100671" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100670" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100669" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100655" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100582" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100568" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100528" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100421" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201200047" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201200027" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201200025" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201200019" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201200014" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201200002" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100603" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100593" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100589" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100588" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100587" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100584" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100579" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100578" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100568" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100560" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100559" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100546" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100545" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100538" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100537" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100533" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100531" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100530" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100529" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100528" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100522" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100510" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100505" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100504" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100499" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100469" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100467" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100438" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100431" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100423" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103918" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103892" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103830" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103816" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103800" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103720" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103708" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103649" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103601" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103552" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103530" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103527" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103509" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103495" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103479" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103465" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103456" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103435" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103418" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103366" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103347" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103342" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103325" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103294" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103280" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103272" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103266" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103262" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103251" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103249" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103242" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103239" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103235" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103232" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103212" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103209" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103185" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103170" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103163" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103161" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103151" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103147" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103088" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103080" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103061" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103051" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103032" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103027" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103026" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103009" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103004" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102963" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102959" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102939" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102936" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102921" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102909" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102903" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102902" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102899" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102898" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102893" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102883" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102861" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102847" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102815" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102783" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102779" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102720" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102709" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102704" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102698" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102682" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102677" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102670" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102646" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102638" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102599" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102572" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102529" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102508" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102474" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102460" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102414" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102407" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102330" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102326" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102261" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102252" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102246" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102236" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102223" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102215" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102207" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102203" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102201" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102193" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102175" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102146" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102137" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102084" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101975" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101963" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101940" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101925" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101918" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101888" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101771" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101514" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101476" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101416" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101262" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101219" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201101040" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201100838" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201002100" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.200901991" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.200901098" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100444" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100394" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100391" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100388" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100366" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100365" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100361" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100358" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100356" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100343" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100329" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100315" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100314" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100313" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100309" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100307" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100275" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100257" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100243" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201200048" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201200042" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100802" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100800" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100793" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100789" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100787" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100767" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100754" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100751" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100750" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100740" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100738" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100737" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100725" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100721" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100716" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100710" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100703" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100689" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100683" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100580" />
 </rdf:Seq>
</items>
</channel>
<item rdf:about="http://dx.doi.org/10.1002/open.201100009">
<title>Opening Up the World of Chemistry</title>
<link>http://dx.doi.org/10.1002/open.201100009</link>
<dc:date>2012-01-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p></p><p> [Editorial]<br /><br /><i>ChemistryOpen</i>, January 2, 2012, DOI: 10.1002/open.201100009. <a href="http://dx.doi.org/10.1002/open.201100009">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/open.201100004">
<title>Determining the Role of the Aromatic Ring of &lt;I&gt;N&lt;/I&gt;-Arylmethyl &lt;I&gt;ent&lt;/I&gt;-conduramine F-1 in their Interactions with &#x3B1;-Glucosidases by Saturation Transfer Difference NMR Spectroscopy Experiments</title>
<link>http://dx.doi.org/10.1002/open.201100004</link>
<dc:creator>Antonio Hern&#xE1;ndez Daranas, Sonia Koteich Khatib, Robert Lysek, Pierre Vogel, Jos&#xE9; A. Gav&#xED;n</dc:creator>
<dc:date>2012-01-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/open201100004.gif" width="216" height="187" alt="Determining the Role of the Aromatic Ring of N-Arylmethyl ent-conduramine F-1 in their Interactions with &alpha;-Glucosidases by Saturation Transfer Difference NMR Spectroscopy Experiments" title="Determining the Role of the Aromatic Ring of N-Arylmethyl ent-conduramine F-1 in their Interactions with &alpha;-Glucosidases by Saturation Transfer Difference NMR Spectroscopy Experiments" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Saturation transfer difference (STD)</B> NMR spectroscopy was used to study the role of aromatic moieties in the inhibition of &alpha;-glucosidases by <I>N</I>-arylmethyl <I>ent</I>-conduramine F-1. STD epitope mapping and molecular docking simulations provide new insights into the structure-based design of drugs targeting this enzyme (see figure).</P>
<p> [Communication]<br />Antonio Hern&#xE1;ndez&#xA0;Daranas, Sonia Koteich&#xA0;Khatib, Robert Lysek, Pierre Vogel, Jos&#xE9; A. Gav&#xED;n<br /><i>ChemistryOpen</i>, January 2, 2012, DOI: 10.1002/open.201100004. <a href="http://dx.doi.org/10.1002/open.201100004">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/open.201100002">
<title>Semi-Synthesis and Analysis of Chemically Modified Zif268 Zinc-Finger Domains</title>
<link>http://dx.doi.org/10.1002/open.201100002</link>
<dc:creator>Friederike Fehr, Andr&#xE9; Nadler, Florian Brodhun, Ivo Feussner, Ulf Diederichsen</dc:creator>
<dc:date>2012-01-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/open201100002.gif" width="164" height="213" alt="Semi-Synthesis and Analysis of Chemically Modified Zif268 Zinc-Finger Domains" title="Semi-Synthesis and Analysis of Chemically Modified Zif268 Zinc-Finger Domains" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The entire zinc-finger domain</B> of Zif268 was synthesized by a semi-synthetic pathway using the expressed protein ligation approach. Despite several modifications, for example, attachment of a fluorophore and introduction of a metal-chelating amino acid within the sequence of the third zinc finger, circular dichroism spectroscopic measurements confirmed zinc-induced folding and intact DNA binding ability.</P>
<p> [Full Paper]<br />Friederike Fehr, Andr&#xE9; Nadler, Florian Brodhun, Ivo Feussner, Ulf Diederichsen<br /><i>ChemistryOpen</i>, January 2, 2012, DOI: 10.1002/open.201100002. <a href="http://dx.doi.org/10.1002/open.201100002">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101842">
<title>Ti/Ni-Based Multimetallic System for the Efficient Allylation of Carbonyl Compounds</title>
<link>http://dx.doi.org/10.1002/ejoc.201101842</link>
<dc:creator>Angela Mart&#xED;nez-Perag&#xF3;n, Alba Mill&#xE1;n, Araceli G. Campa&#xF1;a, Irene Rodr&#xED;guez-M&#xE1;rquez, Sandra Resa, Delia Miguel, Luis Alvarez de Cienfuegos, Juan M. Cuerva</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101842.jpg" width="171" height="114" alt="Ti/Ni-Based Multimetallic System for the Efficient Allylation of Carbonyl Compounds" title="Ti/Ni-Based Multimetallic System for the Efficient Allylation of Carbonyl Compounds" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Angela Mart&#xED;nez-Perag&#xF3;n, Alba Mill&#xE1;n, Araceli G. Campa&#xF1;a, Irene Rodr&#xED;guez-M&#xE1;rquez, Sandra Resa, Delia Miguel, Luis Alvarez de Cienfuegos, Juan M. Cuerva<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101842. <a href="http://dx.doi.org/10.1002/ejoc.201101842">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101835">
<title>Oxidative Homologation of Aldehydes to &#x3B1;-Ketoaldehydes by using Iodoform, &lt;I&gt;o&lt;/I&gt;-Iodoxybenzoic Acid, and Dimethyl Sulfoxide</title>
<link>http://dx.doi.org/10.1002/ejoc.201101835</link>
<dc:creator>Andrea Zall, Dennis Bensinger, Boris Schmidt</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101835.jpg" width="423" height="67" alt="Oxidative Homologation of Aldehydes to &alpha;-Ketoaldehydes by using Iodoform, o-Iodoxybenzoic Acid, and Dimethyl Sulfoxide" title="Oxidative Homologation of Aldehydes to &alpha;-Ketoaldehydes by using Iodoform, o-Iodoxybenzoic Acid, and Dimethyl Sulfoxide" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Andrea Zall, Dennis Bensinger, Boris Schmidt<br /><i>Eur. J. Org. Chem.</i>, January 24, 2012, DOI: 10.1002/ejoc.201101835. <a href="http://dx.doi.org/10.1002/ejoc.201101835">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101830">
<title>Replacement of HMPA in Samarium Diiodide Promoted Cyclizations and Reactions of Organolithium Compounds&lt;P&gt;Dedicated to Professor Dr. Gerhard Erker on the occasion of his 65th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101830</link>
<dc:creator>Mathias Berndt, Alexandra H&#xF6;lemann, Andr&#xE9; Niermann, Christoph Bentz, Reinhold Zimmer, Hans-Ulrich Reissig</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101830.jpg" width="210" height="165" alt="Replacement of HMPA in Samarium Diiodide Promoted Cyclizations and Reactions of Organolithium CompoundsDedicated to Professor Dr. Gerhard Erker on the occasion of his 65th birthday" title="Replacement of HMPA in Samarium Diiodide Promoted Cyclizations and Reactions of Organolithium CompoundsDedicated to Professor Dr. Gerhard Erker on the occasion of his 65th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Mathias Berndt, Alexandra H&#xF6;lemann, Andr&#xE9; Niermann, Christoph Bentz, Reinhold Zimmer, Hans-Ulrich Reissig<br /><i>Eur. J. Org. Chem.</i>, January 25, 2012, DOI: 10.1002/ejoc.201101830. <a href="http://dx.doi.org/10.1002/ejoc.201101830">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101822">
<title>New Linearly and Angularly Fused Quinazolinones: Synthesis through Gold(I)-Catalyzed Cascade Reactions and Anticancer Activities</title>
<link>http://dx.doi.org/10.1002/ejoc.201101822</link>
<dc:creator>Nitin T. Patil, Pediredla G. V. V. Lakshmi, Balasubramanian Sridhar, Sujata Patra, Manika Pal Bhadra, Chitta Ranjan Patra</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101822.jpg" width="213" height="120" alt="New Linearly and Angularly Fused Quinazolinones: Synthesis through Gold(I)-Catalyzed Cascade Reactions and Anticancer Activities" title="New Linearly and Angularly Fused Quinazolinones: Synthesis through Gold(I)-Catalyzed Cascade Reactions and Anticancer Activities" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Nitin T. Patil, Pediredla G. V. V. Lakshmi, Balasubramanian Sridhar, Sujata Patra, Manika Pal Bhadra, Chitta Ranjan Patra<br /><i>Eur. J. Org. Chem.</i>, February 6, 2012, DOI: 10.1002/ejoc.201101822. <a href="http://dx.doi.org/10.1002/ejoc.201101822">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101814">
<title>Synthesis of Isoxazole Triflones</title>
<link>http://dx.doi.org/10.1002/ejoc.201101814</link>
<dc:creator>Hiroyuki Kawai, Yutaka Sugita, Etsuko Tokunaga, Norio Shibata</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101814.jpg" width="428" height="75" alt="Synthesis of Isoxazole Triflones" title="Synthesis of Isoxazole Triflones" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Hiroyuki Kawai, Yutaka Sugita, Etsuko Tokunaga, Norio Shibata<br /><i>Eur. J. Org. Chem.</i>, January 25, 2012, DOI: 10.1002/ejoc.201101814. <a href="http://dx.doi.org/10.1002/ejoc.201101814">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101807">
<title>Stereocontrolled Synthesis of the &lt;I&gt;cis&lt;/I&gt;-Hydroxydecalin System: Towards Biologically Active 19-&lt;I&gt;nor&lt;/I&gt;-Clerodanes</title>
<link>http://dx.doi.org/10.1002/ejoc.201101807</link>
<dc:creator>Paul Malek Mirzayans, Rebecca H. Pouwer, Craig M. Williams, Paul V. Bernhardt</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101807.jpg" width="207" height="91" alt="Stereocontrolled Synthesis of the cis-Hydroxydecalin System: Towards Biologically Active 19-nor-Clerodanes" title="Stereocontrolled Synthesis of the cis-Hydroxydecalin System: Towards Biologically Active 19-nor-Clerodanes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Paul Malek Mirzayans, Rebecca H. Pouwer, Craig M. Williams, Paul V. Bernhardt<br /><i>Eur. J. Org. Chem.</i>, January 26, 2012, DOI: 10.1002/ejoc.201101807. <a href="http://dx.doi.org/10.1002/ejoc.201101807">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101794">
<title>Asymmetric Organocatalytic Michael Addition&#x2013;Cyclization Cascade Reaction of Nitroalkanes with &lt;I&gt;o&lt;/I&gt;-Hydroxycinnamaldehydes</title>
<link>http://dx.doi.org/10.1002/ejoc.201101794</link>
<dc:creator>Kwang-Su Choi, Sung-Gon Kim</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101794.jpg" width="401" height="56" alt="Asymmetric Organocatalytic Michael Addition&ndash;Cyclization Cascade Reaction of Nitroalkanes with o-Hydroxycinnamaldehydes" title="Asymmetric Organocatalytic Michael Addition&ndash;Cyclization Cascade Reaction of Nitroalkanes with o-Hydroxycinnamaldehydes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Kwang-Su Choi, Sung-Gon Kim<br /><i>Eur. J. Org. Chem.</i>, January 13, 2012, DOI: 10.1002/ejoc.201101794. <a href="http://dx.doi.org/10.1002/ejoc.201101794">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101788">
<title>Phomopsinones A&#x2013;D: Four New Pyrenocines from Endophytic Fungus &lt;I&gt;Phomopsis&lt;/I&gt; sp.&lt;P&gt;Biologically Active Secondary Metabolites from Fungi, 51. Part 50: I. N. Siddiqui, A. Zahoor, H. Hussain, I. Ahmed, V. U. Ahmad, D. Padula, S. Draeger, B. Schulz, K. Meier, M. Steiner, T. Kurtan, U. Fl&#xF6;rke, G. Pescitelli, K. Krohn, &lt;I&gt;J. Nat. Prod.&lt;/I&gt; &lt;B&gt;2011&lt;/B&gt;, &lt;I&gt;74&lt;/I&gt;, 365&#x2013;373.&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101788</link>
<dc:creator>Hidayat Hussain, Karsten Krohn, Ishtiaq Ahmed, Siegfried Draeger, Barbara Schulz, Sebastiano Di Pietro, Gennaro Pescitelli</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101788.jpg" width="428" height="82" alt="Phomopsinones A&ndash;D: Four New Pyrenocines from Endophytic Fungus Phomopsis sp.Biologically Active Secondary Metabolites from Fungi, 51. Part 50: I. N. Siddiqui, A. Zahoor, H. Hussain, I. Ahmed, V. U. Ahmad, D. Padula, S. Draeger, B. Schulz, K. Meier, M. Steiner, T. Kurtan, U. Fl&ouml;rke, G. Pescitelli, K. Krohn, J. Nat. Prod. 2011, 74, 365&ndash;373." title="Phomopsinones A&ndash;D: Four New Pyrenocines from Endophytic Fungus Phomopsis sp.Biologically Active Secondary Metabolites from Fungi, 51. Part 50: I. N. Siddiqui, A. Zahoor, H. Hussain, I. Ahmed, V. U. Ahmad, D. Padula, S. Draeger, B. Schulz, K. Meier, M. Steiner, T. Kurtan, U. Fl&ouml;rke, G. Pescitelli, K. Krohn, J. Nat. Prod. 2011, 74, 365&ndash;373." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Hidayat Hussain, Karsten Krohn, Ishtiaq Ahmed, Siegfried Draeger, Barbara Schulz, Sebastiano Di Pietro, Gennaro Pescitelli<br /><i>Eur. J. Org. Chem.</i>, February 1, 2012, DOI: 10.1002/ejoc.201101788. <a href="http://dx.doi.org/10.1002/ejoc.201101788">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101786">
<title>Solvent-Free Tandem Synthesis of 2-Thiazolines and 2-Oxazolines Catalyzed by a Copper Catalyst</title>
<link>http://dx.doi.org/10.1002/ejoc.201101786</link>
<dc:creator>Xiangnan Li, Baoyue Zhou, Jin Zhang, Mengyao She, Shujuan An, Haixia Ge, Cong Li, Bing Yin, Jianli Li, Zhen Shi</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101786.jpg" width="210" height="116" alt="Solvent-Free Tandem Synthesis of 2-Thiazolines and 2-Oxazolines Catalyzed by a Copper Catalyst" title="Solvent-Free Tandem Synthesis of 2-Thiazolines and 2-Oxazolines Catalyzed by a Copper Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Xiangnan Li, Baoyue Zhou, Jin Zhang, Mengyao She, Shujuan An, Haixia Ge, Cong Li, Bing Yin, Jianli Li, Zhen Shi<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101786. <a href="http://dx.doi.org/10.1002/ejoc.201101786">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101770">
<title>Practical Synthesis of Unsymmetrical Diarylacetylenes from Propiolic Acid and Two Different Aryl Bromides</title>
<link>http://dx.doi.org/10.1002/ejoc.201101770</link>
<dc:creator>Stefano Tartaggia, Ottorino De Lucchi, Lukas J. Goo&#xDF;en</dc:creator>
<dc:date>2012-01-18T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101770.jpg" width="200" height="89" alt="Practical Synthesis of Unsymmetrical Diarylacetylenes from Propiolic Acid and Two Different Aryl Bromides" title="Practical Synthesis of Unsymmetrical Diarylacetylenes from Propiolic Acid and Two Different Aryl Bromides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Stefano Tartaggia, Ottorino De Lucchi, Lukas J. Goo&#xDF;en<br /><i>Eur. J. Org. Chem.</i>, January 18, 2012, DOI: 10.1002/ejoc.201101770. <a href="http://dx.doi.org/10.1002/ejoc.201101770">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101765">
<title>Asymmetric Michael Addition Reactions between 3-Substituted Benzofuran-2(3&lt;I&gt;H&lt;/I&gt;)-ones and 1,1-Bis(phenylsulfonyl)ethylene Catalyzed by Bifunctional Catalysts Containing Tertiary Amine and Thiourea Groups</title>
<link>http://dx.doi.org/10.1002/ejoc.201101765</link>
<dc:creator>Xin Li, Yue-Yan Zhang, Xiao-Song Xue, Jia-Lu Jin, Bo-Xuan Tan, Cong Liu, Nan Dong, Jin-Pei Cheng</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101765.jpg" width="331" height="113" alt="Asymmetric Michael Addition Reactions between 3-Substituted Benzofuran-2(3H)-ones and 1,1-Bis(phenylsulfonyl)ethylene Catalyzed by Bifunctional Catalysts Containing Tertiary Amine and Thiourea Groups" title="Asymmetric Michael Addition Reactions between 3-Substituted Benzofuran-2(3H)-ones and 1,1-Bis(phenylsulfonyl)ethylene Catalyzed by Bifunctional Catalysts Containing Tertiary Amine and Thiourea Groups" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Xin Li, Yue-Yan Zhang, Xiao-Song Xue, Jia-Lu Jin, Bo-Xuan Tan, Cong Liu, Nan Dong, Jin-Pei Cheng<br /><i>Eur. J. Org. Chem.</i>, February 6, 2012, DOI: 10.1002/ejoc.201101765. <a href="http://dx.doi.org/10.1002/ejoc.201101765">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101763">
<title>Bis- and Tris-Alkyne Phosphoramidites for Multiple 5&#x27;-Labeling of Oligonucleotides by Click Chemistry</title>
<link>http://dx.doi.org/10.1002/ejoc.201101763</link>
<dc:creator>Caroline Ligeour, Albert Meyer, Jean-Jacques Vasseur, Fran&#xE7;ois Morvan</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101763.jpg" width="204" height="107" alt="Bis- and Tris-Alkyne Phosphoramidites for Multiple 5&#x27;-Labeling of Oligonucleotides by Click Chemistry" title="Bis- and Tris-Alkyne Phosphoramidites for Multiple 5&#x27;-Labeling of Oligonucleotides by Click Chemistry" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Caroline Ligeour, Albert Meyer, Jean-Jacques Vasseur, Fran&#xE7;ois Morvan<br /><i>Eur. J. Org. Chem.</i>, February 6, 2012, DOI: 10.1002/ejoc.201101763. <a href="http://dx.doi.org/10.1002/ejoc.201101763">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101757">
<title>Development of a Solid-Phase Approach to the Natural Product Class of Ahp-Containing Cyclodepsipeptides</title>
<link>http://dx.doi.org/10.1002/ejoc.201101757</link>
<dc:creator>Sara C. Stolze, Michael Meltzer, Michael Ehrmann, Markus Kaiser</dc:creator>
<dc:date>2012-01-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101757.jpg" width="434" height="106" alt="Development of a Solid-Phase Approach to the Natural Product Class of Ahp-Containing Cyclodepsipeptides" title="Development of a Solid-Phase Approach to the Natural Product Class of Ahp-Containing Cyclodepsipeptides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Sara C. Stolze, Michael Meltzer, Michael Ehrmann, Markus Kaiser<br /><i>Eur. J. Org. Chem.</i>, January 23, 2012, DOI: 10.1002/ejoc.201101757. <a href="http://dx.doi.org/10.1002/ejoc.201101757">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101744">
<title>Synthesis of Modified Phenylalanine Peptides by Cross Enyne Metathesis and a Diels&#x2013;Alder Reaction as Key Steps</title>
<link>http://dx.doi.org/10.1002/ejoc.201101744</link>
<dc:creator>Sambasivarao Kotha, Deepti Goyal (n&#xE9;e Bansal), Niranjan Thota, Venu Srinivas</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101744.jpg" width="421" height="111" alt="Synthesis of Modified Phenylalanine Peptides by Cross Enyne Metathesis and a Diels&ndash;Alder Reaction as Key Steps" title="Synthesis of Modified Phenylalanine Peptides by Cross Enyne Metathesis and a Diels&ndash;Alder Reaction as Key Steps" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Sambasivarao Kotha, Deepti Goyal (n&#xE9;e Bansal), Niranjan Thota, Venu Srinivas<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101744. <a href="http://dx.doi.org/10.1002/ejoc.201101744">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101739">
<title>Asymmetric Allylboration of Aldehydes with Pinacol Allylboronates Catalyzed by 1,1&#x27;-Spirobiindane-7,7&#x27;-diol (SPINOL) Based Phosphoric Acids</title>
<link>http://dx.doi.org/10.1002/ejoc.201101739</link>
<dc:creator>Chun-Hui Xing, Yuan-Xi Liao, Yimei Zhang, Darya Sabarova, Monica Bassous, Qiao-Sheng Hu</dc:creator>
<dc:date>2012-01-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101739.jpg" width="204" height="149" alt="Asymmetric Allylboration of Aldehydes with Pinacol Allylboronates Catalyzed by 1,1&#x27;-Spirobiindane-7,7&#x27;-diol (SPINOL) Based Phosphoric Acids" title="Asymmetric Allylboration of Aldehydes with Pinacol Allylboronates Catalyzed by 1,1&#x27;-Spirobiindane-7,7&#x27;-diol (SPINOL) Based Phosphoric Acids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Chun-Hui Xing, Yuan-Xi Liao, Yimei Zhang, Darya Sabarova, Monica Bassous, Qiao-Sheng Hu<br /><i>Eur. J. Org. Chem.</i>, January 16, 2012, DOI: 10.1002/ejoc.201101739. <a href="http://dx.doi.org/10.1002/ejoc.201101739">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101735">
<title>A One-Pot Three-Step Synthesis of &lt;I&gt;Z&lt;/I&gt;-Trisubstituted Olefins from Arylalkynes and Their Cyclization into 4-Aryl-2&lt;I&gt;H&lt;/I&gt;-chromenes</title>
<link>http://dx.doi.org/10.1002/ejoc.201101735</link>
<dc:creator>Evelia Rasolofonjatovo, Bret Tr&#xE9;guier, Olivier Provot, Abdallah Hamze, Jean-Daniel Brion, Mou&#xE2;d Alami</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101735.jpg" width="430" height="80" alt="A One-Pot Three-Step Synthesis of Z-Trisubstituted Olefins from Arylalkynes and Their Cyclization into 4-Aryl-2H-chromenes" title="A One-Pot Three-Step Synthesis of Z-Trisubstituted Olefins from Arylalkynes and Their Cyclization into 4-Aryl-2H-chromenes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Evelia Rasolofonjatovo, Bret Tr&#xE9;guier, Olivier Provot, Abdallah Hamze, Jean-Daniel Brion, Mou&#xE2;d Alami<br /><i>Eur. J. Org. Chem.</i>, January 20, 2012, DOI: 10.1002/ejoc.201101735. <a href="http://dx.doi.org/10.1002/ejoc.201101735">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101722">
<title>Asymmetric Benzoylation of &lt;I&gt;meso&lt;/I&gt;-Hydrobenzoin Using a Reusable Tripodal Imidazoline&#x2013;Pyridine&#x2013;Cu Catalyst</title>
<link>http://dx.doi.org/10.1002/ejoc.201101722</link>
<dc:creator>Takayoshi Arai, Ken Sakagami</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101722.jpg" width="393" height="125" alt="Asymmetric Benzoylation of meso-Hydrobenzoin Using a Reusable Tripodal Imidazoline&ndash;Pyridine&ndash;Cu Catalyst" title="Asymmetric Benzoylation of meso-Hydrobenzoin Using a Reusable Tripodal Imidazoline&ndash;Pyridine&ndash;Cu Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Takayoshi Arai, Ken Sakagami<br /><i>Eur. J. Org. Chem.</i>, January 17, 2012, DOI: 10.1002/ejoc.201101722. <a href="http://dx.doi.org/10.1002/ejoc.201101722">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101715">
<title>A Novel Type of Chiral Triangulane-Based Diphosphane Ligands for Transition Metals&lt;P&gt;See ref.&lt;SUP&gt;1&lt;/SUP&gt;&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101715</link>
<dc:creator>Alexander F. Khlebnikov, Sergei I. Kozhushkov, Dmitry S. Yufit, Heiko Schill, Michael Reggelin, Volker Spohr, Armin de Meijere</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101715.jpg" width="213" height="117" alt="A Novel Type of Chiral Triangulane-Based Diphosphane Ligands for Transition MetalsSee ref.1" title="A Novel Type of Chiral Triangulane-Based Diphosphane Ligands for Transition MetalsSee ref.1" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Alexander F. Khlebnikov, Sergei I. Kozhushkov, Dmitry S. Yufit, Heiko Schill, Michael Reggelin, Volker Spohr, Armin de Meijere<br /><i>Eur. J. Org. Chem.</i>, January 31, 2012, DOI: 10.1002/ejoc.201101715. <a href="http://dx.doi.org/10.1002/ejoc.201101715">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101709">
<title>Cicindeloine from &lt;I&gt;Stenus cicindeloides&lt;/I&gt; &#x2013; Isolation, Structure Elucidation, and Total Synthesis</title>
<link>http://dx.doi.org/10.1002/ejoc.201101709</link>
<dc:creator>Tobias M&#xFC;ller, Matthias G&#xF6;hl, Inka Lusebrink, Konrad Dettner, Karlheinz Seifert</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101709.jpg" width="195" height="143" alt="Cicindeloine from Stenus cicindeloides &ndash; Isolation, Structure Elucidation, and Total Synthesis" title="Cicindeloine from Stenus cicindeloides &ndash; Isolation, Structure Elucidation, and Total Synthesis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Tobias M&#xFC;ller, Matthias G&#xF6;hl, Inka Lusebrink, Konrad Dettner, Karlheinz Seifert<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101709. <a href="http://dx.doi.org/10.1002/ejoc.201101709">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101702">
<title>Synthesis of a Photochromic Fused 2&lt;I&gt;H&lt;/I&gt;-Chromene Capable of Generating a Single Coloured Species</title>
<link>http://dx.doi.org/10.1002/ejoc.201101702</link>
<dc:creator>C&#xE9;u M. Sousa, Jo&#xE3;o Pina, Jo&#xE3;o Seixas de Melo, Jerome Berthet, Stephanie Delbaere, Paulo J. Coelho</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101702.jpg" width="213" height="100" alt="Synthesis of a Photochromic Fused 2H-Chromene Capable of Generating a Single Coloured Species" title="Synthesis of a Photochromic Fused 2H-Chromene Capable of Generating a Single Coloured Species" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />C&#xE9;u M. Sousa, Jo&#xE3;o Pina, Jo&#xE3;o Seixas de Melo, Jerome Berthet, Stephanie Delbaere, Paulo J. Coelho<br /><i>Eur. J. Org. Chem.</i>, February 6, 2012, DOI: 10.1002/ejoc.201101702. <a href="http://dx.doi.org/10.1002/ejoc.201101702">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101699">
<title>A Photodynamic Library of Tetrasulfinylcalix[4]arenes: The Sulfinyl Dance</title>
<link>http://dx.doi.org/10.1002/ejoc.201101699</link>
<dc:creator>Roberta Cacciapaglia, Stefano Di Stefano, Osvaldo Lanzalunga, Leonardo Maugeri, Marco Mazzonna</dc:creator>
<dc:date>2012-01-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101699.jpg" width="263" height="205" alt="A Photodynamic Library of Tetrasulfinylcalix[4]arenes: The Sulfinyl Dance" title="A Photodynamic Library of Tetrasulfinylcalix[4]arenes: The Sulfinyl Dance" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Roberta Cacciapaglia, Stefano Di Stefano, Osvaldo Lanzalunga, Leonardo Maugeri, Marco Mazzonna<br /><i>Eur. J. Org. Chem.</i>, January 11, 2012, DOI: 10.1002/ejoc.201101699. <a href="http://dx.doi.org/10.1002/ejoc.201101699">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101695">
<title>&lt;I&gt;Klebsiella&lt;/I&gt; &lt;I&gt;pneumoniae&lt;/I&gt; (NBRC 3319) Mediated Asymmetric Reduction of &#x3B1;-Substituted &#x3B2;-Oxo Esters and Its Application to the Enantioiselective Synthesis of Small-Ring Carbocycle Derivatives</title>
<link>http://dx.doi.org/10.1002/ejoc.201101695</link>
<dc:creator>Rajib Bhuniya, Tridib Mahapatra, Samik Nanda</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101695.jpg" width="196" height="123" alt="Klebsiella pneumoniae (NBRC 3319) Mediated Asymmetric Reduction of &alpha;-Substituted &beta;-Oxo Esters and Its Application to the Enantioiselective Synthesis of Small-Ring Carbocycle Derivatives" title="Klebsiella pneumoniae (NBRC 3319) Mediated Asymmetric Reduction of &alpha;-Substituted &beta;-Oxo Esters and Its Application to the Enantioiselective Synthesis of Small-Ring Carbocycle Derivatives" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Rajib Bhuniya, Tridib Mahapatra, Samik Nanda<br /><i>Eur. J. Org. Chem.</i>, January 30, 2012, DOI: 10.1002/ejoc.201101695. <a href="http://dx.doi.org/10.1002/ejoc.201101695">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101690">
<title>The Oxy-Cope Rearrangement of Aldol Products. A Combined Experimental and Theoretical Study</title>
<link>http://dx.doi.org/10.1002/ejoc.201101690</link>
<dc:creator>Christian F. Weise, Stefan Immel, Frank Richter, Christoph Schneider</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101690.jpg" width="428" height="152" alt="The Oxy-Cope Rearrangement of Aldol Products. A Combined Experimental and Theoretical Study" title="The Oxy-Cope Rearrangement of Aldol Products. A Combined Experimental and Theoretical Study" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Christian F. Weise, Stefan Immel, Frank Richter, Christoph Schneider<br /><i>Eur. J. Org. Chem.</i>, January 27, 2012, DOI: 10.1002/ejoc.201101690. <a href="http://dx.doi.org/10.1002/ejoc.201101690">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101684">
<title>Stereoselective Olefination and Regiospecific Vicinal Difunctionalization of Imines with &#x3B1;-(Benzothiazol-2-ylsulfonyl) Carbonyl Compounds</title>
<link>http://dx.doi.org/10.1002/ejoc.201101684</link>
<dc:creator>You-Dong Shao, Xue-Song Wu, Shi-Kai Tian</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101684.jpg" width="213" height="180" alt="Stereoselective Olefination and Regiospecific Vicinal Difunctionalization of Imines with &alpha;-(Benzothiazol-2-ylsulfonyl) Carbonyl Compounds" title="Stereoselective Olefination and Regiospecific Vicinal Difunctionalization of Imines with &alpha;-(Benzothiazol-2-ylsulfonyl) Carbonyl Compounds" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />You-Dong Shao, Xue-Song Wu, Shi-Kai Tian<br /><i>Eur. J. Org. Chem.</i>, January 26, 2012, DOI: 10.1002/ejoc.201101684. <a href="http://dx.doi.org/10.1002/ejoc.201101684">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101673">
<title>Total Synthesis of (+)-Aspicilin by an Alkyne-Based Approach and Its Biological Evaluation</title>
<link>http://dx.doi.org/10.1002/ejoc.201101673</link>
<dc:creator>Chada Raji Reddy, Nagavaram Narsimha Rao, Pombala Sujitha, Chityal Ganesh Kumar</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101673.jpg" width="206" height="206" alt="Total Synthesis of (+)-Aspicilin by an Alkyne-Based Approach and Its Biological Evaluation" title="Total Synthesis of (+)-Aspicilin by an Alkyne-Based Approach and Its Biological Evaluation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Chada Raji Reddy, Nagavaram Narsimha Rao, Pombala Sujitha, Chityal Ganesh Kumar<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101673. <a href="http://dx.doi.org/10.1002/ejoc.201101673">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101670">
<title>Palladium-Catalyzed Tandem Reactions of &#x3B2;-(2-Bromophenyl)-&#x3B1;,&#x3B2;-Unsaturated Carbonyl Compounds with 2-Hydroxyphenylboronic Acid: A New Route to Benzo[&lt;I&gt;c&lt;/I&gt;]chromenes</title>
<link>http://dx.doi.org/10.1002/ejoc.201101670</link>
<dc:creator>Qihua Zhu, Xuyan Wang, Yungen Xu</dc:creator>
<dc:date>2012-01-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101670.jpg" width="313" height="61" alt="Palladium-Catalyzed Tandem Reactions of &beta;-(2-Bromophenyl)-&alpha;,&beta;-Unsaturated Carbonyl Compounds with 2-Hydroxyphenylboronic Acid: A New Route to Benzo[c]chromenes" title="Palladium-Catalyzed Tandem Reactions of &beta;-(2-Bromophenyl)-&alpha;,&beta;-Unsaturated Carbonyl Compounds with 2-Hydroxyphenylboronic Acid: A New Route to Benzo[c]chromenes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Qihua Zhu, Xuyan Wang, Yungen Xu<br /><i>Eur. J. Org. Chem.</i>, January 16, 2012, DOI: 10.1002/ejoc.201101670. <a href="http://dx.doi.org/10.1002/ejoc.201101670">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101662">
<title>Synthesis of 6-Substituted 2(1&lt;I&gt;H&lt;/I&gt;)-Pyridon-3-yl &lt;I&gt;C&lt;/I&gt;-2&#x27;-Deoxyribonucleosides</title>
<link>http://dx.doi.org/10.1002/ejoc.201101662</link>
<dc:creator>Hubert Chapuis, Tom&#xE1;&#x161; Kubelka, Nicolas Joubert, Radek Pohl, Michal Hocek</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101662.jpg" width="444" height="99" alt="Synthesis of 6-Substituted 2(1H)-Pyridon-3-yl C-2&#x27;-Deoxyribonucleosides" title="Synthesis of 6-Substituted 2(1H)-Pyridon-3-yl C-2&#x27;-Deoxyribonucleosides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Hubert Chapuis, Tom&#xE1;&#x161; Kubelka, Nicolas Joubert, Radek Pohl, Michal Hocek<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101662. <a href="http://dx.doi.org/10.1002/ejoc.201101662">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101656">
<title>An Efficient Route to Quinolines and Other Compounds by Iron-Catalysed Cross-Dehydrogenative Coupling Reactions of Glycine Derivatives</title>
<link>http://dx.doi.org/10.1002/ejoc.201101656</link>
<dc:creator>Peng Liu, Zhiming Wang, Jue Lin, Xianming Hu</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101656.jpg" width="321" height="131" alt="An Efficient Route to Quinolines and Other Compounds by Iron-Catalysed Cross-Dehydrogenative Coupling Reactions of Glycine Derivatives" title="An Efficient Route to Quinolines and Other Compounds by Iron-Catalysed Cross-Dehydrogenative Coupling Reactions of Glycine Derivatives" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Peng Liu, Zhiming Wang, Jue Lin, Xianming Hu<br /><i>Eur. J. Org. Chem.</i>, January 30, 2012, DOI: 10.1002/ejoc.201101656. <a href="http://dx.doi.org/10.1002/ejoc.201101656">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101648">
<title>Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes</title>
<link>http://dx.doi.org/10.1002/ejoc.201101648</link>
<dc:creator>Junwei Xing, Guihua Chen, Peng Cao, Jian Liao</dc:creator>
<dc:date>2012-01-04T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101648.jpg" width="332" height="80" alt="Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes" title="Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Junwei Xing, Guihua Chen, Peng Cao, Jian Liao<br /><i>Eur. J. Org. Chem.</i>, January 4, 2012, DOI: 10.1002/ejoc.201101648. <a href="http://dx.doi.org/10.1002/ejoc.201101648">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101645">
<title>Preparation of New 1,4-Diazocanes as Scaffolds for Combinatorial Chemistry</title>
<link>http://dx.doi.org/10.1002/ejoc.201101645</link>
<dc:creator>Miriam Penning, Jens Christoffers</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101645.jpg" width="396" height="73" alt="Preparation of New 1,4-Diazocanes as Scaffolds for Combinatorial Chemistry" title="Preparation of New 1,4-Diazocanes as Scaffolds for Combinatorial Chemistry" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Miriam Penning, Jens Christoffers<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101645. <a href="http://dx.doi.org/10.1002/ejoc.201101645">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101636">
<title>Controlling the Macroscopic Chirality of Organic Materials Based on 1,3,5-Trialkynylbenzenes&lt;P&gt;Dedicated to Dr. Helmut Sonnenschein on the occasion of his 60th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101636</link>
<dc:creator>Gunther Hennrich, Bel&#xE9;n Nieto-Ortega, Berta G&#xF3;mez-Lor, Entique Gutierrez, Laura de Vega, Emma Cavero, Francisco J. Ram&#xED;rez, Juan T. L&#xF3;pez Navarrete, Juan Casado</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101636.jpg" width="329" height="204" alt="Controlling the Macroscopic Chirality of Organic Materials Based on 1,3,5-TrialkynylbenzenesDedicated to Dr. Helmut Sonnenschein on the occasion of his 60th birthday" title="Controlling the Macroscopic Chirality of Organic Materials Based on 1,3,5-TrialkynylbenzenesDedicated to Dr. Helmut Sonnenschein on the occasion of his 60th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Gunther Hennrich, Bel&#xE9;n Nieto-Ortega, Berta G&#xF3;mez-Lor, Entique Gutierrez, Laura de Vega, Emma Cavero, Francisco J. Ram&#xED;rez, Juan T. L&#xF3;pez Navarrete, Juan Casado<br /><i>Eur. J. Org. Chem.</i>, January 26, 2012, DOI: 10.1002/ejoc.201101636. <a href="http://dx.doi.org/10.1002/ejoc.201101636">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101634">
<title>Effects of Silyl Substituents on the Palladium-Catalyzed Asymmetric Synthesis of Axially Chiral (Allenylmethyl)silanes and Their S&lt;sub&gt;E&lt;/sub&gt;2&#x27; Chirality Transfer Reactions</title>
<link>http://dx.doi.org/10.1002/ejoc.201101634</link>
<dc:creator>Masamichi Ogasawara, Yonghui Ge, Atsushi Okada, Tamotsu Takahashi</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101634.jpg" width="355" height="67" alt="Effects of Silyl Substituents on the Palladium-Catalyzed Asymmetric Synthesis of Axially Chiral (Allenylmethyl)silanes and Their SE2&#x27; Chirality Transfer Reactions" title="Effects of Silyl Substituents on the Palladium-Catalyzed Asymmetric Synthesis of Axially Chiral (Allenylmethyl)silanes and Their SE2&#x27; Chirality Transfer Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Masamichi Ogasawara, Yonghui Ge, Atsushi Okada, Tamotsu Takahashi<br /><i>Eur. J. Org. Chem.</i>, January 30, 2012, DOI: 10.1002/ejoc.201101634. <a href="http://dx.doi.org/10.1002/ejoc.201101634">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101633">
<title>Selective Saccharide Recognition Using Modular Diboronic Acid Fluorescent Sensors</title>
<link>http://dx.doi.org/10.1002/ejoc.201101633</link>
<dc:creator>Zhitao Xing, Hui-Chen Wang, Yixiang Cheng, Chengjian Zhu, Tony D. James, Jianzhang Zhao</dc:creator>
<dc:date>2012-01-05T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101633.jpg" width="213" height="158" alt="Selective Saccharide Recognition Using Modular Diboronic Acid Fluorescent Sensors" title="Selective Saccharide Recognition Using Modular Diboronic Acid Fluorescent Sensors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Zhitao Xing, Hui-Chen Wang, Yixiang Cheng, Chengjian Zhu, Tony D. James, Jianzhang Zhao<br /><i>Eur. J. Org. Chem.</i>, January 5, 2012, DOI: 10.1002/ejoc.201101633. <a href="http://dx.doi.org/10.1002/ejoc.201101633">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101624">
<title>Promiscuous Behavior of &lt;I&gt;Rhizomucor miehei&lt;/I&gt; Lipase in the Synthesis of &lt;I&gt;N&lt;/I&gt;-Substituted &#x3B2;-Amino Esters</title>
<link>http://dx.doi.org/10.1002/ejoc.201101624</link>
<dc:creator>Leandro N. Monsalve, Florencia Gillanders, Alicia Baldessari</dc:creator>
<dc:date>2011-12-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101624.jpg" width="210" height="140" alt="Promiscuous Behavior of Rhizomucor miehei Lipase in the Synthesis of N-Substituted &beta;-Amino Esters" title="Promiscuous Behavior of Rhizomucor miehei Lipase in the Synthesis of N-Substituted &beta;-Amino Esters" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Leandro N. Monsalve, Florencia Gillanders, Alicia Baldessari<br /><i>Eur. J. Org. Chem.</i>, December 27, 2011, DOI: 10.1002/ejoc.201101624. <a href="http://dx.doi.org/10.1002/ejoc.201101624">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101623">
<title>A BODIPY-Based Highly Selective Fluorescent Chemosensor for Hg&lt;SUP&gt;2+&lt;/SUP&gt; Ions and Its Application in Living Cell Imaging</title>
<link>http://dx.doi.org/10.1002/ejoc.201101623</link>
<dc:creator>Mani Vedamalai, Shu-Pao Wu</dc:creator>
<dc:date>2012-01-04T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101623.jpg" width="315" height="176" alt="A BODIPY-Based Highly Selective Fluorescent Chemosensor for Hg2+ Ions and Its Application in Living Cell Imaging" title="A BODIPY-Based Highly Selective Fluorescent Chemosensor for Hg2+ Ions and Its Application in Living Cell Imaging" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Mani Vedamalai, Shu-Pao Wu<br /><i>Eur. J. Org. Chem.</i>, January 4, 2012, DOI: 10.1002/ejoc.201101623. <a href="http://dx.doi.org/10.1002/ejoc.201101623">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101619">
<title>Dendritic Architectures with Positively Charged Cores and Negatively Charged Shells</title>
<link>http://dx.doi.org/10.1002/ejoc.201101619</link>
<dc:creator>Torsten Schunk, Andreas Hirsch</dc:creator>
<dc:date>2011-12-21T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101619.jpg" width="213" height="228" alt="Dendritic Architectures with Positively Charged Cores and Negatively Charged Shells" title="Dendritic Architectures with Positively Charged Cores and Negatively Charged Shells" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Torsten Schunk, Andreas Hirsch<br /><i>Eur. J. Org. Chem.</i>, December 21, 2011, DOI: 10.1002/ejoc.201101619. <a href="http://dx.doi.org/10.1002/ejoc.201101619">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101615">
<title>1,2,4-Oxadiazole 4-Oxides as Nitrones in 1,3-Dipolar Cycloaddition Reactions to Vinyl Ethers</title>
<link>http://dx.doi.org/10.1002/ejoc.201101615</link>
<dc:creator>Paolo Quadrelli, Fabio Lunghi, Bruna Bovio, William Gautschi, Pierluigi Caramella</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101615.jpg" width="155" height="189" alt="1,2,4-Oxadiazole 4-Oxides as Nitrones in 1,3-Dipolar Cycloaddition Reactions to Vinyl Ethers" title="1,2,4-Oxadiazole 4-Oxides as Nitrones in 1,3-Dipolar Cycloaddition Reactions to Vinyl Ethers" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Paolo Quadrelli, Fabio Lunghi, Bruna Bovio, William Gautschi, Pierluigi Caramella<br /><i>Eur. J. Org. Chem.</i>, January 20, 2012, DOI: 10.1002/ejoc.201101615. <a href="http://dx.doi.org/10.1002/ejoc.201101615">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101614">
<title>Synthetic Studies of Sesquiterpenes with the Dunniane Skeleton</title>
<link>http://dx.doi.org/10.1002/ejoc.201101614</link>
<dc:creator>S&#xF2;nia Par&#xE9;s, Ramon Alib&#xE9;s, Marta Figueredo, Josep Font, Teodor Parella</dc:creator>
<dc:date>2012-01-12T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101614.jpg" width="377" height="67" alt="Synthetic Studies of Sesquiterpenes with the Dunniane Skeleton" title="Synthetic Studies of Sesquiterpenes with the Dunniane Skeleton" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />S&#xF2;nia Par&#xE9;s, Ramon Alib&#xE9;s, Marta Figueredo, Josep Font, Teodor Parella<br /><i>Eur. J. Org. Chem.</i>, January 12, 2012, DOI: 10.1002/ejoc.201101614. <a href="http://dx.doi.org/10.1002/ejoc.201101614">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101609">
<title>Biosynthesis and Total Synthesis Studies on the Jadomycin Family of Natural Products</title>
<link>http://dx.doi.org/10.1002/ejoc.201101609</link>
<dc:creator>Ehesan U. Sharif, George A. O&#x27;Doherty</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101609.jpg" width="370" height="108" alt="Biosynthesis and Total Synthesis Studies on the Jadomycin Family of Natural Products" title="Biosynthesis and Total Synthesis Studies on the Jadomycin Family of Natural Products" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Ehesan U. Sharif, George A. O&#x27;Doherty<br /><i>Eur. J. Org. Chem.</i>, January 13, 2012, DOI: 10.1002/ejoc.201101609. <a href="http://dx.doi.org/10.1002/ejoc.201101609">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101605">
<title>A Carbohydrate-Based Synthesis of the C13&#x2013;C22 Fragment of Amphidinolide X</title>
<link>http://dx.doi.org/10.1002/ejoc.201101605</link>
<dc:creator>Mukund K. Gurjar, Gorakh S. Yellol, Debendra K. Mohapatra</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101605.jpg" width="210" height="151" alt="A Carbohydrate-Based Synthesis of the C13&ndash;C22 Fragment of Amphidinolide X" title="A Carbohydrate-Based Synthesis of the C13&ndash;C22 Fragment of Amphidinolide X" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Mukund K. Gurjar, Gorakh S. Yellol, Debendra K. Mohapatra<br /><i>Eur. J. Org. Chem.</i>, February 6, 2012, DOI: 10.1002/ejoc.201101605. <a href="http://dx.doi.org/10.1002/ejoc.201101605">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101601">
<title>The First Stereoselective Total Synthesis of Putaminoxin E and Its Epimer and Evaluation of Their Biological Properties&lt;P&gt;Synthetic Studies on Natural Products, 53; Part 52: D. B. Shinde, B. S. Kanth, M. Srilatha, B. Das, Synthesis 2011, in press.&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101601</link>
<dc:creator>Chithaluri Sudhakar, Parigi Raghavendar Reddy, Chityal Ganesh Kumar, Pombala Sujitha, Biswanath Das</dc:creator>
<dc:date>2011-12-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101601.jpg" width="86" height="130" alt="The First Stereoselective Total Synthesis of Putaminoxin E and Its Epimer and Evaluation of Their Biological PropertiesSynthetic Studies on Natural Products, 53; Part 52: D. B. Shinde, B. S. Kanth, M. Srilatha, B. Das, Synthesis 2011, in press." title="The First Stereoselective Total Synthesis of Putaminoxin E and Its Epimer and Evaluation of Their Biological PropertiesSynthetic Studies on Natural Products, 53; Part 52: D. B. Shinde, B. S. Kanth, M. Srilatha, B. Das, Synthesis 2011, in press." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Chithaluri Sudhakar, Parigi Raghavendar Reddy, Chityal Ganesh Kumar, Pombala Sujitha, Biswanath Das<br /><i>Eur. J. Org. Chem.</i>, December 9, 2011, DOI: 10.1002/ejoc.201101601. <a href="http://dx.doi.org/10.1002/ejoc.201101601">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101599">
<title>Synthesis, Structure and Conformation of Terphenylene-Derived Oxacalixaromatics&lt;P&gt;Dedicated to Professor Wen-Qi Chen on the occasion of his 80th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101599</link>
<dc:creator>Wen-Jing Hu, Xiao-Li Zhao, Ming-Liang Ma, Fang Guo, Xian-Qiang Mi, Biao Jiang, Ke Wen</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101599.jpg" width="385" height="180" alt="Synthesis, Structure and Conformation of Terphenylene-Derived OxacalixaromaticsDedicated to Professor Wen-Qi Chen on the occasion of his 80th birthday" title="Synthesis, Structure and Conformation of Terphenylene-Derived OxacalixaromaticsDedicated to Professor Wen-Qi Chen on the occasion of his 80th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Wen-Jing Hu, Xiao-Li Zhao, Ming-Liang Ma, Fang Guo, Xian-Qiang Mi, Biao Jiang, Ke Wen<br /><i>Eur. J. Org. Chem.</i>, January 17, 2012, DOI: 10.1002/ejoc.201101599. <a href="http://dx.doi.org/10.1002/ejoc.201101599">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101595">
<title>Regioselective Photochemical C&#x2013;OMe Bond Formation Initiated by One-Electron Transfer and N&#x2013;OMe Bond Fragmentation in Electron Donor&#x2013;Acceptor Systems&lt;P&gt;Dedicated to the memory of Rafael Suau&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101595</link>
<dc:creator>Daniel Collado, Ezequiel Perez-Inestrosa</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101595.jpg" width="436" height="96" alt="Regioselective Photochemical C&ndash;OMe Bond Formation Initiated by One-Electron Transfer and N&ndash;OMe Bond Fragmentation in Electron Donor&ndash;Acceptor SystemsDedicated to the memory of Rafael Suau" title="Regioselective Photochemical C&ndash;OMe Bond Formation Initiated by One-Electron Transfer and N&ndash;OMe Bond Fragmentation in Electron Donor&ndash;Acceptor SystemsDedicated to the memory of Rafael Suau" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Daniel Collado, Ezequiel Perez-Inestrosa<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101595. <a href="http://dx.doi.org/10.1002/ejoc.201101595">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101592">
<title>Complex-Induced Proximity Effect in the Regioselective Lithiation of Pyridine Derivatives</title>
<link>http://dx.doi.org/10.1002/ejoc.201101592</link>
<dc:creator>Jaspreet S. Dhau, Amritpal Singh, Yoganjaneyulu Kasetti, P. V. Bharatam</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101592.jpg" width="292" height="139" alt="Complex-Induced Proximity Effect in the Regioselective Lithiation of Pyridine Derivatives" title="Complex-Induced Proximity Effect in the Regioselective Lithiation of Pyridine Derivatives" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Jaspreet S. Dhau, Amritpal Singh, Yoganjaneyulu Kasetti, P. V. Bharatam<br /><i>Eur. J. Org. Chem.</i>, February 3, 2012, DOI: 10.1002/ejoc.201101592. <a href="http://dx.doi.org/10.1002/ejoc.201101592">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101587">
<title>Assignment of Absolute Configuration of Bis-&#x3B3;-pyrone Polypropionates from Marine Pulmonate Molluscs</title>
<link>http://dx.doi.org/10.1002/ejoc.201101587</link>
<dc:creator>Jian-Rong Wang, Marianna Carbone, Margherita Gavagnin, Attila M&#xE1;ndi, S&#xE1;ndor Antus, Li-Gong Yao, Guido Cimino, Tibor Kurt&#xE1;n, Yue-Wei Guo</dc:creator>
<dc:date>2012-01-18T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101587.jpg" width="198" height="195" alt="Assignment of Absolute Configuration of Bis-&gamma;-pyrone Polypropionates from Marine Pulmonate Molluscs" title="Assignment of Absolute Configuration of Bis-&gamma;-pyrone Polypropionates from Marine Pulmonate Molluscs" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Jian-Rong Wang, Marianna Carbone, Margherita Gavagnin, Attila M&#xE1;ndi, S&#xE1;ndor Antus, Li-Gong Yao, Guido Cimino, Tibor Kurt&#xE1;n, Yue-Wei Guo<br /><i>Eur. J. Org. Chem.</i>, January 18, 2012, DOI: 10.1002/ejoc.201101587. <a href="http://dx.doi.org/10.1002/ejoc.201101587">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101584">
<title>Design of New Tetrazine&#x2013;Triphenylamine Bichromophores &#x2013; Fluorescent Switching by Chemical Oxidation</title>
<link>http://dx.doi.org/10.1002/ejoc.201101584</link>
<dc:creator>Cassandre Quinton, Val&#xE9;rie Alain-Rizzo, C&#xE9;cile Dumas-Verdes, Gilles Clavier, Fabien Miomandre, Pierre Audebert</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101584.jpg" width="213" height="146" alt="Design of New Tetrazine&ndash;Triphenylamine Bichromophores &ndash; Fluorescent Switching by Chemical Oxidation" title="Design of New Tetrazine&ndash;Triphenylamine Bichromophores &ndash; Fluorescent Switching by Chemical Oxidation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Cassandre Quinton, Val&#xE9;rie Alain-Rizzo, C&#xE9;cile Dumas-Verdes, Gilles Clavier, Fabien Miomandre, Pierre Audebert<br /><i>Eur. J. Org. Chem.</i>, January 9, 2012, DOI: 10.1002/ejoc.201101584. <a href="http://dx.doi.org/10.1002/ejoc.201101584">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101583">
<title>Synthesis and Study of Oxadisilole-Fused Benzisoxazoles or Naphthisoxazoles</title>
<link>http://dx.doi.org/10.1002/ejoc.201101583</link>
<dc:creator>Xuyan Ma, Yali Chen, Yajuan Zhang, Di Xu, Weiguo Cao, Jie Chen</dc:creator>
<dc:date>2012-01-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101583.jpg" width="207" height="144" alt="Synthesis and Study of Oxadisilole-Fused Benzisoxazoles or Naphthisoxazoles" title="Synthesis and Study of Oxadisilole-Fused Benzisoxazoles or Naphthisoxazoles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Xuyan Ma, Yali Chen, Yajuan Zhang, Di Xu, Weiguo Cao, Jie Chen<br /><i>Eur. J. Org. Chem.</i>, January 16, 2012, DOI: 10.1002/ejoc.201101583. <a href="http://dx.doi.org/10.1002/ejoc.201101583">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101576">
<title>Synthesis and Evaluation of Lipophilic BTBP Ligands for An/Ln Separation in Nuclear Waste Treatment: The Effect of Alkyl Substitution on Extraction Properties and Implications for Ligand Design</title>
<link>http://dx.doi.org/10.1002/ejoc.201101576</link>
<dc:creator>Frank W. Lewis, Laurence M. Harwood, Michael J. Hudson, Petr Distler, Jan John, Karel Stamberg, Ana N&#xFA;&#xF1;ez, Hitos Gal&#xE1;n, Amparo G. Espartero</dc:creator>
<dc:date>2012-01-12T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101576.jpg" width="213" height="136" alt="Synthesis and Evaluation of Lipophilic BTBP Ligands for An/Ln Separation in Nuclear Waste Treatment: The Effect of Alkyl Substitution on Extraction Properties and Implications for Ligand Design" title="Synthesis and Evaluation of Lipophilic BTBP Ligands for An/Ln Separation in Nuclear Waste Treatment: The Effect of Alkyl Substitution on Extraction Properties and Implications for Ligand Design" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Frank W. Lewis, Laurence M. Harwood, Michael J. Hudson, Petr Distler, Jan John, Karel Stamberg, Ana N&#xFA;&#xF1;ez, Hitos Gal&#xE1;n, Amparo G. Espartero<br /><i>Eur. J. Org. Chem.</i>, January 12, 2012, DOI: 10.1002/ejoc.201101576. <a href="http://dx.doi.org/10.1002/ejoc.201101576">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101563">
<title>Biosynthesis of Defensive Coccinellidae Alkaloids: Incorporation of Fatty Acids in Adaline, Coccinelline, and Harmonine</title>
<link>http://dx.doi.org/10.1002/ejoc.201101563</link>
<dc:creator>Eveline Haulotte, Pascal Laurent, and Jean-Claude Braekman</dc:creator>
<dc:date>2012-01-04T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101563.jpg" width="315" height="124" alt="Biosynthesis of Defensive Coccinellidae Alkaloids: Incorporation of Fatty Acids in Adaline, Coccinelline, and Harmonine" title="Biosynthesis of Defensive Coccinellidae Alkaloids: Incorporation of Fatty Acids in Adaline, Coccinelline, and Harmonine" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Eveline Haulotte, Pascal Laurent, and Jean-Claude Braekman<br /><i>Eur. J. Org. Chem.</i>, January 4, 2012, DOI: 10.1002/ejoc.201101563. <a href="http://dx.doi.org/10.1002/ejoc.201101563">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101543">
<title>An Ammonia-Triggered Stereocontrolled Conversion of a &#x3B3;-Lactone to the Central Tetrahydropyran of Pederin, Psymberin, and Onnamides D&#x2013;F&lt;P&gt;Dedicated to Professor Philip Kocienski, FRS&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101543</link>
<dc:creator>William J. Buffham, Nigel A. Swain, Sarah L. Kostiuk, Th&#xE9;o P. Gon&#xE7;alves, David C. Harrowven</dc:creator>
<dc:date>2012-01-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101543.jpg" width="448" height="123" alt="An Ammonia-Triggered Stereocontrolled Conversion of a &gamma;-Lactone to the Central Tetrahydropyran of Pederin, Psymberin, and Onnamides D&ndash;FDedicated to Professor Philip Kocienski, FRS" title="An Ammonia-Triggered Stereocontrolled Conversion of a &gamma;-Lactone to the Central Tetrahydropyran of Pederin, Psymberin, and Onnamides D&ndash;FDedicated to Professor Philip Kocienski, FRS" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />William J. Buffham, Nigel A. Swain, Sarah L. Kostiuk, Th&#xE9;o P. Gon&#xE7;alves, David C. Harrowven<br /><i>Eur. J. Org. Chem.</i>, January 11, 2012, DOI: 10.1002/ejoc.201101543. <a href="http://dx.doi.org/10.1002/ejoc.201101543">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101540">
<title>&lt;I&gt;N&lt;/I&gt;&lt;SUP&gt;1&lt;/SUP&gt;-Functionalized Indole-Phosphane Oxazoline (IndPHOX) Ligands in Asymmetric Allylic Substitution Reactions</title>
<link>http://dx.doi.org/10.1002/ejoc.201101540</link>
<dc:creator>Yu Wang, Matti J. P. Vaismaa, Kari Rissanen, Robert Franz&#xE9;n</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101540.jpg" width="321" height="58" alt="N1-Functionalized Indole-Phosphane Oxazoline (IndPHOX) Ligands in Asymmetric Allylic Substitution Reactions" title="N1-Functionalized Indole-Phosphane Oxazoline (IndPHOX) Ligands in Asymmetric Allylic Substitution Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Yu Wang, Matti J. P. Vaismaa, Kari Rissanen, Robert Franz&#xE9;n<br /><i>Eur. J. Org. Chem.</i>, January 25, 2012, DOI: 10.1002/ejoc.201101540. <a href="http://dx.doi.org/10.1002/ejoc.201101540">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101539">
<title>Stereoselective Dihydroxylation Reaction of Alkenyl &#x3B2;-&lt;span style="font-variant:small-caps"&gt;D&lt;/span&gt;-Hexopyranosides: A Methodology for the Synthesis of Glycosylglycerol Derivatives and 1-&lt;I&gt;O&lt;/I&gt;-Acyl-3-&lt;I&gt;O&lt;/I&gt;-&#x3B2;-&lt;span style="font-variant:small-caps"&gt;D&lt;/span&gt;-glycosyl-&lt;I&gt;sn&lt;/I&gt;-glycerol Analogues</title>
<link>http://dx.doi.org/10.1002/ejoc.201101539</link>
<dc:creator>Jos&#xE9; M. Vega-P&#xE9;rez, Carlos Palo-Nieto, Ignacio Peri&#xF1;&#xE1;n, Margarita Vega-Holm, Jos&#xE9; M. Calder&#xF3;n-Monta&#xF1;o, Miguel L&#xF3;pez-L&#xE1;zaro, Fernando Iglesias-Guerra</dc:creator>
<dc:date>2011-12-29T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101539.jpg" width="331" height="152" alt="Stereoselective Dihydroxylation Reaction of Alkenyl &beta;-D-Hexopyranosides: A Methodology for the Synthesis of Glycosylglycerol Derivatives and 1-O-Acyl-3-O-&beta;-D-glycosyl-sn-glycerol Analogues" title="Stereoselective Dihydroxylation Reaction of Alkenyl &beta;-D-Hexopyranosides: A Methodology for the Synthesis of Glycosylglycerol Derivatives and 1-O-Acyl-3-O-&beta;-D-glycosyl-sn-glycerol Analogues" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Jos&#xE9; M. Vega-P&#xE9;rez, Carlos Palo-Nieto, Ignacio Peri&#xF1;&#xE1;n, Margarita Vega-Holm, Jos&#xE9; M. Calder&#xF3;n-Monta&#xF1;o, Miguel L&#xF3;pez-L&#xE1;zaro, Fernando Iglesias-Guerra<br /><i>Eur. J. Org. Chem.</i>, December 29, 2011, DOI: 10.1002/ejoc.201101539. <a href="http://dx.doi.org/10.1002/ejoc.201101539">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101535">
<title>The New Age of Electrophilic Perfluoroalkylation Reactions&lt;P&gt;Dedicated to the memory of Professor Lev Yagupolskii&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101535</link>
<dc:creator>Yohan Mac&#xE9;, Emmanuel Magnier</dc:creator>
<dc:date>2012-01-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101535.jpg" width="175" height="130" alt="The New Age of Electrophilic Perfluoroalkylation ReactionsDedicated to the memory of Professor Lev Yagupolskii" title="The New Age of Electrophilic Perfluoroalkylation ReactionsDedicated to the memory of Professor Lev Yagupolskii" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Yohan Mac&#xE9;, Emmanuel Magnier<br /><i>Eur. J. Org. Chem.</i>, January 11, 2012, DOI: 10.1002/ejoc.201101535. <a href="http://dx.doi.org/10.1002/ejoc.201101535">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101529">
<title>Highly Enantioselective Synthesis of Spiro[cyclohexanone-oxindoles] and Spiro[cyclohexanone-pyrazolones] by Asymmetric Cascade [5+1] Double Michael Reactions</title>
<link>http://dx.doi.org/10.1002/ejoc.201101529</link>
<dc:creator>Bin Wu, Jian Chen, Mei-Qiu Li, Jin-Xin Zhang, Xiao-Ping Xu, Shun-Jun Ji, Xing-Wang Wang</dc:creator>
<dc:date>2012-01-04T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101529.jpg" width="377" height="132" alt="Highly Enantioselective Synthesis of Spiro[cyclohexanone-oxindoles] and Spiro[cyclohexanone-pyrazolones] by Asymmetric Cascade [5+1] Double Michael Reactions" title="Highly Enantioselective Synthesis of Spiro[cyclohexanone-oxindoles] and Spiro[cyclohexanone-pyrazolones] by Asymmetric Cascade [5+1] Double Michael Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Bin Wu, Jian Chen, Mei-Qiu Li, Jin-Xin Zhang, Xiao-Ping Xu, Shun-Jun Ji, Xing-Wang Wang<br /><i>Eur. J. Org. Chem.</i>, January 4, 2012, DOI: 10.1002/ejoc.201101529. <a href="http://dx.doi.org/10.1002/ejoc.201101529">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101525">
<title>Recent Advances in the Total Synthesis of Chlorosulfolipids</title>
<link>http://dx.doi.org/10.1002/ejoc.201101525</link>
<dc:creator>Christian Nilewski, Erick M. Carreira</dc:creator>
<dc:date>2012-01-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101525.jpg" width="207" height="186" alt="Recent Advances in the Total Synthesis of Chlorosulfolipids" title="Recent Advances in the Total Synthesis of Chlorosulfolipids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Christian Nilewski, Erick M. Carreira<br /><i>Eur. J. Org. Chem.</i>, January 19, 2012, DOI: 10.1002/ejoc.201101525. <a href="http://dx.doi.org/10.1002/ejoc.201101525">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101518">
<title>Synthesis of Difluoromethyl-Containing &#x3B1;-Acyloxycarboxamide Derivatives through a Passerini Reaction and Desulfonylation</title>
<link>http://dx.doi.org/10.1002/ejoc.201101518</link>
<dc:creator>Jingjing Wu, Wenwen Zhao, Song Cao</dc:creator>
<dc:date>2012-01-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101518.jpg" width="430" height="60" alt="Synthesis of Difluoromethyl-Containing &alpha;-Acyloxycarboxamide Derivatives through a Passerini Reaction and Desulfonylation" title="Synthesis of Difluoromethyl-Containing &alpha;-Acyloxycarboxamide Derivatives through a Passerini Reaction and Desulfonylation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Jingjing Wu, Wenwen Zhao, Song Cao<br /><i>Eur. J. Org. Chem.</i>, January 23, 2012, DOI: 10.1002/ejoc.201101518. <a href="http://dx.doi.org/10.1002/ejoc.201101518">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101509">
<title>Enantioselective Organocatalytic &#x3B1;-Alkylation of Ketones by S&lt;sub&gt;N&lt;/sub&gt;1-Type Reaction of Alcohols</title>
<link>http://dx.doi.org/10.1002/ejoc.201101509</link>
<dc:creator>Maria Trifonidou, Christoforos G. Kokotos</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101509.jpg" width="311" height="113" alt="Enantioselective Organocatalytic &alpha;-Alkylation of Ketones by SN1-Type Reaction of Alcohols" title="Enantioselective Organocatalytic &alpha;-Alkylation of Ketones by SN1-Type Reaction of Alcohols" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Maria Trifonidou, Christoforos G. Kokotos<br /><i>Eur. J. Org. Chem.</i>, January 20, 2012, DOI: 10.1002/ejoc.201101509. <a href="http://dx.doi.org/10.1002/ejoc.201101509">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101505">
<title>An Efficient Multigram Synthesis of Alkannin and Shikonin</title>
<link>http://dx.doi.org/10.1002/ejoc.201101505</link>
<dc:creator>Rubing Wang, Shanshan Zhou, Hudagula Jiang, Xiaogang Zheng, Wen Zhou, Shaoshun Li</dc:creator>
<dc:date>2012-01-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101505.jpg" width="377" height="140" alt="An Efficient Multigram Synthesis of Alkannin and Shikonin" title="An Efficient Multigram Synthesis of Alkannin and Shikonin" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Rubing Wang, Shanshan Zhou, Hudagula Jiang, Xiaogang Zheng, Wen Zhou, Shaoshun Li<br /><i>Eur. J. Org. Chem.</i>, January 11, 2012, DOI: 10.1002/ejoc.201101505. <a href="http://dx.doi.org/10.1002/ejoc.201101505">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101499">
<title>Rapid Room-Temperature &lt;SUP&gt;11&lt;/SUP&gt;C-Methylation of Arylamines with [&lt;SUP&gt;11&lt;/SUP&gt;C]Methyl Iodide Promoted by Solid Inorganic-Bases in DMF</title>
<link>http://dx.doi.org/10.1002/ejoc.201101499</link>
<dc:creator>Lisheng Cai, Rong Xu, Xuelei Guo, Victor W. Pike</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101499.jpg" width="157" height="142" alt="Rapid Room-Temperature 11C-Methylation of Arylamines with [11C]Methyl Iodide Promoted by Solid Inorganic-Bases in DMF" title="Rapid Room-Temperature 11C-Methylation of Arylamines with [11C]Methyl Iodide Promoted by Solid Inorganic-Bases in DMF" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Lisheng Cai, Rong Xu, Xuelei Guo, Victor W. Pike<br /><i>Eur. J. Org. Chem.</i>, January 9, 2012, DOI: 10.1002/ejoc.201101499. <a href="http://dx.doi.org/10.1002/ejoc.201101499">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101498">
<title>Trapping and Analysing Wheland&#x2013;Meisenheimer &#x3C3; Complexes, Usually Labile and Escaping Intermediates</title>
<link>http://dx.doi.org/10.1002/ejoc.201101498</link>
<dc:creator>Luciano Forlani, Carla Boga, Andrea Mazzanti, Nicola Zanna</dc:creator>
<dc:date>2011-12-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101498.jpg" width="424" height="101" alt="Trapping and Analysing Wheland&ndash;Meisenheimer &sigma; Complexes, Usually Labile and Escaping Intermediates" title="Trapping and Analysing Wheland&ndash;Meisenheimer &sigma; Complexes, Usually Labile and Escaping Intermediates" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Luciano Forlani, Carla Boga, Andrea Mazzanti, Nicola Zanna<br /><i>Eur. J. Org. Chem.</i>, December 23, 2011, DOI: 10.1002/ejoc.201101498. <a href="http://dx.doi.org/10.1002/ejoc.201101498">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101495">
<title>Glaser Coupling of 4-Ethynyl[2.2]paracyclophane: The Formation of Two Diastereomers&lt;P&gt;Cyclophanes, 68. Part 67: H. Hopf, H. Hinrichs, L. Ernst, P. G. Jones, V. Boekelheide, &lt;I&gt;Isr. J. Chem&lt;/I&gt;., in press.&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101495</link>
<dc:creator>Henning Hopf, Ina Dix, Vitaly Raev, Ludger Ernst</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101495.jpg" width="165" height="144" alt="Glaser Coupling of 4-Ethynyl[2.2]paracyclophane: The Formation of Two DiastereomersCyclophanes, 68. Part 67: H. Hopf, H. Hinrichs, L. Ernst, P. G. Jones, V. Boekelheide, Isr. J. Chem., in press." title="Glaser Coupling of 4-Ethynyl[2.2]paracyclophane: The Formation of Two DiastereomersCyclophanes, 68. Part 67: H. Hopf, H. Hinrichs, L. Ernst, P. G. Jones, V. Boekelheide, Isr. J. Chem., in press." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Henning Hopf, Ina Dix, Vitaly Raev, Ludger Ernst<br /><i>Eur. J. Org. Chem.</i>, January 26, 2012, DOI: 10.1002/ejoc.201101495. <a href="http://dx.doi.org/10.1002/ejoc.201101495">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101491">
<title>Efficient Synthesis of Arylated Flavones by Site-Selective Suzuki&#x2013;Miyaura Cross-Coupling Reactions of the Bis(triflate) of 5,7- and 7,8-Dihydroxyflavone</title>
<link>http://dx.doi.org/10.1002/ejoc.201101491</link>
<dc:creator>Nadi Eleya, Imran Malik, Sebastian Reimann, Kai Wittler, Martin Hein, Tam&#xE1;s Patonay, Alexander Villinger, Ralf Ludwig, Peter Langer</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101491.jpg" width="370" height="81" alt="Efficient Synthesis of Arylated Flavones by Site-Selective Suzuki&ndash;Miyaura Cross-Coupling Reactions of the Bis(triflate) of 5,7- and 7,8-Dihydroxyflavone" title="Efficient Synthesis of Arylated Flavones by Site-Selective Suzuki&ndash;Miyaura Cross-Coupling Reactions of the Bis(triflate) of 5,7- and 7,8-Dihydroxyflavone" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Nadi Eleya, Imran Malik, Sebastian Reimann, Kai Wittler, Martin Hein, Tam&#xE1;s Patonay, Alexander Villinger, Ralf Ludwig, Peter Langer<br /><i>Eur. J. Org. Chem.</i>, January 30, 2012, DOI: 10.1002/ejoc.201101491. <a href="http://dx.doi.org/10.1002/ejoc.201101491">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101489">
<title>Nonenzymatic Acylative Kinetic Resolution of Racemic Amines and Related Compounds</title>
<link>http://dx.doi.org/10.1002/ejoc.201101489</link>
<dc:creator>Victor P. Krasnov, Dmitry A. Gruzdev, Galina L. Levit</dc:creator>
<dc:date>2011-12-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101489.jpg" width="213" height="184" alt="Nonenzymatic Acylative Kinetic Resolution of Racemic Amines and Related Compounds" title="Nonenzymatic Acylative Kinetic Resolution of Racemic Amines and Related Compounds" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Victor P. Krasnov, Dmitry A. Gruzdev, Galina L. Levit<br /><i>Eur. J. Org. Chem.</i>, December 16, 2011, DOI: 10.1002/ejoc.201101489. <a href="http://dx.doi.org/10.1002/ejoc.201101489">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101484">
<title>Tetrakis(tetrathiafulvalene&#x2013;tetrathiacrown ether)porphyrazine Triads: Synthesis, Photophysical, and Electrochemical Properties</title>
<link>http://dx.doi.org/10.1002/ejoc.201101484</link>
<dc:creator>Ruibin Hou, Bao Li, Keli Zhong, Hongda Li, Long-Yi Jin, Bingzhu Yin</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101484.jpg" width="213" height="217" alt="Tetrakis(tetrathiafulvalene&ndash;tetrathiacrown ether)porphyrazine Triads: Synthesis, Photophysical, and Electrochemical Properties" title="Tetrakis(tetrathiafulvalene&ndash;tetrathiacrown ether)porphyrazine Triads: Synthesis, Photophysical, and Electrochemical Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Ruibin Hou, Bao Li, Keli Zhong, Hongda Li, Long-Yi Jin, Bingzhu Yin<br /><i>Eur. J. Org. Chem.</i>, January 9, 2012, DOI: 10.1002/ejoc.201101484. <a href="http://dx.doi.org/10.1002/ejoc.201101484">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101480">
<title>Polynuclear Copper(I) Complexes with Chelating Bis- and Tris-&lt;I&gt;N&lt;/I&gt;-Heterocyclic Carbene Ligands: Catalytic Activity in Nitrene and Carbene Transfer Reactions</title>
<link>http://dx.doi.org/10.1002/ejoc.201101480</link>
<dc:creator>Cristina Tubaro, Andrea Biffis, Riccardo Gava, Elena Scattolin, Andrea Volpe, Marino Basato, M. Mar D&#xED;az-Requejo, Pedro J. Perez</dc:creator>
<dc:date>2012-01-18T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101480.jpg" width="213" height="182" alt="Polynuclear Copper(I) Complexes with Chelating Bis- and Tris-N-Heterocyclic Carbene Ligands: Catalytic Activity in Nitrene and Carbene Transfer Reactions" title="Polynuclear Copper(I) Complexes with Chelating Bis- and Tris-N-Heterocyclic Carbene Ligands: Catalytic Activity in Nitrene and Carbene Transfer Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Cristina Tubaro, Andrea Biffis, Riccardo Gava, Elena Scattolin, Andrea Volpe, Marino Basato, M. Mar D&#xED;az-Requejo, Pedro J. Perez<br /><i>Eur. J. Org. Chem.</i>, January 18, 2012, DOI: 10.1002/ejoc.201101480. <a href="http://dx.doi.org/10.1002/ejoc.201101480">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101477">
<title>Towards the Total Synthesis of Mycaperoxide B: Probing Biosynthetic Rationale</title>
<link>http://dx.doi.org/10.1002/ejoc.201101477</link>
<dc:creator>Eduarda M. P. Silva, Richard J. Pye, Geoffrey D. Brown, Laurence M. Harwood</dc:creator>
<dc:date>2011-12-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101477.jpg" width="409" height="75" alt="Towards the Total Synthesis of Mycaperoxide B: Probing Biosynthetic Rationale" title="Towards the Total Synthesis of Mycaperoxide B: Probing Biosynthetic Rationale" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Eduarda M. P. Silva, Richard J. Pye, Geoffrey D. Brown, Laurence M. Harwood<br /><i>Eur. J. Org. Chem.</i>, December 27, 2011, DOI: 10.1002/ejoc.201101477. <a href="http://dx.doi.org/10.1002/ejoc.201101477">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101470">
<title>&lt;I&gt;N&lt;/I&gt;-Acylpyrroles: More Than Amides</title>
<link>http://dx.doi.org/10.1002/ejoc.201101470</link>
<dc:creator>Anna M. Goldys, Christopher S. P. McErlean</dc:creator>
<dc:date>2011-12-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101470.jpg" width="195" height="138" alt="N-Acylpyrroles: More Than Amides" title="N-Acylpyrroles: More Than Amides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Anna M. Goldys, Christopher S. P. McErlean<br /><i>Eur. J. Org. Chem.</i>, December 20, 2011, DOI: 10.1002/ejoc.201101470. <a href="http://dx.doi.org/10.1002/ejoc.201101470">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101463">
<title>Sulfur&#x2013;Nitrogen and Carbon&#x2013;Nitrogen Bond Formation by Intermolecular Imination and Amidation without Catalyst</title>
<link>http://dx.doi.org/10.1002/ejoc.201101463</link>
<dc:creator>Wen Bo Ma, Sheng Nan Li, Zhong Hua Zhou, Heng Shui Shen, Xue Li, Qiu Sun, Ling He, Ying Xue</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101463.jpg" width="207" height="111" alt="Sulfur&ndash;Nitrogen and Carbon&ndash;Nitrogen Bond Formation by Intermolecular Imination and Amidation without Catalyst" title="Sulfur&ndash;Nitrogen and Carbon&ndash;Nitrogen Bond Formation by Intermolecular Imination and Amidation without Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Wen Bo Ma, Sheng Nan Li, Zhong Hua Zhou, Heng Shui Shen, Xue Li, Qiu Sun, Ling He, Ying Xue<br /><i>Eur. J. Org. Chem.</i>, January 26, 2012, DOI: 10.1002/ejoc.201101463. <a href="http://dx.doi.org/10.1002/ejoc.201101463">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101462">
<title>Studies on the Diastereoselective Intramolecular Pauson&#x2013;Khand Reaction on Regioisomeric Chiral Perhydrobenzoxazines Derived from (&#x2013;)-8-Aminomenthol</title>
<link>http://dx.doi.org/10.1002/ejoc.201101462</link>
<dc:creator>Alicia Maestro, Rafael Pedrosa, Alfonso P&#xE9;rez-Encabo, Juan J. P&#xE9;rez-Rueda</dc:creator>
<dc:date>2011-12-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101462.jpg" width="206" height="197" alt="Studies on the Diastereoselective Intramolecular Pauson&ndash;Khand Reaction on Regioisomeric Chiral Perhydrobenzoxazines Derived from (&ndash;)-8-Aminomenthol" title="Studies on the Diastereoselective Intramolecular Pauson&ndash;Khand Reaction on Regioisomeric Chiral Perhydrobenzoxazines Derived from (&ndash;)-8-Aminomenthol" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Alicia Maestro, Rafael Pedrosa, Alfonso P&#xE9;rez-Encabo, Juan J. P&#xE9;rez-Rueda<br /><i>Eur. J. Org. Chem.</i>, December 27, 2011, DOI: 10.1002/ejoc.201101462. <a href="http://dx.doi.org/10.1002/ejoc.201101462">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101454">
<title>Copper-Catalyzed Cascade Reaction of 4-Iodopyrazole Derivatives with Amidines for the Synthesis of Pyrazolo[4,3-&lt;I&gt;d&lt;/I&gt;]pyrimidine Derivatives&lt;P&gt;CDRI Communication Number 8161&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101454</link>
<dc:creator>Maloy Nayak, Neeraj Rastogi, Sanjay Batra</dc:creator>
<dc:date>2012-01-10T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101454.jpg" width="213" height="102" alt="Copper-Catalyzed Cascade Reaction of 4-Iodopyrazole Derivatives with Amidines for the Synthesis of Pyrazolo[4,3-d]pyrimidine DerivativesCDRI Communication Number 8161" title="Copper-Catalyzed Cascade Reaction of 4-Iodopyrazole Derivatives with Amidines for the Synthesis of Pyrazolo[4,3-d]pyrimidine DerivativesCDRI Communication Number 8161" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Maloy Nayak, Neeraj Rastogi, Sanjay Batra<br /><i>Eur. J. Org. Chem.</i>, January 10, 2012, DOI: 10.1002/ejoc.201101454. <a href="http://dx.doi.org/10.1002/ejoc.201101454">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101450">
<title>Synthesis, Spectroscopic and Thermal Characterization of Azido-1,2,4-triazoles: A Class of Heteroarenes with a High Nitrogen Content</title>
<link>http://dx.doi.org/10.1002/ejoc.201101450</link>
<dc:creator>Paolo Cardillo, Marco Dellavedova, Lucia Gigante, Angelo Lunghi, Christian Pasturenzi, Elisabetta Salatelli, Paolo Zanirato</dc:creator>
<dc:date>2011-12-29T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101450.jpg" width="213" height="184" alt="Synthesis, Spectroscopic and Thermal Characterization of Azido-1,2,4-triazoles: A Class of Heteroarenes with a High Nitrogen Content" title="Synthesis, Spectroscopic and Thermal Characterization of Azido-1,2,4-triazoles: A Class of Heteroarenes with a High Nitrogen Content" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Paolo Cardillo, Marco Dellavedova, Lucia Gigante, Angelo Lunghi, Christian Pasturenzi, Elisabetta Salatelli, Paolo Zanirato<br /><i>Eur. J. Org. Chem.</i>, December 29, 2011, DOI: 10.1002/ejoc.201101450. <a href="http://dx.doi.org/10.1002/ejoc.201101450">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101449">
<title>A Synthetic Overview of Radiolabeled Compounds for &#x3B2;-Amyloid Targeting</title>
<link>http://dx.doi.org/10.1002/ejoc.201101449</link>
<dc:creator>Goreti Ribeiro Morais, Ant&#xF3;nio Paulo, Isabel Santos</dc:creator>
<dc:date>2011-12-28T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101449.jpg" width="272" height="160" alt="A Synthetic Overview of Radiolabeled Compounds for &beta;-Amyloid Targeting" title="A Synthetic Overview of Radiolabeled Compounds for &beta;-Amyloid Targeting" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Goreti Ribeiro Morais, Ant&#xF3;nio Paulo, Isabel Santos<br /><i>Eur. J. Org. Chem.</i>, December 28, 2011, DOI: 10.1002/ejoc.201101449. <a href="http://dx.doi.org/10.1002/ejoc.201101449">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101442">
<title>New Anthracene Derivatives &#x2013; Structure Elucidation and Antimicrobial Activity</title>
<link>http://dx.doi.org/10.1002/ejoc.201101442</link>
<dc:creator>Abdessamad Debbab, Amal H. Aly, Ruangelie Edrada-Ebel, Victor Wray, Alexander Pretsch, Gennaro Pescitelli, Tibor Kurtan, Peter Proksch</dc:creator>
<dc:date>2012-01-10T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101442.jpg" width="213" height="161" alt="New Anthracene Derivatives &ndash; Structure Elucidation and Antimicrobial Activity" title="New Anthracene Derivatives &ndash; Structure Elucidation and Antimicrobial Activity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Abdessamad Debbab, Amal H. Aly, Ruangelie Edrada-Ebel, Victor Wray, Alexander Pretsch, Gennaro Pescitelli, Tibor Kurtan, Peter Proksch<br /><i>Eur. J. Org. Chem.</i>, January 10, 2012, DOI: 10.1002/ejoc.201101442. <a href="http://dx.doi.org/10.1002/ejoc.201101442">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101434">
<title>Site-Directed Spin Labelling of Nucleic Acids</title>
<link>http://dx.doi.org/10.1002/ejoc.201101434</link>
<dc:creator>Sandip A. Shelke, Snorri Th. Sigurdsson</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101434.jpg" width="213" height="211" alt="Site-Directed Spin Labelling of Nucleic Acids" title="Site-Directed Spin Labelling of Nucleic Acids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Sandip A. Shelke, Snorri Th. Sigurdsson<br /><i>Eur. J. Org. Chem.</i>, January 13, 2012, DOI: 10.1002/ejoc.201101434. <a href="http://dx.doi.org/10.1002/ejoc.201101434">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101421">
<title>Segment Solid-Phase Total Synthesis of the Anthelmintic Cyclooctadepsipeptides PF1022A and Emodepside</title>
<link>http://dx.doi.org/10.1002/ejoc.201101421</link>
<dc:creator>J&#xFC;rgen Scherkenbeck, Sebastian L&#xFC;ttenberg, Monika Ludwig, Karin Br&#xFC;cher, Andreas Kotthaus</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101421.jpg" width="151" height="114" alt="Segment Solid-Phase Total Synthesis of the Anthelmintic Cyclooctadepsipeptides PF1022A and Emodepside" title="Segment Solid-Phase Total Synthesis of the Anthelmintic Cyclooctadepsipeptides PF1022A and Emodepside" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />J&#xFC;rgen Scherkenbeck, Sebastian L&#xFC;ttenberg, Monika Ludwig, Karin Br&#xFC;cher, Andreas Kotthaus<br /><i>Eur. J. Org. Chem.</i>, January 24, 2012, DOI: 10.1002/ejoc.201101421. <a href="http://dx.doi.org/10.1002/ejoc.201101421">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101356">
<title>Concave Annelated Terpyridines&lt;P&gt;Concave Reagents, 61; Part 60: D. Stoltenberg, S. L&#xFC;thje, O. Winkelmann, C. N&#xE4;ther, U. L&#xFC;ning, &lt;I&gt;Eur. J. Org. Chem.&lt;/I&gt; &lt;B&gt;2011&lt;/B&gt;, 5845&#x2013;5859.&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101356</link>
<dc:creator>Ulrich L&#xFC;ning, Timo Liebig</dc:creator>
<dc:date>2012-01-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101356.jpg" width="101" height="84" alt="Concave Annelated TerpyridinesConcave Reagents, 61; Part 60: D. Stoltenberg, S. L&uuml;thje, O. Winkelmann, C. N&auml;ther, U. L&uuml;ning, Eur. J. Org. Chem. 2011, 5845&ndash;5859." title="Concave Annelated TerpyridinesConcave Reagents, 61; Part 60: D. Stoltenberg, S. L&uuml;thje, O. Winkelmann, C. N&auml;ther, U. L&uuml;ning, Eur. J. Org. Chem. 2011, 5845&ndash;5859." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Ulrich L&#xFC;ning, Timo Liebig<br /><i>Eur. J. Org. Chem.</i>, January 11, 2012, DOI: 10.1002/ejoc.201101356. <a href="http://dx.doi.org/10.1002/ejoc.201101356">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101320">
<title>Silicone-Supported &lt;I&gt;Cinchona&lt;/I&gt; Alkaloid Derivatives as Insoluble Organocatalysts in the Enantioselective Dimerization of Ketenes</title>
<link>http://dx.doi.org/10.1002/ejoc.201101320</link>
<dc:creator>Damiano Cancogni, Alessandro Mandoli, Ravindra P. Jumde, Dario Pini</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101320.jpg" width="210" height="132" alt="Silicone-Supported Cinchona Alkaloid Derivatives as Insoluble Organocatalysts in the Enantioselective Dimerization of Ketenes" title="Silicone-Supported Cinchona Alkaloid Derivatives as Insoluble Organocatalysts in the Enantioselective Dimerization of Ketenes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Damiano Cancogni, Alessandro Mandoli, Ravindra P. Jumde, Dario Pini<br /><i>Eur. J. Org. Chem.</i>, January 25, 2012, DOI: 10.1002/ejoc.201101320. <a href="http://dx.doi.org/10.1002/ejoc.201101320">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101301">
<title>Facial Selectivity in the Diels&#x2013;Alder Reactions of 2,2-Disubstituted Cyclopent-4-ene-1,3-dione Derivatives and a Computational Examination of the Facial Selectivity of the Diels&#x2013;Alder Reactions of Structurally Related Dienes and Dienophiles</title>
<link>http://dx.doi.org/10.1002/ejoc.201101301</link>
<dc:creator>Pei-Ying Liu, Yong-Jin Wu, Cory C. Pye, Paul D. Thornton, Raymond A. Poirier, D. Jean Burnell</dc:creator>
<dc:date>2011-12-28T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101301.jpg" width="280" height="87" alt="Facial Selectivity in the Diels&ndash;Alder Reactions of 2,2-Disubstituted Cyclopent-4-ene-1,3-dione Derivatives and a Computational Examination of the Facial Selectivity of the Diels&ndash;Alder Reactions of Structurally Related Dienes and Dienophiles" title="Facial Selectivity in the Diels&ndash;Alder Reactions of 2,2-Disubstituted Cyclopent-4-ene-1,3-dione Derivatives and a Computational Examination of the Facial Selectivity of the Diels&ndash;Alder Reactions of Structurally Related Dienes and Dienophiles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Pei-Ying Liu, Yong-Jin Wu, Cory C. Pye, Paul D. Thornton, Raymond A. Poirier, D. Jean Burnell<br /><i>Eur. J. Org. Chem.</i>, December 28, 2011, DOI: 10.1002/ejoc.201101301. <a href="http://dx.doi.org/10.1002/ejoc.201101301">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101293">
<title>P&#x2013;C Cross-Coupling Onto Enamides: Versatile Synthesis of &#x3B1;-Enamido Phosphane Derivatives</title>
<link>http://dx.doi.org/10.1002/ejoc.201101293</link>
<dc:creator>Monika Cieslikiewicz, Alexis Bouet, Sylvain Jug&#xE9;, Martial Toffano, J&#xE9;r&#xF4;me Bayardon, Caroline West, Krzystof Lewinski, Isabelle Gillaizeau</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101293.jpg" width="195" height="124" alt="P&ndash;C Cross-Coupling Onto Enamides: Versatile Synthesis of &alpha;-Enamido Phosphane Derivatives" title="P&ndash;C Cross-Coupling Onto Enamides: Versatile Synthesis of &alpha;-Enamido Phosphane Derivatives" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Monika Cieslikiewicz, Alexis Bouet, Sylvain Jug&#xE9;, Martial Toffano, J&#xE9;r&#xF4;me Bayardon, Caroline West, Krzystof Lewinski, Isabelle Gillaizeau<br /><i>Eur. J. Org. Chem.</i>, January 13, 2012, DOI: 10.1002/ejoc.201101293. <a href="http://dx.doi.org/10.1002/ejoc.201101293">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101269">
<title>Protecting Group Free Formal Total Synthesis of the Antitubercular Agent Erogorgiaene</title>
<link>http://dx.doi.org/10.1002/ejoc.201101269</link>
<dc:creator>Jhillu S. Yadav, Bodakuntla Thirupathaiah,, Ahmad Al Khazim Al Ghamdi</dc:creator>
<dc:date>2011-11-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101269.jpg" width="302" height="100" alt="Protecting Group Free Formal Total Synthesis of the Antitubercular Agent Erogorgiaene" title="Protecting Group Free Formal Total Synthesis of the Antitubercular Agent Erogorgiaene" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Jhillu S. Yadav, Bodakuntla Thirupathaiah,, Ahmad Al Khazim Al Ghamdi<br /><i>Eur. J. Org. Chem.</i>, November 3, 2011, DOI: 10.1002/ejoc.201101269. <a href="http://dx.doi.org/10.1002/ejoc.201101269">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101258">
<title>Cu-Catalyzed Enantioselective 1,4-Additions of Aryl-Grignard Reagents to Cyclohexenone in the Presence of TADDOL-Derived Phosphane-Phosphite Ligands&lt;P&gt;Dedicated to Professor Mohammed A. Omary&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101258</link>
<dc:creator>Qaseem Naeemi, Mehmet Dindaro&amp;gbreve;lu, Darius P. Kranz, Janna Velder, Hans-G&#xFC;nther Schmalz</dc:creator>
<dc:date>2011-12-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101258.jpg" width="170" height="171" alt="Cu-Catalyzed Enantioselective 1,4-Additions of Aryl-Grignard Reagents to Cyclohexenone in the Presence of TADDOL-Derived Phosphane-Phosphite LigandsDedicated to Professor Mohammed A. Omary" title="Cu-Catalyzed Enantioselective 1,4-Additions of Aryl-Grignard Reagents to Cyclohexenone in the Presence of TADDOL-Derived Phosphane-Phosphite LigandsDedicated to Professor Mohammed A. Omary" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Qaseem Naeemi, Mehmet Dindaro&gbreve;lu, Darius P. Kranz, Janna Velder, Hans-G&#xFC;nther Schmalz<br /><i>Eur. J. Org. Chem.</i>, December 23, 2011, DOI: 10.1002/ejoc.201101258. <a href="http://dx.doi.org/10.1002/ejoc.201101258">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101240">
<title>Anthracene-Labeled 1,2,3-Triazole-Linked Bispyridinium Amide for Selective Sensing of H&lt;sub&gt;2&lt;/sub&gt;PO&lt;sub&gt;4&lt;/sub&gt;&lt;SUP&gt;&#x2013;&lt;/SUP&gt; by Fluorescence and Gel Formation</title>
<link>http://dx.doi.org/10.1002/ejoc.201101240</link>
<dc:creator>Kumaresh Ghosh, Avik Ranjan Sarkar, Asoke P. Chattopadhyay</dc:creator>
<dc:date>2012-01-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101240.jpg" width="195" height="207" alt="Anthracene-Labeled 1,2,3-Triazole-Linked Bispyridinium Amide for Selective Sensing of H2PO4&ndash; by Fluorescence and Gel Formation" title="Anthracene-Labeled 1,2,3-Triazole-Linked Bispyridinium Amide for Selective Sensing of H2PO4&ndash; by Fluorescence and Gel Formation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Kumaresh Ghosh, Avik Ranjan Sarkar, Asoke P. Chattopadhyay<br /><i>Eur. J. Org. Chem.</i>, January 16, 2012, DOI: 10.1002/ejoc.201101240. <a href="http://dx.doi.org/10.1002/ejoc.201101240">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101231">
<title>Phenanthroline- and Terpyridine-Substituted Tetralactam Macrocycles: A Facile Route to Rigid Di- and Trivalent Receptors and Interlocked Molecules</title>
<link>http://dx.doi.org/10.1002/ejoc.201101231</link>
<dc:creator>Egor V. Dzyuba, Bilge Baytekin, Dominik Sattler, Christoph A. Schalley</dc:creator>
<dc:date>2011-12-28T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101231.jpg" width="213" height="138" alt="Phenanthroline- and Terpyridine-Substituted Tetralactam Macrocycles: A Facile Route to Rigid Di- and Trivalent Receptors and Interlocked Molecules" title="Phenanthroline- and Terpyridine-Substituted Tetralactam Macrocycles: A Facile Route to Rigid Di- and Trivalent Receptors and Interlocked Molecules" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Egor V. Dzyuba, Bilge Baytekin, Dominik Sattler, Christoph A. Schalley<br /><i>Eur. J. Org. Chem.</i>, December 28, 2011, DOI: 10.1002/ejoc.201101231. <a href="http://dx.doi.org/10.1002/ejoc.201101231">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101230">
<title>New Directions in Ketene Chemistry: The Land of Opportunity</title>
<link>http://dx.doi.org/10.1002/ejoc.201101230</link>
<dc:creator>Annette D. Allen, Thomas T. Tidwell</dc:creator>
<dc:date>2011-11-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101230.jpg" width="207" height="64" alt="New Directions in Ketene Chemistry: The Land of Opportunity" title="New Directions in Ketene Chemistry: The Land of Opportunity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Annette D. Allen, Thomas T. Tidwell<br /><i>Eur. J. Org. Chem.</i>, November 11, 2011, DOI: 10.1002/ejoc.201101230. <a href="http://dx.doi.org/10.1002/ejoc.201101230">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101222">
<title>Regioselective Photochemical Rearrangement of &lt;I&gt;N&lt;/I&gt;-Mesyloxylactams</title>
<link>http://dx.doi.org/10.1002/ejoc.201101222</link>
<dc:creator>Simon Pichette, Samuel Aubert-Nicol, Jean Lessard, Claude Spino</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101222.jpg" width="306" height="92" alt="Regioselective Photochemical Rearrangement of N-Mesyloxylactams" title="Regioselective Photochemical Rearrangement of N-Mesyloxylactams" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Simon Pichette, Samuel Aubert-Nicol, Jean Lessard, Claude Spino<br /><i>Eur. J. Org. Chem.</i>, January 9, 2012, DOI: 10.1002/ejoc.201101222. <a href="http://dx.doi.org/10.1002/ejoc.201101222">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101133">
<title>Synthesis of the Indolic Pentacyclic Core of Manadomanzamine A Following Biogenetically Based Strategies&lt;P&gt;Dedicated to the memory of Fran&#xE7;ois Tillequin&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejoc.201101133</link>
<dc:creator>Lok-Hang Yan, Philippe Nuhant, Isabelle Sinigaglia, Yann Fromentin, Christian Marazano, Bernard Delpech, Erwan Poupon</dc:creator>
<dc:date>2012-01-04T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejoc201101133.jpg" width="444" height="95" alt="Synthesis of the Indolic Pentacyclic Core of Manadomanzamine A Following Biogenetically Based StrategiesDedicated to the memory of Fran&ccedil;ois Tillequin" title="Synthesis of the Indolic Pentacyclic Core of Manadomanzamine A Following Biogenetically Based StrategiesDedicated to the memory of Fran&ccedil;ois Tillequin" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Lok-Hang Yan, Philippe Nuhant, Isabelle Sinigaglia, Yann Fromentin, Christian Marazano, Bernard Delpech, Erwan Poupon<br /><i>Eur. J. Org. Chem.</i>, January 4, 2012, DOI: 10.1002/ejoc.201101133. <a href="http://dx.doi.org/10.1002/ejoc.201101133">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201200024">
<title>Activation of Gas-Phase Uranyl Diacetone Alcohol Coordination Complexes by Spectator Ligand Addition</title>
<link>http://dx.doi.org/10.1002/ejic.201200024</link>
<dc:creator>Daniel Rios, John K. Gibson</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201200024.jpg" width="428" height="117" alt="Activation of Gas-Phase Uranyl Diacetone Alcohol Coordination Complexes by Spectator Ligand Addition" title="Activation of Gas-Phase Uranyl Diacetone Alcohol Coordination Complexes by Spectator Ligand Addition" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Daniel Rios, John K. Gibson<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201200024. <a href="http://dx.doi.org/10.1002/ejic.201200024">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101385">
<title>Bidentate and Tetradentate &#x3B2;-Aminovinyl Trifluoromethylated Ketones and Their Copper(II) Complexes: Synthesis, Characterization and Redox Chemistry</title>
<link>http://dx.doi.org/10.1002/ejic.201101385</link>
<dc:creator>Nicolas Chopin, Maurice M&#xE9;debielle, Guillaume Pilet</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101385.jpg" width="210" height="154" alt="Bidentate and Tetradentate &beta;-Aminovinyl Trifluoromethylated Ketones and Their Copper(II) Complexes: Synthesis, Characterization and Redox Chemistry" title="Bidentate and Tetradentate &beta;-Aminovinyl Trifluoromethylated Ketones and Their Copper(II) Complexes: Synthesis, Characterization and Redox Chemistry" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Nicolas Chopin, Maurice M&#xE9;debielle, Guillaume Pilet<br /><i>Eur. J. Inorg. Chem.</i>, January 27, 2012, DOI: 10.1002/ejic.201101385. <a href="http://dx.doi.org/10.1002/ejic.201101385">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101364">
<title>Structure&#x2013;Relaxivity Relationships among Targeted MR Contrast Agents</title>
<link>http://dx.doi.org/10.1002/ejic.201101364</link>
<dc:creator>Peter Caravan, Zhaoda Zhang</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101364.jpg" width="188" height="169" alt="Structure&ndash;Relaxivity Relationships among Targeted MR Contrast Agents" title="Structure&ndash;Relaxivity Relationships among Targeted MR Contrast Agents" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Peter Caravan, Zhaoda Zhang<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201101364. <a href="http://dx.doi.org/10.1002/ejic.201101364">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101342">
<title>Diene Dissolution of the Heavier Alkaline Earth Metals</title>
<link>http://dx.doi.org/10.1002/ejic.201101342</link>
<dc:creator>Olaf Michel, Hiroshi Kaneko, Hayato Tsurugi, Koji Yamamoto, Karl W. T&#xF6;rnroos, Reiner Anwander, Kazushi Mashima</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101342.jpg" width="206" height="142" alt="Diene Dissolution of the Heavier Alkaline Earth Metals" title="Diene Dissolution of the Heavier Alkaline Earth Metals" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Olaf Michel, Hiroshi Kaneko, Hayato Tsurugi, Koji Yamamoto, Karl W. T&#xF6;rnroos, Reiner Anwander, Kazushi Mashima<br /><i>Eur. J. Inorg. Chem.</i>, January 13, 2012, DOI: 10.1002/ejic.201101342. <a href="http://dx.doi.org/10.1002/ejic.201101342">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101339">
<title>Synthesis, Reactivity and Ring-Opening Polymerization of a Tin-Bridged &lt;I&gt;ansa&lt;/I&gt;-Cycloheptatrienyl-Cyclopentadienyl Titanium Sandwich Complex</title>
<link>http://dx.doi.org/10.1002/ejic.201101339</link>
<dc:creator>Alain C. Tagne Kuate, Constantin G. Daniliuc, Peter G. Jones, Matthias Tamm</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101339.jpg" width="175" height="102" alt="Synthesis, Reactivity and Ring-Opening Polymerization of a Tin-Bridged ansa-Cycloheptatrienyl-Cyclopentadienyl Titanium Sandwich Complex" title="Synthesis, Reactivity and Ring-Opening Polymerization of a Tin-Bridged ansa-Cycloheptatrienyl-Cyclopentadienyl Titanium Sandwich Complex" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Alain C. Tagne Kuate, Constantin G. Daniliuc, Peter G. Jones, Matthias Tamm<br /><i>Eur. J. Inorg. Chem.</i>, January 27, 2012, DOI: 10.1002/ejic.201101339. <a href="http://dx.doi.org/10.1002/ejic.201101339">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101329">
<title>Room-Temperature Sol&#x2013;Gel Synthesis of Sodium Hexaniobate in an Immiscible Hexane&#x2013;Water System and Its Conversion into NaNbO&lt;sub&gt;3&lt;/sub&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201101329</link>
<dc:creator>Masahiro Tanaka, Shinobu Fujihara</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101329.jpg" width="213" height="109" alt="Room-Temperature Sol&ndash;Gel Synthesis of Sodium Hexaniobate in an Immiscible Hexane&ndash;Water System and Its Conversion into NaNbO3" title="Room-Temperature Sol&ndash;Gel Synthesis of Sodium Hexaniobate in an Immiscible Hexane&ndash;Water System and Its Conversion into NaNbO3" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Masahiro Tanaka, Shinobu Fujihara<br /><i>Eur. J. Inorg. Chem.</i>, February 6, 2012, DOI: 10.1002/ejic.201101329. <a href="http://dx.doi.org/10.1002/ejic.201101329">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101326">
<title>Isolation of a New &lt;I&gt;C&lt;/I&gt;&lt;sub&gt;s&lt;/sub&gt;-Symmetrized Mo&lt;sub&gt;3&lt;/sub&gt;(&#x3BC;&lt;sub&gt;3&lt;/sub&gt;-S)(&#x3BC;-S)(&#x3BC;-S&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt; Structural Type Through Complementary Association with a Cubane-Type Mo&lt;sub&gt;3&lt;/sub&gt;NiS&lt;sub&gt;4&lt;/sub&gt; Cluster</title>
<link>http://dx.doi.org/10.1002/ejic.201101326</link>
<dc:creator>Rita Hernandez-Molina, Javier Gonzalez-Platas, Cristian Vicent</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101326.jpg" width="311" height="189" alt="Isolation of a New Cs-Symmetrized Mo3(&mu;3-S)(&mu;-S)(&mu;-S2)2 Structural Type Through Complementary Association with a Cubane-Type Mo3NiS4 Cluster" title="Isolation of a New Cs-Symmetrized Mo3(&mu;3-S)(&mu;-S)(&mu;-S2)2 Structural Type Through Complementary Association with a Cubane-Type Mo3NiS4 Cluster" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Rita Hernandez-Molina, Javier Gonzalez-Platas, Cristian Vicent<br /><i>Eur. J. Inorg. Chem.</i>, February 6, 2012, DOI: 10.1002/ejic.201101326. <a href="http://dx.doi.org/10.1002/ejic.201101326">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101315">
<title>Structure&#x2013;Photoluminescence Quenching Relationships of Iridium(III)&#x2013;Tris(phenylpyridine) Complexes</title>
<link>http://dx.doi.org/10.1002/ejic.201101315</link>
<dc:creator>Albert Ruggi, Matteo Mauro, Federico Polo, David N. Reinhoudt, Luisa De Cola, Aldrik H. Velders</dc:creator>
<dc:date>2012-01-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101315.jpg" width="213" height="163" alt="Structure&ndash;Photoluminescence Quenching Relationships of Iridium(III)&ndash;Tris(phenylpyridine) Complexes" title="Structure&ndash;Photoluminescence Quenching Relationships of Iridium(III)&ndash;Tris(phenylpyridine) Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Albert Ruggi, Matteo Mauro, Federico Polo, David N. Reinhoudt, Luisa De Cola, Aldrik H. Velders<br /><i>Eur. J. Inorg. Chem.</i>, January 11, 2012, DOI: 10.1002/ejic.201101315. <a href="http://dx.doi.org/10.1002/ejic.201101315">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101296">
<title>Gd-Aminoethyl-DO3A Complexes: A Novel Class of pH-Sensitive MRI Contrast Agents</title>
<link>http://dx.doi.org/10.1002/ejic.201101296</link>
<dc:creator>Giovanni B. Giovenzana, Roberto Negri, Gabriele A. Rolla, Lorenzo Tei</dc:creator>
<dc:date>2012-01-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101296.jpg" width="330" height="93" alt="Gd-Aminoethyl-DO3A Complexes: A Novel Class of pH-Sensitive MRI Contrast Agents" title="Gd-Aminoethyl-DO3A Complexes: A Novel Class of pH-Sensitive MRI Contrast Agents" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Giovanni B. Giovenzana, Roberto Negri, Gabriele A. Rolla, Lorenzo Tei<br /><i>Eur. J. Inorg. Chem.</i>, January 23, 2012, DOI: 10.1002/ejic.201101296. <a href="http://dx.doi.org/10.1002/ejic.201101296">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101294">
<title>Influence of &lt;I&gt;gem&lt;/I&gt;-Dimethyl Substitution on the Stability, Kinetics and Relaxometric Properties of PDTA Complexes</title>
<link>http://dx.doi.org/10.1002/ejic.201101294</link>
<dc:creator>Attila Forg&#xE1;cs, Giovanni B. Giovenzana, Mauro Botta, Ern&#x151; Br&#xFC;cher, Imre T&#xF3;th, Zsolt Baranyai</dc:creator>
<dc:date>2012-02-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101294.jpg" width="195" height="115" alt="Influence of gem-Dimethyl Substitution on the Stability, Kinetics and Relaxometric Properties of PDTA Complexes" title="Influence of gem-Dimethyl Substitution on the Stability, Kinetics and Relaxometric Properties of PDTA Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Attila Forg&#xE1;cs, Giovanni B. Giovenzana, Mauro Botta, Ern&#x151; Br&#xFC;cher, Imre T&#xF3;th, Zsolt Baranyai<br /><i>Eur. J. Inorg. Chem.</i>, February 7, 2012, DOI: 10.1002/ejic.201101294. <a href="http://dx.doi.org/10.1002/ejic.201101294">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101292">
<title>Single-Strand Molecular Wheels and Coordination Polymers in Copper(II) Benzoate Chemistry by the Employment of &#x3B1;-Benzoin Oxime and Azides: Synthesis, Structures, and Magnetic Characterization</title>
<link>http://dx.doi.org/10.1002/ejic.201101292</link>
<dc:creator>Theocharis C. Stamatatos, Gina Vlahopoulou, Catherine P. Raptopoulou, Vassilis Psycharis, Albert Escuer, George Christou, Spyros P. Perlepes</dc:creator>
<dc:date>2012-01-10T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101292.jpg" width="253" height="187" alt="Single-Strand Molecular Wheels and Coordination Polymers in Copper(II) Benzoate Chemistry by the Employment of &alpha;-Benzoin Oxime and Azides: Synthesis, Structures, and Magnetic Characterization" title="Single-Strand Molecular Wheels and Coordination Polymers in Copper(II) Benzoate Chemistry by the Employment of &alpha;-Benzoin Oxime and Azides: Synthesis, Structures, and Magnetic Characterization" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Theocharis C. Stamatatos, Gina Vlahopoulou, Catherine P. Raptopoulou, Vassilis Psycharis, Albert Escuer, George Christou, Spyros P. Perlepes<br /><i>Eur. J. Inorg. Chem.</i>, January 10, 2012, DOI: 10.1002/ejic.201101292. <a href="http://dx.doi.org/10.1002/ejic.201101292">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101291">
<title>Chemical Exchange Saturation Transfer Is Unaffected by Modest Changes in Pressure</title>
<link>http://dx.doi.org/10.1002/ejic.201101291</link>
<dc:creator>Benjamin C. Webber, Christiane E. Carney, Mark Woods</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101291.jpg" width="167" height="161" alt="Chemical Exchange Saturation Transfer Is Unaffected by Modest Changes in Pressure" title="Chemical Exchange Saturation Transfer Is Unaffected by Modest Changes in Pressure" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Benjamin C. Webber, Christiane E. Carney, Mark Woods<br /><i>Eur. J. Inorg. Chem.</i>, January 9, 2012, DOI: 10.1002/ejic.201101291. <a href="http://dx.doi.org/10.1002/ejic.201101291">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101277">
<title>Ca&lt;sub&gt;2&lt;/sub&gt;NiSn&lt;sub&gt;2&lt;/sub&gt; &#x2013; A Polymorphic Intermetallic Phase: Atomic and Electronic Structure as well as a Topological Description of the Phase Transition by a Sigmatropic-Type Rearrangement of Ni and Sn Atoms</title>
<link>http://dx.doi.org/10.1002/ejic.201101277</link>
<dc:creator>Lisa Siggelkow, Viktor Hlukhyy, Thomas F. F&#xE4;ssler</dc:creator>
<dc:date>2012-01-12T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101277.jpg" width="213" height="182" alt="Ca2NiSn2 &ndash; A Polymorphic Intermetallic Phase: Atomic and Electronic Structure as well as a Topological Description of the Phase Transition by a Sigmatropic-Type Rearrangement of Ni and Sn Atoms" title="Ca2NiSn2 &ndash; A Polymorphic Intermetallic Phase: Atomic and Electronic Structure as well as a Topological Description of the Phase Transition by a Sigmatropic-Type Rearrangement of Ni and Sn Atoms" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Lisa Siggelkow, Viktor Hlukhyy, Thomas F. F&#xE4;ssler<br /><i>Eur. J. Inorg. Chem.</i>, January 12, 2012, DOI: 10.1002/ejic.201101277. <a href="http://dx.doi.org/10.1002/ejic.201101277">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101263">
<title>Molecular Structure of a Hydridoniobocene Complex [Nb(&#x3B7;&lt;SUP&gt;5&lt;/SUP&gt;-C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;SiMe&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;(H)&lt;sub&gt;3&lt;/sub&gt;] and Its Use as Catalyst for the Ring-Opening Polymerization of Cyclic Esters</title>
<link>http://dx.doi.org/10.1002/ejic.201101263</link>
<dc:creator>Carlos Alonso-Moreno, Antonio Anti&#xF1;olo, Joaqu&#xED;n C. Garc&#xED;a-Mart&#xED;nez, Santiago Garc&#xED;a-Yuste, Isabel L&#xF3;pez-Solera, Antonio Otero, Juan C. P&#xE9;rez-Flores, Maria T. Tercero-Morales</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101263.jpg" width="195" height="171" alt="Molecular Structure of a Hydridoniobocene Complex [Nb(&eta;5-C5H4SiMe3)2(H)3] and Its Use as Catalyst for the Ring-Opening Polymerization of Cyclic Esters" title="Molecular Structure of a Hydridoniobocene Complex [Nb(&eta;5-C5H4SiMe3)2(H)3] and Its Use as Catalyst for the Ring-Opening Polymerization of Cyclic Esters" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Carlos Alonso-Moreno, Antonio Anti&#xF1;olo, Joaqu&#xED;n C. Garc&#xED;a-Mart&#xED;nez, Santiago Garc&#xED;a-Yuste, Isabel L&#xF3;pez-Solera, Antonio Otero, Juan C. P&#xE9;rez-Flores, Maria T. Tercero-Morales<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201101263. <a href="http://dx.doi.org/10.1002/ejic.201101263">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101257">
<title>Amide and Urea Ferrocene-Containing Macrocycles Capable of the Electrochemical Sensing of Anions</title>
<link>http://dx.doi.org/10.1002/ejic.201101257</link>
<dc:creator>Nicholas H. Evans, Christopher J. Serpell, Kirsten E. Christensen, Paul D. Beer</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101257.jpg" width="213" height="88" alt="Amide and Urea Ferrocene-Containing Macrocycles Capable of the Electrochemical Sensing of Anions" title="Amide and Urea Ferrocene-Containing Macrocycles Capable of the Electrochemical Sensing of Anions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Nicholas H. Evans, Christopher J. Serpell, Kirsten E. Christensen, Paul D. Beer<br /><i>Eur. J. Inorg. Chem.</i>, January 17, 2012, DOI: 10.1002/ejic.201101257. <a href="http://dx.doi.org/10.1002/ejic.201101257">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101254">
<title>Silver Melonates and Coordination Modes of the Multidentate [C&lt;sub&gt;6&lt;/sub&gt;N&lt;sub&gt;7&lt;/sub&gt;(NCN)&lt;sub&gt;3&lt;/sub&gt;]&lt;SUP&gt;3&#x2013;&lt;/SUP&gt; Anion</title>
<link>http://dx.doi.org/10.1002/ejic.201101254</link>
<dc:creator>Corinna Clauss, Uwe B&#xF6;hme, Anke Schwarzer, Edwin Kroke</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101254.jpg" width="213" height="165" alt="Silver Melonates and Coordination Modes of the Multidentate [C6N7(NCN)3]3&ndash; Anion" title="Silver Melonates and Coordination Modes of the Multidentate [C6N7(NCN)3]3&ndash; Anion" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Corinna Clauss, Uwe B&#xF6;hme, Anke Schwarzer, Edwin Kroke<br /><i>Eur. J. Inorg. Chem.</i>, January 13, 2012, DOI: 10.1002/ejic.201101254. <a href="http://dx.doi.org/10.1002/ejic.201101254">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101253">
<title>Application of Nickel Complexes Modified by Tridentate &lt;I&gt;O&lt;/I&gt;,&lt;I&gt;N&lt;/I&gt;,&lt;I&gt;O&#x27;&lt;/I&gt;-Ligands as Precatalysts in Nickel-Catalyzed C(sp&lt;SUP&gt;2&lt;/SUP&gt;)&#x2013;C(sp&lt;SUP&gt;3&lt;/SUP&gt;) Bond Formations</title>
<link>http://dx.doi.org/10.1002/ejic.201101253</link>
<dc:creator>Chika I. Someya, Shigeyoshi Inoue, Sebastian Krackl, Elisabeth Irran, Stephan Enthaler</dc:creator>
<dc:date>2012-02-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101253.jpg" width="415" height="59" alt="Application of Nickel Complexes Modified by Tridentate O,N,O&#x27;-Ligands as Precatalysts in Nickel-Catalyzed C(sp2)&ndash;C(sp3) Bond Formations" title="Application of Nickel Complexes Modified by Tridentate O,N,O&#x27;-Ligands as Precatalysts in Nickel-Catalyzed C(sp2)&ndash;C(sp3) Bond Formations" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Chika I. Someya, Shigeyoshi Inoue, Sebastian Krackl, Elisabeth Irran, Stephan Enthaler<br /><i>Eur. J. Inorg. Chem.</i>, February 7, 2012, DOI: 10.1002/ejic.201101253. <a href="http://dx.doi.org/10.1002/ejic.201101253">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101249">
<title>Coordinating Properties of Pyrone and Pyridinone Derivatives, Tropolone and Catechol toward the VO&lt;SUP&gt;2+&lt;/SUP&gt; Ion: An Experimental and Computational Approach</title>
<link>http://dx.doi.org/10.1002/ejic.201101249</link>
<dc:creator>Daniele Sanna, P&#xE9;ter Bugly&#xF3;, Linda B&#xED;r&#xF3;, Giovanni Micera, Eugenio Garribba</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101249.jpg" width="280" height="149" alt="Coordinating Properties of Pyrone and Pyridinone Derivatives, Tropolone and Catechol toward the VO2+ Ion: An Experimental and Computational Approach" title="Coordinating Properties of Pyrone and Pyridinone Derivatives, Tropolone and Catechol toward the VO2+ Ion: An Experimental and Computational Approach" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Daniele Sanna, P&#xE9;ter Bugly&#xF3;, Linda B&#xED;r&#xF3;, Giovanni Micera, Eugenio Garribba<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201101249. <a href="http://dx.doi.org/10.1002/ejic.201101249">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101244">
<title>2D Magnetic Frames Obtained by the Microwave-Assisted Chemistry Approach</title>
<link>http://dx.doi.org/10.1002/ejic.201101244</link>
<dc:creator>Oana Pascu, Mart&#xED; Gich, Gervasi Herranz, Anna Roig</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101244.jpg" width="245" height="72" alt="2D Magnetic Frames Obtained by the Microwave-Assisted Chemistry Approach" title="2D Magnetic Frames Obtained by the Microwave-Assisted Chemistry Approach" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Oana Pascu, Mart&#xED; Gich, Gervasi Herranz, Anna Roig<br /><i>Eur. J. Inorg. Chem.</i>, January 9, 2012, DOI: 10.1002/ejic.201101244. <a href="http://dx.doi.org/10.1002/ejic.201101244">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101230">
<title>Derivatives of Photosensitive CORM-S1 &#x2013; CO Complexes of Iron and Ruthenium with the (OC)&lt;sub&gt;2&lt;/sub&gt;M(S&#x2013;C&#x2013;C&#x2013;NH&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt; Fragment</title>
<link>http://dx.doi.org/10.1002/ejic.201101230</link>
<dc:creator>Vaneza P. Lorett Vel&#xE1;squez, Taghreed M. A. Jazzazi, Astrid Malassa, Helmar G&#xF6;rls, Guido Gessner, Stefan H. Heinemann, Matthias Westerhausen</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101230.jpg" width="155" height="149" alt="Derivatives of Photosensitive CORM-S1 &ndash; CO Complexes of Iron and Ruthenium with the (OC)2M(S&ndash;C&ndash;C&ndash;NH2)2 Fragment" title="Derivatives of Photosensitive CORM-S1 &ndash; CO Complexes of Iron and Ruthenium with the (OC)2M(S&ndash;C&ndash;C&ndash;NH2)2 Fragment" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Vaneza P. Lorett Vel&#xE1;squez, Taghreed M. A. Jazzazi, Astrid Malassa, Helmar G&#xF6;rls, Guido Gessner, Stefan H. Heinemann, Matthias Westerhausen<br /><i>Eur. J. Inorg. Chem.</i>, January 31, 2012, DOI: 10.1002/ejic.201101230. <a href="http://dx.doi.org/10.1002/ejic.201101230">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101227">
<title>Fe&lt;SUP&gt;III&lt;/SUP&gt; Spin-Crossover Complexes with Photoisomerizable Ligands: Experimental and Theoretical Studies on the Ligand-Driven Light-Induced Spin Change Effect</title>
<link>http://dx.doi.org/10.1002/ejic.201101227</link>
<dc:creator>Alexander Bannwarth, Sven Olaf Schmidt, Gerhard Peters, Frank D. S&#xF6;nnichsen, Wulf Thimm, Rainer Herges, Felix Tuczek</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101227.jpg" width="124" height="164" alt="FeIII Spin-Crossover Complexes with Photoisomerizable Ligands: Experimental and Theoretical Studies on the Ligand-Driven Light-Induced Spin Change Effect" title="FeIII Spin-Crossover Complexes with Photoisomerizable Ligands: Experimental and Theoretical Studies on the Ligand-Driven Light-Induced Spin Change Effect" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Alexander Bannwarth, Sven Olaf Schmidt, Gerhard Peters, Frank D. S&#xF6;nnichsen, Wulf Thimm, Rainer Herges, Felix Tuczek<br /><i>Eur. J. Inorg. Chem.</i>, January 27, 2012, DOI: 10.1002/ejic.201101227. <a href="http://dx.doi.org/10.1002/ejic.201101227">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101223">
<title>Synthesis of Oligomeric Zinc Complexes with Bicyclic and Acyclic Guanidinate Ligands&lt;P&gt;Dedicated to Prof. Dr. mult. Alois Haas on the occasion of his 80th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201101223</link>
<dc:creator>Christiane Neuh&#xE4;user, Matthias Reinmuth, Elisabeth Kaifer, Hans-J&#xF6;rg Himmel</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101223.jpg" width="187" height="149" alt="Synthesis of Oligomeric Zinc Complexes with Bicyclic and Acyclic Guanidinate LigandsDedicated to Prof. Dr. mult. Alois Haas on the occasion of his 80th birthday" title="Synthesis of Oligomeric Zinc Complexes with Bicyclic and Acyclic Guanidinate LigandsDedicated to Prof. Dr. mult. Alois Haas on the occasion of his 80th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Christiane Neuh&#xE4;user, Matthias Reinmuth, Elisabeth Kaifer, Hans-J&#xF6;rg Himmel<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201101223. <a href="http://dx.doi.org/10.1002/ejic.201101223">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101220">
<title>Functional Heterometallic Layered Hybrid Magnets by Double Ion-Exchange</title>
<link>http://dx.doi.org/10.1002/ejic.201101220</link>
<dc:creator>Emilie Delahaye, S&#xE9;raphin Eyele-Mezui, Mayoro Diop, C&#xE9;dric Leuvrey, Dominique Foix, Danielle Gonbeau, Pierre Rabu, Guillaume Rogez</dc:creator>
<dc:date>2012-01-12T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101220.jpg" width="272" height="124" alt="Functional Heterometallic Layered Hybrid Magnets by Double Ion-Exchange" title="Functional Heterometallic Layered Hybrid Magnets by Double Ion-Exchange" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Emilie Delahaye, S&#xE9;raphin Eyele-Mezui, Mayoro Diop, C&#xE9;dric Leuvrey, Dominique Foix, Danielle Gonbeau, Pierre Rabu, Guillaume Rogez<br /><i>Eur. J. Inorg. Chem.</i>, January 12, 2012, DOI: 10.1002/ejic.201101220. <a href="http://dx.doi.org/10.1002/ejic.201101220">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101219">
<title>A Cyano-Bridged Vanadium&#x2013;Niobium Bimetal Assembly Exhibiting a High Curie Temperature of 210 K</title>
<link>http://dx.doi.org/10.1002/ejic.201101219</link>
<dc:creator>Kenta Imoto, Miho Takemura, Hiroko Tokoro, Shin-ichi Ohkoshi</dc:creator>
<dc:date>2011-12-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101219.jpg" width="206" height="208" alt="A Cyano-Bridged Vanadium&ndash;Niobium Bimetal Assembly Exhibiting a High Curie Temperature of 210 K" title="A Cyano-Bridged Vanadium&ndash;Niobium Bimetal Assembly Exhibiting a High Curie Temperature of 210 K" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Kenta Imoto, Miho Takemura, Hiroko Tokoro, Shin-ichi Ohkoshi<br /><i>Eur. J. Inorg. Chem.</i>, December 19, 2011, DOI: 10.1002/ejic.201101219. <a href="http://dx.doi.org/10.1002/ejic.201101219">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101202">
<title>Di-, Tetra-, Penta- and Polynuclear Zinc Complexes Supported by a Flexible Tetradentate Schiff Base Ligand</title>
<link>http://dx.doi.org/10.1002/ejic.201101202</link>
<dc:creator>David J. D. Wilson, Christine M. Beavers, Anne F. Richards</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101202.jpg" width="283" height="158" alt="Di-, Tetra-, Penta- and Polynuclear Zinc Complexes Supported by a Flexible Tetradentate Schiff Base Ligand" title="Di-, Tetra-, Penta- and Polynuclear Zinc Complexes Supported by a Flexible Tetradentate Schiff Base Ligand" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />David J. D. Wilson, Christine M. Beavers, Anne F. Richards<br /><i>Eur. J. Inorg. Chem.</i>, January 24, 2012, DOI: 10.1002/ejic.201101202. <a href="http://dx.doi.org/10.1002/ejic.201101202">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101197">
<title>Expected and Unconventional Ag&lt;SUP&gt;+&lt;/SUP&gt; Binding Modes in Heteronuclear Pt,Ag Coordination Polymers Derived from &lt;I&gt;trans&lt;/I&gt;-[Pt(methylamine)&lt;sub&gt;2&lt;/sub&gt;(pyrazole)&lt;sub&gt;2&lt;/sub&gt;]&lt;SUP&gt;2+&lt;/SUP&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201101197</link>
<dc:creator>Pilar Brandi-Blanco, Pablo J. Sanz Miguel, Bernhard Lippert</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101197.jpg" width="136" height="141" alt="Expected and Unconventional Ag+ Binding Modes in Heteronuclear Pt,Ag Coordination Polymers Derived from trans-[Pt(methylamine)2(pyrazole)2]2+" title="Expected and Unconventional Ag+ Binding Modes in Heteronuclear Pt,Ag Coordination Polymers Derived from trans-[Pt(methylamine)2(pyrazole)2]2+" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Pilar Brandi-Blanco, Pablo J. Sanz Miguel, Bernhard Lippert<br /><i>Eur. J. Inorg. Chem.</i>, January 30, 2012, DOI: 10.1002/ejic.201101197. <a href="http://dx.doi.org/10.1002/ejic.201101197">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101191">
<title>Ferrocenyl Maleimides &#x2013; Synthesis, (Spectro-)Electrochemistry, and Solvatochromism</title>
<link>http://dx.doi.org/10.1002/ejic.201101191</link>
<dc:creator>Alexander Hildebrandt, Steve W. Lehrich, Dieter Schaarschmidt, Romy Jaeschke, Katja Schreiter, Stefan Spange, Heinrich Lang</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101191.jpg" width="210" height="134" alt="Ferrocenyl Maleimides &ndash; Synthesis, (Spectro-)Electrochemistry, and Solvatochromism" title="Ferrocenyl Maleimides &ndash; Synthesis, (Spectro-)Electrochemistry, and Solvatochromism" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Alexander Hildebrandt, Steve W. Lehrich, Dieter Schaarschmidt, Romy Jaeschke, Katja Schreiter, Stefan Spange, Heinrich Lang<br /><i>Eur. J. Inorg. Chem.</i>, January 31, 2012, DOI: 10.1002/ejic.201101191. <a href="http://dx.doi.org/10.1002/ejic.201101191">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101187">
<title>[V&lt;sub&gt;15&lt;/sub&gt;Ge&lt;sub&gt;6&lt;/sub&gt;O&lt;sub&gt;42&lt;/sub&gt;S&lt;sub&gt;6&lt;/sub&gt;(H&lt;sub&gt;2&lt;/sub&gt;O)]&lt;SUP&gt;12&#x2013;&lt;/SUP&gt;, a Thiogermanatopolyoxovanadate Cluster Featuring the Spin Topology of the Molecular Magnet [V&lt;sub&gt;15&lt;/sub&gt;As&lt;sub&gt;6&lt;/sub&gt;O&lt;sub&gt;42&lt;/sub&gt;(H&lt;sub&gt;2&lt;/sub&gt;O)]&lt;SUP&gt;6&#x2013;&lt;/SUP&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201101187</link>
<dc:creator>Jing Wang, Christian N&#xE4;ther, Paul K&#xF6;gerler, Wolfgang Bensch</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101187.jpg" width="195" height="134" alt="[V15Ge6O42S6(H2O)]12&ndash;, a Thiogermanatopolyoxovanadate Cluster Featuring the Spin Topology of the Molecular Magnet [V15As6O42(H2O)]6&ndash;" title="[V15Ge6O42S6(H2O)]12&ndash;, a Thiogermanatopolyoxovanadate Cluster Featuring the Spin Topology of the Molecular Magnet [V15As6O42(H2O)]6&ndash;" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Jing Wang, Christian N&#xE4;ther, Paul K&#xF6;gerler, Wolfgang Bensch<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201101187. <a href="http://dx.doi.org/10.1002/ejic.201101187">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101183">
<title>A Facile Approach for Transferring PbS Colloidal Photonic Structures into Alkanol Solutions and Composite Solid Films</title>
<link>http://dx.doi.org/10.1002/ejic.201101183</link>
<dc:creator>Chunguang Li, Tianyu Bai, Tao Li, Feifei Li, Wenjun Dong, Zhan Shi, Shouhua Feng</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101183.jpg" width="213" height="125" alt="A Facile Approach for Transferring PbS Colloidal Photonic Structures into Alkanol Solutions and Composite Solid Films" title="A Facile Approach for Transferring PbS Colloidal Photonic Structures into Alkanol Solutions and Composite Solid Films" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Chunguang Li, Tianyu Bai, Tao Li, Feifei Li, Wenjun Dong, Zhan Shi, Shouhua Feng<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201101183. <a href="http://dx.doi.org/10.1002/ejic.201101183">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101181">
<title>Structural Conformation and Optical and Electrochemical Properties of Imidazolyl-Substituted Naphthalenediimide and Its Hg&lt;SUP&gt;II&lt;/SUP&gt;, Cd&lt;SUP&gt;II&lt;/SUP&gt;, and Cu&lt;SUP&gt;II&lt;/SUP&gt; Halide Complexes</title>
<link>http://dx.doi.org/10.1002/ejic.201101181</link>
<dc:creator>Jia-Jian Jiang, Cheng Yan, Mei Pan, Zi Wang, Hai-Ying Deng, Jian-Rong He, Qing-Yuan Yang, Lei Fu, Xian-Fang Xu, Cheng-Yong Su</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101181.jpg" width="191" height="92" alt="Structural Conformation and Optical and Electrochemical Properties of Imidazolyl-Substituted Naphthalenediimide and Its HgII, CdII, and CuII Halide Complexes" title="Structural Conformation and Optical and Electrochemical Properties of Imidazolyl-Substituted Naphthalenediimide and Its HgII, CdII, and CuII Halide Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Jia-Jian Jiang, Cheng Yan, Mei Pan, Zi Wang, Hai-Ying Deng, Jian-Rong He, Qing-Yuan Yang, Lei Fu, Xian-Fang Xu, Cheng-Yong Su<br /><i>Eur. J. Inorg. Chem.</i>, January 26, 2012, DOI: 10.1002/ejic.201101181. <a href="http://dx.doi.org/10.1002/ejic.201101181">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101178">
<title>The Nature of Spin Crossover and Coordination Core Distortion in a Family of Binuclear Iron(II) Complexes with Bipyridyl-Like Bridging Ligands</title>
<link>http://dx.doi.org/10.1002/ejic.201101178</link>
<dc:creator>Galina S. Matouzenko, Erwann Jeanneau, Alexander Yu. Verat, Yannick de Gaetano</dc:creator>
<dc:date>2012-01-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101178.jpg" width="311" height="98" alt="The Nature of Spin Crossover and Coordination Core Distortion in a Family of Binuclear Iron(II) Complexes with Bipyridyl-Like Bridging Ligands" title="The Nature of Spin Crossover and Coordination Core Distortion in a Family of Binuclear Iron(II) Complexes with Bipyridyl-Like Bridging Ligands" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Galina S. Matouzenko, Erwann Jeanneau, Alexander Yu. Verat, Yannick de Gaetano<br /><i>Eur. J. Inorg. Chem.</i>, January 23, 2012, DOI: 10.1002/ejic.201101178. <a href="http://dx.doi.org/10.1002/ejic.201101178">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101169">
<title>The Development of Iron(II) Complexes as ParaCEST MRI Contrast Agents</title>
<link>http://dx.doi.org/10.1002/ejic.201101169</link>
<dc:creator>Sarina J. Dorazio, Janet R. Morrow</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101169.jpg" width="195" height="120" alt="The Development of Iron(II) Complexes as ParaCEST MRI Contrast Agents" title="The Development of Iron(II) Complexes as ParaCEST MRI Contrast Agents" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Sarina J. Dorazio, Janet R. Morrow<br /><i>Eur. J. Inorg. Chem.</i>, January 13, 2012, DOI: 10.1002/ejic.201101169. <a href="http://dx.doi.org/10.1002/ejic.201101169">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101167">
<title>Conjugation to Biocompatible Dendrimers Increases Lanthanide &lt;I&gt;T&lt;/I&gt;&lt;sub&gt;2&lt;/sub&gt; Relaxivity of Hydroxypyridinone Complexes for Magnetic Resonance Imaging</title>
<link>http://dx.doi.org/10.1002/ejic.201101167</link>
<dc:creator>Piper J. Klemm, William C. Floyd III, Christopher M. Andolina, Jean M. J. Fr&#xE9;chet, Kenneth N. Raymond</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101167.jpg" width="195" height="111" alt="Conjugation to Biocompatible Dendrimers Increases Lanthanide T2 Relaxivity of Hydroxypyridinone Complexes for Magnetic Resonance Imaging" title="Conjugation to Biocompatible Dendrimers Increases Lanthanide T2 Relaxivity of Hydroxypyridinone Complexes for Magnetic Resonance Imaging" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Piper J. Klemm, William C. Floyd III, Christopher M. Andolina, Jean M. J. Fr&#xE9;chet, Kenneth N. Raymond<br /><i>Eur. J. Inorg. Chem.</i>, February 6, 2012, DOI: 10.1002/ejic.201101167. <a href="http://dx.doi.org/10.1002/ejic.201101167">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101164">
<title>The Solution Structure and Dynamics of MRI Probes Based on Lanthanide(III) DOTA as Investigated by DFT and NMR Spectroscopy</title>
<link>http://dx.doi.org/10.1002/ejic.201101164</link>
<dc:creator>Carlos Platas-Iglesias</dc:creator>
<dc:date>2011-12-21T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101164.jpg" width="213" height="167" alt="The Solution Structure and Dynamics of MRI Probes Based on Lanthanide(III) DOTA as Investigated by DFT and NMR Spectroscopy" title="The Solution Structure and Dynamics of MRI Probes Based on Lanthanide(III) DOTA as Investigated by DFT and NMR Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Carlos Platas-Iglesias<br /><i>Eur. J. Inorg. Chem.</i>, December 21, 2011, DOI: 10.1002/ejic.201101164. <a href="http://dx.doi.org/10.1002/ejic.201101164">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101162">
<title>New Bisaqua Picolinate-Based Gadolinium Complexes as MRI Contrast Agents with Substantial High-Field Relaxivities</title>
<link>http://dx.doi.org/10.1002/ejic.201101162</link>
<dc:creator>Aline M. Nonat, Christelle Gateau, Pascal H. Fries, Lothar Helm, Marinella Mazzanti</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101162.jpg" width="370" height="130" alt="New Bisaqua Picolinate-Based Gadolinium Complexes as MRI Contrast Agents with Substantial High-Field Relaxivities" title="New Bisaqua Picolinate-Based Gadolinium Complexes as MRI Contrast Agents with Substantial High-Field Relaxivities" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Aline M. Nonat, Christelle Gateau, Pascal H. Fries, Lothar Helm, Marinella Mazzanti<br /><i>Eur. J. Inorg. Chem.</i>, January 13, 2012, DOI: 10.1002/ejic.201101162. <a href="http://dx.doi.org/10.1002/ejic.201101162">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101159">
<title>PTA-Stabilized Ruthenium and Platinum Nanoparticles: Characterization and Investigation in Aqueous Biphasic Hydrogenation Catalysis</title>
<link>http://dx.doi.org/10.1002/ejic.201101159</link>
<dc:creator>Pierre-Jean Deboutti&#xE8;re, Yannick Coppel, Audrey Denicourt-Nowicki, Alain Roucoux, Bruno Chaudret, Karine Philippot</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101159.jpg" width="192" height="108" alt="PTA-Stabilized Ruthenium and Platinum Nanoparticles: Characterization and Investigation in Aqueous Biphasic Hydrogenation Catalysis" title="PTA-Stabilized Ruthenium and Platinum Nanoparticles: Characterization and Investigation in Aqueous Biphasic Hydrogenation Catalysis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Pierre-Jean Deboutti&#xE8;re, Yannick Coppel, Audrey Denicourt-Nowicki, Alain Roucoux, Bruno Chaudret, Karine Philippot<br /><i>Eur. J. Inorg. Chem.</i>, February 6, 2012, DOI: 10.1002/ejic.201101159. <a href="http://dx.doi.org/10.1002/ejic.201101159">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101158">
<title>Catalytic Hydrocarbon Functionalization with Gold Complexes Containing N-Heterocyclic Carbene Ligands with Pendant Donor Groups</title>
<link>http://dx.doi.org/10.1002/ejic.201101158</link>
<dc:creator>Manuela Delgado-Rebollo, Alvaro Beltr&#xE1;n, Auxiliadora Prieto, M. Mar D&#xED;az-Requejo, Antonio M. Echavarren, Pedro J. P&#xE9;rez</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101158.jpg" width="210" height="109" alt="Catalytic Hydrocarbon Functionalization with Gold Complexes Containing N-Heterocyclic Carbene Ligands with Pendant Donor Groups" title="Catalytic Hydrocarbon Functionalization with Gold Complexes Containing N-Heterocyclic Carbene Ligands with Pendant Donor Groups" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Manuela Delgado-Rebollo, Alvaro Beltr&#xE1;n, Auxiliadora Prieto, M. Mar D&#xED;az-Requejo, Antonio M. Echavarren, Pedro J. P&#xE9;rez<br /><i>Eur. J. Inorg. Chem.</i>, January 9, 2012, DOI: 10.1002/ejic.201101158. <a href="http://dx.doi.org/10.1002/ejic.201101158">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101142">
<title>Hexaphosphine: A Multifaceted Ligand for Transition Metal Coordination&lt;P&gt;Dedicated to Professor Philippe Meunier on the occasion of his 65th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201101142</link>
<dc:creator>Radomyr V. Smaliy, Matthieu Beaup&#xE9;rin, Arnaud Mielle, Philippe Richard, H&#xE9;l&#xE8;ne Cattey, Aleksandr N. Kostyuk, Jean-Cyrille Hierso</dc:creator>
<dc:date>2011-12-15T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101142.jpg" width="175" height="183" alt="Hexaphosphine: A Multifaceted Ligand for Transition Metal CoordinationDedicated to Professor Philippe Meunier on the occasion of his 65th birthday" title="Hexaphosphine: A Multifaceted Ligand for Transition Metal CoordinationDedicated to Professor Philippe Meunier on the occasion of his 65th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Radomyr V. Smaliy, Matthieu Beaup&#xE9;rin, Arnaud Mielle, Philippe Richard, H&#xE9;l&#xE8;ne Cattey, Aleksandr N. Kostyuk, Jean-Cyrille Hierso<br /><i>Eur. J. Inorg. Chem.</i>, December 15, 2011, DOI: 10.1002/ejic.201101142. <a href="http://dx.doi.org/10.1002/ejic.201101142">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101137">
<title>Blood-Pool and Targeting MRI Contrast Agents: From Gd-Chelates to Gd-Nanoparticles</title>
<link>http://dx.doi.org/10.1002/ejic.201101137</link>
<dc:creator>Gang Ho Lee, Yongmin Chang, Tae-Jeong Kim</dc:creator>
<dc:date>2012-01-04T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101137.jpg" width="175" height="195" alt="Blood-Pool and Targeting MRI Contrast Agents: From Gd-Chelates to Gd-Nanoparticles" title="Blood-Pool and Targeting MRI Contrast Agents: From Gd-Chelates to Gd-Nanoparticles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Gang Ho Lee, Yongmin Chang, Tae-Jeong Kim<br /><i>Eur. J. Inorg. Chem.</i>, January 4, 2012, DOI: 10.1002/ejic.201101137. <a href="http://dx.doi.org/10.1002/ejic.201101137">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101136">
<title>Synthesis and Characterization of Surface-Functionalized Layered Titanate Nanosheets Using Lamellar Self-Assembly as a Template</title>
<link>http://dx.doi.org/10.1002/ejic.201101136</link>
<dc:creator>Keizo Nakagawa, Kazuki Yamaguchi, Keiji Yamada, Ken-Ichiro Sotowa, Shigeru Sugiyama, Motonari Adachi</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101136.jpg" width="155" height="155" alt="Synthesis and Characterization of Surface-Functionalized Layered Titanate Nanosheets Using Lamellar Self-Assembly as a Template" title="Synthesis and Characterization of Surface-Functionalized Layered Titanate Nanosheets Using Lamellar Self-Assembly as a Template" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Keizo Nakagawa, Kazuki Yamaguchi, Keiji Yamada, Ken-Ichiro Sotowa, Shigeru Sugiyama, Motonari Adachi<br /><i>Eur. J. Inorg. Chem.</i>, February 6, 2012, DOI: 10.1002/ejic.201101136. <a href="http://dx.doi.org/10.1002/ejic.201101136">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101121">
<title>Pompon-Like MnF&lt;sub&gt;2&lt;/sub&gt; Nanostructures from a Single-Source Precursor through Atmospheric Pressure Chemical Vapor Deposition</title>
<link>http://dx.doi.org/10.1002/ejic.201101121</link>
<dc:creator>Graziella Malandrino, Roberta G. Toro, Maria R. Catalano, Maria E. Fragal&#xE0;, Patrizia Rossi, Paola Paoli</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101121.jpg" width="213" height="109" alt="Pompon-Like MnF2 Nanostructures from a Single-Source Precursor through Atmospheric Pressure Chemical Vapor Deposition" title="Pompon-Like MnF2 Nanostructures from a Single-Source Precursor through Atmospheric Pressure Chemical Vapor Deposition" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Graziella Malandrino, Roberta G. Toro, Maria R. Catalano, Maria E. Fragal&#xE0;, Patrizia Rossi, Paola Paoli<br /><i>Eur. J. Inorg. Chem.</i>, February 6, 2012, DOI: 10.1002/ejic.201101121. <a href="http://dx.doi.org/10.1002/ejic.201101121">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101119">
<title>Synthesis and Structure of Silver Amino-Arenesulfonates</title>
<link>http://dx.doi.org/10.1002/ejic.201101119</link>
<dc:creator>Madleen Busse, Philip C. Andrews, Peter C. Junk</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101119.jpg" width="213" height="181" alt="Synthesis and Structure of Silver Amino-Arenesulfonates" title="Synthesis and Structure of Silver Amino-Arenesulfonates" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Madleen Busse, Philip C. Andrews, Peter C. Junk<br /><i>Eur. J. Inorg. Chem.</i>, January 31, 2012, DOI: 10.1002/ejic.201101119. <a href="http://dx.doi.org/10.1002/ejic.201101119">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101110">
<title>Silica Nanoparticles for Bimodal MRI&#x2013;Optical Imaging by Grafting Gd&lt;SUP&gt;3+&lt;/SUP&gt; and Eu&lt;SUP&gt;3+&lt;/SUP&gt;/Tb&lt;SUP&gt;3+&lt;/SUP&gt; Complexes</title>
<link>http://dx.doi.org/10.1002/ejic.201101110</link>
<dc:creator>Sonia L. C. Pinho, Henrique Faneca, Carlos F. G. C. Geraldes, Jo&#xE3;o Rocha, Lu&#xED;s D. Carlos, Marie-H&#xE9;l&#xE8;ne Delville</dc:creator>
<dc:date>2012-01-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101110.jpg" width="213" height="148" alt="Silica Nanoparticles for Bimodal MRI&ndash;Optical Imaging by Grafting Gd3+ and Eu3+/Tb3+ Complexes" title="Silica Nanoparticles for Bimodal MRI&ndash;Optical Imaging by Grafting Gd3+ and Eu3+/Tb3+ Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Sonia L. C. Pinho, Henrique Faneca, Carlos F. G. C. Geraldes, Jo&#xE3;o Rocha, Lu&#xED;s D. Carlos, Marie-H&#xE9;l&#xE8;ne Delville<br /><i>Eur. J. Inorg. Chem.</i>, January 19, 2012, DOI: 10.1002/ejic.201101110. <a href="http://dx.doi.org/10.1002/ejic.201101110">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101103">
<title>Syntheses and Structural Study of Novel Tetranuclear Bis(phenoxido)-Bridged Cu&lt;SUP&gt;II&lt;/SUP&gt; Metal&#x2013;Organic Macrocycles</title>
<link>http://dx.doi.org/10.1002/ejic.201101103</link>
<dc:creator>Antti Riisi&#xF6;, Mikko M. H&#xE4;nninen, Reijo Sillanp&#xE4;&#xE4;</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101103.jpg" width="210" height="135" alt="Syntheses and Structural Study of Novel Tetranuclear Bis(phenoxido)-Bridged CuII Metal&ndash;Organic Macrocycles" title="Syntheses and Structural Study of Novel Tetranuclear Bis(phenoxido)-Bridged CuII Metal&ndash;Organic Macrocycles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Antti Riisi&#xF6;, Mikko M. H&#xE4;nninen, Reijo Sillanp&#xE4;&#xE4;<br /><i>Eur. J. Inorg. Chem.</i>, January 27, 2012, DOI: 10.1002/ejic.201101103. <a href="http://dx.doi.org/10.1002/ejic.201101103">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101099">
<title>Synthesis, Structural Characterization, and Catalytic Performance of a Vanadium-Based Metal&#x2013;Organic Framework (COMOC-3)</title>
<link>http://dx.doi.org/10.1002/ejic.201101099</link>
<dc:creator>Ying-Ya Liu, Karen Leus, Maciej Grzywa, David Weinberger, Katrien Strubbe, Henk Vrielinck, Rik Van Deun, Dirk Volkmer, Veronique Van Speybroeck, Pascal Van Der Voort</dc:creator>
<dc:date>2011-12-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101099.jpg" width="389" height="106" alt="Synthesis, Structural Characterization, and Catalytic Performance of a Vanadium-Based Metal&ndash;Organic Framework (COMOC-3)" title="Synthesis, Structural Characterization, and Catalytic Performance of a Vanadium-Based Metal&ndash;Organic Framework (COMOC-3)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Ying-Ya Liu, Karen Leus, Maciej Grzywa, David Weinberger, Katrien Strubbe, Henk Vrielinck, Rik Van Deun, Dirk Volkmer, Veronique Van Speybroeck, Pascal Van Der Voort<br /><i>Eur. J. Inorg. Chem.</i>, December 16, 2011, DOI: 10.1002/ejic.201101099. <a href="http://dx.doi.org/10.1002/ejic.201101099">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101096">
<title>New Octahedral, Head&#x2013;Tail Iron(II) Complexes with Spin Crossover Properties</title>
<link>http://dx.doi.org/10.1002/ejic.201101096</link>
<dc:creator>Stephan Schlamp, Peter Thoma, Birgit Weber</dc:creator>
<dc:date>2011-12-08T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101096.jpg" width="331" height="142" alt="New Octahedral, Head&ndash;Tail Iron(II) Complexes with Spin Crossover Properties" title="New Octahedral, Head&ndash;Tail Iron(II) Complexes with Spin Crossover Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Stephan Schlamp, Peter Thoma, Birgit Weber<br /><i>Eur. J. Inorg. Chem.</i>, December 8, 2011, DOI: 10.1002/ejic.201101096. <a href="http://dx.doi.org/10.1002/ejic.201101096">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101088">
<title>Peculiarities of Vibrational Spectra and Electronic Structure of the Five-Membered Metallacyclocumulenes of the Group 4 Metals</title>
<link>http://dx.doi.org/10.1002/ejic.201101088</link>
<dc:creator>Rinat R. Aysin, Larissa A. Leites, Vladimir V. Burlakov, Vladimir B. Shur, Torsten Beweries, Uwe Rosenthal</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101088.jpg" width="155" height="166" alt="Peculiarities of Vibrational Spectra and Electronic Structure of the Five-Membered Metallacyclocumulenes of the Group 4 Metals" title="Peculiarities of Vibrational Spectra and Electronic Structure of the Five-Membered Metallacyclocumulenes of the Group 4 Metals" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Rinat R. Aysin, Larissa A. Leites, Vladimir V. Burlakov, Vladimir B. Shur, Torsten Beweries, Uwe Rosenthal<br /><i>Eur. J. Inorg. Chem.</i>, January 25, 2012, DOI: 10.1002/ejic.201101088. <a href="http://dx.doi.org/10.1002/ejic.201101088">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101075">
<title>K&lt;sub&gt;&#x3B2;&lt;/sub&gt; Detected High-Resolution XANES of Fe&lt;SUP&gt;II&lt;/SUP&gt; and Fe&lt;SUP&gt;III&lt;/SUP&gt; Models of the 2-His-1-Carboxylate Motif: Analysis of the Carboxylate Binding Mode</title>
<link>http://dx.doi.org/10.1002/ejic.201101075</link>
<dc:creator>Ana Mijovilovich, Hisashi Hayashi, Naomi Kawamura, Hitoshi Osawa, Pieter C. A. Bruijnincx, Robertus J. M. Klein Gebbink, Frank M. F. de Groot, Bert M. Weckhuysen</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101075.jpg" width="335" height="143" alt="K&beta; Detected High-Resolution XANES of FeII and FeIII Models of the 2-His-1-Carboxylate Motif: Analysis of the Carboxylate Binding Mode" title="K&beta; Detected High-Resolution XANES of FeII and FeIII Models of the 2-His-1-Carboxylate Motif: Analysis of the Carboxylate Binding Mode" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Ana Mijovilovich, Hisashi Hayashi, Naomi Kawamura, Hitoshi Osawa, Pieter C. A. Bruijnincx, Robertus J. M. Klein Gebbink, Frank M. F. de Groot, Bert M. Weckhuysen<br /><i>Eur. J. Inorg. Chem.</i>, January 30, 2012, DOI: 10.1002/ejic.201101075. <a href="http://dx.doi.org/10.1002/ejic.201101075">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101073">
<title>Rhodium (Thiophosphinoyl)(trimethylsilyl)methanide and Bis(thiophosphinoyl)methanide Complexes: S~S vs. C~S Coordination&lt;P&gt;Dedicated to the memory of our friend and colleague Pascal Le Floch&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201101073</link>
<dc:creator>Hadrien Heuclin, Sophie Carenco, Xavier-Fr&#xE9;d&#xE9;ric Le Goff, Nicolas M&#xE9;zailles</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101073.jpg" width="175" height="134" alt="Rhodium (Thiophosphinoyl)(trimethylsilyl)methanide and Bis(thiophosphinoyl)methanide Complexes: S~S vs. C~S CoordinationDedicated to the memory of our friend and colleague Pascal Le Floch" title="Rhodium (Thiophosphinoyl)(trimethylsilyl)methanide and Bis(thiophosphinoyl)methanide Complexes: S~S vs. C~S CoordinationDedicated to the memory of our friend and colleague Pascal Le Floch" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Hadrien Heuclin, Sophie Carenco, Xavier-Fr&#xE9;d&#xE9;ric Le Goff, Nicolas M&#xE9;zailles<br /><i>Eur. J. Inorg. Chem.</i>, January 27, 2012, DOI: 10.1002/ejic.201101073. <a href="http://dx.doi.org/10.1002/ejic.201101073">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101066">
<title>Crystal-Phase- and Morphology-Controlled Synthesis of Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; Nanomaterials</title>
<link>http://dx.doi.org/10.1002/ejic.201101066</link>
<dc:creator>Xiaoling Mou, Yong Li, Bingsen Zhang, Lide Yao, Xuejiao Wei, Dang Sheng Su, Wenjie Shen</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101066.jpg" width="175" height="159" alt="Crystal-Phase- and Morphology-Controlled Synthesis of Fe2O3 Nanomaterials" title="Crystal-Phase- and Morphology-Controlled Synthesis of Fe2O3 Nanomaterials" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Xiaoling Mou, Yong Li, Bingsen Zhang, Lide Yao, Xuejiao Wei, Dang Sheng Su, Wenjie Shen<br /><i>Eur. J. Inorg. Chem.</i>, January 26, 2012, DOI: 10.1002/ejic.201101066. <a href="http://dx.doi.org/10.1002/ejic.201101066">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101064">
<title>Synthesis of Mesoporous Zirconium Organophosphonate Solid-Acid Catalysts</title>
<link>http://dx.doi.org/10.1002/ejic.201101064</link>
<dc:creator>Xiu-Zhen Lin, Zhong-Yong Yuan</dc:creator>
<dc:date>2011-12-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101064.jpg" width="213" height="165" alt="Synthesis of Mesoporous Zirconium Organophosphonate Solid-Acid Catalysts" title="Synthesis of Mesoporous Zirconium Organophosphonate Solid-Acid Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Xiu-Zhen Lin, Zhong-Yong Yuan<br /><i>Eur. J. Inorg. Chem.</i>, December 6, 2011, DOI: 10.1002/ejic.201101064. <a href="http://dx.doi.org/10.1002/ejic.201101064">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101060">
<title>One-Dimensional 3d&#x2013;3d&#x2013;4f Trimetallic Assemblies Consisting of Cu&lt;SUP&gt;II&lt;/SUP&gt;&lt;sub&gt;2&lt;/sub&gt;Ln&lt;SUP&gt;III&lt;/SUP&gt; Trinuclear Complexes and Hexacyanometallate</title>
<link>http://dx.doi.org/10.1002/ejic.201101060</link>
<dc:creator>Takuya Shiga, Akio Mishima, Kunihisa Sugimoto, Hisashi Okawa, Hiroki Oshio, Masaaki Ohba</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101060.jpg" width="370" height="125" alt="One-Dimensional 3d&ndash;3d&ndash;4f Trimetallic Assemblies Consisting of CuII2LnIII Trinuclear Complexes and Hexacyanometallate" title="One-Dimensional 3d&ndash;3d&ndash;4f Trimetallic Assemblies Consisting of CuII2LnIII Trinuclear Complexes and Hexacyanometallate" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Takuya Shiga, Akio Mishima, Kunihisa Sugimoto, Hisashi Okawa, Hiroki Oshio, Masaaki Ohba<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201101060. <a href="http://dx.doi.org/10.1002/ejic.201101060">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101058">
<title>Synthesis and Characterization of Gold Nanostars as Filler of Tunneling Conductive Polymer Composites</title>
<link>http://dx.doi.org/10.1002/ejic.201101058</link>
<dc:creator>Stefano Stassi, Valentina Cauda, Giancarlo Canavese, Diego Manfredi, Candido Fabrizio Pirri</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101058.jpg" width="191" height="147" alt="Synthesis and Characterization of Gold Nanostars as Filler of Tunneling Conductive Polymer Composites" title="Synthesis and Characterization of Gold Nanostars as Filler of Tunneling Conductive Polymer Composites" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Stefano Stassi, Valentina Cauda, Giancarlo Canavese, Diego Manfredi, Candido Fabrizio Pirri<br /><i>Eur. J. Inorg. Chem.</i>, January 31, 2012, DOI: 10.1002/ejic.201101058. <a href="http://dx.doi.org/10.1002/ejic.201101058">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101057">
<title>Thiolato-Bridged Arene&#x2013;Ruthenium Complexes: Synthesis, Molecular Structure, Reactivity, and Anticancer Activity of the Dinuclear Complexes [(arene)&lt;sub&gt;2&lt;/sub&gt;Ru&lt;sub&gt;2&lt;/sub&gt;(SR)&lt;sub&gt;2&lt;/sub&gt;Cl&lt;sub&gt;2&lt;/sub&gt;]&lt;P&gt;Dedicated to Dr. Hubert Le Bozec on the occasion of his 60th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201101057</link>
<dc:creator>Anne-Flore Ibao, Micha&#xEB;l Gras, Bruno Therrien, Georg S&#xFC;ss-Fink, Olivier Zava, Paul J. Dyson</dc:creator>
<dc:date>2011-12-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101057.jpg" width="360" height="146" alt="Thiolato-Bridged Arene&ndash;Ruthenium Complexes: Synthesis, Molecular Structure, Reactivity, and Anticancer Activity of the Dinuclear Complexes [(arene)2Ru2(SR)2Cl2]Dedicated to Dr. Hubert Le Bozec on the occasion of his 60th birthday" title="Thiolato-Bridged Arene&ndash;Ruthenium Complexes: Synthesis, Molecular Structure, Reactivity, and Anticancer Activity of the Dinuclear Complexes [(arene)2Ru2(SR)2Cl2]Dedicated to Dr. Hubert Le Bozec on the occasion of his 60th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Anne-Flore Ibao, Micha&#xEB;l Gras, Bruno Therrien, Georg S&#xFC;ss-Fink, Olivier Zava, Paul J. Dyson<br /><i>Eur. J. Inorg. Chem.</i>, December 16, 2011, DOI: 10.1002/ejic.201101057. <a href="http://dx.doi.org/10.1002/ejic.201101057">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101056">
<title>MOFs for Use in Adsorption Heat Pump Processes</title>
<link>http://dx.doi.org/10.1002/ejic.201101056</link>
<dc:creator>Stefan K. Henninger, Felix Jeremias, Harry Kummer, Christoph Janiak</dc:creator>
<dc:date>2011-12-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101056.jpg" width="175" height="175" alt="MOFs for Use in Adsorption Heat Pump Processes" title="MOFs for Use in Adsorption Heat Pump Processes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Stefan K. Henninger, Felix Jeremias, Harry Kummer, Christoph Janiak<br /><i>Eur. J. Inorg. Chem.</i>, December 13, 2011, DOI: 10.1002/ejic.201101056. <a href="http://dx.doi.org/10.1002/ejic.201101056">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101054">
<title>Synthesis and Characterization of New Pentacoordinate Iron-Based Aryloxide Complexes</title>
<link>http://dx.doi.org/10.1002/ejic.201101054</link>
<dc:creator>Yvens Ch&#xE9;r&#xE9;mond, Aur&#xE9;lien Crochet, Katharina M. Fromm</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101054.jpg" width="428" height="70" alt="Synthesis and Characterization of New Pentacoordinate Iron-Based Aryloxide Complexes" title="Synthesis and Characterization of New Pentacoordinate Iron-Based Aryloxide Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Yvens Ch&#xE9;r&#xE9;mond, Aur&#xE9;lien Crochet, Katharina M. Fromm<br /><i>Eur. J. Inorg. Chem.</i>, January 24, 2012, DOI: 10.1002/ejic.201101054. <a href="http://dx.doi.org/10.1002/ejic.201101054">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101050">
<title>The Question of &lt;I&gt;cis&lt;/I&gt; versus &lt;I&gt;trans&lt;/I&gt; Configuration in Octahedral Metal Diketonates: An In-Depth Investigation on Diorganobis(4-acyl-5-pyrazolonato)tin(IV) Complexes</title>
<link>http://dx.doi.org/10.1002/ejic.201101050</link>
<dc:creator>Francesco Caruso, Eric J. Chan, John V. Hanna, Fabio Marchetti, Claudio Pettinari, Corrado Di Nicola, Riccardo Pettinari, Adriano Pizzabiocca, Gregory J. Rees, David Quigley, Miriam Rossi, Brian W. Skelton, Alexandre N. Sobolev, Allan H. White</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101050.jpg" width="206" height="155" alt="The Question of cis versus trans Configuration in Octahedral Metal Diketonates: An In-Depth Investigation on Diorganobis(4-acyl-5-pyrazolonato)tin(IV) Complexes" title="The Question of cis versus trans Configuration in Octahedral Metal Diketonates: An In-Depth Investigation on Diorganobis(4-acyl-5-pyrazolonato)tin(IV) Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Francesco Caruso, Eric J. Chan, John V. Hanna, Fabio Marchetti, Claudio Pettinari, Corrado Di Nicola, Riccardo Pettinari, Adriano Pizzabiocca, Gregory J. Rees, David Quigley, Miriam Rossi, Brian W. Skelton, Alexandre N. Sobolev, Allan H. White<br /><i>Eur. J. Inorg. Chem.</i>, January 17, 2012, DOI: 10.1002/ejic.201101050. <a href="http://dx.doi.org/10.1002/ejic.201101050">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101048">
<title>Synthesis of Stable Ruthenium Olefin Metathesis Catalysts with Mixed Anionic Ligands</title>
<link>http://dx.doi.org/10.1002/ejic.201101048</link>
<dc:creator>Rafa&#x142; Gawin, Karol Grela</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101048.jpg" width="195" height="151" alt="Synthesis of Stable Ruthenium Olefin Metathesis Catalysts with Mixed Anionic Ligands" title="Synthesis of Stable Ruthenium Olefin Metathesis Catalysts with Mixed Anionic Ligands" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Rafa&#x142; Gawin, Karol Grela<br /><i>Eur. J. Inorg. Chem.</i>, January 31, 2012, DOI: 10.1002/ejic.201101048. <a href="http://dx.doi.org/10.1002/ejic.201101048">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101040">
<title>Spin-Crossover Behaviors Based on Intermolecular Interactions for Cobalt(II) Complexes with Long Alkyl Chains</title>
<link>http://dx.doi.org/10.1002/ejic.201101040</link>
<dc:creator>Yasuka Komatsu, Kazuya Kato, Yuuki Yamamoto, Hidenobu Kamihata, Young Hoon Lee, Akira Fuyuhiro, Satoshi Kawata, Shinya Hayami</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101040.jpg" width="311" height="88" alt="Spin-Crossover Behaviors Based on Intermolecular Interactions for Cobalt(II) Complexes with Long Alkyl Chains" title="Spin-Crossover Behaviors Based on Intermolecular Interactions for Cobalt(II) Complexes with Long Alkyl Chains" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Yasuka Komatsu, Kazuya Kato, Yuuki Yamamoto, Hidenobu Kamihata, Young Hoon Lee, Akira Fuyuhiro, Satoshi Kawata, Shinya Hayami<br /><i>Eur. J. Inorg. Chem.</i>, January 9, 2012, DOI: 10.1002/ejic.201101040. <a href="http://dx.doi.org/10.1002/ejic.201101040">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101038">
<title>Hierarchical Hydroxyapatite Microspheres Composed of Nanorods and Their Competitive Sorption Behavior for Heavy Metal Ions</title>
<link>http://dx.doi.org/10.1002/ejic.201101038</link>
<dc:creator>Ronghai Zhu, Xiaoyong Lai, Jonathan E. Halpert, Ranbo Yu, Dan Wang</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101038.jpg" width="159" height="121" alt="Hierarchical Hydroxyapatite Microspheres Composed of Nanorods and Their Competitive Sorption Behavior for Heavy Metal Ions" title="Hierarchical Hydroxyapatite Microspheres Composed of Nanorods and Their Competitive Sorption Behavior for Heavy Metal Ions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Ronghai Zhu, Xiaoyong Lai, Jonathan E. Halpert, Ranbo Yu, Dan Wang<br /><i>Eur. J. Inorg. Chem.</i>, January 27, 2012, DOI: 10.1002/ejic.201101038. <a href="http://dx.doi.org/10.1002/ejic.201101038">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101036">
<title>Nickel-Catalyzed Cross-Coupling with Pincer Ligands</title>
<link>http://dx.doi.org/10.1002/ejic.201101036</link>
<dc:creator>Zhong-Xia Wang, Ning Liu</dc:creator>
<dc:date>2012-01-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101036.jpg" width="213" height="68" alt="Nickel-Catalyzed Cross-Coupling with Pincer Ligands" title="Nickel-Catalyzed Cross-Coupling with Pincer Ligands" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Zhong-Xia Wang, Ning Liu<br /><i>Eur. J. Inorg. Chem.</i>, January 16, 2012, DOI: 10.1002/ejic.201101036. <a href="http://dx.doi.org/10.1002/ejic.201101036">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101033">
<title>A Systematic Study of Electrochemical and Spectral Properties for the Electronic Interactions in Porphyrin&#x2013;Triphenylamine Conjugates</title>
<link>http://dx.doi.org/10.1002/ejic.201101033</link>
<dc:creator>Chih-Yen Huang, Chao-Yen Hsu, Luo-Yi Yang, Chia-Jung Lee, Te-Fang Yang, Chia-Chan Hsu, Chung-Hsiu Ke, Yuhlong Oliver Su</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101033.jpg" width="331" height="86" alt="A Systematic Study of Electrochemical and Spectral Properties for the Electronic Interactions in Porphyrin&ndash;Triphenylamine Conjugates" title="A Systematic Study of Electrochemical and Spectral Properties for the Electronic Interactions in Porphyrin&ndash;Triphenylamine Conjugates" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Chih-Yen Huang, Chao-Yen Hsu, Luo-Yi Yang, Chia-Jung Lee, Te-Fang Yang, Chia-Chan Hsu, Chung-Hsiu Ke, Yuhlong Oliver Su<br /><i>Eur. J. Inorg. Chem.</i>, January 30, 2012, DOI: 10.1002/ejic.201101033. <a href="http://dx.doi.org/10.1002/ejic.201101033">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101026">
<title>Ruthenium(III) Cyclometalates Obtained by Site-Specific Orthometallation and Their Reactivity with Nitric Oxide: Photoinduced Release and Estimation of NO Liberated from the Ruthenium Nitrosyl Complexes</title>
<link>http://dx.doi.org/10.1002/ejic.201101026</link>
<dc:creator>Kaushik Ghosh, Sushil Kumar, Rajan Kumar, Udai P. Singh</dc:creator>
<dc:date>2012-01-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101026.jpg" width="409" height="189" alt="Ruthenium(III) Cyclometalates Obtained by Site-Specific Orthometallation and Their Reactivity with Nitric Oxide: Photoinduced Release and Estimation of NO Liberated from the Ruthenium Nitrosyl Complexes" title="Ruthenium(III) Cyclometalates Obtained by Site-Specific Orthometallation and Their Reactivity with Nitric Oxide: Photoinduced Release and Estimation of NO Liberated from the Ruthenium Nitrosyl Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Kaushik Ghosh, Sushil Kumar, Rajan Kumar, Udai P. Singh<br /><i>Eur. J. Inorg. Chem.</i>, January 23, 2012, DOI: 10.1002/ejic.201101026. <a href="http://dx.doi.org/10.1002/ejic.201101026">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201101014">
<title>Synthesis of &#x3B2;-Hydroxy and &#x3B2;-Amino Ketones from Allylic Alcohols Catalyzed by Ru(&#x3B7;&lt;SUP&gt;5&lt;/SUP&gt;-C&lt;sub&gt;5&lt;/sub&gt;Ph&lt;sub&gt;5&lt;/sub&gt;)(CO)&lt;sub&gt;2&lt;/sub&gt;Cl</title>
<link>http://dx.doi.org/10.1002/ejic.201101014</link>
<dc:creator>Agnieszka Bartoszewicz, Martina M. Je&#x17C;owska, K&#xE9;vin Laymand, Juri M&#xF6;bus, Bel&#xE9;n Mart&#xED;n-Matute</dc:creator>
<dc:date>2011-12-29T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201101014.jpg" width="210" height="100" alt="Synthesis of &beta;-Hydroxy and &beta;-Amino Ketones from Allylic Alcohols Catalyzed by Ru(&eta;5-C5Ph5)(CO)2Cl" title="Synthesis of &beta;-Hydroxy and &beta;-Amino Ketones from Allylic Alcohols Catalyzed by Ru(&eta;5-C5Ph5)(CO)2Cl" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Agnieszka Bartoszewicz, Martina M. Je&#x17C;owska, K&#xE9;vin Laymand, Juri M&#xF6;bus, Bel&#xE9;n Mart&#xED;n-Matute<br /><i>Eur. J. Inorg. Chem.</i>, December 29, 2011, DOI: 10.1002/ejic.201101014. <a href="http://dx.doi.org/10.1002/ejic.201101014">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100992">
<title>Kinetic and Mechanistic Studies on the Reactions of the Reduced Vitamin B&lt;sub&gt;12&lt;/sub&gt; Complex Cob(I)alamin with Nitrite and Nitrate&lt;P&gt;Dedicated to the memory of Dr. Edwin S. Gould&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201100992</link>
<dc:creator>Noah T. Plymale, Rohan S. Dassanayake, Hanaa A. Hassanin, Nicola E. Brasch</dc:creator>
<dc:date>2011-12-14T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100992.jpg" width="283" height="115" alt="Kinetic and Mechanistic Studies on the Reactions of the Reduced Vitamin B12 Complex Cob(I)alamin with Nitrite and NitrateDedicated to the memory of Dr. Edwin S. Gould" title="Kinetic and Mechanistic Studies on the Reactions of the Reduced Vitamin B12 Complex Cob(I)alamin with Nitrite and NitrateDedicated to the memory of Dr. Edwin S. Gould" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Noah T. Plymale, Rohan S. Dassanayake, Hanaa A. Hassanin, Nicola E. Brasch<br /><i>Eur. J. Inorg. Chem.</i>, December 14, 2011, DOI: 10.1002/ejic.201100992. <a href="http://dx.doi.org/10.1002/ejic.201100992">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100990">
<title>Cyclopentadienyl-, Indenyl- and Fluorenyl-Functionalized N-Heterocyclic Carbene Metal Complexes: Synthesis and Catalytic Applications</title>
<link>http://dx.doi.org/10.1002/ejic.201100990</link>
<dc:creator>Beatriz Royo, Eduardo Peris</dc:creator>
<dc:date>2011-11-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100990.jpg" width="155" height="107" alt="Cyclopentadienyl-, Indenyl- and Fluorenyl-Functionalized N-Heterocyclic Carbene Metal Complexes: Synthesis and Catalytic Applications" title="Cyclopentadienyl-, Indenyl- and Fluorenyl-Functionalized N-Heterocyclic Carbene Metal Complexes: Synthesis and Catalytic Applications" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Beatriz Royo, Eduardo Peris<br /><i>Eur. J. Inorg. Chem.</i>, November 30, 2011, DOI: 10.1002/ejic.201100990. <a href="http://dx.doi.org/10.1002/ejic.201100990">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100988">
<title>Graphitic Carbon Nanocapsules: Scaled Preparation, Formation Mechanism, and Use as an Excellent Support for Methanol Electro-oxidation</title>
<link>http://dx.doi.org/10.1002/ejic.201100988</link>
<dc:creator>Lei Wang, Chungui Tian, Hongxing Zhang, Honggang Fu</dc:creator>
<dc:date>2012-01-18T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100988.jpg" width="370" height="78" alt="Graphitic Carbon Nanocapsules: Scaled Preparation, Formation Mechanism, and Use as an Excellent Support for Methanol Electro-oxidation" title="Graphitic Carbon Nanocapsules: Scaled Preparation, Formation Mechanism, and Use as an Excellent Support for Methanol Electro-oxidation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Lei Wang, Chungui Tian, Hongxing Zhang, Honggang Fu<br /><i>Eur. J. Inorg. Chem.</i>, January 18, 2012, DOI: 10.1002/ejic.201100988. <a href="http://dx.doi.org/10.1002/ejic.201100988">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100981">
<title>Synthesis and Reactivity of Ester-Functionalized 5-Membered Rh&lt;SUP&gt;I&lt;/SUP&gt;-&#x3BA;&lt;SUP&gt;2&lt;/SUP&gt;-C,O-Chelates and Their Relevance in Rh(cod)-Mediated Carbene Polymerization</title>
<link>http://dx.doi.org/10.1002/ejic.201100981</link>
<dc:creator>Markus Finger, Martin Lutz, Joost N. H. Reek, Bas de Bruin</dc:creator>
<dc:date>2011-12-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100981.jpg" width="155" height="127" alt="Synthesis and Reactivity of Ester-Functionalized 5-Membered RhI-&kappa;2-C,O-Chelates and Their Relevance in Rh(cod)-Mediated Carbene Polymerization" title="Synthesis and Reactivity of Ester-Functionalized 5-Membered RhI-&kappa;2-C,O-Chelates and Their Relevance in Rh(cod)-Mediated Carbene Polymerization" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Markus Finger, Martin Lutz, Joost N. H. Reek, Bas de Bruin<br /><i>Eur. J. Inorg. Chem.</i>, December 23, 2011, DOI: 10.1002/ejic.201100981. <a href="http://dx.doi.org/10.1002/ejic.201100981">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100968">
<title>Cationic Group 4 Metallocene&#x2013;(&lt;I&gt;o&lt;/I&gt;-Phosphanylaryl)oxido Complexes: Synthetic Routes to Transition-Metal Frustrated Lewis Pairs</title>
<link>http://dx.doi.org/10.1002/ejic.201100968</link>
<dc:creator>Andy M. Chapman, Mairi F. Haddow, Duncan F. Wass</dc:creator>
<dc:date>2011-12-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100968.jpg" width="195" height="117" alt="Cationic Group 4 Metallocene&ndash;(o-Phosphanylaryl)oxido Complexes: Synthetic Routes to Transition-Metal Frustrated Lewis Pairs" title="Cationic Group 4 Metallocene&ndash;(o-Phosphanylaryl)oxido Complexes: Synthetic Routes to Transition-Metal Frustrated Lewis Pairs" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Andy M. Chapman, Mairi F. Haddow, Duncan F. Wass<br /><i>Eur. J. Inorg. Chem.</i>, December 9, 2011, DOI: 10.1002/ejic.201100968. <a href="http://dx.doi.org/10.1002/ejic.201100968">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100956">
<title>Unexpected Outcomes of the Oxidation of (Pentafluorophenyl)triphenylphosphanegold(I)</title>
<link>http://dx.doi.org/10.1002/ejic.201100956</link>
<dc:creator>Manuel Hofer, Cristina Nevado</dc:creator>
<dc:date>2011-11-28T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100956.jpg" width="428" height="56" alt="Unexpected Outcomes of the Oxidation of (Pentafluorophenyl)triphenylphosphanegold(I)" title="Unexpected Outcomes of the Oxidation of (Pentafluorophenyl)triphenylphosphanegold(I)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Manuel Hofer, Cristina Nevado<br /><i>Eur. J. Inorg. Chem.</i>, November 28, 2011, DOI: 10.1002/ejic.201100956. <a href="http://dx.doi.org/10.1002/ejic.201100956">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100954">
<title>An NMR Study of the Oxidative Degradation of Cp*Ir Catalysts for Water Oxidation: Evidence for a Preliminary Attack on the Quaternary Carbon Atom of the &#x2013;C&#x2013;CH&lt;sub&gt;3&lt;/sub&gt; Moiety</title>
<link>http://dx.doi.org/10.1002/ejic.201100954</link>
<dc:creator>Cristiano Zuccaccia, Gianfranco Bellachioma, Sandra Bola&#xF1;o, Luca Rocchigiani, Arianna Savini, Alceo Macchioni</dc:creator>
<dc:date>2011-11-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100954.jpg" width="296" height="66" alt="An NMR Study of the Oxidative Degradation of Cp*Ir Catalysts for Water Oxidation: Evidence for a Preliminary Attack on the Quaternary Carbon Atom of the &ndash;C&ndash;CH3 Moiety" title="An NMR Study of the Oxidative Degradation of Cp*Ir Catalysts for Water Oxidation: Evidence for a Preliminary Attack on the Quaternary Carbon Atom of the &ndash;C&ndash;CH3 Moiety" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Cristiano Zuccaccia, Gianfranco Bellachioma, Sandra Bola&#xF1;o, Luca Rocchigiani, Arianna Savini, Alceo Macchioni<br /><i>Eur. J. Inorg. Chem.</i>, November 30, 2011, DOI: 10.1002/ejic.201100954. <a href="http://dx.doi.org/10.1002/ejic.201100954">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100951">
<title>Influence of Morphology and Texture of CeO&lt;sub&gt;2&lt;/sub&gt; on YBa&lt;sub&gt;2&lt;/sub&gt;Cu&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt; (YBCO) Growth and BaCeO&lt;sub&gt;3&lt;/sub&gt; Formation in Solution-Derived Synthesis</title>
<link>http://dx.doi.org/10.1002/ejic.201100951</link>
<dc:creator>Nigel Van de Velde, Tom Bruggeman, Lander Stove, Glenn Pollefeyt, Oliver Brunkahl, Isabel Van Driessche</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100951.jpg" width="155" height="119" alt="Influence of Morphology and Texture of CeO2 on YBa2Cu3O7 (YBCO) Growth and BaCeO3 Formation in Solution-Derived Synthesis" title="Influence of Morphology and Texture of CeO2 on YBa2Cu3O7 (YBCO) Growth and BaCeO3 Formation in Solution-Derived Synthesis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Nigel Van de Velde, Tom Bruggeman, Lander Stove, Glenn Pollefeyt, Oliver Brunkahl, Isabel Van Driessche<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201100951. <a href="http://dx.doi.org/10.1002/ejic.201100951">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100942">
<title>New Structural Features in Tetranuclear Iron Carbonyl Thiocarbonyls: Exotriangular Iron Atoms and Six-Electron-Donoating Thiocarbonyl Groups Bridging Four Iron Atoms</title>
<link>http://dx.doi.org/10.1002/ejic.201100942</link>
<dc:creator>Zhong Zhang, Qian-shu Li, R. Bruce King, Henry F. Schaefer, III </dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100942.jpg" width="210" height="135" alt="New Structural Features in Tetranuclear Iron Carbonyl Thiocarbonyls: Exotriangular Iron Atoms and Six-Electron-Donoating Thiocarbonyl Groups Bridging Four Iron Atoms" title="New Structural Features in Tetranuclear Iron Carbonyl Thiocarbonyls: Exotriangular Iron Atoms and Six-Electron-Donoating Thiocarbonyl Groups Bridging Four Iron Atoms" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Zhong Zhang, Qian-shu Li, R. Bruce King, Henry F. Schaefer, III <br /><i>Eur. J. Inorg. Chem.</i>, January 17, 2012, DOI: 10.1002/ejic.201100942. <a href="http://dx.doi.org/10.1002/ejic.201100942">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100940">
<title>Chelating C4-Bound Imidazolylidene Complexes through Oxidative Addition of Imidazolium Salts to Palladium(0)</title>
<link>http://dx.doi.org/10.1002/ejic.201100940</link>
<dc:creator>Anneke Kr&#xFC;ger, Evelyne Kluser, Helge M&#xFC;ller-Bunz, Antonia Neels, Martin Albrecht</dc:creator>
<dc:date>2011-11-10T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100940.jpg" width="448" height="72" alt="Chelating C4-Bound Imidazolylidene Complexes through Oxidative Addition of Imidazolium Salts to Palladium(0)" title="Chelating C4-Bound Imidazolylidene Complexes through Oxidative Addition of Imidazolium Salts to Palladium(0)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Anneke Kr&#xFC;ger, Evelyne Kluser, Helge M&#xFC;ller-Bunz, Antonia Neels, Martin Albrecht<br /><i>Eur. J. Inorg. Chem.</i>, November 10, 2011, DOI: 10.1002/ejic.201100940. <a href="http://dx.doi.org/10.1002/ejic.201100940">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100936">
<title>Fabrication of a 3D Hierarchical Flower-Like MgO Microsphere and Its Application as Heterogeneous Catalyst</title>
<link>http://dx.doi.org/10.1002/ejic.201100936</link>
<dc:creator>Yang Qu, Wei Zhou, Zhiyu Ren, Kai Pan, Chungui Tian, Yang Liu, Shanshan Feng, Youzhen Dong, Honggang Fu</dc:creator>
<dc:date>2012-01-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100936.jpg" width="389" height="89" alt="Fabrication of a 3D Hierarchical Flower-Like MgO Microsphere and Its Application as Heterogeneous Catalyst" title="Fabrication of a 3D Hierarchical Flower-Like MgO Microsphere and Its Application as Heterogeneous Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Yang Qu, Wei Zhou, Zhiyu Ren, Kai Pan, Chungui Tian, Yang Liu, Shanshan Feng, Youzhen Dong, Honggang Fu<br /><i>Eur. J. Inorg. Chem.</i>, January 16, 2012, DOI: 10.1002/ejic.201100936. <a href="http://dx.doi.org/10.1002/ejic.201100936">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100932">
<title>The Nature of the Barrier to Phosphane Dissociation from Grubbs Olefin Metathesis Catalysts</title>
<link>http://dx.doi.org/10.1002/ejic.201100932</link>
<dc:creator>Yury Minenkov, Giovanni Occhipinti, Wouter Heyndrickx, Vidar R. Jensen</dc:creator>
<dc:date>2011-12-21T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100932.jpg" width="213" height="109" alt="The Nature of the Barrier to Phosphane Dissociation from Grubbs Olefin Metathesis Catalysts" title="The Nature of the Barrier to Phosphane Dissociation from Grubbs Olefin Metathesis Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Yury Minenkov, Giovanni Occhipinti, Wouter Heyndrickx, Vidar R. Jensen<br /><i>Eur. J. Inorg. Chem.</i>, December 21, 2011, DOI: 10.1002/ejic.201100932. <a href="http://dx.doi.org/10.1002/ejic.201100932">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100931">
<title>Ruthenium Acetate Complexes as Versatile Probes of Metal&#x2013;Ligand Interactions: Insight into the Ligand Effects of Vinylidene, Carbene, Carbonyl, Nitrosyl and Isocyanide</title>
<link>http://dx.doi.org/10.1002/ejic.201100931</link>
<dc:creator>Christine E. Welby, Thomas O. Eschemann, Christopher A. Unsworth, Elizabeth J. Smith, Robert J. Thatcher, Adrian C. Whitwood, Jason M. Lynam</dc:creator>
<dc:date>2011-12-21T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100931.jpg" width="175" height="93" alt="Ruthenium Acetate Complexes as Versatile Probes of Metal&ndash;Ligand Interactions: Insight into the Ligand Effects of Vinylidene, Carbene, Carbonyl, Nitrosyl and Isocyanide" title="Ruthenium Acetate Complexes as Versatile Probes of Metal&ndash;Ligand Interactions: Insight into the Ligand Effects of Vinylidene, Carbene, Carbonyl, Nitrosyl and Isocyanide" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Christine E. Welby, Thomas O. Eschemann, Christopher A. Unsworth, Elizabeth J. Smith, Robert J. Thatcher, Adrian C. Whitwood, Jason M. Lynam<br /><i>Eur. J. Inorg. Chem.</i>, December 21, 2011, DOI: 10.1002/ejic.201100931. <a href="http://dx.doi.org/10.1002/ejic.201100931">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100929">
<title>Dinuclear and Mononuclear Chromium Acetylide Complexes&lt;P&gt;Dedicated to Professor Gerhard Erker on the occasion of his 65th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201100929</link>
<dc:creator>Carolina Egler-Lucas, Olivier Blacque, Koushik Venkatesan, Alberto L&#xF3;pez-Hern&#xE1;ndez, Heinz Berke</dc:creator>
<dc:date>2011-12-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100929.jpg" width="377" height="110" alt="Dinuclear and Mononuclear Chromium Acetylide ComplexesDedicated to Professor Gerhard Erker on the occasion of his 65th birthday" title="Dinuclear and Mononuclear Chromium Acetylide ComplexesDedicated to Professor Gerhard Erker on the occasion of his 65th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Carolina Egler-Lucas, Olivier Blacque, Koushik Venkatesan, Alberto L&#xF3;pez-Hern&#xE1;ndez, Heinz Berke<br /><i>Eur. J. Inorg. Chem.</i>, December 2, 2011, DOI: 10.1002/ejic.201100929. <a href="http://dx.doi.org/10.1002/ejic.201100929">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100928">
<title>Arene Exchange in the Ruthenium&#x2013;Naphthalene Complex [CpRu(C&lt;sub&gt;10&lt;/sub&gt;H&lt;sub&gt;8&lt;/sub&gt;)]&lt;SUP&gt;+&lt;/SUP&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201100928</link>
<dc:creator>Dmitry S. Perekalin, Eduard E. Karslyan, Pavel V. Petrovskii, Alexandra O. Borissova, Konstantin A. Lyssenko, Alexander R. Kudinov</dc:creator>
<dc:date>2011-11-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100928.jpg" width="195" height="79" alt="Arene Exchange in the Ruthenium&ndash;Naphthalene Complex [CpRu(C10H8)]+" title="Arene Exchange in the Ruthenium&ndash;Naphthalene Complex [CpRu(C10H8)]+" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Dmitry S. Perekalin, Eduard E. Karslyan, Pavel V. Petrovskii, Alexandra O. Borissova, Konstantin A. Lyssenko, Alexander R. Kudinov<br /><i>Eur. J. Inorg. Chem.</i>, November 23, 2011, DOI: 10.1002/ejic.201100928. <a href="http://dx.doi.org/10.1002/ejic.201100928">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100927">
<title>Unique Type of BF&lt;sub&gt;2&lt;/sub&gt;-Capped Tetraoxobenzene &#x3C0;-Complexes of &#x201C;Cp*M&#x201D;: Novel Organometallic Backbones for the Self-Assembly of Porous Networks</title>
<link>http://dx.doi.org/10.1002/ejic.201100927</link>
<dc:creator>Jamal Moussa, Aur&#xE9;lie Damas, Lise-Marie Chamoreau, Marie Noelle Rager, Hani Amouri</dc:creator>
<dc:date>2011-10-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100927.jpg" width="187" height="175" alt="Unique Type of BF2-Capped Tetraoxobenzene &pi;-Complexes of &ldquo;Cp*M&rdquo;: Novel Organometallic Backbones for the Self-Assembly of Porous Networks" title="Unique Type of BF2-Capped Tetraoxobenzene &pi;-Complexes of &ldquo;Cp*M&rdquo;: Novel Organometallic Backbones for the Self-Assembly of Porous Networks" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Jamal Moussa, Aur&#xE9;lie Damas, Lise-Marie Chamoreau, Marie Noelle Rager, Hani Amouri<br /><i>Eur. J. Inorg. Chem.</i>, October 24, 2011, DOI: 10.1002/ejic.201100927. <a href="http://dx.doi.org/10.1002/ejic.201100927">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100925">
<title>Synthesis of Ir[&#x3BC;&lt;SUP&gt;2&lt;/SUP&gt;-(&lt;I&gt;N&lt;/I&gt;-&lt;I&gt;N&lt;/I&gt;)]M (M = Ir and Ru) Homo- and Heterobimetallic Complexes through a Condensation Reaction of &lt;I&gt;N&lt;/I&gt;-Amino and Formyl Groups Bound to Mononuclear (&#x3B7;&lt;SUP&gt;&lt;I&gt;n&lt;/I&gt;&lt;/SUP&gt;-C&lt;I&gt;&lt;sub&gt;n&lt;/sub&gt;&lt;/I&gt;Me&lt;I&gt;&lt;sub&gt;n&lt;/sub&gt;&lt;/I&gt;)M Units (&lt;I&gt;n&lt;/I&gt; = 5 for M = Ir; &lt;I&gt;n&lt;/I&gt; = 6 for M = Ru)</title>
<link>http://dx.doi.org/10.1002/ejic.201100925</link>
<dc:creator>Keisuke Nakao, Gyeongshin Choi, Yuki Konishi, Hayato Tsurugi, Kazushi Mashima</dc:creator>
<dc:date>2011-12-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100925.jpg" width="207" height="145" alt="Synthesis of Ir[&mu;2-(N-N)]M (M = Ir and Ru) Homo- and Heterobimetallic Complexes through a Condensation Reaction of N-Amino and Formyl Groups Bound to Mononuclear (&eta;n-CnMen)M Units (n = 5 for M = Ir; n = 6 for M = Ru)" title="Synthesis of Ir[&mu;2-(N-N)]M (M = Ir and Ru) Homo- and Heterobimetallic Complexes through a Condensation Reaction of N-Amino and Formyl Groups Bound to Mononuclear (&eta;n-CnMen)M Units (n = 5 for M = Ir; n = 6 for M = Ru)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Keisuke Nakao, Gyeongshin Choi, Yuki Konishi, Hayato Tsurugi, Kazushi Mashima<br /><i>Eur. J. Inorg. Chem.</i>, December 7, 2011, DOI: 10.1002/ejic.201100925. <a href="http://dx.doi.org/10.1002/ejic.201100925">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100919">
<title>Synthesis and Characterization of Dioxidodiphenylrhenium(VII) Propionate</title>
<link>http://dx.doi.org/10.1002/ejic.201100919</link>
<dc:creator>Stefan Huber, Mirza Cokoja, Markus Drees, Wolfgang A. Herrmann, Fritz E. K&#xFC;hn</dc:creator>
<dc:date>2011-10-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100919.jpg" width="195" height="125" alt="Synthesis and Characterization of Dioxidodiphenylrhenium(VII) Propionate" title="Synthesis and Characterization of Dioxidodiphenylrhenium(VII) Propionate" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />Stefan Huber, Mirza Cokoja, Markus Drees, Wolfgang A. Herrmann, Fritz E. K&#xFC;hn<br /><i>Eur. J. Inorg. Chem.</i>, October 25, 2011, DOI: 10.1002/ejic.201100919. <a href="http://dx.doi.org/10.1002/ejic.201100919">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100917">
<title>Synthesis, Structure and Reactivity of Iridium Hydrido Fluorido Complexes</title>
<link>http://dx.doi.org/10.1002/ejic.201100917</link>
<dc:creator>Paul Kl&#xE4;ring, Ann-Katrin Jungton, Thomas Braun, Carsten M&#xFC;ller</dc:creator>
<dc:date>2011-12-21T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100917.jpg" width="377" height="68" alt="Synthesis, Structure and Reactivity of Iridium Hydrido Fluorido Complexes" title="Synthesis, Structure and Reactivity of Iridium Hydrido Fluorido Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Paul Kl&#xE4;ring, Ann-Katrin Jungton, Thomas Braun, Carsten M&#xFC;ller<br /><i>Eur. J. Inorg. Chem.</i>, December 21, 2011, DOI: 10.1002/ejic.201100917. <a href="http://dx.doi.org/10.1002/ejic.201100917">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100905">
<title>Straightforward Synthesis of Dipyrido-Annelated NHC-Palladium(II) Complexes by Oxidative Addition&lt;P&gt;Dedicated to Robert Weiss on the occasion of his 70th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201100905</link>
<dc:creator>Verena Gierz, Alexander Seyboldt, C&#xE4;cilia Maichle-M&#xF6;ssmer, Roland Fr&#xF6;hlich, Frank Rominger, Doris Kunz</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100905.jpg" width="302" height="87" alt="Straightforward Synthesis of Dipyrido-Annelated NHC-Palladium(II) Complexes by Oxidative AdditionDedicated to Robert Weiss on the occasion of his 70th birthday" title="Straightforward Synthesis of Dipyrido-Annelated NHC-Palladium(II) Complexes by Oxidative AdditionDedicated to Robert Weiss on the occasion of his 70th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Verena Gierz, Alexander Seyboldt, C&#xE4;cilia Maichle-M&#xF6;ssmer, Roland Fr&#xF6;hlich, Frank Rominger, Doris Kunz<br /><i>Eur. J. Inorg. Chem.</i>, January 17, 2012, DOI: 10.1002/ejic.201100905. <a href="http://dx.doi.org/10.1002/ejic.201100905">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100904">
<title>New Acylhydrido- and Diacylrhodium(III) Organocomplexes Derived from 8-Quinolinecarbaldehyde and/or &lt;I&gt;o&lt;/I&gt;-(Diphenylphosphanyl)benzaldehyde</title>
<link>http://dx.doi.org/10.1002/ejic.201100904</link>
<dc:creator>Montserrat Barqu&#xED;n, Mar&#xED;a A. Garralda, Ricardo Hern&#xE1;ndez, Lourdes Ibarlucea, Claudio Mendicute-Fierro, M. Carmen Torralba, M. Rosario Torres, Virginia San Nacianceno, Itziar Zumeta</dc:creator>
<dc:date>2011-12-14T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100904.jpg" width="202" height="205" alt="New Acylhydrido- and Diacylrhodium(III) Organocomplexes Derived from 8-Quinolinecarbaldehyde and/or o-(Diphenylphosphanyl)benzaldehyde" title="New Acylhydrido- and Diacylrhodium(III) Organocomplexes Derived from 8-Quinolinecarbaldehyde and/or o-(Diphenylphosphanyl)benzaldehyde" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Montserrat Barqu&#xED;n, Mar&#xED;a A. Garralda, Ricardo Hern&#xE1;ndez, Lourdes Ibarlucea, Claudio Mendicute-Fierro, M. Carmen Torralba, M. Rosario Torres, Virginia San Nacianceno, Itziar Zumeta<br /><i>Eur. J. Inorg. Chem.</i>, December 14, 2011, DOI: 10.1002/ejic.201100904. <a href="http://dx.doi.org/10.1002/ejic.201100904">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100894">
<title>Lanthanide Complexes as Paramagnetic Probes for &lt;SUP&gt;19&lt;/SUP&gt;F Magnetic Resonance</title>
<link>http://dx.doi.org/10.1002/ejic.201100894</link>
<dc:creator>Peter Harvey, Ilya Kuprov, David Parker</dc:creator>
<dc:date>2011-11-08T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100894.jpg" width="195" height="185" alt="Lanthanide Complexes as Paramagnetic Probes for 19F Magnetic Resonance" title="Lanthanide Complexes as Paramagnetic Probes for 19F Magnetic Resonance" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Peter Harvey, Ilya Kuprov, David Parker<br /><i>Eur. J. Inorg. Chem.</i>, November 8, 2011, DOI: 10.1002/ejic.201100894. <a href="http://dx.doi.org/10.1002/ejic.201100894">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100890">
<title>Hydroalumination of Bis(alkynyl)silanes: Generation of Chelating Lewis Acids, Their Application in the Coordination of Chloride Ions and a 1,1-Carbalumination Reaction</title>
<link>http://dx.doi.org/10.1002/ejic.201100890</link>
<dc:creator>Werner Uhl, Denis Heller, Jutta K&#xF6;sters, Ernst-Ulrich W&#xFC;rthwein, Nugzar Ghavtadze</dc:creator>
<dc:date>2011-11-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100890.jpg" width="116" height="110" alt="Hydroalumination of Bis(alkynyl)silanes: Generation of Chelating Lewis Acids, Their Application in the Coordination of Chloride Ions and a 1,1-Carbalumination Reaction" title="Hydroalumination of Bis(alkynyl)silanes: Generation of Chelating Lewis Acids, Their Application in the Coordination of Chloride Ions and a 1,1-Carbalumination Reaction" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Werner Uhl, Denis Heller, Jutta K&#xF6;sters, Ernst-Ulrich W&#xFC;rthwein, Nugzar Ghavtadze<br /><i>Eur. J. Inorg. Chem.</i>, November 7, 2011, DOI: 10.1002/ejic.201100890. <a href="http://dx.doi.org/10.1002/ejic.201100890">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100856">
<title>Group 10 Metal Complexes of a Ferrocene-Based N-Heterocyclic Carbene: Syntheses, Structures and Catalytic Applications&lt;P&gt;Dedicated to Professor Dirk Steinborn on the occasion of his 65th birthday&lt;/P&gt;</title>
<link>http://dx.doi.org/10.1002/ejic.201100856</link>
<dc:creator>Ulrich Siemeling, Christian F&#xE4;rber, Clemens Bruhn, Sven F&#xFC;rmeier, Tim Schulz, Michael Kurlemann, Sandra Tripp</dc:creator>
<dc:date>2011-10-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100856.jpg" width="175" height="118" alt="Group 10 Metal Complexes of a Ferrocene-Based N-Heterocyclic Carbene: Syntheses, Structures and Catalytic ApplicationsDedicated to Professor Dirk Steinborn on the occasion of his 65th birthday" title="Group 10 Metal Complexes of a Ferrocene-Based N-Heterocyclic Carbene: Syntheses, Structures and Catalytic ApplicationsDedicated to Professor Dirk Steinborn on the occasion of his 65th birthday" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Ulrich Siemeling, Christian F&#xE4;rber, Clemens Bruhn, Sven F&#xFC;rmeier, Tim Schulz, Michael Kurlemann, Sandra Tripp<br /><i>Eur. J. Inorg. Chem.</i>, October 17, 2011, DOI: 10.1002/ejic.201100856. <a href="http://dx.doi.org/10.1002/ejic.201100856">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100853">
<title>Structural Heterogeneity of Ag&lt;SUP&gt;I&lt;/SUP&gt; Complexes with a Flexible 1,2-Bis[(imidazol-2-yl)thiomethyl]benzene Ligand and Issues Regarding the Phase Purity of the Bulk Material</title>
<link>http://dx.doi.org/10.1002/ejic.201100853</link>
<dc:creator>Liliana Dobrza&#x144;ska</dc:creator>
<dc:date>2012-01-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100853.jpg" width="213" height="169" alt="Structural Heterogeneity of AgI Complexes with a Flexible 1,2-Bis[(imidazol-2-yl)thiomethyl]benzene Ligand and Issues Regarding the Phase Purity of the Bulk Material" title="Structural Heterogeneity of AgI Complexes with a Flexible 1,2-Bis[(imidazol-2-yl)thiomethyl]benzene Ligand and Issues Regarding the Phase Purity of the Bulk Material" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Liliana Dobrza&#x144;ska<br /><i>Eur. J. Inorg. Chem.</i>, January 23, 2012, DOI: 10.1002/ejic.201100853. <a href="http://dx.doi.org/10.1002/ejic.201100853">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100806">
<title>Two Environmentally Friendly Energetic Compounds, [Mn(AZT)&lt;sub&gt;4&lt;/sub&gt;(H&lt;sub&gt;2&lt;/sub&gt;O)&lt;sub&gt;2&lt;/sub&gt;](PA)&lt;sub&gt;2&lt;/sub&gt;&#xB7;4H&lt;sub&gt;2&lt;/sub&gt;O and [Co(AZT)&lt;sub&gt;2&lt;/sub&gt;(H&lt;sub&gt;2&lt;/sub&gt;O)&lt;sub&gt;4&lt;/sub&gt;](PA)&lt;sub&gt;2&lt;/sub&gt;, Based on 3-Azido-1,2,4-triazole (AZT) and Picrate (PA)</title>
<link>http://dx.doi.org/10.1002/ejic.201100806</link>
<dc:creator>Bi-Dong Wu, Jian-Guo Zhang, Tong-Lai Zhang, Li Yang, Zun-Ning Zhou</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100806.jpg" width="213" height="145" alt="Two Environmentally Friendly Energetic Compounds, [Mn(AZT)4(H2O)2](PA)2&middot;4H2O and [Co(AZT)2(H2O)4](PA)2, Based on 3-Azido-1,2,4-triazole (AZT) and Picrate (PA)" title="Two Environmentally Friendly Energetic Compounds, [Mn(AZT)4(H2O)2](PA)2&middot;4H2O and [Co(AZT)2(H2O)4](PA)2, Based on 3-Azido-1,2,4-triazole (AZT) and Picrate (PA)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Full Paper]<br />Bi-Dong Wu, Jian-Guo Zhang, Tong-Lai Zhang, Li Yang, Zun-Ning Zhou<br /><i>Eur. J. Inorg. Chem.</i>, February 3, 2012, DOI: 10.1002/ejic.201100806. <a href="http://dx.doi.org/10.1002/ejic.201100806">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100762">
<title>Cyclopentadienyl&#x2013;NHC Iron Complexes for Solvent-Free Catalytic Hydrosilylation of Aldehydes and Ketones</title>
<link>http://dx.doi.org/10.1002/ejic.201100762</link>
<dc:creator>David B&#xE9;zier, Fan Jiang, Thierry Roisnel, Jean-Baptiste Sortais, Christophe Darcel</dc:creator>
<dc:date>2011-10-14T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100762.jpg" width="213" height="148" alt="Cyclopentadienyl&ndash;NHC Iron Complexes for Solvent-Free Catalytic Hydrosilylation of Aldehydes and Ketones" title="Cyclopentadienyl&ndash;NHC Iron Complexes for Solvent-Free Catalytic Hydrosilylation of Aldehydes and Ketones" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Short Communication]<br />David B&#xE9;zier, Fan Jiang, Thierry Roisnel, Jean-Baptiste Sortais, Christophe Darcel<br /><i>Eur. J. Inorg. Chem.</i>, October 14, 2011, DOI: 10.1002/ejic.201100762. <a href="http://dx.doi.org/10.1002/ejic.201100762">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100609">
<title>[&lt;I&gt;n&lt;/I&gt;]Borametalloarenophanes (&lt;I&gt;n&lt;/I&gt; = 1, 2): Strained Systems with Uncommon Reactivity Patterns</title>
<link>http://dx.doi.org/10.1002/ejic.201100609</link>
<dc:creator>Holger Braunschweig, Thomas Kupfer</dc:creator>
<dc:date>2011-10-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/ejic201100609.jpg" width="311" height="85" alt="[n]Borametalloarenophanes (n = 1, 2): Strained Systems with Uncommon Reactivity Patterns" title="[n]Borametalloarenophanes (n = 1, 2): Strained Systems with Uncommon Reactivity Patterns" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><p> [Microreview]<br />Holger Braunschweig, Thomas Kupfer<br /><i>Eur. J. Inorg. Chem.</i>, October 27, 2011, DOI: 10.1002/ejic.201100609. <a href="http://dx.doi.org/10.1002/ejic.201100609">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100688">
<title>Synthesis of Furfural from Xylose, Xylan, and Biomass Using AlCl&lt;sub&gt;3&lt;/sub&gt;&#xB7;6&#xA0;H&lt;sub&gt;2&lt;/sub&gt;O in Biphasic Media via Xylose Isomerization to Xylulose</title>
<link>http://dx.doi.org/10.1002/cssc.201100688</link>
<dc:creator>Yu Yang, Chang-Wei Hu, Mahdi M. Abu-Omar</dc:creator>
<dc:date>2012-02-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100688.gif" width="170" height="195" alt="Synthesis of Furfural from Xylose, Xylan, and Biomass Using AlCl3&middot;6&nbsp;H2O in Biphasic Media via Xylose Isomerization to Xylulose" title="Synthesis of Furfural from Xylose, Xylan, and Biomass Using AlCl3&middot;6&nbsp;H2O in Biphasic Media via Xylose Isomerization to Xylulose" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Aluminum in microwaves:</B> AlCl<sub>3</sub><B>&middot;</B>6&nbsp;H<sub>2</sub>O successively hydrolyzes biomass hemicellulose to xylose, isomerizes xylose to xylulose, and dehydrates xylulose to furfural under microwave heating at 160&nbsp;&deg;C with yields in the range of 38&ndash;64&nbsp;%, depending on the biomass feedstock. The use of a biphasic medium allows the recycling of AlCl<sub>3</sub><B>&middot;</B>6&nbsp;H<sub>2</sub>O (which remains in the aqueous phase) for multiple cycles without loss of activity or selectivity (see figure).</P>
<p> [Full Paper]<br />Yu Yang, Chang-Wei Hu, Mahdi M. Abu-Omar<br /><i>ChemSusChem</i>, February 7, 2012, DOI: 10.1002/cssc.201100688. <a href="http://dx.doi.org/10.1002/cssc.201100688">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100631">
<title>Solid Acid-Catalyzed Cellulose Hydrolysis Monitored by In&#xA0;Situ ATR-IR Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cssc.201100631</link>
<dc:creator>Joseph Zakzeski, Ruud J. H. Grisel, Arjan T. Smit, Bert M. Weckhuysen</dc:creator>
<dc:date>2012-02-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100631.gif" width="215" height="196" alt="Solid Acid-Catalyzed Cellulose Hydrolysis Monitored by In&nbsp;Situ ATR-IR Spectroscopy" title="Solid Acid-Catalyzed Cellulose Hydrolysis Monitored by In&nbsp;Situ ATR-IR Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Vibrating acids:</B> The solid acid-catalyzed hydrolysis of cellulose has been studied by using in&nbsp;situ ATR-IR spectroscopy. It is possible to monitor the formation and consumption of important products and intermediates by their distinctive vibrational characteristics under the reaction conditions.</P>
<p> [Full Paper]<br />Joseph Zakzeski, Ruud J. H. Grisel, Arjan T. Smit, Bert M. Weckhuysen<br /><i>ChemSusChem</i>, February 7, 2012, DOI: 10.1002/cssc.201100631. <a href="http://dx.doi.org/10.1002/cssc.201100631">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100629">
<title>Improved Li-Storage Performance of Li&lt;sub&gt;4&lt;/sub&gt;Ti&lt;sub&gt;5&lt;/sub&gt;O&lt;sub&gt;12&lt;/sub&gt; Coated with C-N Compounds Derived from Pyrolysis of Urea through a Low-Temperature Approach</title>
<link>http://dx.doi.org/10.1002/cssc.201100629</link>
<dc:creator>Huilin Pan, Liang Zhao, Yong-Sheng Hu, Hong Li, Liquan Chen</dc:creator>
<dc:date>2011-12-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100629.gif" width="211" height="160" alt="Improved Li-Storage Performance of Li4Ti5O12 Coated with C-N Compounds Derived from Pyrolysis of Urea through a Low-Temperature Approach" title="Improved Li-Storage Performance of Li4Ti5O12 Coated with C-N Compounds Derived from Pyrolysis of Urea through a Low-Temperature Approach" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The wonders of urea:</B> The porous Li<sub>4</sub>Ti<sub>5</sub>O<sub>12</sub> coated with C-N compound is prepared by pyrolysis of urea at a rather low temperature of 400&nbsp;&deg;C. The coated Li<sub>4</sub>Ti<sub>5</sub>O<sub>12</sub> sample shows improved rate performance and excellent capacity retention after 2000 cycles at a current rate of 2C in a half cell.</P>
<p> [Communication]<br />Huilin Pan, Liang Zhao, Yong-Sheng Hu, Hong Li, Liquan Chen<br /><i>ChemSusChem</i>, December 6, 2011, DOI: 10.1002/cssc.201100629. <a href="http://dx.doi.org/10.1002/cssc.201100629">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100609">
<title>Hollow Carbon Nanospheres with a High Rate Capability for Lithium-Based Batteries</title>
<link>http://dx.doi.org/10.1002/cssc.201100609</link>
<dc:creator>Kun Tang, Robin J. White, Xiaoke Mu, Maria-Magdalena Titirici, Peter A. van Aken, Joachim Maier</dc:creator>
<dc:date>2012-01-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100609.gif" width="207" height="187" alt="Hollow Carbon Nanospheres with a High Rate Capability for Lithium-Based Batteries" title="Hollow Carbon Nanospheres with a High Rate Capability for Lithium-Based Batteries" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Higher spheres:</B> Hollow carbon nanospheres are prepared from glucose through a facile, sustainable hydrothermal method. Their morphology provides fast electron and lithium ion transport, which is reflected in a superior rate capability (100&nbsp;mAh&nbsp;g<SUP>&minus;1</SUP> at 50&nbsp;C) and good cycle stability. Nevertheless, these results provide direct evidence that not only lithium-ion insertion/extraction to the carbon layers occurs, but also that a surface reaction contributes to the high rate performance.</P>
<p> [Communication]<br />Kun Tang, Robin J. White, Xiaoke Mu, Maria-Magdalena Titirici, Peter A. van&#xA0;Aken, Joachim Maier<br /><i>ChemSusChem</i>, January 19, 2012, DOI: 10.1002/cssc.201100609. <a href="http://dx.doi.org/10.1002/cssc.201100609">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100608">
<title>Conversion of Hemicellulose to Furfural and Levulinic Acid using Biphasic Reactors with Alkylphenol Solvents</title>
<link>http://dx.doi.org/10.1002/cssc.201100608</link>
<dc:creator>Elif I. G&#xFC;rb&#xFC;z, Stephanie G. Wettstein, James A. Dumesic</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100608.gif" width="215" height="157" alt="Conversion of Hemicellulose to Furfural and Levulinic Acid using Biphasic Reactors with Alkylphenol Solvents" title="Conversion of Hemicellulose to Furfural and Levulinic Acid using Biphasic Reactors with Alkylphenol Solvents" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Plans with plants:</B> The hemicellulose fraction of lignocellulosic biomass is converted to furfural and levulinic acid using biphasic reactors with alkylphenol solvents that selectively partition furanic compounds from acidic aqueous solutions. The furfural and levulinic acid products are valuable compounds for a variety of chemical applications, and they serve as precursors for the synthesis of liquid transportation fuels.</P>
<p> [Communication]<br />Elif I. G&#xFC;rb&#xFC;z, Stephanie G. Wettstein, James A. Dumesic<br /><i>ChemSusChem</i>, January 24, 2012, DOI: 10.1002/cssc.201100608. <a href="http://dx.doi.org/10.1002/cssc.201100608">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100585">
<title>Amine Synthesis through Mild Catalytic Hydrosilylation of Imines using Polymethylhydroxysiloxane and [RuCl&lt;sub&gt;2&lt;/sub&gt;(arene)]&lt;sub&gt;2&lt;/sub&gt; Catalysts</title>
<link>http://dx.doi.org/10.1002/cssc.201100585</link>
<dc:creator>Bin Li, Jean-Baptiste Sortais, Christophe Darcel, Pierre H. Dixneuf</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100585.gif" width="429" height="100" alt="Amine Synthesis through Mild Catalytic Hydrosilylation of Imines using Polymethylhydroxysiloxane and [RuCl2(arene)]2 Catalysts" title="Amine Synthesis through Mild Catalytic Hydrosilylation of Imines using Polymethylhydroxysiloxane and [RuCl2(arene)]2 Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Tolerate silicone!</B> The stable [RuCl<sub>2</sub>(<I>p</I>-cymene]<sub>2</sub> complex is an efficient catalyst for the direct chemoselective hydrosilylation of functionalized aldimines and ketimines into amines, using polymethylhydroxysiloxane as an inexpensive, stable, and safe hydrosilane source. The catalysis operates in ethanol, under air at room temperature, and tolerates the ketone ester and alkene functionality.</P>
<p> [Communication]<br />Bin Li, Jean-Baptiste Sortais, Christophe Darcel, Pierre H. Dixneuf<br /><i>ChemSusChem</i>, February 3, 2012, DOI: 10.1002/cssc.201100585. <a href="http://dx.doi.org/10.1002/cssc.201100585">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100570">
<title>A Solid-Supported Organocatalyst for Continuous-Flow Enantioselective Aldol Reactions</title>
<link>http://dx.doi.org/10.1002/cssc.201100570</link>
<dc:creator>Carles Ayats, Andrea H. Henseler, Miquel A. Peric&#xE0;s</dc:creator>
<dc:date>2012-01-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100570.gif" width="216" height="138" alt="A Solid-Supported Organocatalyst for Continuous-Flow Enantioselective Aldol Reactions" title="A Solid-Supported Organocatalyst for Continuous-Flow Enantioselective Aldol Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Go with the flow!</B> A novel 4-(1-triazolyl)proline immobilized onto 8&nbsp;% DVB-PS catalyzes highly stereoselective aldol reactions under continuous flow conditions with very low catalyst loading (TON up to 61). Up to four different enantiomerically pure aldol products can be sequentially produced in gram amounts with the same catalyst sample.</P>
<p> [Full Paper]<br />Carles Ayats, Andrea H. Henseler, Miquel A. Peric&#xE0;s<br /><i>ChemSusChem</i>, January 2, 2012, DOI: 10.1002/cssc.201100570. <a href="http://dx.doi.org/10.1002/cssc.201100570">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100530">
<title>A High-Energy-Density Redox Flow Battery based on Zinc/Polyhalide Chemistry</title>
<link>http://dx.doi.org/10.1002/cssc.201100530</link>
<dc:creator>Liqun Zhang , Qinzhi Lai, Jianlu Zhang, Huamin Zhang</dc:creator>
<dc:date>2012-01-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100530.gif" width="217" height="136" alt="A High-Energy-Density Redox Flow Battery based on Zinc/Polyhalide Chemistry" title="A High-Energy-Density Redox Flow Battery based on Zinc/Polyhalide Chemistry" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Zn and the Art of Battery Development:</B> A zinc/polyhalide redox flow battery employs Br<SUP>&minus;</SUP>/ClBr<SUP>2&minus;</SUP> and Zn/Zn<SUP>2+</SUP> redox couples in its positive and negative half-cells, respectively. The performance of the battery is evaluated by charge&ndash;discharge cycling tests and reveals a high energy efficiency of 81%, based on a Coulombic efficiency of 96% and voltage efficiency of 84%. The new battery technology can provide high performance and energy density at an acceptable cost.</P>
<p> [Communication]<br />Liqun Zhang&#xA0;, Qinzhi Lai, Jianlu Zhang, Huamin Zhang<br /><i>ChemSusChem</i>, January 19, 2012, DOI: 10.1002/cssc.201100530. <a href="http://dx.doi.org/10.1002/cssc.201100530">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100525">
<title>CO Oxidation at the Perimeters of an FeO/Pt(111) Interface and how Water Promotes the Activity: A First-Principles Study</title>
<link>http://dx.doi.org/10.1002/cssc.201100525</link>
<dc:creator>Xiang-Kui Gu, Runhai Ouyang, Dapeng Sun, Hai-Yan Su, Wei-Xue Li</dc:creator>
<dc:date>2011-12-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100525.gif" width="215" height="157" alt="CO Oxidation at the Perimeters of an FeO/Pt(111) Interface and how Water Promotes the Activity: A First-Principles Study" title="CO Oxidation at the Perimeters of an FeO/Pt(111) Interface and how Water Promotes the Activity: A First-Principles Study" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>An active ensemble:</B> The Pt-Fe cation ensemble hosted in the perimeters of FeO islands supported on Pt provides active sites for O<sub>2</sub> and H<sub>2</sub>O activation free from CO poison. The Pt-Fe cation ensemble is highly active for CO oxidation, the activity of which is further promoted by water (see picture).</P>
<p> [Full Paper]<br />Xiang-Kui Gu, Runhai Ouyang, Dapeng Sun, Hai-Yan Su, Wei-Xue Li<br /><i>ChemSusChem</i>, December 9, 2011, DOI: 10.1002/cssc.201100525. <a href="http://dx.doi.org/10.1002/cssc.201100525">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100523">
<title>Mechanistic Investigation on the Formation and Dehydrogenation of Calcium Amidoborane Ammoniate</title>
<link>http://dx.doi.org/10.1002/cssc.201100523</link>
<dc:creator>Yong Shen Chua, Wen Li, Wendy J. Shaw, Guotao Wu, Tom Autrey, Zhitao Xiong, Ming Wah Wong, Ping Chen</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100523.gif" width="210" height="165" alt="Mechanistic Investigation on the Formation and Dehydrogenation of Calcium Amidoborane Ammoniate" title="Mechanistic Investigation on the Formation and Dehydrogenation of Calcium Amidoborane Ammoniate" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Amidoborane ammoniate formation</B> is investigated by using isotopic labeling techniques. The formation of Ca(NH<sub>2</sub>BH<sub>3</sub>)<sub>2</sub><B>&middot;</B>2&nbsp;NH<sub>3</sub> is initiated by proton transfer from NH<sub>3</sub>BH<sub>3</sub> to NH<sub>2</sub><SUP>&minus;</SUP> (amide), forming Ca(NH<sub>3</sub>)<SUP>2+</SUP> and anionic [NH<sub>2</sub>BH<sub>3</sub>]<SUP>&minus;</SUP> groups. The dehydrogenation of the ammoniate, which occurs at lower temperatures, is a result of the participation of NH<sub>3</sub> in the dehydrogenation process via the combination of (NH<sub>3</sub>)H<SUP><I>&delta;</I>+</SUP>&middot;&middot;&middot;H<SUP><I>&delta;</I>&minus;</SUP>(NH<sub>2</sub>BH<sub>3</sub><SUP>&minus;</SUP>).</P>
<p> [Full Paper]<br />Yong Shen Chua, Wen Li, Wendy J. Shaw, Guotao Wu, Tom Autrey, Zhitao Xiong, Ming Wah Wong, Ping Chen<br /><i>ChemSusChem</i>, January 31, 2012, DOI: 10.1002/cssc.201100523. <a href="http://dx.doi.org/10.1002/cssc.201100523">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100468">
<title>Application of the Sol&#x2013;Gel Technique to Develop Synthetic Calcium-Based Sorbents with Excellent Carbon Dioxide Capture Characteristics</title>
<link>http://dx.doi.org/10.1002/cssc.201100468</link>
<dc:creator>Marcin Broda, Agnieszka M. Kierzkowska, Christoph R. M&#xFC;ller</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100468.gif" width="216" height="204" alt="Application of the Sol&ndash;Gel Technique to Develop Synthetic Calcium-Based Sorbents with Excellent Carbon Dioxide Capture Characteristics" title="Application of the Sol&ndash;Gel Technique to Develop Synthetic Calcium-Based Sorbents with Excellent Carbon Dioxide Capture Characteristics" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Catch your breath</B>: We report the development of synthetic calcium-based CO<sub>2</sub> sorbents using a sol&ndash;gel technique. We are able to synthesize a nanostructured material that possesses a high surface area and pore volume and shows excellent CO<sub>2</sub> capture characteristics over many cycles (see picture).</P>
<p> [Full Paper]<br />Marcin Broda, Agnieszka M. Kierzkowska, Christoph R. M&#xFC;ller<br /><i>ChemSusChem</i>, February 1, 2012, DOI: 10.1002/cssc.201100468. <a href="http://dx.doi.org/10.1002/cssc.201100468">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100445">
<title>Transfer of the Epoxidation of Soybean Oil from Batch to Flow Chemistry Guided by Cost and Environmental Issues</title>
<link>http://dx.doi.org/10.1002/cssc.201100445</link>
<dc:creator>Dana Kralisch, Ina Streckmann, Denise Ott, Ulich Krtschil, Elio Santacesaria, Martino Di Serio, Vincenzo Russo, Lucrezia De Carlo, Walter Linhart, Engelbert Christian, Bruno Cortese, Mart H. J. M. de Croon, Volker Hessel</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100445.gif" width="216" height="163" alt="Transfer of the Epoxidation of Soybean Oil from Batch to Flow Chemistry Guided by Cost and Environmental Issues" title="Transfer of the Epoxidation of Soybean Oil from Batch to Flow Chemistry Guided by Cost and Environmental Issues" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Transfer window:</B> A holistic concept for sustainable process development through process intensification due to microprocess technology in combination with novel process windows is presented. Process modeling and simulation linked with simplified cost and lifecycle assessment provide valuable information to guide the ongoing design of a continuously running pilot-process for the epoxidation of soybean oil (see picture).</P>
<p> [Full Paper]<br />Dana Kralisch, Ina Streckmann, Denise Ott, Ulich Krtschil, Elio Santacesaria, Martino Di&#xA0;Serio, Vincenzo Russo, Lucrezia De&#xA0;Carlo, Walter Linhart, Engelbert Christian, Bruno Cortese, Mart H. J. M. de&#xA0;Croon, Volker Hessel<br /><i>ChemSusChem</i>, January 27, 2012, DOI: 10.1002/cssc.201100445. <a href="http://dx.doi.org/10.1002/cssc.201100445">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100444">
<title>Application of Metal-Based Reagents and Catalysts in Microstructured Flow Devices</title>
<link>http://dx.doi.org/10.1002/cssc.201100444</link>
<dc:creator>Tamilselvi Chinnusamy, Salprima Yudha S , Markus Hager, Peter Kreitmeier, Oliver Reiser</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100444.gif" width="385" height="102" alt="Application of Metal-Based Reagents and Catalysts in Microstructured Flow Devices" title="Application of Metal-Based Reagents and Catalysts in Microstructured Flow Devices" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Down and up:</B> Downscaling reaction vessels and moving to a continuous flow approach have not only advanced many reactions with respect to efficiency and safety, but also offer a reliable solution for upscaling chemical transformations. Examples in this Minireview demonstrate the use of sensitive metal-based reagents, substrates, and catalysts at extreme temperatures.</P>
<p> [Minireview]<br />Tamilselvi Chinnusamy, Salprima Yudha&#xA0;S&#xA0;, Markus Hager, Peter Kreitmeier, Oliver Reiser<br /><i>ChemSusChem</i>, January 24, 2012, DOI: 10.1002/cssc.201100444. <a href="http://dx.doi.org/10.1002/cssc.201100444">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100431">
<title>A Capsule Catalyst with a Zeolite Membrane Prepared by Direct Liquid Membrane Crystallization</title>
<link>http://dx.doi.org/10.1002/cssc.201100431</link>
<dc:creator>Chunlin Li, Hengyong Xu, Yuko Kido, Yoshiharu Yoneyama, Yoshifumi Suehiro, Noritatsu Tsubaki</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100431.gif" width="211" height="94" alt="A Capsule Catalyst with a Zeolite Membrane Prepared by Direct Liquid Membrane Crystallization" title="A Capsule Catalyst with a Zeolite Membrane Prepared by Direct Liquid Membrane Crystallization" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A sheltered existence:</B> Direct liquid-membrane crystallization is used as a low-cost, low-waste, yet highly effective method to prepare a catalyst encapsulated by a H-&beta; zeolite. Through vapor&ndash;liquid exchange, a continuous and sufficient, but not excessive supply of both water and template is the key part of this method.</P>
<p> [Communication]<br />Chunlin Li, Hengyong Xu, Yuko Kido, Yoshiharu Yoneyama, Yoshifumi Suehiro, Noritatsu Tsubaki<br /><i>ChemSusChem</i>, January 27, 2012, DOI: 10.1002/cssc.201100431. <a href="http://dx.doi.org/10.1002/cssc.201100431">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100430">
<title>Flexible and Platinum-Free Dye-Sensitized Solar Cells with Conducting-Polymer-Coated Graphene Counter Electrodes</title>
<link>http://dx.doi.org/10.1002/cssc.201100430</link>
<dc:creator>Kun Seok Lee, Youngbin Lee, Jun Young Lee, Jong-Hyun Ahn, Jong Hyeok Park</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100430.gif" width="194" height="192" alt="Flexible and Platinum-Free Dye-Sensitized Solar Cells with Conducting-Polymer-Coated Graphene Counter Electrodes" title="Flexible and Platinum-Free Dye-Sensitized Solar Cells with Conducting-Polymer-Coated Graphene Counter Electrodes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Always wear a coat:</B> On a plastic substrate graphene is coated with a conducting polymer (PEDOT), resulting in a flexible composite film. The film is used as counter electrode in dye-sensitized solar cells (DSSCs) instead of platinum/transparent conducting oxides (TCOs). The performance of the TCO- and platinum-free counter electrode rivals that of convenential DSSCs.</P>
<p> [Communication]<br />Kun Seok Lee, Youngbin Lee, Jun Young Lee, Jong-Hyun Ahn, Jong Hyeok Park<br /><i>ChemSusChem</i>, January 13, 2012, DOI: 10.1002/cssc.201100430. <a href="http://dx.doi.org/10.1002/cssc.201100430">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100427">
<title>Design of Cellulose Dissolving Ionic Liquids Inspired by Nature</title>
<link>http://dx.doi.org/10.1002/cssc.201100427</link>
<dc:creator>Kazutaka Ohira, Yoshikazu Abe, Motoi Kawatsura, Kazuhiko Suzuki, Masahiro Mizuno, Yoshihiko Amano, Toshiyuki Itoh</dc:creator>
<dc:date>2012-01-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100427.gif" width="214" height="196" alt="Design of Cellulose Dissolving Ionic Liquids Inspired by Nature" title="Design of Cellulose Dissolving Ionic Liquids Inspired by Nature" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Stimulating the hunger of enzymes:</B> The design of an ionic liquid that have the ability to dissolve cellulose has been attempted from the viewpoint of a cellulase. <I>N</I>,<I>N</I>-diethyl-<I>N</I>-(2-methoxyethyl)-<I>N</I>-methylammonium alanine ([N<sub>221ME</sub>][Ala]) is a good solvent for cellulose. Dissolution in [N<sub>221ME</sub>][Ala] converts the crystalline structure of cellulose from Type&nbsp;I to II, which is known to be a form easily digested by cellulases.</P>
<p> [Communication]<br />Kazutaka Ohira, Yoshikazu Abe, Motoi Kawatsura, Kazuhiko Suzuki, Masahiro Mizuno, Yoshihiko Amano, Toshiyuki Itoh<br /><i>ChemSusChem</i>, January 19, 2012, DOI: 10.1002/cssc.201100427. <a href="http://dx.doi.org/10.1002/cssc.201100427">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100423">
<title>Sequential Continuous flow Processes for the Oxidation of Amines and Azides by using HOF&#xB7;MeCN</title>
<link>http://dx.doi.org/10.1002/cssc.201100423</link>
<dc:creator>Christopher B. McPake, Christopher B. Murray, Graham Sandford</dc:creator>
<dc:date>2011-12-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100423.gif" width="430" height="75" alt="Sequential Continuous flow Processes for the Oxidation of Amines and Azides by using HOF&middot;MeCN" title="Sequential Continuous flow Processes for the Oxidation of Amines and Azides by using HOF&middot;MeCN" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Oxidation in flow:</B> The oxidation of amines and azides to the corresponding nitrated systems by using fluorine gas, water and acetonitrile by sequential gas&ndash;liquid/liquid&ndash;liquid continuous flow procedures are reported.</P>
<p> [Full Paper]<br />Christopher B. McPake, Christopher B. Murray, Graham Sandford<br /><i>ChemSusChem</i>, December 13, 2011, DOI: 10.1002/cssc.201100423. <a href="http://dx.doi.org/10.1002/cssc.201100423">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100418">
<title>Development of Polymeric Palladium-Nanoparticle Membrane-Installed Microflow Devices and their Application in Hydrodehalogenation</title>
<link>http://dx.doi.org/10.1002/cssc.201100418</link>
<dc:creator>Yoichi M. A. Yamada, Toshihiro Watanabe, Aya Ohno, Yasuhiro Uozumi</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100418.gif" width="216" height="197" alt="Development of Polymeric Palladium-Nanoparticle Membrane-Installed Microflow Devices and their Application in Hydrodehalogenation" title="Development of Polymeric Palladium-Nanoparticle Membrane-Installed Microflow Devices and their Application in Hydrodehalogenation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Streamlined nanoparticles:</B> We developed a variety of polymeric Pd nanoparticle membrane-installed microflow devices. Instantaneous hydrodehalogenation of aryl halides can be achieved at short residence times and moderate temperatures using a safe, nonexplosive aqueous sodium formate to quantitatively afford the corresponding hydrodehalogenated products. PCB and PBB can also be fully decomposed under similar conditions to give a biphenyl.</P>
<p> [Full Paper]<br />Yoichi M. A. Yamada, Toshihiro Watanabe, Aya Ohno, Yasuhiro Uozumi<br /><i>ChemSusChem</i>, January 13, 2012, DOI: 10.1002/cssc.201100418. <a href="http://dx.doi.org/10.1002/cssc.201100418">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100415">
<title>New Biobased High Functionality Polyols and Their Use in Polyurethane Coatings</title>
<link>http://dx.doi.org/10.1002/cssc.201100415</link>
<dc:creator>Xiao Pan, Dean C. Webster</dc:creator>
<dc:date>2012-01-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100415.gif" width="213" height="191" alt="New Biobased High Functionality Polyols and Their Use in Polyurethane Coatings" title="New Biobased High Functionality Polyols and Their Use in Polyurethane Coatings" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Sweet resins</B>: Sucrose soyate based polyols are made from sucrose esters of soybean oil through epoxidation and epoxide ring-opening reactions (see picture). These new biobased high functionality polyols are biomacromolecules with an innovative structural concept: well-defined compact structure, rigid sucrose core, and high hydroxyl group functionality.</P>
<p> [Full Paper]<br />Xiao Pan, Dean C. Webster<br /><i>ChemSusChem</i>, January 23, 2012, DOI: 10.1002/cssc.201100415. <a href="http://dx.doi.org/10.1002/cssc.201100415">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100389">
<title>Recent Changes in Patenting Behavior in Microprocess Technology and its Possible Use for Gas&#x2013;Liquid Reactions and the Oxidation of Glucose</title>
<link>http://dx.doi.org/10.1002/cssc.201100389</link>
<dc:creator>Ivana Dencic, Volker Hessel, Mart H. J. M. de Croon, Jan Meuldijk, Christianus W. J. van der Doelen, Kasper Koch</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100389.gif" width="215" height="127" alt="Recent Changes in Patenting Behavior in Microprocess Technology and its Possible Use for Gas&ndash;Liquid Reactions and the Oxidation of Glucose" title="Recent Changes in Patenting Behavior in Microprocess Technology and its Possible Use for Gas&ndash;Liquid Reactions and the Oxidation of Glucose" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>It got patential flow:</B> Patenting behavior in microprocess technology has been changed during the last five years. The importance of multiphase reactions in chemical and pharmaceutical industry is shown by an increased number of device and process patents in this field. However, reviewed patents indicate that dealing with solid catalyst and flow control are still challenging tasks.</P>
<p> [Review]<br />Ivana Dencic, Volker Hessel, Mart H. J. M. de&#xA0;Croon, Jan Meuldijk, Christianus W. J. van&#xA0;der&#xA0;Doelen, Kasper Koch<br /><i>ChemSusChem</i>, January 25, 2012, DOI: 10.1002/cssc.201100389. <a href="http://dx.doi.org/10.1002/cssc.201100389">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100376">
<title>Practical Synthesis of Photochromic Diarylethenes in Integrated Flow microreactor Systems</title>
<link>http://dx.doi.org/10.1002/cssc.201100376</link>
<dc:creator>Tatsuro Asai, Atsushi Takata, Aiichiro Nagaki, Jun-ichi Yoshida</dc:creator>
<dc:date>2011-11-08T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100376.gif" width="216" height="167" alt="Practical Synthesis of Photochromic Diarylethenes in Integrated Flow microreactor Systems" title="Practical Synthesis of Photochromic Diarylethenes in Integrated Flow microreactor Systems" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Too successful to be cool</B>: An effective method for the synthesis of photochromic diarylethenes has been developed by using integrated flow microreactor systems. Reactions can be conducted without the need for cryogenic conditions by using these systems (see picture). The synthesis of unsymmetrical diarylethenes, which is difficult to achieve by using conventional macro batch systems, has also been accomplished.</P>
<p> [Full Paper]<br />Tatsuro Asai, Atsushi Takata, Aiichiro Nagaki, Jun-ichi Yoshida<br /><i>ChemSusChem</i>, November 8, 2011, DOI: 10.1002/cssc.201100376. <a href="http://dx.doi.org/10.1002/cssc.201100376">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100373">
<title>Room-Temperature, Acid-Catalyzed [2+2] Cycloadditions: Suppression of Side Reactions by using a Flow Microreactor System</title>
<link>http://dx.doi.org/10.1002/cssc.201100373</link>
<dc:creator>Kei Kurahashi, Yoshiji Takemoto, Kiyosei Takasu</dc:creator>
<dc:date>2011-10-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100373.gif" width="200" height="130" alt="Room-Temperature, Acid-Catalyzed [2+2] Cycloadditions: Suppression of Side Reactions by using a Flow Microreactor System" title="Room-Temperature, Acid-Catalyzed [2+2] Cycloadditions: Suppression of Side Reactions by using a Flow Microreactor System" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Added value:</B> The [2+2] cycloaddition of silyl enol ethers with &alpha;,&beta;-unsaturated esters, catalyzed by the superstrong acid triflic imide (Tf<sub>2</sub>NH), at room temperature in a flow microreactor system is reported. The micororeactor method achieves the [2+2] cycloaddition of unstable silyl enol ethers and acrylates, which is unsuccessful batch reactors, even at room temperature.</P>
<p> [Communication]<br />Kei Kurahashi, Yoshiji Takemoto, Kiyosei Takasu<br /><i>ChemSusChem</i>, October 27, 2011, DOI: 10.1002/cssc.201100373. <a href="http://dx.doi.org/10.1002/cssc.201100373">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100372">
<title>Ritter Reactions in Flow</title>
<link>http://dx.doi.org/10.1002/cssc.201100372</link>
<dc:creator>Logan Audiger, Kevin Watts, Simon C. Elmore, Richard I. Robinson, Thomas Wirth</dc:creator>
<dc:date>2011-12-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100372.gif" width="299" height="91" alt="Ritter Reactions in Flow" title="Ritter Reactions in Flow" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Flow me a Ritter:</B> Ritter reactions are performed in a simple microreactor setup using <I>tert</I>-butylacetate as versatile carbocation source. The protocol avoids the handling of large amounts of hot concentrated sulfuric acid as low concentrations are optimal for rapid access <I>tert</I>-butyl- or diphenylmethyl-protected amides.</P>
<p> [Communication]<br />Logan Audiger, Kevin Watts, Simon C. Elmore, Richard I. Robinson, Thomas Wirth<br /><i>ChemSusChem</i>, December 1, 2011, DOI: 10.1002/cssc.201100372. <a href="http://dx.doi.org/10.1002/cssc.201100372">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100370">
<title>Solid-Supported Gallium Triflate: An Efficient Catalyst for the Three-component Ketonic Strecker Reaction</title>
<link>http://dx.doi.org/10.1002/cssc.201100370</link>
<dc:creator>Charlotte Wiles, Paul Watts</dc:creator>
<dc:date>2011-12-08T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100370.gif" width="216" height="195" alt="Solid-Supported Gallium Triflate: An Efficient Catalyst for the Three-component Ketonic Strecker Reaction" title="Solid-Supported Gallium Triflate: An Efficient Catalyst for the Three-component Ketonic Strecker Reaction" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Trifle gallium supporters:</B> A solidsupported gallium triflate derivative is synthesized and screened for activity towards the ketonic Strecker reaction. The target &alpha;-aminonitriles are obtained in higher yield and purity compared to reactions reported in literature, for which the analogous homogeneous catalyst is used.</P>
<p> [Full Paper]<br />Charlotte Wiles, Paul Watts<br /><i>ChemSusChem</i>, December 8, 2011, DOI: 10.1002/cssc.201100370. <a href="http://dx.doi.org/10.1002/cssc.201100370">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100366">
<title>Highly Proton-Selective Biopolymer Layer-Coated Ion-Exchange Membrane for Direct Methanol Fuel Cells</title>
<link>http://dx.doi.org/10.1002/cssc.201100366</link>
<dc:creator>Sanna Kotrappanavar Nataraj, Chen-Hao Wang, Hsin-Chih Huang, He-Yun Du, Sea-Fu Wang, Ying-Chu Chen, Li-Chyong Chen, Kuei-Hsien Chen</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100366.gif" width="214" height="132" alt="Highly Proton-Selective Biopolymer Layer-Coated Ion-Exchange Membrane for Direct Methanol Fuel Cells" title="Highly Proton-Selective Biopolymer Layer-Coated Ion-Exchange Membrane for Direct Methanol Fuel Cells" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Peels of an onion:</B> New composite proton exchange membranes prepared through layer-by-layer coating of a biopolymer has shown superior methanol barrier properties, while maintaining a high affinity to proton transfer same time. The highly selective skin layer in the composite system significantly increases the fuel utilization efficiency in direct methanol fuel cells (DMFCs).</P>
<p> [Communication]<br />Sanna Kotrappanavar Nataraj, Chen-Hao Wang, Hsin-Chih Huang, He-Yun Du, Sea-Fu Wang, Ying-Chu Chen, Li-Chyong Chen, Kuei-Hsien Chen<br /><i>ChemSusChem</i>, February 3, 2012, DOI: 10.1002/cssc.201100366. <a href="http://dx.doi.org/10.1002/cssc.201100366">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100342">
<title>Prilezhaev Dihydroxylation of Olefins in a Continuous Flow Process</title>
<link>http://dx.doi.org/10.1002/cssc.201100342</link>
<dc:creator>Bas A. M. W. van den Broek, Ren&#xE9; Becker, Florian K&#xF6;ssl, Mari&#xEB;lle M. E. Delville, Pieter J. Nieuwland, Kaspar Koch, Floris P. J. T. Rutjes</dc:creator>
<dc:date>2011-12-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100342.gif" width="367" height="98" alt="Prilezhaev Dihydroxylation of Olefins in a Continuous Flow Process" title="Prilezhaev Dihydroxylation of Olefins in a Continuous Flow Process" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Olefins go with the flow:</B> Prilezhaev dihydroxylation can be performed on a large scale in continuous flow microreactor systems in the oxidation of terminal and internal olefins. Major drivers for a continuous flow process include better control, improved safety, and a faster overall process, leading to a significantly higher throughput.</P>
<p> [Full Paper]<br />Bas A. M. W. van&#xA0;den&#xA0;Broek, Ren&#xE9; Becker, Florian K&#xF6;ssl, Mari&#xEB;lle M. E. Delville, Pieter J. Nieuwland, Kaspar Koch, Floris P. J. T. Rutjes<br /><i>ChemSusChem</i>, December 1, 2011, DOI: 10.1002/cssc.201100342. <a href="http://dx.doi.org/10.1002/cssc.201100342">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100339">
<title>The Oxygen-Mediated Synthesis of 1,3-Butadiynes in Continuous Flow: Using Teflon AF-2400 to Effect Gas/Liquid Contact</title>
<link>http://dx.doi.org/10.1002/cssc.201100339</link>
<dc:creator>Trine P. Petersen, Anastasios Polyzos , Matthew O&#x2019;Brien, Trond Ulven, Ian R. Baxendale, Steven V. Ley</dc:creator>
<dc:date>2011-09-21T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100339.gif" width="371" height="99" alt="The Oxygen-Mediated Synthesis of 1,3-Butadiynes in Continuous Flow: Using Teflon AF-2400 to Effect Gas/Liquid Contact" title="The Oxygen-Mediated Synthesis of 1,3-Butadiynes in Continuous Flow: Using Teflon AF-2400 to Effect Gas/Liquid Contact" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The gas is always greener:</B> A continuous flow Glaser&ndash;Hay coupling reaction system, mediated by molecular oxygen, is developed based on a tube-in-tube gas/liquid reactor/injector. The system uses a semi-permeable Teflon AF-2400 membrane to effect rapid gas/liquid contact in flow, affording homogeneous solutions of oxygen. Measurements of out-gassing downstream of the back-pressure regulator indicate the onset of saturation is reached after ca. 16 seconds.</P>
<p> [Communication]<br />Trine P. Petersen, Anastasios Polyzos&#xA0;, Matthew O&#x2019;Brien, Trond Ulven, Ian R. Baxendale, Steven V. Ley<br /><i>ChemSusChem</i>, September 21, 2011, DOI: 10.1002/cssc.201100339. <a href="http://dx.doi.org/10.1002/cssc.201100339">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100332">
<title>Highly Efficient 1,4-Addition of Aldehydes to Nitroolefins: Organocatalysis in Continuous Flow by Solid-Supported Peptidic Catalysts</title>
<link>http://dx.doi.org/10.1002/cssc.201100332</link>
<dc:creator>S&#xE1;ndor B. &#xD6;tv&#xF6;s, Istv&#xE1;n M. M&#xE1;ndity, Ferenc F&#xFC;l&#xF6;p</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100332.gif" width="215" height="142" alt="Highly Efficient 1,4-Addition of Aldehydes to Nitroolefins: Organocatalysis in Continuous Flow by Solid-Supported Peptidic Catalysts" title="Highly Efficient 1,4-Addition of Aldehydes to Nitroolefins: Organocatalysis in Continuous Flow by Solid-Supported Peptidic Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Michael&rsquo;s peptides:</B> A simple and efficient continuous flow technique has been developed for the organocatalytic Michael reactions using solid-supported peptidic catalysts, readily synthesized and immobilized in one single step. Synthetically useful chiral &gamma;-nitroaldehydes have been obtained in excellent yields and stereoselectivities within short reaction times, while catalyst reusability, the ease of product isolation, and facile scale-up enhances the efficacy of the technique.</P>
<p> [Communication]<br />S&#xE1;ndor B. &#xD6;tv&#xF6;s, Istv&#xE1;n M. M&#xE1;ndity, Ferenc F&#xFC;l&#xF6;p<br /><i>ChemSusChem</i>, February 1, 2012, DOI: 10.1002/cssc.201100332. <a href="http://dx.doi.org/10.1002/cssc.201100332">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100286">
<title>Homogeneous Photocatalytic Reactions with Organometallic and Coordination Compounds&#x2014;Perspectives for Sustainable Chemistry</title>
<link>http://dx.doi.org/10.1002/cssc.201100286</link>
<dc:creator>Norbert Hoffmann</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100286.gif" width="216" height="197" alt="Homogeneous Photocatalytic Reactions with Organometallic and Coordination Compounds&mdash;Perspectives for Sustainable Chemistry" title="Homogeneous Photocatalytic Reactions with Organometallic and Coordination Compounds&mdash;Perspectives for Sustainable Chemistry" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Solar powered:</B> Photochemical conditions significantly alter the outcome of chemical reactions. Consequently, the scope of catalytic transformations with organometallic and coordination compounds is also considerably enlarged. This article provides a short overview on such reactions and their application to organic synthesis. The review also indicates synergistic effects of photochemistry and catalysis with perspectives for a sustainable chemistry.</P>
<p> [Review]<br />Norbert Hoffmann<br /><i>ChemSusChem</i>, January 27, 2012, DOI: 10.1002/cssc.201100286. <a href="http://dx.doi.org/10.1002/cssc.201100286">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100281">
<title>Hydrogen Evolution from Water/Alcohol Mixtures: Effective In&#xA0;Situ Generation of an Active Au/TiO&lt;sub&gt;2&lt;/sub&gt; catalyst</title>
<link>http://dx.doi.org/10.1002/cssc.201100281</link>
<dc:creator>Felix G&#xE4;rtner, Sebastian Losse, Albert Boddien, Marga-Martina Pohl, Stefania Denurra, Henrik Junge, Matthias Beller</dc:creator>
<dc:date>2011-10-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100281.gif" width="213" height="160" alt="Hydrogen Evolution from Water/Alcohol Mixtures: Effective In&nbsp;Situ Generation of an Active Au/TiO2 catalyst" title="Hydrogen Evolution from Water/Alcohol Mixtures: Effective In&nbsp;Situ Generation of an Active Au/TiO2 catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Gold standard:</B> Au/TiO<sub>2</sub> catalysts, easily prepared in&nbsp;situ from different Au precursors and TiO<sub>2</sub>, generate hydrogen from water/alcohol mixtures. Different alcohols, and even glucose, can serve as sacrificial reductants. The best system produces hydrogen on a liter scale, and is stable for more than two days. Deuteration studies show that proton reduction is likely the rate-limiting step in this reaction.</P>
<p> [Communication]<br />Felix G&#xE4;rtner, Sebastian Losse, Albert Boddien, Marga-Martina Pohl, Stefania Denurra, Henrik Junge, Matthias Beller<br /><i>ChemSusChem</i>, October 27, 2011, DOI: 10.1002/cssc.201100281. <a href="http://dx.doi.org/10.1002/cssc.201100281">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100262">
<title>Organocatalyzed Epoxidation of Alkenes in Continuous Flow using a Multi-Jet Oscillating Disk Reactor</title>
<link>http://dx.doi.org/10.1002/cssc.201100262</link>
<dc:creator>Raffaele Spaccini, Lucia Liguori, Carlo Punta, Hans-Ren&#xE9; Bj&#xF8;rsvik</dc:creator>
<dc:date>2011-10-12T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100262.gif" width="211" height="125" alt="Organocatalyzed Epoxidation of Alkenes in Continuous Flow using a Multi-Jet Oscillating Disk Reactor" title="Organocatalyzed Epoxidation of Alkenes in Continuous Flow using a Multi-Jet Oscillating Disk Reactor" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The times are changing:</B> A batch process, the Minisci epoxidation, is transformed into a continuous-flow protocol for the selective aerobic radical epoxidation of alkenes. The use of a novel reactor type allows to considerably shorten reactor residence times. Experimental results suggest that two different reaction mechanisms exist for the oxidation: one for the batch conditions and a different one for the flow synthesis protocol.</P>
<p> [Communication]<br />Raffaele Spaccini, Lucia Liguori, Carlo Punta, Hans-Ren&#xE9; Bj&#xF8;rsvik<br /><i>ChemSusChem</i>, October 12, 2011, DOI: 10.1002/cssc.201100262. <a href="http://dx.doi.org/10.1002/cssc.201100262">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100257">
<title>Energy from Plants and Microorganisms: Progress in Plant&#x2013;Microbial Fuel Cells</title>
<link>http://dx.doi.org/10.1002/cssc.201100257</link>
<dc:creator>Huan Deng, Zheng Chen, Feng Zhao</dc:creator>
<dc:date>2011-12-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cssc201100257.gif" width="176" height="191" alt="Energy from Plants and Microorganisms: Progress in Plant&ndash;Microbial Fuel Cells" title="Energy from Plants and Microorganisms: Progress in Plant&ndash;Microbial Fuel Cells" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Down to the roots:</B> Plant&ndash;microbial fuel cells convert solar energy into electrical power by using microorganisms, which degrade root exudates and pollutants at the anode and pass the electrons to acceptors at the cathode. This setup can provide auxiliary power while reducing the emission of greenhouse gas, that is, methane, from fields.</P>
<p> [Minireview]<br />Huan Deng, Zheng Chen, Feng Zhao<br /><i>ChemSusChem</i>, December 9, 2011, DOI: 10.1002/cssc.201100257. <a href="http://dx.doi.org/10.1002/cssc.201100257">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201190001">
<title>ChemPlusChem &#x2013; A Genuinely Multidisciplinary Journal of Chemistry &amp; Materials</title>
<link>http://dx.doi.org/10.1002/cplu.201190001</link>
<dc:date>2011-09-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p></p><p> [Call for Papers]<br /><br /><i>ChemPlusChem</i>, September 26, 2011, DOI: 10.1002/cplu.201190001. <a href="http://dx.doi.org/10.1002/cplu.201190001">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100083">
<title>Porous Frameworks Based on Carborane&#x2013;Ln&lt;sub&gt;2&lt;/sub&gt;(CO&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;6&lt;/sub&gt;: Architecture Influenced by Lanthanide Contraction and Selective CO&lt;sub&gt;2&lt;/sub&gt; Capture</title>
<link>http://dx.doi.org/10.1002/cplu.201100083</link>
<dc:creator>Sheng-Li Huang, Yue-Jian Lin, Wei-Bin Yu, Guo-Xin Jin</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100083.gif" width="190" height="185" alt="Porous Frameworks Based on Carborane&ndash;Ln2(CO2)6: Architecture Influenced by Lanthanide Contraction and Selective CO2 Capture" title="Porous Frameworks Based on Carborane&ndash;Ln2(CO2)6: Architecture Influenced by Lanthanide Contraction and Selective CO2 Capture" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Cast your net widely</B>: Three distinct structure types of porous frameworks based on carborane&ndash;Ln<sub>2</sub>(CO<sub>2</sub>)<sub>6</sub> (structure type&nbsp;I with Schl&auml;fli symbol of 4<SUP>4</SUP>&middot;6<SUP>2</SUP>, structure type&nbsp;II with Schl&auml;fli symbol of (4<SUP>8</SUP>&middot;6<SUP>6</SUP>&middot;8)(4<SUP>8</SUP>&middot;6<SUP>6</SUP>&middot;8), and structure type&nbsp;III with Schl&auml;fli symbol of 4<SUP>12</SUP>&middot;6<SUP>3</SUP>) have been synthesized and structurally characterized (see figure). Gas sorption was studied and selective CO<sub>2</sub> capture over CH<sub>4</sub> and N<sub>2</sub> was observed.</P>
<p> [Full Paper]<br />Sheng-Li Huang, Yue-Jian Lin, Wei-Bin Yu, Guo-Xin Jin<br /><i>ChemPlusChem</i>, January 25, 2012, DOI: 10.1002/cplu.201100083. <a href="http://dx.doi.org/10.1002/cplu.201100083">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100080">
<title>Scaffold-Optimized Dendrimers for the Detection of the Triacetone Triperoxide Explosive Using Quartz Crystal Microbalances</title>
<link>http://dx.doi.org/10.1002/cplu.201100080</link>
<dc:creator>Daniel Lubczyk, Matthias Grill, Martin Baumgarten, Siegfried R. Waldvogel, Klaus M&#xFC;llen</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100080.gif" width="211" height="206" alt="Scaffold-Optimized Dendrimers for the Detection of the Triacetone Triperoxide Explosive Using Quartz Crystal Microbalances" title="Scaffold-Optimized Dendrimers for the Detection of the Triacetone Triperoxide Explosive Using Quartz Crystal Microbalances" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Affinity and selectivity</B>: The online detection of the explosive triacetone triperoxide (TATP) is an utmost challenge in security research. The great number of events wherein TATP was involved underlines the significance of solutions to trace that particular explosive material. New optimized functionalized polyphenylene dendrimers (see structure) have been synthesized that can be used as powerful affinity systems to trace TATP on a ppb level.</P>
<p> [Communication]<br />Daniel Lubczyk, Matthias Grill, Martin Baumgarten, Siegfried R. Waldvogel, Klaus M&#xFC;llen<br /><i>ChemPlusChem</i>, January 25, 2012, DOI: 10.1002/cplu.201100080. <a href="http://dx.doi.org/10.1002/cplu.201100080">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100076">
<title>Identifying the Decomposition Product of Single-Source Precursors: Towards Water-Soluble Quantum Dots</title>
<link>http://dx.doi.org/10.1002/cplu.201100076</link>
<dc:creator>Mark Green, Lydia Sandiford, Kirsty M. Anderson, Yongmin Ma</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100076.gif" width="216" height="174" alt="Identifying the Decomposition Product of Single-Source Precursors: Towards Water-Soluble Quantum Dots" title="Identifying the Decomposition Product of Single-Source Precursors: Towards Water-Soluble Quantum Dots" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>On the dot</B>: A water-soluble single-source precursor has been used in the synthesis of CdS quantum dots passivated with a nucleotide in an aqueous one-pot reaction (see figure). The crystal structure of the decomposition product of a single-source precursor, 3-methyl-5-(1,2,3,4-tetra hydroxybutyl)oxazolidine-2-thione is also presented. A new decomposition mechanism is suggested that compliments existing routes.</P>
<p> [Communication]<br />Mark Green, Lydia Sandiford, Kirsty M. Anderson, Yongmin Ma<br /><i>ChemPlusChem</i>, January 31, 2012, DOI: 10.1002/cplu.201100076. <a href="http://dx.doi.org/10.1002/cplu.201100076">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100074">
<title>Synthesis and Stability of Highly Crystalline and Stable Iron/Iron Oxide Core/Shell Nanoparticles for Biomedical Applications</title>
<link>http://dx.doi.org/10.1002/cplu.201100074</link>
<dc:creator>Soshan Cheong, Peter Ferguson, Ian F. Hermans, Guy N. L. Jameson, Sujay Prabakar, David A. J. Herman, Richard D. Tilley</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100074.gif" width="198" height="99" alt="Synthesis and Stability of Highly Crystalline and Stable Iron/Iron Oxide Core/Shell Nanoparticles for Biomedical Applications" title="Synthesis and Stability of Highly Crystalline and Stable Iron/Iron Oxide Core/Shell Nanoparticles for Biomedical Applications" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Strike while the iron is hot</B>: Stable core/shell nanoparticles of single-crystal iron core are shown to produce much greater contrast enhancement in magnetic resonance imaging of cells, compared to that produced by pure iron oxides without increase in cytotoxicity (see TEM image of iron/iron oxide nanoparticles).</P>
<p> [Full Paper]<br />Soshan Cheong, Peter Ferguson, Ian F. Hermans, Guy N. L. Jameson, Sujay Prabakar, David A. J. Herman, Richard D. Tilley<br /><i>ChemPlusChem</i>, January 20, 2012, DOI: 10.1002/cplu.201100074. <a href="http://dx.doi.org/10.1002/cplu.201100074">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100070">
<title>Influence of the Second Coordination Shell on the XANES Spectra of the Zn&lt;SUP&gt;2+&lt;/SUP&gt; Ion in Water and Methanol.</title>
<link>http://dx.doi.org/10.1002/cplu.201100070</link>
<dc:creator>Valentina Migliorati, Andrea Zitolo, Giovanni Chillemi, Paola D&#x27;Angelo</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100070.gif" width="371" height="142" alt="Influence of the Second Coordination Shell on the XANES Spectra of the Zn2+ Ion in Water and Methanol." title="Influence of the Second Coordination Shell on the XANES Spectra of the Zn2+ Ion in Water and Methanol." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Come out of your shell</B>: Molecular dynamics simulations and X-ray absorption near-edge structure (XANES) spectroscopy have been used to investigate the coordination properties of the Zn<SUP>2+</SUP> ion in water and methanol (see graphs; Zn&nbsp;cyan). XANES is sensitive to water molecules in the second hydration shell, meanwhile second-shell methanol molecules provide a negligible contribution. This finding is related to the different structuring ability of the two solvents.</P>
<p> [Full Paper]<br />Valentina Migliorati, Andrea Zitolo, Giovanni Chillemi, Paola D&#x27;Angelo<br /><i>ChemPlusChem</i>, January 26, 2012, DOI: 10.1002/cplu.201100070. <a href="http://dx.doi.org/10.1002/cplu.201100070">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100069">
<title>(&#x2212;)-(1&lt;I&gt;R&lt;/I&gt;,2&lt;I&gt;R&lt;/I&gt;,7&lt;I&gt;S,&lt;/I&gt;8a&lt;I&gt;R&lt;/I&gt;)-1,2,7-Trihydroxyindolizidine ((&#x2212;)-7&lt;I&gt;S&lt;/I&gt;-OH-Lentiginosine): Synthesis and Proapoptotic Activity</title>
<link>http://dx.doi.org/10.1002/cplu.201100069</link>
<dc:creator>Franca M. Cordero, Paola Bonanno, Bhushan B. Khairnar, Francesca Cardona, Alberto Brandi, Beatrice Macchi, Antonella Minutolo, Sandro Grelli, Antonio Mastino</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100069.gif" width="272" height="85" alt="(&minus;)-(1R,2R,7S,8aR)-1,2,7-Trihydroxyindolizidine ((&minus;)-7S-OH-Lentiginosine): Synthesis and Proapoptotic Activity" title="(&minus;)-(1R,2R,7S,8aR)-1,2,7-Trihydroxyindolizidine ((&minus;)-7S-OH-Lentiginosine): Synthesis and Proapoptotic Activity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Indolizidine alkaloids</B>: Highly selective and reproducible <I>tert</I>-butylation of enantiopure <I>N</I>-benzyl dihydroxypyrrolidine was exploited in an improved synthesis of 3,4-bis-<I>tert</I>-butoxypyrroline <I>N</I>-oxide for the synthesis of (&minus;)-7<I>S</I>-OH-lentiginosine (see scheme; Bn=benzyl). The introduction of an additional hydroxy group on C7 of the non-natural lentiginosine provides another example of an efficient apoptosis inducer with low cytotoxicity.</P>
<p> [Full Paper]<br />Franca M. Cordero, Paola Bonanno, Bhushan B. Khairnar, Francesca Cardona, Alberto Brandi, Beatrice Macchi, Antonella Minutolo, Sandro Grelli, Antonio Mastino<br /><i>ChemPlusChem</i>, February 6, 2012, DOI: 10.1002/cplu.201100069. <a href="http://dx.doi.org/10.1002/cplu.201100069">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100068">
<title>Sequential Immobilization of Enzymes in Microfluidic Channels for Cascade Reactions</title>
<link>http://dx.doi.org/10.1002/cplu.201100068</link>
<dc:creator>Sara Fornera, Phillip Kuhn, Dario Lombardi, A. Dieter Schl&#xFC;ter, Petra S. Dittrich, Peter Walde</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100068.gif" width="217" height="181" alt="Sequential Immobilization of Enzymes in Microfluidic Channels for Cascade Reactions" title="Sequential Immobilization of Enzymes in Microfluidic Channels for Cascade Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Go with the flow</B>: A flow-through microfluidic reactor system was developed that contained the three enzymes, &beta;-galactosidase (&beta;-Gal), glucose oxidase (GOD), and peroxidase (HRP), immobilized with a polycationic dendronized polymer in a predetermined sequence on a single chip for the conduction of an enzymatic cascade reaction. The desired enzyme localization within the microchannels of the chip could be achieved with a micromechanical valve system.</P>
<p> [Communication]<br />Sara Fornera, Phillip Kuhn, Dario Lombardi, A. Dieter Schl&#xFC;ter, Petra S. Dittrich, Peter Walde<br /><i>ChemPlusChem</i>, January 20, 2012, DOI: 10.1002/cplu.201100068. <a href="http://dx.doi.org/10.1002/cplu.201100068">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100066">
<title>Facile One-pot Synthesis of ZnO/SnO&lt;sub&gt;2&lt;/sub&gt; Heterojunction Photocatalysts with Excellent Photocatalytic Activity and Photostability</title>
<link>http://dx.doi.org/10.1002/cplu.201100066</link>
<dc:creator>Lirong Zheng, Yuanhui Zheng, Chongqi Chen, Yingying Zhan, Xinyi Lin, Qi Zheng, Kemei Wei</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100066.gif" width="151" height="151" alt="Facile One-pot Synthesis of ZnO/SnO2 Heterojunction Photocatalysts with Excellent Photocatalytic Activity and Photostability" title="Facile One-pot Synthesis of ZnO/SnO2 Heterojunction Photocatalysts with Excellent Photocatalytic Activity and Photostability" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>It&#x27;s all about performance</B>: ZnO/SnO<sub>2</sub> heterojunction nanocatalysts (see the formation of a ZnO/SnO<sub>2</sub> heterojunction in the TEM image) with excellent photocatalytic performances have been synthesized through a simple one-pot solvothermal method. The relationship between their structure and photocatalytic performances, especially antiphotocorrosion property, has been systematically studied.</P>
<p> [Full Paper]<br />Lirong Zheng, Yuanhui Zheng, Chongqi Chen, Yingying Zhan, Xinyi Lin, Qi Zheng, Kemei Wei<br /><i>ChemPlusChem</i>, January 25, 2012, DOI: 10.1002/cplu.201100066. <a href="http://dx.doi.org/10.1002/cplu.201100066">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100055">
<title>DNA &#x201C;Nanolamps&#x201D;: &#x201C;Clicked&#x201D; DNA Conjugates with Photon Upconverting Nanoparticles as Highly Emissive Biomaterial</title>
<link>http://dx.doi.org/10.1002/cplu.201100055</link>
<dc:creator>Moritz M. Rubner, Daniela E. Achatz, Heike S. Mader, Judith A. Stolwijk, Joachim Wegener, Gregory S. Harms, Otto S. Wolfbeis, Hans-Achim Wagenknecht</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100055.gif" width="158" height="165" alt="DNA &ldquo;Nanolamps&rdquo;: &ldquo;Clicked&rdquo; DNA Conjugates with Photon Upconverting Nanoparticles as Highly Emissive Biomaterial" title="DNA &ldquo;Nanolamps&rdquo;: &ldquo;Clicked&rdquo; DNA Conjugates with Photon Upconverting Nanoparticles as Highly Emissive Biomaterial" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Upconverting DNA:</B> Upconversion nanoparticles are ligated to oligonucleotides by using &ldquo;click&rdquo;-type cycloaddition (see figure). Excitation in the near-infrared region yields bright luminescence of the DNA conjugates in the visible range.</P>
<p> [Full Paper]<br />Moritz M. Rubner, Daniela E. Achatz, Heike S. Mader, Judith A. Stolwijk, Joachim Wegener, Gregory S. Harms, Otto S. Wolfbeis, Hans-Achim Wagenknecht<br /><i>ChemPlusChem</i>, January 25, 2012, DOI: 10.1002/cplu.201100055. <a href="http://dx.doi.org/10.1002/cplu.201100055">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100051">
<title>Facile and Low-Cost Synthesis of Large-Area Pure V&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt; Nanosheets for High-Capacity and High-Rate Lithium Storage over a Wide Temperature Range</title>
<link>http://dx.doi.org/10.1002/cplu.201100051</link>
<dc:creator>Zhong-li Wang, Dan Xu, Li-min Wang, Xin-bo Zhang</dc:creator>
<dc:date>2012-01-09T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100051.gif" width="215" height="170" alt="Facile and Low-Cost Synthesis of Large-Area Pure V2O5 Nanosheets for High-Capacity and High-Rate Lithium Storage over a Wide Temperature Range" title="Facile and Low-Cost Synthesis of Large-Area Pure V2O5 Nanosheets for High-Capacity and High-Rate Lithium Storage over a Wide Temperature Range" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Layer upon layer</B>: Pure V<sub>2</sub>O<sub>5</sub> nanosheets (see figure; C) have been successfully synthesized by a novel and facile dissolution&ndash;splitting method using low-cost raw materials (A). The as-prepared product exhibits enhanced lithium storage properties including good cycling and rate performance, 144&nbsp;mAh&nbsp;g<SUP>&minus;1</SUP> at 10&nbsp;C and 95&nbsp;mAh&nbsp;g<SUP>&minus;1</SUP> at 20&nbsp;C, as well as high reversible capacity, 290&nbsp;mAh&nbsp;g<SUP>&minus;1</SUP>.</P>
<p> [Full Paper]<br />Zhong-li Wang, Dan Xu, Li-min Wang, Xin-bo Zhang<br /><i>ChemPlusChem</i>, January 9, 2012, DOI: 10.1002/cplu.201100051. <a href="http://dx.doi.org/10.1002/cplu.201100051">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100044">
<title>Tweezer-like Complexes of Crown Ethers with Divalent Metals: Probing Cation-Size-Dependent Conformations by Vibrational Spectroscopy in the Gas Phase</title>
<link>http://dx.doi.org/10.1002/cplu.201100044</link>
<dc:creator>Francisco G&#xE1;mez, Paola Hurtado, Said Hamad, Bruno Mart&#xED;nez-Haya, Giel Berden, Jos Oomens</dc:creator>
<dc:date>2012-01-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100044.gif" width="328" height="100" alt="Tweezer-like Complexes of Crown Ethers with Divalent Metals: Probing Cation-Size-Dependent Conformations by Vibrational Spectroscopy in the Gas Phase" title="Tweezer-like Complexes of Crown Ethers with Divalent Metals: Probing Cation-Size-Dependent Conformations by Vibrational Spectroscopy in the Gas Phase" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Molecular tweezers in the gas phase</B>: Isolated tweezer-like ternary complexes comprising two [18]crown-6 cyclic ether molecules and one divalent cation of varying size (Cu<SUP>2+</SUP>, Ca<SUP>2+</SUP>, Ba<SUP>2+</SUP>; see structures) have been investigated by means of laser vibrational action spectroscopy and computations. A remarkable dependence of the structure of the complexes with the size of the cation is observed.</P>
<p> [Full Paper]<br />Francisco G&#xE1;mez, Paola Hurtado, Said Hamad, Bruno Mart&#xED;nez-Haya, Giel Berden, Jos Oomens<br /><i>ChemPlusChem</i>, January 11, 2012, DOI: 10.1002/cplu.201100044. <a href="http://dx.doi.org/10.1002/cplu.201100044">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100040">
<title>One-Step Decatungstate-Photomediated PEGylation of Single-Walled Carbon Nanotubes</title>
<link>http://dx.doi.org/10.1002/cplu.201100040</link>
<dc:creator>Davide Ravelli, Sara Montanaro, Corrado Tomasi, Pietro Galinetto, Eliana Quartarone, Daniele Merli, Piercarlo Mustarelli, Maurizio Fagnoni</dc:creator>
<dc:date>2012-02-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100040.gif" width="249" height="133" alt="One-Step Decatungstate-Photomediated PEGylation of Single-Walled Carbon Nanotubes" title="One-Step Decatungstate-Photomediated PEGylation of Single-Walled Carbon Nanotubes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Off the wall</B>: A straightforward PEGylation of single-walled carbon nanotubes (SWCNTs) has been performed by photomediated addition of various PEG derivatives onto the nanotube surfaces. The reaction was promoted both by UV and by solar light and took place under very mild conditions using commercial PEGs as PEGylating agents (see figure). Interestingly, the functionalization caused a partial dissolution of the resulting CNTs in the reaction medium.</P>
<p> [Full Paper]<br />Davide Ravelli, Sara Montanaro, Corrado Tomasi, Pietro Galinetto, Eliana Quartarone, Daniele Merli, Piercarlo Mustarelli, Maurizio Fagnoni<br /><i>ChemPlusChem</i>, February 7, 2012, DOI: 10.1002/cplu.201100040. <a href="http://dx.doi.org/10.1002/cplu.201100040">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100039">
<title>Surface Functionalization and Characterization of TiO&lt;sub&gt;2&lt;/sub&gt; with Cibacron Blue Dye: An Affinity Column for Proteins</title>
<link>http://dx.doi.org/10.1002/cplu.201100039</link>
<dc:creator>Chilukuri Subbalakshmi, Manaswita Nag, Sunkara V. Manorama</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100039.gif" width="216" height="150" alt="Surface Functionalization and Characterization of TiO2 with Cibacron Blue Dye: An Affinity Column for Proteins" title="Surface Functionalization and Characterization of TiO2 with Cibacron Blue Dye: An Affinity Column for Proteins" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Get a load of this!</B> The purification of lactic dehydrogenase (LHD) using an affinity column of TiO<sub>2</sub> functionalized with Cibacron blue dye is illustrated. The large capacity of the TiO<sub>2</sub>&ndash;CB NP microtip column for proteins, its stability at room temperature, and low cost of preparation suggest that TiO<sub>2</sub>&ndash;CB NPs are useful for rapid protein purification. The two-step procedure results in the recovery of over 90&nbsp;% of the protein loaded.</P>
<p> [Full Paper]<br />Chilukuri Subbalakshmi, Manaswita Nag, Sunkara V. Manorama<br /><i>ChemPlusChem</i>, January 20, 2012, DOI: 10.1002/cplu.201100039. <a href="http://dx.doi.org/10.1002/cplu.201100039">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100036">
<title>A Molecular Lock and Key: &#x201C;Unlocked&#x2013;Locked&#x201D; Conformational Switching of a Receptor by Anions</title>
<link>http://dx.doi.org/10.1002/cplu.201100036</link>
<dc:creator>Sasanka Dalapati, Md. Akhtarul Alam, Sankar Jana, Rajat Saha, Saptarshi Biswas, Nikhil Guchhait</dc:creator>
<dc:date>2012-01-04T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100036.gif" width="212" height="111" alt="A Molecular Lock and Key: &ldquo;Unlocked&ndash;Locked&rdquo; Conformational Switching of a Receptor by Anions" title="A Molecular Lock and Key: &ldquo;Unlocked&ndash;Locked&rdquo; Conformational Switching of a Receptor by Anions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Lock up your valuables</B>: Receptor <B>1</B> acts as a &ldquo;molecular lock&rdquo; and anions act as &ldquo;keys&rdquo;; H<sub>2</sub>PO<sub>4</sub><SUP>&minus;</SUP> can &ldquo;lock&rdquo; <B>1</B> by switching it from its &ldquo;unlocked&rdquo; conformation, however, the structurally similar HSO<sub>4</sub><SUP>&minus;</SUP> cannot &ldquo;lock&rdquo; receptor <B>1</B> as evidenced by single-crystal X-ray analysis (see scheme). The &ldquo;unlocked&ndash;locked&rdquo; conformational switching of <B>1</B> was investigated by monitoring changes in fluorescence intensity in the presence of different anions.</P>
<p> [Communication]<br />Sasanka Dalapati, Md. Akhtarul Alam, Sankar Jana, Rajat Saha, Saptarshi Biswas, Nikhil Guchhait<br /><i>ChemPlusChem</i>, January 4, 2012, DOI: 10.1002/cplu.201100036. <a href="http://dx.doi.org/10.1002/cplu.201100036">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100035">
<title>A Brief Summary of the Synthesis of Polyester Building-Block Chemicals and Biofuels from 5-Hydroxymethylfurfural</title>
<link>http://dx.doi.org/10.1002/cplu.201100035</link>
<dc:creator>Saikat Dutta, Sudipta De, Basudeb Saha</dc:creator>
<dc:date>2012-02-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100035.gif" width="216" height="140" alt="A Brief Summary of the Synthesis of Polyester Building-Block Chemicals and Biofuels from 5-Hydroxymethylfurfural" title="A Brief Summary of the Synthesis of Polyester Building-Block Chemicals and Biofuels from 5-Hydroxymethylfurfural" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Out of the woods</B>: Considerable advances have been made for the synthesis of furan-based polyester building blocks, especially 2,5-furandicarboxylic acid (FDCA), by using nanoparticulate gold catalysts. This Minireview discuss the fundamental aspects of using nanoparticulate catalysts for the aerobic oxidation of biomass-derived 5-hydroxymethylfurfural (HMF) into FDCA and selective transformation of HMF into potential biofuels (DMF=2,5-dimethylfuran).</P>
<p> [Minireview]<br />Saikat Dutta, Sudipta De, Basudeb Saha<br /><i>ChemPlusChem</i>, February 2, 2012, DOI: 10.1002/cplu.201100035. <a href="http://dx.doi.org/10.1002/cplu.201100035">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100021">
<title>Palladium Nanoparticles Supported on Mixed-Linker Metal&#x2013;Organic Frameworks as Highly Active Catalysts for Heck Reactions</title>
<link>http://dx.doi.org/10.1002/cplu.201100021</link>
<dc:creator>Yuanbiao Huang, Shuiying Gao, Tianfu Liu, Jian L&#xFC;, Xi Lin, Hongfang Li, Rong Cao</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100021.gif" width="256" height="130" alt="Palladium Nanoparticles Supported on Mixed-Linker Metal&ndash;Organic Frameworks as Highly Active Catalysts for Heck Reactions" title="Palladium Nanoparticles Supported on Mixed-Linker Metal&ndash;Organic Frameworks as Highly Active Catalysts for Heck Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Like a MOF to a flame</B>: A facile ion-exchange approach for the preparation of palladium nanoparticles (Pd&nbsp;NPs) catalysts supported on amine-functionalized, mixed-linker metal&ndash;organic frameworks based on MIL-53(Al) has been developed. These well-dispersed Pd&nbsp;NPs drastically enhance N<sub>2</sub> adsorption and show high activity and selectivity for Heck reactions (see scheme). The Pd&nbsp;NPs catalysts exhibit high stability and can be easily recovered and reused.</P>
<p> [Full Paper]<br />Yuanbiao Huang, Shuiying Gao, Tianfu Liu, Jian L&#xFC;, Xi Lin, Hongfang Li, Rong Cao<br /><i>ChemPlusChem</i>, January 17, 2012, DOI: 10.1002/cplu.201100021. <a href="http://dx.doi.org/10.1002/cplu.201100021">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100008">
<title>Fabrication of Soft Submicrospheres by Sequential Boronate Esterification and Their Dynamic Behavior</title>
<link>http://dx.doi.org/10.1002/cplu.201100008</link>
<dc:creator>Ryuhei Nishiyabu, Shiori Teraoka, Yusuke Matsushima, Yuji Kubo</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201100008.gif" width="294" height="93" alt="Fabrication of Soft Submicrospheres by Sequential Boronate Esterification and Their Dynamic Behavior" title="Fabrication of Soft Submicrospheres by Sequential Boronate Esterification and Their Dynamic Behavior" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Pyridine-assisted</B> sequential boronate esterification of benzene-1,4-diboronic acid and 1,2,4,5-tetrahydroxybenzene has led to hierarchically structured submicrospheres. The dynamic covalent functionality of the boronate ester linkage enables not only reversible formation by a pH switch but also morphological transformation of the submicrospheres by constitutional exchange reactions (see figure).</P>
<p> [Full Paper]<br />Ryuhei Nishiyabu, Shiori Teraoka, Yusuke Matsushima, Yuji Kubo<br /><i>ChemPlusChem</i>, January 26, 2012, DOI: 10.1002/cplu.201100008. <a href="http://dx.doi.org/10.1002/cplu.201100008">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201101018">
<title>H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;-Aided Seed-Mediated Synthesis of Silver Nanoplates with Improved Yield and Efficiency</title>
<link>http://dx.doi.org/10.1002/cphc.201101018</link>
<dc:creator>Na Li, Qiao Zhang, Sean Quinlivan, James Goebl, Yang Gan, Yadong Yin</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201101018.gif" width="191" height="160" alt="H2O2-Aided Seed-Mediated Synthesis of Silver Nanoplates with Improved Yield and Efficiency" title="H2O2-Aided Seed-Mediated Synthesis of Silver Nanoplates with Improved Yield and Efficiency" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Nanoplates:</B> Hydrogen peroxide is added in a seed-mediated growth process for producing silver nanoplates (see graphic) with not only significantly improved synthetic yield, but also greatly shortened reaction time and much enhanced reproducibility.</P>
<p> [Communication]<br />Na Li, Qiao Zhang, Sean Quinlivan, James Goebl, Yang Gan, Yadong Yin<br /><i>ChemPhysChem</i>, February 1, 2012, DOI: 10.1002/cphc.201101018. <a href="http://dx.doi.org/10.1002/cphc.201101018">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100996">
<title>Do Cation&#xB7;&#xB7;&#xB7;&#x3C0; Interactions Always Need to be 1:1?</title>
<link>http://dx.doi.org/10.1002/cphc.201100996</link>
<dc:creator>Sharon Achamma Abraham, Deepthi Jose, Ayan Datta</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100996.gif" width="411" height="124" alt="Do Cation&middot;&middot;&middot;&pi; Interactions Always Need to be 1:1?" title="Do Cation&middot;&middot;&middot;&pi; Interactions Always Need to be 1:1?" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The more the better:</B> Calculations and crystal-structure analyses show that a single electron-rich aromatic ring can simultaneously bind to two cations on its top and bottom &pi; surfaces (see picture).</P>
<p> [Communication]<br />Sharon Achamma Abraham, Deepthi Jose, Ayan Datta<br /><i>ChemPhysChem</i>, January 20, 2012, DOI: 10.1002/cphc.201100996. <a href="http://dx.doi.org/10.1002/cphc.201100996">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100983">
<title>Reaction Pathways from Single-Molecule Trajectories</title>
<link>http://dx.doi.org/10.1002/cphc.201100983</link>
<dc:creator>Haifeng Yuan, Michel Orrit</dc:creator>
<dc:date>2012-01-12T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100983.gif" width="179" height="90" alt="Reaction Pathways from Single-Molecule Trajectories" title="Reaction Pathways from Single-Molecule Trajectories" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A good sign:</B> Signal-pair histograms map transitions between different states of a single molecule (see picture) and open new opportunities for the reconstruction of kinetic pathways.</P>
<p> [Highlight]<br />Haifeng Yuan, Michel Orrit<br /><i>ChemPhysChem</i>, January 12, 2012, DOI: 10.1002/cphc.201100983. <a href="http://dx.doi.org/10.1002/cphc.201100983">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100959">
<title>Can Aromaticity Coexist with Diradical Character? An Ab&#xA0;Initio Valence Bond Study of S&lt;sub&gt;2&lt;/sub&gt;N&lt;sub&gt;2&lt;/sub&gt; and Related 6&#x3C0;-Electron Four-Membered Rings E&lt;sub&gt;2&lt;/sub&gt;N&lt;sub&gt;2&lt;/sub&gt; and E&lt;sub&gt;4&lt;/sub&gt;&lt;SUP&gt;2+&lt;/SUP&gt; (E=S, Se, Te)</title>
<link>http://dx.doi.org/10.1002/cphc.201100959</link>
<dc:creator>Beno&#xEE;t Bra&#xEF;da, Aur&#xE9;lien Lo, Philippe C. Hiberty</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100959.gif" width="208" height="215" alt="Can Aromaticity Coexist with Diradical Character? An Ab&nbsp;Initio Valence Bond Study of S2N2 and Related 6&pi;-Electron Four-Membered Rings E2N2 and E42+ (E=S, Se, Te)" title="Can Aromaticity Coexist with Diradical Character? An Ab&nbsp;Initio Valence Bond Study of S2N2 and Related 6&pi;-Electron Four-Membered Rings E2N2 and E42+ (E=S, Se, Te)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Radical ideas about diradicals:</B> A series of 6&pi;-electron 4-center species, E<sub>2</sub>N<sub>2</sub> and E<sub>4</sub><SUP>2+</SUP> (E=S, Se, Te; see picture) is studied by means of ab&nbsp;initio valence bond methods. It is shown that aromaticity and diradical character do not exclude each other, contrary to what is usually claimed.</P>
<p> [Article]<br />Beno&#xEE;t Bra&#xEF;da, Aur&#xE9;lien Lo, Philippe C. Hiberty<br /><i>ChemPhysChem</i>, January 24, 2012, DOI: 10.1002/cphc.201100959. <a href="http://dx.doi.org/10.1002/cphc.201100959">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100948">
<title>Photoinduced Electron Transfer in Zinc Naphthalocyanine&#x2013;Naphthalenediimide Supramolecular Dyads</title>
<link>http://dx.doi.org/10.1002/cphc.201100948</link>
<dc:creator>Mohamed E. El-Khouly, Andrey G. Moiseev, Art van der Est, Shunichi Fukuzumi</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100948.gif" width="193" height="116" alt="Photoinduced Electron Transfer in Zinc Naphthalocyanine&ndash;Naphthalenediimide Supramolecular Dyads" title="Photoinduced Electron Transfer in Zinc Naphthalocyanine&ndash;Naphthalenediimide Supramolecular Dyads" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Long live the dyads:</B> Efficient electron transfer and relatively long-lived charge-separated states are achieved of light-harvesting zinc naphthalocyanine:naphthalenediimide supramolecular dyads utilizing the femtosecond transient absorption technique in toluene.</P>
<p> [Article]<br />Mohamed E. El-Khouly, Andrey G. Moiseev, Art van&#xA0;der&#xA0;Est, Shunichi Fukuzumi<br /><i>ChemPhysChem</i>, January 31, 2012, DOI: 10.1002/cphc.201100948. <a href="http://dx.doi.org/10.1002/cphc.201100948">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100936">
<title>Reaction Dynamics: Rules Change with Molecular Size</title>
<link>http://dx.doi.org/10.1002/cphc.201100936</link>
<dc:creator>Markus Meuwly</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100936.gif" width="167" height="164" alt="Reaction Dynamics: Rules Change with Molecular Size" title="Reaction Dynamics: Rules Change with Molecular Size" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Playing by the rules:</B> A combined experimental/atomistic simulation approach is a powerful means to better understand chemical reactivity (see picture) and to best take advantage of mode-specific processes, highlighted herein.</P>
<p> [Highlight]<br />Markus Meuwly<br /><i>ChemPhysChem</i>, January 17, 2012, DOI: 10.1002/cphc.201100936. <a href="http://dx.doi.org/10.1002/cphc.201100936">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100929">
<title>Coherent Motion Reveals Non-Ergodic Nature of Internal Conversion between Excited States</title>
<link>http://dx.doi.org/10.1002/cphc.201100929</link>
<dc:creator>Thomas S. Kuhlman, Theis I. S&#xF8;lling, Klaus B. M&#xF8;ller</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100929.gif" width="189" height="152" alt="Coherent Motion Reveals Non-Ergodic Nature of Internal Conversion between Excited States" title="Coherent Motion Reveals Non-Ergodic Nature of Internal Conversion between Excited States" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Inherently non-ergodic:</B> The nature of a fundamental process such as internal conversion is inherently more complex than simple models might suggest. By following the vibrational dynamics during a transition between two electronic states, the complex nature can be disentangled and it is revealed how specific low-frequency modes play a significant role revealing the non-ergodic behavior (see picture).</P>
<p> [Article]<br />Thomas S. Kuhlman, Theis I. S&#xF8;lling, Klaus B. M&#xF8;ller<br /><i>ChemPhysChem</i>, January 25, 2012, DOI: 10.1002/cphc.201100929. <a href="http://dx.doi.org/10.1002/cphc.201100929">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100916">
<title>Defining a Polymethine Dye for Fluorescence Anisotropy Applications in the Near-Infrared Spectral Range</title>
<link>http://dx.doi.org/10.1002/cphc.201100916</link>
<dc:creator>Tiffany P. Gustafson, Qian Cao, Samuel Achilefu, Mikhail Y. Berezin</dc:creator>
<dc:date>2012-02-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100916.gif" width="196" height="116" alt="Defining a Polymethine Dye for Fluorescence Anisotropy Applications in the Near-Infrared Spectral Range" title="Defining a Polymethine Dye for Fluorescence Anisotropy Applications in the Near-Infrared Spectral Range" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>This dye does it!</B> Fluorescence anisotropy in the near-infrared (NIR) spectral range is challenging because appropriate NIR fluorescent labels still need to be identified. Polymethine fluorescent dyes are evaluated for this purpose. The most promising label (LS601) is then utilized in conjugation reactions to demonstrate the feasibility of fluorescence anisotropy in the NIR range (see picture).</P>
<p> [Article]<br />Tiffany P. Gustafson, Qian Cao, Samuel Achilefu, Mikhail Y. Berezin<br /><i>ChemPhysChem</i>, February 2, 2012, DOI: 10.1002/cphc.201100916. <a href="http://dx.doi.org/10.1002/cphc.201100916">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100903">
<title>Electron Transfer and Switching in Rigid [2]Rotaxanes Adsorbed on TiO&lt;sub&gt;2&lt;/sub&gt; Nanoparticles</title>
<link>http://dx.doi.org/10.1002/cphc.201100903</link>
<dc:creator>Elena Lestini, Kirill Nikitin, Jacek K. Stolarczyk, Donald Fitzmaurice</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100903.gif" width="187" height="176" alt="Electron Transfer and Switching in Rigid [2]Rotaxanes Adsorbed on TiO2 Nanoparticles" title="Electron Transfer and Switching in Rigid [2]Rotaxanes Adsorbed on TiO2 Nanoparticles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Peeling back the layers:</B> In contrast with findings in the solution phase, shuttling of the crown ether ring is inhibited in a rigid bistable [2]rotaxane when adsorbed on a TiO<sub>2</sub> nanoparticle (see picture). The results are analysed in terms of the donor&ndash;bridge&ndash;acceptor electron transfer formalism and presence of an electrical double layer.</P>
<p> [Article]<br />Elena Lestini, Kirill Nikitin, Jacek K. Stolarczyk, Donald Fitzmaurice<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100903. <a href="http://dx.doi.org/10.1002/cphc.201100903">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100894">
<title>Removing Polyvinylpyrrolidone from Catalytic Pt Nanoparticles without Modification of Superficial Order</title>
<link>http://dx.doi.org/10.1002/cphc.201100894</link>
<dc:creator>J. Monz&#xF3;, M. T. M. Koper, P. Rodriguez</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100894.gif" width="200" height="197" alt="Removing Polyvinylpyrrolidone from Catalytic Pt Nanoparticles without Modification of Superficial Order" title="Removing Polyvinylpyrrolidone from Catalytic Pt Nanoparticles without Modification of Superficial Order" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Clean catalysts:</B> A facile and novel chemical method is introduced for cleaning Pt nanoparticles with preferential orientation. The method is based on the idea that the decomposition of hydrogen peroxide may aid in removing organic components from the Pt-nanoparticle surface, and does not introduce any major loss of superficial structure.</P>
<p> [Article]<br />J. Monz&#xF3;, M. T. M. Koper, P. Rodriguez<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100894. <a href="http://dx.doi.org/10.1002/cphc.201100894">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100888">
<title>Supramolecular Systems Based on Novel Mono- and Dicationic Pyrimidinic Amphiphiles and Oligonucleotides: A Self-Organization and Complexation Study</title>
<link>http://dx.doi.org/10.1002/cphc.201100888</link>
<dc:creator>Lucia Zakharova, Mikhail Voronin, Vyacheslav Semenov, Dinar Gabdrakhmanov, Victor Syakaev, Yuri Gogolev, Rashit Giniyatullin, Svetlana Lukashenko, Vladimir Reznik, Shamil Latypov, Alexander Konovalov, Yuri Zuev</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100888.gif" width="196" height="67" alt="Supramolecular Systems Based on Novel Mono- and Dicationic Pyrimidinic Amphiphiles and Oligonucleotides: A Self-Organization and Complexation Study" title="Supramolecular Systems Based on Novel Mono- and Dicationic Pyrimidinic Amphiphiles and Oligonucleotides: A Self-Organization and Complexation Study" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Novel mono- and dicationic pyrimidinic surfactants</B> are synthesized and their aggregation behavior is studied by methods of tensiometry and nuclear magnetic resonance self-diffusion. To estimate their potentiality as gene delivery agents, the complexation with oligonucleotides is explored (see picture).</P>
<p> [Article]<br />Lucia Zakharova, Mikhail Voronin, Vyacheslav Semenov, Dinar Gabdrakhmanov, Victor Syakaev, Yuri Gogolev, Rashit Giniyatullin, Svetlana Lukashenko, Vladimir Reznik, Shamil Latypov, Alexander Konovalov, Yuri Zuev<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100888. <a href="http://dx.doi.org/10.1002/cphc.201100888">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100879">
<title>Structure&#x2013;Property Relationships in Ionic Liquids: A Study of the Anion Dependence in Vaporization Enthalpies of Imidazolium-Based Ionic Liquids</title>
<link>http://dx.doi.org/10.1002/cphc.201100879</link>
<dc:creator>Dzmitry H. Zaitsau, Koichi Fumino, Vladimir N. Emel&#x27;yanenko, Andrei V. Yermalayeu, Ralf Ludwig , Sergey P. Verevkin</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100879.gif" width="170" height="181" alt="Structure&ndash;Property Relationships in Ionic Liquids: A Study of the Anion Dependence in Vaporization Enthalpies of Imidazolium-Based Ionic Liquids" title="Structure&ndash;Property Relationships in Ionic Liquids: A Study of the Anion Dependence in Vaporization Enthalpies of Imidazolium-Based Ionic Liquids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Depend or not depend:</B> The quartz crystal microbalance and far-IR spectroscopy are used to determine vaporization enthalpies, &Delta;<sub>l</sub><SUP>g</SUP><I>H</I>&deg;<sub>m</sub>, for a series of ionic liquids (ILs) [C<sub>2</sub>mim][X] (see picture). Dependences of vaporization enthalpies on physicochemical parameters specific for anions are revealed and a simple group-contribution method is developed for predicting vaporization enthalpies of alkyl imidazolium-based ILs.</P>
<p> [Article]<br />Dzmitry H. Zaitsau, Koichi Fumino, Vladimir N. Emel&#x27;yanenko, Andrei V. Yermalayeu, Ralf Ludwig&#xA0;, Sergey P. Verevkin<br /><i>ChemPhysChem</i>, February 1, 2012, DOI: 10.1002/cphc.201100879. <a href="http://dx.doi.org/10.1002/cphc.201100879">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100876">
<title>Coordination Environment of Highly Concentrated Solutions of Cu&lt;SUP&gt;II&lt;/SUP&gt; in Ionic Liquids through a Multidisciplinary Approach</title>
<link>http://dx.doi.org/10.1002/cphc.201100876</link>
<dc:creator>Stefano Caporali, Cinzia Chiappe, Tiziana Ghilardi, Christian Silvio Pomelli, Calogero Pinzino</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100876.gif" width="118" height="196" alt="Coordination Environment of Highly Concentrated Solutions of CuII in Ionic Liquids through a Multidisciplinary Approach" title="Coordination Environment of Highly Concentrated Solutions of CuII in Ionic Liquids through a Multidisciplinary Approach" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Counteranion complexation ability</B> determines the nature of the complexes in concentrated solutions of Cu<SUP>II</SUP> salts in imidazolium-based ionic liquids (ILs), whereas the salt/IL molar ratio plays only a marginal role, according to spectroscopic and electrochemical studies. DFT calculations suggest that [CuCl<sub>3</sub>]<SUP>&minus;</SUP> and [CuCl<sub>4</sub>]<SUP>2&minus;</SUP> are the dominant Cu<SUP>II</SUP> species when the counteranion is Cl<SUP>&minus;</SUP> (see picture).</P>
<p> [Article]<br />Stefano Caporali, Cinzia Chiappe, Tiziana Ghilardi, Christian Silvio Pomelli, Calogero Pinzino<br /><i>ChemPhysChem</i>, February 6, 2012, DOI: 10.1002/cphc.201100876. <a href="http://dx.doi.org/10.1002/cphc.201100876">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100873">
<title>An in&#xA0;Situ STM and DTS Study of the Extremely Pure [EMIM]FAP/Au(111) Interface</title>
<link>http://dx.doi.org/10.1002/cphc.201100873</link>
<dc:creator>Natalia Borisenko, Sherif Zein El Abedin, Frank Endres</dc:creator>
<dc:date>2011-12-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100873.gif" width="196" height="184" alt="An in&nbsp;Situ STM and DTS Study of the Extremely Pure [EMIM]FAP/Au(111) Interface" title="An in&nbsp;Situ STM and DTS Study of the Extremely Pure [EMIM]FAP/Au(111) Interface" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Ionic liquid adlayers:</B> An in&nbsp;situ STM study of extremely pure 1-ethyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate on Au(111) shows potential-dependent surface structures that can be ascribed to cation and/or anion adsorption.</P>
<p> [Article]<br />Natalia Borisenko, Sherif Zein&#xA0;El&#xA0;Abedin, Frank Endres<br /><i>ChemPhysChem</i>, December 30, 2011, DOI: 10.1002/cphc.201100873. <a href="http://dx.doi.org/10.1002/cphc.201100873">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100872">
<title>Determination of LFER Descriptors of 30 Cations of Ionic Liquids&#x2014;Progress in Understanding Their Molecular Interaction Potentials</title>
<link>http://dx.doi.org/10.1002/cphc.201100872</link>
<dc:creator>Chul-Woong Cho, Christian Jungnickel, Stefan Stolte, Ulrich Preiss, J&#xFC;rgen Arning, Johannes Ranke, Ingo Krossing, Jorg Th&#xF6;ming</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100872.gif" width="192" height="150" alt="Determination of LFER Descriptors of 30 Cations of Ionic Liquids&mdash;Progress in Understanding Their Molecular Interaction Potentials" title="Determination of LFER Descriptors of 30 Cations of Ionic Liquids&mdash;Progress in Understanding Their Molecular Interaction Potentials" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Clarifying interactions:</B> The LFER descriptors for the excess molar refractivity and the molar volume are calculated in silico and for hydrogen-bonding acidity and basicity, and the polarizability/dipolarity of ionic liquid cations are experimentally determined through high-performance liquid chromatography measurements. A parameter is successfully added to account for the charge of the ILs (see picture).</P>
<p> [Article]<br />Chul-Woong Cho, Christian Jungnickel, Stefan Stolte, Ulrich Preiss, J&#xFC;rgen Arning, Johannes Ranke, Ingo Krossing, Jorg Th&#xF6;ming<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100872. <a href="http://dx.doi.org/10.1002/cphc.201100872">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100868">
<title>Cation&#x2013;&#x3C0; Interactions between a Free-Base Porphyrin and an Ionic Liquid: A Computational Study</title>
<link>http://dx.doi.org/10.1002/cphc.201100868</link>
<dc:creator>Zhen Cao, Shu Li, Tianying Yan</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100868.gif" width="194" height="176" alt="Cation&ndash;&pi; Interactions between a Free-Base Porphyrin and an Ionic Liquid: A Computational Study" title="Cation&ndash;&pi; Interactions between a Free-Base Porphyrin and an Ionic Liquid: A Computational Study" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Cation&ndash;&pi; stacking</B>: A free-base porphyrin (FBP) is sandwiched between two 1-butyl-3-methylimidazolium (BMIM<SUP>+</SUP>) cations with a slipped-parallel alignment in an ionic liquid, due to the cation&ndash;&pi; interactions between the FBP and BMIM<SUP>+</SUP>.</P>
<p> [Article]<br />Zhen Cao, Shu Li, Tianying Yan<br /><i>ChemPhysChem</i>, January 17, 2012, DOI: 10.1002/cphc.201100868. <a href="http://dx.doi.org/10.1002/cphc.201100868">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100864">
<title>Role of Hydrocarbon Radicals CH&lt;sub&gt;&lt;I&gt;x&lt;/I&gt;&lt;/sub&gt; (&lt;I&gt;x&lt;/I&gt;=1, 2, 3) in Graphene Growth: A Theoretical Perspective</title>
<link>http://dx.doi.org/10.1002/cphc.201100864</link>
<dc:creator>Chong Wang, Bo Xiao, Yi-hong Ding</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100864.gif" width="165" height="192" alt="Role of Hydrocarbon Radicals CHx (x=1, 2, 3) in Graphene Growth: A Theoretical Perspective" title="Role of Hydrocarbon Radicals CHx (x=1, 2, 3) in Graphene Growth: A Theoretical Perspective" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Growing well:</B> Many outstanding properties of graphene are blocked by the existence of structural defects (see picture). An important healing mechanism that takes place during the growth of this material via plasma-enhanced chemical vapor decomposition (PECVD) is proposed. The three-step process is based on the incorporation of C&nbsp;atoms from hydrocarbon radicals into the single-vacancy defects of graphene.</P>
<p> [Article]<br />Chong Wang, Bo Xiao, Yi-hong Ding<br /><i>ChemPhysChem</i>, January 31, 2012, DOI: 10.1002/cphc.201100864. <a href="http://dx.doi.org/10.1002/cphc.201100864">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100857">
<title>In Situ Observation of the Thermally Induced Growth of Platinum-Nanoparticle Catalysts Using High-Temperature X-ray Diffraction</title>
<link>http://dx.doi.org/10.1002/cphc.201100857</link>
<dc:creator>Fr&#xE9;d&#xE9;ric Hasch&#xE9;, Mehtap Oezaslan, Peter Strasser</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100857.gif" width="195" height="149" alt="In Situ Observation of the Thermally Induced Growth of Platinum-Nanoparticle Catalysts Using High-Temperature X-ray Diffraction" title="In Situ Observation of the Thermally Induced Growth of Platinum-Nanoparticle Catalysts Using High-Temperature X-ray Diffraction" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Stable catalysts:</B> The thermal durability of carbon-supported nanoparticles below 3&nbsp;nm is examined using high-temperature X-ray diffraction. The effects of surface area, Pt loading, temperature, and gas environment on the particle growth are identified (see graph). The study provides a guideline for designing enhanced, long-term thermally stable nanoparticle catalysts.</P>
<p> [Article]<br />Fr&#xE9;d&#xE9;ric Hasch&#xE9;, Mehtap Oezaslan, Peter Strasser<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100857. <a href="http://dx.doi.org/10.1002/cphc.201100857">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100843">
<title>Further Insight into the Photostability of the Pyrene Fluorophore in Halogenated Solvents</title>
<link>http://dx.doi.org/10.1002/cphc.201100843</link>
<dc:creator>Jordi Aguilera-Sigalat, Jaime Sanchez-SanMart&#xED;n, Carlos E. Agudelo-Morales, Elena Zaballos, Raquel E. Galian, Julia P&#xE9;rez-Prieto</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100843.gif" width="195" height="102" alt="Further Insight into the Photostability of the Pyrene Fluorophore in Halogenated Solvents" title="Further Insight into the Photostability of the Pyrene Fluorophore in Halogenated Solvents" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The use of dichloromethane</B> can be an excellent alternative to chloroform when the good solubility properties of halogenated solvents are needed applying pyrene systems as fluorescent probes. The reason for this lies in the different reactivity of chloromethyl and dichloromethyl radicals towards pyrene and oxygen.</P>
<p> [Article]<br />Jordi Aguilera-Sigalat, Jaime Sanchez-SanMart&#xED;n, Carlos E. Agudelo-Morales, Elena Zaballos, Raquel E. Galian, Julia P&#xE9;rez-Prieto<br /><i>ChemPhysChem</i>, January 24, 2012, DOI: 10.1002/cphc.201100843. <a href="http://dx.doi.org/10.1002/cphc.201100843">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100842">
<title>Nanoconfinement Effects: Glucose Oxidase Reaction Kinetics in Nanofluidics</title>
<link>http://dx.doi.org/10.1002/cphc.201100842</link>
<dc:creator>Chen Wang, Zhen-Huan Sheng, Jun Ouyang, Jing-Juan Xu, Hong-Yuan Chen, Xing-Hua Xia</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100842.gif" width="192" height="85" alt="Nanoconfinement Effects: Glucose Oxidase Reaction Kinetics in Nanofluidics" title="Nanoconfinement Effects: Glucose Oxidase Reaction Kinetics in Nanofluidics" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Size-tunable nanofluidic devices</B> coupled to an electrochemical detector are fabricated and used to study the reaction kinetics of glucose oxidase confined in nanochannels (see picture). Significant channel-size-dependent effects are observed, demonstrating the influence of spatial confinement on the enzyme reaction kinetics.</P>
<p> [Article]<br />Chen Wang, Zhen-Huan Sheng, Jun Ouyang, Jing-Juan Xu, Hong-Yuan Chen, Xing-Hua Xia<br /><i>ChemPhysChem</i>, February 6, 2012, DOI: 10.1002/cphc.201100842. <a href="http://dx.doi.org/10.1002/cphc.201100842">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100833">
<title>&lt;I&gt;Ortho&lt;/I&gt;-Functionalized Perylenediimides for Highly Fluorescent Water-Soluble Dyes</title>
<link>http://dx.doi.org/10.1002/cphc.201100833</link>
<dc:creator>Glauco Battagliarin, Melari Davies, Stephan Mackowiak, Chen Li, Klaus M&#xFC;llen</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100833.gif" width="187" height="94" alt="Ortho-Functionalized Perylenediimides for Highly Fluorescent Water-Soluble Dyes" title="Ortho-Functionalized Perylenediimides for Highly Fluorescent Water-Soluble Dyes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Clearly visible:</B> A water-soluble and highly fluorescent perylenediimide is synthesized via ruthenium-catalyzed alkylation with outstanding yields (see scheme). For the first time, the possibility to use phosphonate derivatives in a Murai-type reaction is demonstrated.</P>
<p> [Communication]<br />Glauco Battagliarin, Melari Davies, Stephan Mackowiak, Chen Li, Klaus M&#xFC;llen<br /><i>ChemPhysChem</i>, January 13, 2012, DOI: 10.1002/cphc.201100833. <a href="http://dx.doi.org/10.1002/cphc.201100833">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100832">
<title>Determination of Hydrogen-Bond-Accepting and &#x2013;Donating Abilities of Ionic Liquids with Halogeno Complex Anions by Means of &lt;SUP&gt;1&lt;/SUP&gt;H&#xA0;NMR Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cphc.201100832</link>
<dc:creator>Ralf Lungwitz, Stefan Spange</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100832.gif" width="187" height="182" alt="Determination of Hydrogen-Bond-Accepting and &ndash;Donating Abilities of Ionic Liquids with Halogeno Complex Anions by Means of 1H&nbsp;NMR Spectroscopy" title="Determination of Hydrogen-Bond-Accepting and &ndash;Donating Abilities of Ionic Liquids with Halogeno Complex Anions by Means of 1H&nbsp;NMR Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Two for the price of one:</B> The imidazolium cation serves both as part of the ionic liquid (IL) and as an NMR probe. Hydrogen-bond-accepting (HBA) and donating (HBD) abilities of ILs with halogeno complex anions (X<SUP>&minus;</SUP>) are determined by means of <SUP>1</SUP>H&nbsp;NMR spectroscopy (see picture). The chemical shift of the H(2) atom is a function of the HBA strength of the anion.</P>
<p> [Article]<br />Ralf Lungwitz, Stefan Spange<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100832. <a href="http://dx.doi.org/10.1002/cphc.201100832">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100829">
<title>X-Ray Photoelectron Spectroscopy of Ferrocenyl- and Ferrocenium-Based Ionic Liquids</title>
<link>http://dx.doi.org/10.1002/cphc.201100829</link>
<dc:creator>Alasdair W. Taylor, Peter Licence</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100829.gif" width="185" height="111" alt="X-Ray Photoelectron Spectroscopy of Ferrocenyl- and Ferrocenium-Based Ionic Liquids" title="X-Ray Photoelectron Spectroscopy of Ferrocenyl- and Ferrocenium-Based Ionic Liquids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Look sharp!</B> X-ray photoelectron spectroscopy is used to study a series of five 1-(ferrocenylmethyl)-3-methylimidazolium- and 1-(ferroceniummethyl)-3-methylimidazolium-based salts (see picture). All samples emit good photoelectron fluxes with sharp, well-resolved photoelectron peaks.</P>
<p> [Article]<br />Alasdair W. Taylor, Peter Licence<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100829. <a href="http://dx.doi.org/10.1002/cphc.201100829">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100820">
<title>Linking Single-Molecule Blinking to Chromophore Structure and Redox Potentials</title>
<link>http://dx.doi.org/10.1002/cphc.201100820</link>
<dc:creator>Ingo H. Stein, Stella Capone, Jochem H. Smit, Fabian Baumann, Thorben Cordes, Philip Tinnefeld</dc:creator>
<dc:date>2011-12-08T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100820.gif" width="192" height="192" alt="Linking Single-Molecule Blinking to Chromophore Structure and Redox Potentials" title="Linking Single-Molecule Blinking to Chromophore Structure and Redox Potentials" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The missing link:</B> Blinking of three dyes from a homologous series (Cy3, Cy5, Cy7) is studied (see picture). The underlying radical anion states are induced by controlling the oxygen concentration and by adding the reductant ascorbic acid. For different conditions the OFF-state lifetime always increases in the order Cy3&lt;Cy5&lt;Cy7. Off-state lifetimes are related to higher reduction potentials as well as chromophore size.</P>
<p> [Article]<br />Ingo H. Stein, Stella Capone, Jochem H. Smit, Fabian Baumann, Thorben Cordes, Philip Tinnefeld<br /><i>ChemPhysChem</i>, December 8, 2011, DOI: 10.1002/cphc.201100820. <a href="http://dx.doi.org/10.1002/cphc.201100820">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100813">
<title>Demonstration of Photoluminescence and Metal-Enhanced Fluorescence of Exfoliated MoS&lt;sub&gt;2&lt;/sub&gt;</title>
<link>http://dx.doi.org/10.1002/cphc.201100813</link>
<dc:creator>Kangfu Zhou, Yihua Zhu, Xiaoling Yang, Jinghong Zhou, Chunzhong Li</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100813.gif" width="194" height="101" alt="Demonstration of Photoluminescence and Metal-Enhanced Fluorescence of Exfoliated MoS2" title="Demonstration of Photoluminescence and Metal-Enhanced Fluorescence of Exfoliated MoS2" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Thinly spread:</B> Ultrathin layers of exfoliated MoS<sub>2</sub> exhibit remarkable photoluminescence which is absence in bulk MoS<sub>2</sub>. The intensity of the fluorescence is further enhanced by Ag@SiO<sub>2</sub> core/shell composites due to on metal-enhanced fluorescence (see picture).</P>
<p> [Communication]<br />Kangfu Zhou, Yihua Zhu, Xiaoling Yang, Jinghong Zhou, Chunzhong Li<br /><i>ChemPhysChem</i>, January 13, 2012, DOI: 10.1002/cphc.201100813. <a href="http://dx.doi.org/10.1002/cphc.201100813">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100810">
<title>NMR Investigation of Imidazolium-Based Ionic Liquids and Their Aqueous Mixtures</title>
<link>http://dx.doi.org/10.1002/cphc.201100810</link>
<dc:creator>Flaminia Cesare Marincola, Cristina Piras, Olga Russina, Lorenzo Gontrani, Giuseppe Saba, Adolfo Lai</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100810.gif" width="212" height="129" alt="NMR Investigation of Imidazolium-Based Ionic Liquids and Their Aqueous Mixtures" title="NMR Investigation of Imidazolium-Based Ionic Liquids and Their Aqueous Mixtures" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Holding water:</B> The interaction of water with the ionic liquids (ILs) 1-hexyl- and 1-octyl-3-methylimidazolium bromide, at IL concentrations above the critical aggregation concentration, is investigated by NMR spectroscopy (see figure). Water influences the environment close to the polar region of ILs at the lowest water content. Upon increasing the water fraction, the IL molecules form aggregates where contacts occur between the polar and apolar regions.</P>
<p> [Article]<br />Flaminia Cesare&#xA0;Marincola, Cristina Piras, Olga Russina, Lorenzo Gontrani, Giuseppe Saba, Adolfo Lai<br /><i>ChemPhysChem</i>, January 20, 2012, DOI: 10.1002/cphc.201100810. <a href="http://dx.doi.org/10.1002/cphc.201100810">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100807">
<title>Diffusive Shielding Stabilizes Bulk Nanobubble Clusters</title>
<link>http://dx.doi.org/10.1002/cphc.201100807</link>
<dc:creator>Joost H. Weijs, James R. T. Seddon, Detlef Lohse</dc:creator>
<dc:date>2012-01-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100807.gif" width="191" height="192" alt="Diffusive Shielding Stabilizes Bulk Nanobubble Clusters" title="Diffusive Shielding Stabilizes Bulk Nanobubble Clusters" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Small, but tough:</B> Bulk nanobubble clusters can be stable under specific conditions. MD simulations (see picture) of binary mixtures of simple (Lennard-Jones) fluids are used to show this.</P>
<p> [Article]<br />Joost H. Weijs, James R. T. Seddon, Detlef Lohse<br /><i>ChemPhysChem</i>, January 2, 2012, DOI: 10.1002/cphc.201100807. <a href="http://dx.doi.org/10.1002/cphc.201100807">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100806">
<title>Water-Soluble Monodispersed Lanthanide Oxide Submicrospheres: PVP-Assisted Hydrothermal Synthesis, Size-Control and Luminescence Properties</title>
<link>http://dx.doi.org/10.1002/cphc.201100806</link>
<dc:creator>Ying Cui, Xiaoyong Lai, Li Li, Zhudong Hu, Shuo Wang, Jonathan E. Halpert, Ranbo Yu, Dan Wang</dc:creator>
<dc:date>2011-12-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100806.gif" width="196" height="82" alt="Water-Soluble Monodispersed Lanthanide Oxide Submicrospheres: PVP-Assisted Hydrothermal Synthesis, Size-Control and Luminescence Properties" title="Water-Soluble Monodispersed Lanthanide Oxide Submicrospheres: PVP-Assisted Hydrothermal Synthesis, Size-Control and Luminescence Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Easy!</B> A facile hydrothermal synthetic route is presented to prepare a class of monodispersed lanthanide-based compound submicrospheres with controllable size (see picture). The method only employs raw lanthanide oxides as starting material, urea as precipitator and poly(<I>N</I>-vinyl-2-pyrrolidone) as surfactant.</P>
<p> [Article]<br />Ying Cui, Xiaoyong Lai, Li Li, Zhudong Hu, Shuo Wang, Jonathan E. Halpert, Ranbo Yu, Dan Wang<br /><i>ChemPhysChem</i>, December 23, 2011, DOI: 10.1002/cphc.201100806. <a href="http://dx.doi.org/10.1002/cphc.201100806">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100796">
<title>In Situ Formation of One-Dimensional Assemblies of Gold Nanoparticles in Confined Media</title>
<link>http://dx.doi.org/10.1002/cphc.201100796</link>
<dc:creator>Jorge Carballido-Landeira, Sonia Goy-L&#xF3;pez, Alberto P. Mu&#xF1;uzuri, Pablo Taboada, V&#xED;ctor Mosquera</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100796.gif" width="192" height="154" alt="In Situ Formation of One-Dimensional Assemblies of Gold Nanoparticles in Confined Media" title="In Situ Formation of One-Dimensional Assemblies of Gold Nanoparticles in Confined Media" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Assemble!</B> One dimensional Au nanoparticles arrays are created upon solvent drying onto a solid support by exploiting the aurophilic attraction between Au ions complexed to a coordinating ligand, such as oleylamine, and the subsequent formation of polymeric bundles (see picture).</P>
<p> [Article]<br />Jorge Carballido-Landeira, Sonia Goy-L&#xF3;pez, Alberto P. Mu&#xF1;uzuri, Pablo Taboada, V&#xED;ctor Mosquera<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100796. <a href="http://dx.doi.org/10.1002/cphc.201100796">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100788">
<title>Absorption, Luminescence, and Sizing of Organic Dye Nanoparticles and of Patterns Formed Upon Dewetting</title>
<link>http://dx.doi.org/10.1002/cphc.201100788</link>
<dc:creator>Alexander Gaiduk, Mustafa Yorulmaz, El&#xE9;na Ishow, Michel Orrit</dc:creator>
<dc:date>2011-12-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100788.gif" width="195" height="105" alt="Absorption, Luminescence, and Sizing of Organic Dye Nanoparticles and of Patterns Formed Upon Dewetting" title="Absorption, Luminescence, and Sizing of Organic Dye Nanoparticles and of Patterns Formed Upon Dewetting" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Labyrinthine:</B> Quantitative insight into phototphysics of organic dye nanoparticles and the dewetting induced patterns formed from a push&ndash;pull triarylamine dye is obtained by using simultaneous absorption and fluorescence microscopy (see picture). The quantum yield of organic nanoparticles and the number of molecules forming the nanoparticles and patterns are deduced.</P>
<p> [Article]<br />Alexander Gaiduk, Mustafa Yorulmaz, El&#xE9;na Ishow, Michel Orrit<br /><i>ChemPhysChem</i>, December 19, 2011, DOI: 10.1002/cphc.201100788. <a href="http://dx.doi.org/10.1002/cphc.201100788">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100785">
<title>Probing the Electronic State of a Single Coronene Molecule by the Emission from Proximate Fluorophores</title>
<link>http://dx.doi.org/10.1002/cphc.201100785</link>
<dc:creator>Burkhard F&#xFC;ckel, Gerald Hinze, Jishan Wu, Klaus M&#xFC;llen, Thomas Basch&#xE9;</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100785.gif" width="360" height="124" alt="Probing the Electronic State of a Single Coronene Molecule by the Emission from Proximate Fluorophores" title="Probing the Electronic State of a Single Coronene Molecule by the Emission from Proximate Fluorophores" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Long time, no see:</B> The long triplet state lifetime of hexa-<I>peri</I>-hexabenzocoronene (blue) appears as dark states in the emission of the perylenemonoimide periphery (green).</P>
<p> [Article]<br />Burkhard F&#xFC;ckel, Gerald Hinze, Jishan Wu, Klaus M&#xFC;llen, Thomas Basch&#xE9;<br /><i>ChemPhysChem</i>, January 17, 2012, DOI: 10.1002/cphc.201100785. <a href="http://dx.doi.org/10.1002/cphc.201100785">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100783">
<title>Laser Control of Zeolite Nucleation</title>
<link>http://dx.doi.org/10.1002/cphc.201100783</link>
<dc:creator>Marta Navarro, Alvaro Mayoral, Ester Mateo, Ruth Lahoz, Germ&#xE1;n F. de la Fuente, Joaqu&#xED;n Coronas</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100783.gif" width="114" height="196" alt="Laser Control of Zeolite Nucleation" title="Laser Control of Zeolite Nucleation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Cut down to size:</B> Presursor solutions for the synthesis of zeolites are irradiated by means of a Nd-YAG laser (see picture). Upon a hydrothermal treatment, the zeolite crystal size exponentially decreased as a function of laser irradiation time.</P>
<p> [Article]<br />Marta Navarro, Alvaro Mayoral, Ester Mateo, Ruth Lahoz, Germ&#xE1;n F. de&#xA0;la&#xA0;Fuente, Joaqu&#xED;n Coronas<br /><i>ChemPhysChem</i>, January 20, 2012, DOI: 10.1002/cphc.201100783. <a href="http://dx.doi.org/10.1002/cphc.201100783">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100781">
<title>Photobleaching and Blinking of TAMRA Induced by Mn&lt;SUP&gt;2+&lt;/SUP&gt;</title>
<link>http://dx.doi.org/10.1002/cphc.201100781</link>
<dc:creator>Elana M. S. Stennett, Gerdenis Kodis, Marcia Levitus</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100781.gif" width="204" height="173" alt="Photobleaching and Blinking of TAMRA Induced by Mn2+" title="Photobleaching and Blinking of TAMRA Induced by Mn2+" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Blinking and bleaching:</B> Coordination of Mn<SUP>2+</SUP> to DNA induces intersystem crossing, causing fluctuations in the fluorescence intensity and accelerated photobleaching.</P>
<p> [Communication]<br />Elana M. S. Stennett, Gerdenis Kodis, Marcia Levitus<br /><i>ChemPhysChem</i>, February 1, 2012, DOI: 10.1002/cphc.201100781. <a href="http://dx.doi.org/10.1002/cphc.201100781">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100780">
<title>Properties of Oligothiophene Dendrimers as a Function of Molecular Architecture and Generation Number</title>
<link>http://dx.doi.org/10.1002/cphc.201100780</link>
<dc:creator>Esther C&#xF3;rdova-Mateo , Francisco Rodr&#xED;guez-Ropero, Oscar Bertran, Carlos Alem&#xE1;n </dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100780.gif" width="193" height="160" alt="Properties of Oligothiophene Dendrimers as a Function of Molecular Architecture and Generation Number" title="Properties of Oligothiophene Dendrimers as a Function of Molecular Architecture and Generation Number" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>All-thiophene dendrimers</B> are investigated with regard to their molecular geometries and electronic structure by means of DFT and TD-DFT calculations, which are used to examine the dependence of properties such as the lowest &pi;&ndash;&pi;* transition energy <I>&epsilon;</I><sub>g</sub> on molecular dimensions (number of thiophene rings <I>n</I>) and symmetric versus unsymmetric architecture (fractions of &alpha;&ndash;&alpha; and &alpha;&ndash;&beta; linkages <I>&chi;</I><sub>&alpha;&ndash;&alpha;</sub> and <I>&chi;</I><sub>&alpha;&ndash;&beta;</sub>; see picture).</P>
<p> [Article]<br />Esther C&#xF3;rdova-Mateo&#xA0;, Francisco Rodr&#xED;guez-Ropero, Oscar Bertran, Carlos Alem&#xE1;n&#xA0;<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100780. <a href="http://dx.doi.org/10.1002/cphc.201100780">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100776">
<title>The Effect of Temperature on Single-Polypeptide Adsorption</title>
<link>http://dx.doi.org/10.1002/cphc.201100776</link>
<dc:creator>Sandra Kienle, Susanne Liese, Nadine Schwierz, Roland R. Netz, Thorsten Hugel</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100776.gif" width="216" height="129" alt="The Effect of Temperature on Single-Polypeptide Adsorption" title="The Effect of Temperature on Single-Polypeptide Adsorption" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Compensating Mechanisms:</B> The temperature-dependent desorption of single polypeptides from hydrophobic surfaces, studied by means of atomic force microscopy and molecular dynamics simulations, shows a strong compensation mechanism between the different contributions to the desorption force. This is reminiscent of the protein-folding process, where large entropic and enthalpic contributions compensate each other, resulting in a small free-energy difference between the folded and unfolded states.</P>
<p> [Article]<br />Sandra Kienle, Susanne Liese, Nadine Schwierz, Roland R. Netz, Thorsten Hugel<br /><i>ChemPhysChem</i>, January 31, 2012, DOI: 10.1002/cphc.201100776. <a href="http://dx.doi.org/10.1002/cphc.201100776">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100774">
<title>Probing the Chemical Functionalization of Single-Walled Carbon Nanotubes with Multiple Carbon Ad-Dimer Defects</title>
<link>http://dx.doi.org/10.1002/cphc.201100774</link>
<dc:creator>Dong-Lai Wang , Hong-Liang Xu, Zhong-Min Su, Shabbir Muhammad, Dong-Yan Hou</dc:creator>
<dc:date>2012-02-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100774.gif" width="191" height="152" alt="Probing the Chemical Functionalization of Single-Walled Carbon Nanotubes with Multiple Carbon Ad-Dimer Defects" title="Probing the Chemical Functionalization of Single-Walled Carbon Nanotubes with Multiple Carbon Ad-Dimer Defects" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Drying-tube-shaped SWCNTs</B> with multiple carbon ad-dimer defects, constructed by inserting C<sub>2</sub> units into armchair (<I>n</I>,<I>n</I>,<I>m</I>) single-walled carbon nanotubes (<I>n</I>=4&ndash;8) with <I>m</I>=7 and 13 C layers, and their hydrogenated, fluorinated, and chlorinated derivatives are investigated by DFT. Chemisorption of H, F, or Cl atoms on these SWCNTs is exothermic, and reaction energies <I>E</I><sub>r</sub> increase with increasing <I>n</I> (see picture).</P>
<p> [Article]<br />Dong-Lai Wang&#xA0;, Hong-Liang Xu, Zhong-Min Su, Shabbir Muhammad, Dong-Yan Hou<br /><i>ChemPhysChem</i>, February 2, 2012, DOI: 10.1002/cphc.201100774. <a href="http://dx.doi.org/10.1002/cphc.201100774">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100772">
<title>Electron Transport through Single &#x3C0;-Conjugated Molecules Bridging between Metal Electrodes</title>
<link>http://dx.doi.org/10.1002/cphc.201100772</link>
<dc:creator>Manabu Kiguchi, Satoshi Kaneko</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100772.gif" width="155" height="175" alt="Electron Transport through Single &pi;-Conjugated Molecules Bridging between Metal Electrodes" title="Electron Transport through Single &pi;-Conjugated Molecules Bridging between Metal Electrodes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>One and all:</B> Electron transport through a single molecule between metal electrodes is a topic of great interest in the development of nanoscale molecular electronic devices. &pi;-Conjugated molecules have attracted attention due to their unique properties. The fabrication and electron-transport properties of the single &pi;-conjugated molecule junction (see picture) are discussed.</P>
<p> [Review]<br />Manabu Kiguchi, Satoshi Kaneko<br /><i>ChemPhysChem</i>, February 6, 2012, DOI: 10.1002/cphc.201100772. <a href="http://dx.doi.org/10.1002/cphc.201100772">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100771">
<title>Spectroscopic Properties of Gold Nanoparticles at the Single-Particle Level in Biological Environments</title>
<link>http://dx.doi.org/10.1002/cphc.201100771</link>
<dc:creator>Laura C. Estrada, Enrico Gratton</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100771.gif" width="196" height="84" alt="Spectroscopic Properties of Gold Nanoparticles at the Single-Particle Level in Biological Environments" title="Spectroscopic Properties of Gold Nanoparticles at the Single-Particle Level in Biological Environments" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Trap and track:</B> The orbital tracking method (OTM) allows us to simultaneously track single nanoparticles (NPs) and spectroscopically characterize their emission while diffusing even inside cells. As the NPs are always trapped by the laser, a detail spectroscopic characterization of the NPs can be done, even if the NPs are moving in three dimensions and along microns (see picture).</P>
<p> [Article]<br />Laura C. Estrada, Enrico Gratton<br /><i>ChemPhysChem</i>, February 1, 2012, DOI: 10.1002/cphc.201100771. <a href="http://dx.doi.org/10.1002/cphc.201100771">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100770">
<title>Chromophores in Conjugated Polymers&#x2014;All Straight?</title>
<link>http://dx.doi.org/10.1002/cphc.201100770</link>
<dc:creator>John M. Lupton</dc:creator>
<dc:date>2011-12-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100770.gif" width="213" height="95" alt="Chromophores in Conjugated Polymers&mdash;All Straight?" title="Chromophores in Conjugated Polymers&mdash;All Straight?" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>What shape is it?</B> Single-molecule and ensemble time-resolved studies support the notion that the &pi;-bond in large macromolecules, such as conjugated polymers, is remarkably persistent in space: even individual chromophores can be bent and twisted, so that caution is warranted when interpreting a wide range of polarization-based spectroscopies.</P>
<p> [Concept]<br />John M. Lupton<br /><i>ChemPhysChem</i>, December 16, 2011, DOI: 10.1002/cphc.201100770. <a href="http://dx.doi.org/10.1002/cphc.201100770">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100765">
<title>Peptide&#x2013;Antibody Complex as Handle for Single-Molecule Cut &amp; Paste</title>
<link>http://dx.doi.org/10.1002/cphc.201100765</link>
<dc:creator>Mathias Strackharn, Stefan W. Stahl, Philip M. D. Severin, Thomas Nicolaus, Hermann E. Gaub</dc:creator>
<dc:date>2011-12-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100765.gif" width="199" height="193" alt="Peptide&ndash;Antibody Complex as Handle for Single-Molecule Cut &amp; Paste" title="Peptide&ndash;Antibody Complex as Handle for Single-Molecule Cut &amp; Paste" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Molecule-by-molecule arrangement</B> of proteins, for example, in enzymatic networks of predefined composition and proximity, is a major goal that may be accomplished by the single-molecule cut-and-paste technique (SMC&amp;P). For this purpose, co-expressed anchors and handles as protein tags should be employed. As a first step in this direction, the authors develop an SMC&amp;P design which exploits an antibody&ndash;peptide complex as a molecular handle.</P>
<p> [Communication]<br />Mathias Strackharn, Stefan W. Stahl, Philip M. D. Severin, Thomas Nicolaus, Hermann E. Gaub<br /><i>ChemPhysChem</i>, December 19, 2011, DOI: 10.1002/cphc.201100765. <a href="http://dx.doi.org/10.1002/cphc.201100765">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100748">
<title>Measurement and Applications of Long-Range Heteronuclear Scalar Couplings: Recent Experimental and Theoretical Developments</title>
<link>http://dx.doi.org/10.1002/cphc.201100748</link>
<dc:creator>Nilamoni Nath, Lokesh, Nagarajarao Suryaprakash</dc:creator>
<dc:date>2012-02-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100748.gif" width="185" height="186" alt="Measurement and Applications of Long-Range Heteronuclear Scalar Couplings: Recent Experimental and Theoretical Developments" title="Measurement and Applications of Long-Range Heteronuclear Scalar Couplings: Recent Experimental and Theoretical Developments" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Coupling at a distance</B>: The advantages and limitations of a number of NMR techniques for the measurement of long-range heteronuclear couplings are discussed. The use of <SUP><I>n</I></SUP><I>J</I><sub>XY</sub> couplings (see picture) in conjunction with theoretical calculations allows conclusions to be reached on the hyperconjugation, configurational analysis, and effect of the electronegativity of substituents.</P>
<p> [Minireview]<br />Nilamoni Nath, Lokesh, Nagarajarao Suryaprakash<br /><i>ChemPhysChem</i>, February 2, 2012, DOI: 10.1002/cphc.201100748. <a href="http://dx.doi.org/10.1002/cphc.201100748">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100745">
<title>Conjugation-Promoted Reaction of Open-Cage Fullerene: A Density Functional Theory Study</title>
<link>http://dx.doi.org/10.1002/cphc.201100745</link>
<dc:creator>Yong Guo, Jingjing Yan, Niveen M. Khashab</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100745.gif" width="414" height="98" alt="Conjugation-Promoted Reaction of Open-Cage Fullerene: A Density Functional Theory Study" title="Conjugation-Promoted Reaction of Open-Cage Fullerene: A Density Functional Theory Study" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Not that classical:</B> The reaction of a carbonyl group on the fullerene orifice with triethyl phosphite most likely proceeds following the Abramov reaction to firstly form a classical product. However, this product is not stable and turns into an experimental product as the conversion transition state is stabilized by fullerene conjugation (see picture).</P>
<p> [Article]<br />Yong Guo, Jingjing Yan, Niveen M. Khashab<br /><i>ChemPhysChem</i>, January 20, 2012, DOI: 10.1002/cphc.201100745. <a href="http://dx.doi.org/10.1002/cphc.201100745">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100743">
<title>Mapping of Surface-Enhanced Fluorescence on Metal Nanoparticles using Super-Resolution Photoactivation Localization Microscopy</title>
<link>http://dx.doi.org/10.1002/cphc.201100743</link>
<dc:creator>Hongzhen Lin, Silvia P. Centeno, Liang Su, Bart Kenens, Susana Rocha, Michel Sliwa, Johan Hofkens, Hiroshi Uji-i</dc:creator>
<dc:date>2011-12-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100743.gif" width="190" height="206" alt="Mapping of Surface-Enhanced Fluorescence on Metal Nanoparticles using Super-Resolution Photoactivation Localization Microscopy" title="Mapping of Surface-Enhanced Fluorescence on Metal Nanoparticles using Super-Resolution Photoactivation Localization Microscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Maps on metals:</B> Photoactivation localization microscopy (PALM) is applied to study suface-enhanced fluorescence (SEF) on metal nanostructures (SEF-PALM), see picture. The detection of fluorescence from individual single molecules can be used to image the point-spread function and spatial distribution of the fluorescence emitted in the vicinity of a metal surface.</P>
<p> [Article]<br />Hongzhen Lin, Silvia P. Centeno, Liang Su, Bart Kenens, Susana Rocha, Michel Sliwa, Johan Hofkens, Hiroshi Uji-i<br /><i>ChemPhysChem</i>, December 19, 2011, DOI: 10.1002/cphc.201100743. <a href="http://dx.doi.org/10.1002/cphc.201100743">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100737">
<title>Organic&#x2013;Organic Heterostructures: Concepts and Applications</title>
<link>http://dx.doi.org/10.1002/cphc.201100737</link>
<dc:creator>Alexander Hinderhofer, Frank Schreiber</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100737.gif" width="190" height="136" alt="Organic&ndash;Organic Heterostructures: Concepts and Applications" title="Organic&ndash;Organic Heterostructures: Concepts and Applications" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Less is more:</B> Basic concepts, examples and applications of organic&ndash;organic heterostructures are reviewed (see picture). Heterostructures in the monolayer regime, including nanostructuring concepts and systems involving self-assembled monolayers, as well as various other architectures, including superlattices, are discussed.</P>
<p> [Review]<br />Alexander Hinderhofer, Frank Schreiber<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100737. <a href="http://dx.doi.org/10.1002/cphc.201100737">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100732">
<title>The Surface Chemistry of Water on Fe(100): A Density Functional Theory Study</title>
<link>http://dx.doi.org/10.1002/cphc.201100732</link>
<dc:creator>Ashriti Govender, Daniel Curulla Ferr&#xE9;, J. W. Niemantsverdriet</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100732.gif" width="194" height="219" alt="The Surface Chemistry of Water on Fe(100): A Density Functional Theory Study" title="The Surface Chemistry of Water on Fe(100): A Density Functional Theory Study" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Holding water:</B> In the formation of water by hydrogenation of atomic oxygen, the oxygen preferentially adsorbs at the four-fold hollow site, the hydroxyl group prefers the bridge site in a tilted configuration, and water is most stable when adsorbed at the top site with the two O-H bonds parallel to the Fe surface (see picture). Adsorption energies, optimised structures and vibrational frequencies of O, OH and H<sub>2</sub>O for several adsorption modes are presented.</P>
<p> [Article]<br />Ashriti Govender, Daniel Curulla&#xA0;Ferr&#xE9;, J. W. Niemantsverdriet<br /><i>ChemPhysChem</i>, February 1, 2012, DOI: 10.1002/cphc.201100732. <a href="http://dx.doi.org/10.1002/cphc.201100732">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100731">
<title>Comparison of Low-Frequency Spectra between Aromatic and Nonaromatic Cation Based Ionic Liquids Using Femtosecond Raman-Induced Kerr Effect Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cphc.201100731</link>
<dc:creator>Hideaki Shirota</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100731.gif" width="387" height="85" alt="Comparison of Low-Frequency Spectra between Aromatic and Nonaromatic Cation Based Ionic Liquids Using Femtosecond Raman-Induced Kerr Effect Spectroscopy" title="Comparison of Low-Frequency Spectra between Aromatic and Nonaromatic Cation Based Ionic Liquids Using Femtosecond Raman-Induced Kerr Effect Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Bass notes:</B> Low-frequency spectra below 200&nbsp;cm<SUP>&minus;1</SUP> of aromatic and nonaromatic cation based ionic liquids using femtosecond Raman-induced Kerr effect spectroscopy (see picture) are reviewed. The differences in the spectral line shape between two types of ionic liquids are discussed, and the relationships between the first moment of the broad spectral band and the bulk properties are compared.</P>
<p> [Minireview]<br />Hideaki Shirota<br /><i>ChemPhysChem</i>, January 17, 2012, DOI: 10.1002/cphc.201100731. <a href="http://dx.doi.org/10.1002/cphc.201100731">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100730">
<title>A Theoretical Investigation Into the 1,3-Dipolar Cycloaddition of Azidotrimethylsilane Onto Nanographene</title>
<link>http://dx.doi.org/10.1002/cphc.201100730</link>
<dc:creator>Yanli Yuan, Peiyu Chen, Xingye Ren, Hongming Wang</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100730.gif" width="189" height="154" alt="A Theoretical Investigation Into the 1,3-Dipolar Cycloaddition of Azidotrimethylsilane Onto Nanographene" title="A Theoretical Investigation Into the 1,3-Dipolar Cycloaddition of Azidotrimethylsilane Onto Nanographene" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Where to react?:</B> Calculations reveal that the 1,3-dipolar cycloaddition of azidotrimethylsilane onto nanographene (NG) occurs through a two-step reaction mechanism. The reactivity of NG is discussed in detail, revealing that it is the electron density at the functionalization site (see picture) which dominates the reactivity rather than the energetic effect. As a result, the edge area is calculated to be much more reactive than the centre.</P>
<p> [Article]<br />Yanli Yuan, Peiyu Chen, Xingye Ren, Hongming Wang<br /><i>ChemPhysChem</i>, February 3, 2012, DOI: 10.1002/cphc.201100730. <a href="http://dx.doi.org/10.1002/cphc.201100730">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100727">
<title>Instantaneous Normal Mode Analysis of a Series of Model Molten Salts</title>
<link>http://dx.doi.org/10.1002/cphc.201100727</link>
<dc:creator>Hualin Li, Mark N. Kobrak</dc:creator>
<dc:date>2012-01-12T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100727.gif" width="176" height="193" alt="Instantaneous Normal Mode Analysis of a Series of Model Molten Salts" title="Instantaneous Normal Mode Analysis of a Series of Model Molten Salts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Dynamics of a fused salt</B> were previously shown to be affected by the mass and charge distributions of its component ions. These studies are now extended by using instantaneous normal mode analysis to explore how changes in ionic structure affect translational and rotational dynamics in a series of model salts, in which the charge distribution is modified by the addition of dummy atoms.</P>
<p> [Article]<br />Hualin Li, Mark N. Kobrak<br /><i>ChemPhysChem</i>, January 12, 2012, DOI: 10.1002/cphc.201100727. <a href="http://dx.doi.org/10.1002/cphc.201100727">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100721">
<title>Solute-Induced Microstructural Transition from Weak Aggregates towards a Curved Film of Surface-Active Extractants</title>
<link>http://dx.doi.org/10.1002/cphc.201100721</link>
<dc:creator>Philippe Guilbaud, Thomas Zemb</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100721.gif" width="262" height="95" alt="Solute-Induced Microstructural Transition from Weak Aggregates towards a Curved Film of Surface-Active Extractants" title="Solute-Induced Microstructural Transition from Weak Aggregates towards a Curved Film of Surface-Active Extractants" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Reverse micelles?</B> The transition from weak aggregation to water-poor reverse micelles triggered by the presence of extracted ion pairs is modeled using molecular dynamics simulations (see picture). The presence of the ion induces a polar/apolar segregation and the formation of a curved film microstructure consistent with the classical inverse micelle.</P>
<p> [Communication]<br />Philippe Guilbaud, Thomas Zemb<br /><i>ChemPhysChem</i>, January 17, 2012, DOI: 10.1002/cphc.201100721. <a href="http://dx.doi.org/10.1002/cphc.201100721">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100720">
<title>Bayesian-Inference-Based Fluorescence Correlation Spectroscopy and Single-Molecule Burst Analysis Reveal the Influence of Dye Selection on DNA Hairpin Dynamics</title>
<link>http://dx.doi.org/10.1002/cphc.201100720</link>
<dc:creator>Wolfgang K&#xFC;gel, Adam Muschielok, Jens Michaelis</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100720.gif" width="194" height="175" alt="Bayesian-Inference-Based Fluorescence Correlation Spectroscopy and Single-Molecule Burst Analysis Reveal the Influence of Dye Selection on DNA Hairpin Dynamics" title="Bayesian-Inference-Based Fluorescence Correlation Spectroscopy and Single-Molecule Burst Analysis Reveal the Influence of Dye Selection on DNA Hairpin Dynamics" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Dynamic studies:</B> Fluorescence correlation spectroscopy (FCS) data are globally analyzed using the Bayesian inference. This approach is applied, in combination with the results from single-molecule burst analysis, to investigate the influence of various labels on DNA hairpin kinetics as a function of the salt concentration.</P>
<p> [Article]<br />Wolfgang K&#xFC;gel, Adam Muschielok, Jens Michaelis<br /><i>ChemPhysChem</i>, January 25, 2012, DOI: 10.1002/cphc.201100720. <a href="http://dx.doi.org/10.1002/cphc.201100720">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100717">
<title>Effect of Ionic Liquid on Diffusion in P123 Gel: Fluorescence Correlation Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cphc.201100717</link>
<dc:creator>Amit Kumar Mandal, Supratik Sen Mojumdar, Atanu Kumar Das, Kankan Bhattacharyya</dc:creator>
<dc:date>2012-01-05T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100717.gif" width="150" height="211" alt="Effect of Ionic Liquid on Diffusion in P123 Gel: Fluorescence Correlation Spectroscopy" title="Effect of Ionic Liquid on Diffusion in P123 Gel: Fluorescence Correlation Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Fluorescent subterfuge:</B> The effect of two room-temperature ionic liquids (RTILs) on the diffusion of three fluorescent dyes in the gel phase of a triblock copolymer (see picture) was studied by using fluorescence correlation spectroscopy. It is shown that the RTIL affects the structure of the gel by modifying the size of the micellar aggregates and by penetrating the core.</P>
<p> [Article]<br />Amit Kumar Mandal, Supratik Sen&#xA0;Mojumdar, Atanu Kumar Das, Kankan Bhattacharyya<br /><i>ChemPhysChem</i>, January 5, 2012, DOI: 10.1002/cphc.201100717. <a href="http://dx.doi.org/10.1002/cphc.201100717">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100714">
<title>Effect of Surface Hydrophobicity on the Formation and Stability of Oxygen Nanobubbles</title>
<link>http://dx.doi.org/10.1002/cphc.201100714</link>
<dc:creator>Gang Pan, Bo Yang</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100714.gif" width="191" height="158" alt="Effect of Surface Hydrophobicity on the Formation and Stability of Oxygen Nanobubbles" title="Effect of Surface Hydrophobicity on the Formation and Stability of Oxygen Nanobubbles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The formation mechanism of a nanoscale gas state</B> is studied on modified inorganic clay surfaces (see picture). The results suggest that a nanoscale gas state can be formed on both hydrophobic and hydrophilic particle surfaces, but that the stability of the surface nanoscale gas state can vary greatly depending on the hydrophobicity of the solid surfaces.</P>
<p> [Article]<br />Gang Pan, Bo Yang<br /><i>ChemPhysChem</i>, January 24, 2012, DOI: 10.1002/cphc.201100714. <a href="http://dx.doi.org/10.1002/cphc.201100714">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100711">
<title>Formation Principles and Ligand Dynamics of Nanoassemblies of CdSe Quantum Dots and Functionalised Dye Molecules</title>
<link>http://dx.doi.org/10.1002/cphc.201100711</link>
<dc:creator>Thomas Blaudeck, Eduard I. Zenkevich, Mohamed Abdel-Mottaleb, Klementyna Szwaykowska, Danny Kowerko, Frank Cichos, Christian von Borczyskowski</dc:creator>
<dc:date>2011-12-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100711.gif" width="215" height="202" alt="Formation Principles and Ligand Dynamics of Nanoassemblies of CdSe Quantum Dots and Functionalised Dye Molecules" title="Formation Principles and Ligand Dynamics of Nanoassemblies of CdSe Quantum Dots and Functionalised Dye Molecules" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Quenching the glow!</B> The size-dependent photoluminescence quenching of semiconductor quantum dots by functionalised dye molecules in solution is analysed with respect to F&ouml;rster resonance energy transfer (FRET) and non-FRET contributions (see picture). By this approach, assembly formation and ligand dynamics can be studied at extremely low concentrations of quantum dots and dye molecules.</P>
<p> [Article]<br />Thomas Blaudeck, Eduard I. Zenkevich, Mohamed Abdel-Mottaleb, Klementyna Szwaykowska, Danny Kowerko, Frank Cichos, Christian von&#xA0;Borczyskowski<br /><i>ChemPhysChem</i>, December 23, 2011, DOI: 10.1002/cphc.201100711. <a href="http://dx.doi.org/10.1002/cphc.201100711">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100708">
<title>&#x3B2;-Fragmentation of Tertiary Alkoxyl Radicals: G3(MP2)-RAD and Natural Bond Orbital Investigations</title>
<link>http://dx.doi.org/10.1002/cphc.201100708</link>
<dc:creator>Sylvain R. A. Marque, Didier Siri</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100708.gif" width="194" height="137" alt="&beta;-Fragmentation of Tertiary Alkoxyl Radicals: G3(MP2)-RAD and Natural Bond Orbital Investigations" title="&beta;-Fragmentation of Tertiary Alkoxyl Radicals: G3(MP2)-RAD and Natural Bond Orbital Investigations" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Amazing lone pair effect:</B> G3 (MP2)-RAD investigations combined with DFT calculations and NBO analysis shows that the &beta;-fragmentation of tertiary alkoxyl radicals R<sub>1</sub>R<sub>2</sub>YCO<SUP>.</SUP> (see picture) shows a banana bond at the TS (np,O&rarr;&beta;-LUMO) when Y bears a lone pair, in sharp contrast with the &sigma;*<sub>C-C</sub>&rarr;&beta;-LUMO interaction for the conventional homolytic C-Y bond cleavage.</P>
<p> [Communication]<br />Sylvain R. A. Marque, Didier Siri<br /><i>ChemPhysChem</i>, January 30, 2012, DOI: 10.1002/cphc.201100708. <a href="http://dx.doi.org/10.1002/cphc.201100708">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100686">
<title>Three-Dimensional Super-Resolution Imaging of the Midplane Protein FtsZ in Live &lt;I&gt;Caulobacter crescentus&lt;/I&gt; Cells Using Astigmatism</title>
<link>http://dx.doi.org/10.1002/cphc.201100686</link>
<dc:creator>Julie S. Biteen, Erin D. Goley, Lucy Shapiro, W. E. Moerner</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100686.gif" width="390" height="98" alt="Three-Dimensional Super-Resolution Imaging of the Midplane Protein FtsZ in Live Caulobacter crescentus Cells Using Astigmatism" title="Three-Dimensional Super-Resolution Imaging of the Midplane Protein FtsZ in Live Caulobacter crescentus Cells Using Astigmatism" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>3D is here to stay:</B> Three-dimensional super-resolution astigmatic optical imaging provides images of the FtsZ Z-ring in bacterial cells in various stages of the cell cycle. The picture shows, left to right: live stalked cell, live pre-divisional cell, fixed stalked cell, fixed pre-divisional cell. Scale bar: 200&nbsp;nm.</P>
<p> [Article]<br />Julie S. Biteen, Erin D. Goley, Lucy Shapiro, W. E. Moerner<br /><i>ChemPhysChem</i>, January 20, 2012, DOI: 10.1002/cphc.201100686. <a href="http://dx.doi.org/10.1002/cphc.201100686">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100681">
<title>Classical Reactive Molecular Dynamics Implementations: State of the Art</title>
<link>http://dx.doi.org/10.1002/cphc.201100681</link>
<dc:creator>Karim Farah, Florian M&#xFC;ller-Plathe, Michael C. B&#xF6;hm</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100681.gif" width="193" height="155" alt="Classical Reactive Molecular Dynamics Implementations: State of the Art" title="Classical Reactive Molecular Dynamics Implementations: State of the Art" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Reactive molecular dynamics</B> (RMD) simulations are used to investigate the time evolution, governed by empirical potential energy functions, of reactive systems (see graphic). RMD approaches are the only methods that allow the study of chemical reactions in large condensed-phase systems. Exciting microscopic insights into chemical reactions in condensed phases are discussed in this review.</P>
<p> [Minireview]<br />Karim Farah, Florian M&#xFC;ller-Plathe, Michael C. B&#xF6;hm<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100681. <a href="http://dx.doi.org/10.1002/cphc.201100681">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100680">
<title>Lipid Diffusion within Black Lipid Membranes Measured with Dual-Focus Fluorescence Correlation Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cphc.201100680</link>
<dc:creator>Kerstin Wei&#xDF;, J&#xF6;rg Enderlein</dc:creator>
<dc:date>2012-01-17T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100680.gif" width="193" height="156" alt="Lipid Diffusion within Black Lipid Membranes Measured with Dual-Focus Fluorescence Correlation Spectroscopy" title="Lipid Diffusion within Black Lipid Membranes Measured with Dual-Focus Fluorescence Correlation Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Watch them glow:</B> A description and theoretical evaluation of dual-focus fluorescence correlation spectroscopy as a tool for measuring diffusion within lipid bilayers is presented (see picture). The method is applied to a study of the dependence of lipid diffusion on lipid and buffer composition with regard to the ionic strength of the buffer, particularly concerning the influence of mono- and divalent ions.</P>
<p> [Article]<br />Kerstin Wei&#xDF;, J&#xF6;rg Enderlein<br /><i>ChemPhysChem</i>, January 17, 2012, DOI: 10.1002/cphc.201100680. <a href="http://dx.doi.org/10.1002/cphc.201100680">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100677">
<title>Breathing Particles for Controlling Thermo-Sequential On/Off Drug Delivery</title>
<link>http://dx.doi.org/10.1002/cphc.201100677</link>
<dc:creator>Anne-Claire Le Meur, Cyril Aymonier, Val&#xE9;rie H&#xE9;roguez</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100677.gif" width="199" height="135" alt="Breathing Particles for Controlling Thermo-Sequential On/Off Drug Delivery" title="Breathing Particles for Controlling Thermo-Sequential On/Off Drug Delivery" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Two for three:</B> An original combination of two thermoresponsive polymers organized inside a single submicron particle is developed to release drug following a three-step process, which consists of a first spontaneous release at room temperature followed by two possible thermosensitive effects.</P>
<p> [Communication]<br />Anne-Claire Le Meur, Cyril Aymonier, Val&#xE9;rie H&#xE9;roguez<br /><i>ChemPhysChem</i>, January 24, 2012, DOI: 10.1002/cphc.201100677. <a href="http://dx.doi.org/10.1002/cphc.201100677">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100674">
<title>Comprehensive Photophysical Behaviour of Ethynyl Fluorenes and Ethynyl Anthracenes Investigated by Fast and Ultrafast Time-Resolved Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cphc.201100674</link>
<dc:creator>Benedetta Carlotti, Rebecca Flamini, Anna Spalletti, Assunta Marrocchi, Fausto Elisei</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100674.gif" width="196" height="166" alt="Comprehensive Photophysical Behaviour of Ethynyl Fluorenes and Ethynyl Anthracenes Investigated by Fast and Ultrafast Time-Resolved Spectroscopy" title="Comprehensive Photophysical Behaviour of Ethynyl Fluorenes and Ethynyl Anthracenes Investigated by Fast and Ultrafast Time-Resolved Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>State secrets</B>: The photophysical behaviour of ethynyl fluorenes and ethynyl anthracenes is modulated by the molecular structure and solvent polarity. The rate constants of the decay channels are modified by the relative energies of the optical singlet state (<SUP>1</SUP>LE*), the charge-transfer singlet state (<SUP>1</SUP>CT*), and an upper triplet of n,&pi;* nature (see picture).</P>
<p> [Article]<br />Benedetta Carlotti, Rebecca Flamini, Anna Spalletti, Assunta Marrocchi, Fausto Elisei<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100674. <a href="http://dx.doi.org/10.1002/cphc.201100674">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100671">
<title>Optical Modulation and Selective Recovery of Cy5 Fluorescence</title>
<link>http://dx.doi.org/10.1002/cphc.201100671</link>
<dc:creator>Chaoyang Fan, Jung-Cheng Hsiang, Robert M. Dickson</dc:creator>
<dc:date>2011-11-15T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100671.gif" width="206" height="151" alt="Optical Modulation and Selective Recovery of Cy5 Fluorescence" title="Optical Modulation and Selective Recovery of Cy5 Fluorescence" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Photoinduced isomerization</B> of Cy5 from <I>trans</I> to <I>cis</I> can be quickly reversed with long-wavelength secondary illumination. Modulating this co-illumination directly encodes the modulation waveform on the higher energy Cy5 fluorescence, enabling its selective recovery even in the presence of overwhelming background. This low-energy, reversible, long-lived dark state makes Cy5 an excellent dye for synchronously amplified fluorescence image recovery (SAFIRe).</P>
<p> [Article]<br />Chaoyang Fan, Jung-Cheng Hsiang, Robert M. Dickson<br /><i>ChemPhysChem</i>, November 15, 2011, DOI: 10.1002/cphc.201100671. <a href="http://dx.doi.org/10.1002/cphc.201100671">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100670">
<title>Tip-Enhanced Near-Field Optical Microscopy of Quasi-1&#xA0;D Nanostructures</title>
<link>http://dx.doi.org/10.1002/cphc.201100670</link>
<dc:creator>Miriam B&#xF6;hmler, Achim Hartschuh</dc:creator>
<dc:date>2011-12-08T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100670.gif" width="188" height="187" alt="Tip-Enhanced Near-Field Optical Microscopy of Quasi-1&nbsp;D Nanostructures" title="Tip-Enhanced Near-Field Optical Microscopy of Quasi-1&nbsp;D Nanostructures" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>High-resolution imaging</B> and spectroscopy of single CdSe nanowires and carbon nanotubes using tip-enhanced near-field optical microscopy increases the optical excitation and emission rates within a nanoscale sample volume. The resulting signal enhancement for Raman scattering and photoluminescence as well as the tip&ndash;sample-distance dependence are investigated.</P>
<p> [Communication]<br />Miriam B&#xF6;hmler, Achim Hartschuh<br /><i>ChemPhysChem</i>, December 8, 2011, DOI: 10.1002/cphc.201100670. <a href="http://dx.doi.org/10.1002/cphc.201100670">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100669">
<title>Long-Range Transport of Giant Vesicles along Microtubule Networks</title>
<link>http://dx.doi.org/10.1002/cphc.201100669</link>
<dc:creator>Christoph Herold, C&#xE9;cile Leduc, Robert Stock, Stefan Diez, Petra Schwille</dc:creator>
<dc:date>2011-12-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100669.gif" width="203" height="178" alt="Long-Range Transport of Giant Vesicles along Microtubule Networks" title="Long-Range Transport of Giant Vesicles along Microtubule Networks" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Moving giant vesicles:</B> In a biomimetic assay, giant unilamellar vesicles with membrane-anchored kinesin-1 motor proteins are transported along a two-dimensional microtubule network (see picture). In this assay, cooperatively acting motor proteins enable long traveling distances up to the millimeter range.</P>
<p> [Article]<br />Christoph Herold, C&#xE9;cile Leduc, Robert Stock, Stefan Diez, Petra Schwille<br /><i>ChemPhysChem</i>, December 23, 2011, DOI: 10.1002/cphc.201100669. <a href="http://dx.doi.org/10.1002/cphc.201100669">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100655">
<title>What Determines the Rate of Excited-State Intramolecular Electron-Transfer Reaction of 4-(&lt;I&gt;N&lt;/I&gt;,&lt;I&gt;N&lt;/I&gt;&#x27;-dimethylamino)benzonitrile in Room Temperature Ionic Liquids? A Study in [bmim][PF&lt;sub&gt;6&lt;/sub&gt;]</title>
<link>http://dx.doi.org/10.1002/cphc.201100655</link>
<dc:creator>Kotni Santhosh, Anunay Samanta</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100655.gif" width="193" height="117" alt="What Determines the Rate of Excited-State Intramolecular Electron-Transfer Reaction of 4-(N,N&#x27;-dimethylamino)benzonitrile in Room Temperature Ionic Liquids? A Study in [bmim][PF6]" title="What Determines the Rate of Excited-State Intramolecular Electron-Transfer Reaction of 4-(N,N&#x27;-dimethylamino)benzonitrile in Room Temperature Ionic Liquids? A Study in [bmim][PF6]" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Electron transfer faster than solvation:</B> The rate of excited-state intramolecular electron-transfer reaction of DMABN in [bmim][PF<sub>6</sub>] is not determined by the dynamics of solvation.</P>
<p> [Article]<br />Kotni Santhosh, Anunay Samanta<br /><i>ChemPhysChem</i>, January 13, 2012, DOI: 10.1002/cphc.201100655. <a href="http://dx.doi.org/10.1002/cphc.201100655">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100582">
<title>Influence of the Number of Anchoring Groups on the Electronic and Mechanical Properties of Benzene-, Anthracene- and Pentacene-Based Molecular Devices</title>
<link>http://dx.doi.org/10.1002/cphc.201100582</link>
<dc:creator>Ana Mart&#xED;n-Lasanta, Delia Miguel, Trinidad Garc&#xED;a, Juan A. L&#xF3;pez-Villanueva, Salvador Rodr&#xED;guez-Bol&#xED;var, Francisco M. G&#xF3;mez-Campos, Elena Bu&#xF1;uel, Diego J. C&#xE1;rdenas, Luis Alvarez de Cienfuegos, Juan M. Cuerva</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100582.gif" width="192" height="138" alt="Influence of the Number of Anchoring Groups on the Electronic and Mechanical Properties of Benzene-, Anthracene- and Pentacene-Based Molecular Devices" title="Influence of the Number of Anchoring Groups on the Electronic and Mechanical Properties of Benzene-, Anthracene- and Pentacene-Based Molecular Devices" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Better connections</B>: Calculations show that increasing the number of anchoring groups in model acenes leads to higher conductivity as well as mechanical and current stability (see picture; C gray, H white, S yellow) in molecule&ndash;Au electrode contacts. The results have implications for stochastic on/off switching (blinking), which is a major problem of single-molecule electronic devices.</P>
<p> [Article]<br />Ana Mart&#xED;n-Lasanta, Delia Miguel, Trinidad Garc&#xED;a, Juan A. L&#xF3;pez-Villanueva, Salvador Rodr&#xED;guez-Bol&#xED;var, Francisco M. G&#xF3;mez-Campos, Elena Bu&#xF1;uel, Diego J. C&#xE1;rdenas, Luis Alvarez de&#xA0;Cienfuegos, Juan M. Cuerva<br /><i>ChemPhysChem</i>, January 24, 2012, DOI: 10.1002/cphc.201100582. <a href="http://dx.doi.org/10.1002/cphc.201100582">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100568">
<title>Isomerisation of CF&lt;sub&gt;2&lt;/sub&gt;ClCH&lt;sub&gt;2&lt;/sub&gt;Cl and CFCl&lt;sub&gt;2&lt;/sub&gt;CH&lt;sub&gt;2&lt;/sub&gt;F by Interchange of Cl and F Atoms with Analysis of the Unimolecular Reactions of Both Molecules</title>
<link>http://dx.doi.org/10.1002/cphc.201100568</link>
<dc:creator>Sarah A. Solaka, Sara E. Boshamer, Caroline L. Parworth, George L. Heard, D. W. Setser, Bert E. Holmes</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100568.gif" width="352" height="105" alt="Isomerisation of CF2ClCH2Cl and CFCl2CH2F by Interchange of Cl and F Atoms with Analysis of the Unimolecular Reactions of Both Molecules" title="Isomerisation of CF2ClCH2Cl and CFCl2CH2F by Interchange of Cl and F Atoms with Analysis of the Unimolecular Reactions of Both Molecules" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Shall we switch partners?</B> The F&ndash;Cl interchange reaction is an important unimolecular pathway for some hydrochlorofluorocarbons as illustrated by an experimental and computational investigation for the CH<sub>2</sub>ClCF<sub>2</sub>Cl&ndash;CH<sub>2</sub>FCFCl<sub>2</sub> pair (see picture).</P>
<p> [Article]<br />Sarah A. Solaka, Sara E. Boshamer, Caroline L. Parworth, George L. Heard, D. W. Setser, Bert E. Holmes<br /><i>ChemPhysChem</i>, January 27, 2012, DOI: 10.1002/cphc.201100568. <a href="http://dx.doi.org/10.1002/cphc.201100568">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100528">
<title>Electron Correlation in Real Time</title>
<link>http://dx.doi.org/10.1002/cphc.201100528</link>
<dc:creator>Giuseppe Sansone, Thomas Pfeifer, Konstantinos Simeonidis, Alexander I. Kuleff</dc:creator>
<dc:date>2011-12-08T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100528.gif" width="196" height="196" alt="Electron Correlation in Real Time" title="Electron Correlation in Real Time" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Ultrafast electron dynamics</B>: Electron correlation plays a key role in the relaxation mechanisms that characterize excited states of neutral or ionized atoms and molecules obtained by absorption of extreme ultraviolet (XUV) or X-ray radiation. The possibilities offered by femtosecond and attosecond XUV pulses (see picture) to investigate how electron correlations can influence and drive multielectron dynamics in atoms and molecules are presented.</P>
<p> [Minireview]<br />Giuseppe Sansone, Thomas Pfeifer, Konstantinos Simeonidis, Alexander I. Kuleff<br /><i>ChemPhysChem</i>, December 8, 2011, DOI: 10.1002/cphc.201100528. <a href="http://dx.doi.org/10.1002/cphc.201100528">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100421">
<title>Effect of an Ionic liquid on the Unfolding of Human Serum Albumin: A Fluorescence Correlation Spectroscopy Study</title>
<link>http://dx.doi.org/10.1002/cphc.201100421</link>
<dc:creator>Dibyendu Kumar Das, Atanu Kumar Das, Amit Kumar Mandal, Tridib Mondal, Kankan Bhattacharyya</dc:creator>
<dc:date>2011-09-16T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201100421.gif" width="419" height="163" alt="Effect of an Ionic liquid on the Unfolding of Human Serum Albumin: A Fluorescence Correlation Spectroscopy Study" title="Effect of an Ionic liquid on the Unfolding of Human Serum Albumin: A Fluorescence Correlation Spectroscopy Study" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Fluorescence fluctuations:</B> The effect of a room temperature ionic liquid (RTIL) on the unfolding of human serum albumin (HSA) is studied by fluorescence correlation spectroscopy (see picture). The use of a denaturant (GdnHCl) in the presence of the RTIL causes significant changes in the structure and the time constants of the conformational fluctuations.</P>
<p> [Article]<br />Dibyendu Kumar&#xA0;Das, Atanu Kumar&#xA0;Das, Amit Kumar&#xA0;Mandal, Tridib Mondal, Kankan Bhattacharyya<br /><i>ChemPhysChem</i>, September 16, 2011, DOI: 10.1002/cphc.201100421. <a href="http://dx.doi.org/10.1002/cphc.201100421">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200047">
<title>HIV-1 Integrase: Mechanism and Inhibitor Design Edited by Nouri Neamati.</title>
<link>http://dx.doi.org/10.1002/cmdc.201200047</link>
<dc:creator>Maurizio Botta</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201200047.gif" width="106" height="144" alt="HIV-1 Integrase: Mechanism and Inhibitor Design Edited by Nouri Neamati." title="HIV-1 Integrase: Mechanism and Inhibitor Design Edited by Nouri Neamati." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P>John Wiley &amp; Sons, Hoboken 2011. 384&nbsp;pp., hardcover $&nbsp;119.99.&mdash;ISBN&nbsp;978-0-47018-474-5</P>
<p> [Book Review]<br />Maurizio Botta<br /><i>ChemMedChem</i>, February 6, 2012, DOI: 10.1002/cmdc.201200047. <a href="http://dx.doi.org/10.1002/cmdc.201200047">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200027">
<title>Drug Metabolism and Pharmacokinetics Quick Guide By Siamak&#xA0;C. Khojasteh, Harvey Wong and Cornelis&#xA0;E.&#xA0;C.&#xA0;A. Hop.</title>
<link>http://dx.doi.org/10.1002/cmdc.201200027</link>
<dc:creator>Andy Davis</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201200027.gif" width="106" height="172" alt="Drug Metabolism and Pharmacokinetics Quick Guide By Siamak&nbsp;C. Khojasteh, Harvey Wong and Cornelis&nbsp;E.&nbsp;C.&nbsp;A. Hop." title="Drug Metabolism and Pharmacokinetics Quick Guide By Siamak&nbsp;C. Khojasteh, Harvey Wong and Cornelis&nbsp;E.&nbsp;C.&nbsp;A. Hop." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P>Springer, Heidelberg 2011. xii+214&nbsp;pp., softcover &euro;42.75.&mdash;ISBN&nbsp;978-1-4419-5628-6</P>
<p> [Book Review]<br />Andy Davis<br /><i>ChemMedChem</i>, January 27, 2012, DOI: 10.1002/cmdc.201200027. <a href="http://dx.doi.org/10.1002/cmdc.201200027">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200025">
<title>Discovery of [(2&lt;I&gt;R&lt;/I&gt;,5&lt;I&gt;R&lt;/I&gt;)-5-{[(5-Fluoropyridin-2-yl)oxy]methyl}-2-methylpiperidin-1-yl][5-methyl-2-(pyrimidin-2-yl)phenyl]methanone (MK-6096): A Dual Orexin Receptor Antagonist with Potent Sleep-Promoting Properties</title>
<link>http://dx.doi.org/10.1002/cmdc.201200025</link>
<dc:creator>Paul J. Coleman, John D. Schreier, Christopher D. Cox, Michael J. Breslin, David B. Whitman, Michael J. Bogusky, Georgia B. McGaughey, Rodney A. Bednar, Wei Lemaire, Scott M. Doran, Steven V. Fox, Susan L. Garson, Anthony L. Gotter, C. Meacham Harrell, Duane R. Reiss, Tamara D. Cabalu, Donghui Cui, Thomayant Prueksaritanont, Joanne Stevens, Pamela L. Tannenbaum, Richard G. Ball, Joyce Stellabott, Steven D. Young, George D. Hartman, Christopher J. Winrow, John J. Renger</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201200025.gif" width="192" height="161" alt="Discovery of [(2R,5R)-5-{[(5-Fluoropyridin-2-yl)oxy]methyl}-2-methylpiperidin-1-yl][5-methyl-2-(pyrimidin-2-yl)phenyl]methanone (MK-6096): A Dual Orexin Receptor Antagonist with Potent Sleep-Promoting Properties" title="Discovery of [(2R,5R)-5-{[(5-Fluoropyridin-2-yl)oxy]methyl}-2-methylpiperidin-1-yl][5-methyl-2-(pyrimidin-2-yl)phenyl]methanone (MK-6096): A Dual Orexin Receptor Antagonist with Potent Sleep-Promoting Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Exploring DORAs:</B> Orexin receptor antagonism has been identified as a new mechanism for treating insomnia with clinical proof of concept. The design of MK-6096 was partly driven by understanding the conformational properties anticipated to be favorable for high orexin receptor activity. MK-6096 represents a novel therapy for treating insomnia and other disorders related to sleep/wake dysregulation.</P>
<p> [Full Paper]<br />Paul J. Coleman, John D. Schreier, Christopher D. Cox, Michael J. Breslin, David B. Whitman, Michael J. Bogusky, Georgia B. McGaughey, Rodney A. Bednar, Wei Lemaire, Scott M. Doran, Steven V. Fox, Susan L. Garson, Anthony L. Gotter, C. Meacham Harrell, Duane R. Reiss, Tamara D. Cabalu, Donghui Cui, Thomayant Prueksaritanont, Joanne Stevens, Pamela L. Tannenbaum, Richard G. Ball, Joyce Stellabott, Steven D. Young, George D. Hartman, Christopher J. Winrow, John J. Renger<br /><i>ChemMedChem</i>, February 3, 2012, DOI: 10.1002/cmdc.201200025. <a href="http://dx.doi.org/10.1002/cmdc.201200025">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200019">
<title>Chiral Drugs: Chemistry and Biological Action Edited by Guo-Qiang Lin, Qi-Dong You and Jie-Fei Cheng.</title>
<link>http://dx.doi.org/10.1002/cmdc.201200019</link>
<dc:creator>Thorleif Anthonsen</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201200019.gif" width="106" height="159" alt="Chiral Drugs: Chemistry and Biological Action Edited by Guo-Qiang Lin, Qi-Dong You and Jie-Fei Cheng." title="Chiral Drugs: Chemistry and Biological Action Edited by Guo-Qiang Lin, Qi-Dong You and Jie-Fei Cheng." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P>John Wiley &amp; Sons, Hoboken 2011. 472&nbsp;pp., hardcover $&nbsp;149.95.&mdash;ISBN&nbsp;978-0-470-58720-1</P>
<p> [Book Review]<br />Thorleif Anthonsen<br /><i>ChemMedChem</i>, February 1, 2012, DOI: 10.1002/cmdc.201200019. <a href="http://dx.doi.org/10.1002/cmdc.201200019">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200014">
<title>Sulfonimidamides as Sulfonamides Bioisosteres: Rational Evaluation through Synthetic, in Vitro, and in Vivo Studies with &#x3B3;-Secretase Inhibitors</title>
<link>http://dx.doi.org/10.1002/cmdc.201200014</link>
<dc:creator>Fernando Sehgelmeble, Juliette Janson, Colin Ray, Susanne Rosqvist, Susanne Gustavsson, Linda I. Nilsson, Alexander Minidis, J&#xF6;rg Holenz, Didier Rotticci, Johan Lundkvist, Per I. Arvidsson</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201200014.gif" width="151" height="76" alt="Sulfonimidamides as Sulfonamides Bioisosteres: Rational Evaluation through Synthetic, in Vitro, and in Vivo Studies with &gamma;-Secretase Inhibitors" title="Sulfonimidamides as Sulfonamides Bioisosteres: Rational Evaluation through Synthetic, in Vitro, and in Vivo Studies with &gamma;-Secretase Inhibitors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The proof of the pudding:</B> A proof-of-concept study using &gamma;-secretase inhibitors as a model has shown that sulfonimidamides act as bioisosteres for sulfonamides. Detailed in&nbsp;vitro and in&nbsp;vivo profiling reveal that the sulfonimidamide motif imparts desirable properties such as decreased lipophilicity and plasma protein binding, accompanied by increased solubility. Our data support a wider use of this unique functional group in the design of new pharmacologically active agents.</P>
<p> [Communication]<br />Fernando Sehgelmeble, Juliette Janson, Colin Ray, Susanne Rosqvist, Susanne Gustavsson, Linda I. Nilsson, Alexander Minidis, J&#xF6;rg Holenz, Didier Rotticci, Johan Lundkvist, Per I. Arvidsson<br /><i>ChemMedChem</i>, February 3, 2012, DOI: 10.1002/cmdc.201200014. <a href="http://dx.doi.org/10.1002/cmdc.201200014">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200002">
<title>Synthesis and Evaluation of 1-Amino-6-halo-&#x3B2;-carbolines as Antimalarial and Antiprion Agents</title>
<link>http://dx.doi.org/10.1002/cmdc.201200002</link>
<dc:creator>Mark J. Thompson, Jennifer C. Louth, Susan M. Little, Matthew P. Jackson, Yohan Boursereau, Beining Chen, Iain Coldham</dc:creator>
<dc:date>2012-01-24T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201200002.gif" width="452" height="90" alt="Synthesis and Evaluation of 1-Amino-6-halo-&beta;-carbolines as Antimalarial and Antiprion Agents" title="Synthesis and Evaluation of 1-Amino-6-halo-&beta;-carbolines as Antimalarial and Antiprion Agents" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Parasites and problem proteins!</B> Malaria and Creutzfeldt&ndash;Jakob disease (CJD), two very different conditions, may have a common therapeutic agent class in the 6-halo-&beta;-carbolines. Synthesis of a compound library and screening against two strains of <I>Plasmodium falciparum</I> and in an in vitro model of prion disease revealed these agents as potential candidates for further development as both antiprion and antimalarial drugs.</P>
<p> [Full Paper]<br />Mark J. Thompson, Jennifer C. Louth, Susan M. Little, Matthew P. Jackson, Yohan Boursereau, Beining Chen, Iain Coldham<br /><i>ChemMedChem</i>, January 24, 2012, DOI: 10.1002/cmdc.201200002. <a href="http://dx.doi.org/10.1002/cmdc.201200002">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100603">
<title>A 2,6-Disubstituted 4-Anilinoquinazoline Derivative Facilitates Cardiomyogenesis of Embryonic Stem Cells</title>
<link>http://dx.doi.org/10.1002/cmdc.201100603</link>
<dc:creator>Guofang Shen, Ying Hu, Jianwei Wu, Ke Jin, Danyan Zhu, Yandong Zhang, Yongping Yu, Yijia Lou</dc:creator>
<dc:date>2012-02-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100603.gif" width="165" height="150" alt="A 2,6-Disubstituted 4-Anilinoquinazoline Derivative Facilitates Cardiomyogenesis of Embryonic Stem Cells" title="A 2,6-Disubstituted 4-Anilinoquinazoline Derivative Facilitates Cardiomyogenesis of Embryonic Stem Cells" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Cardiomyogenic agents:</B> We explored the effects of EGFR inhibitors on cardiomyogenesis of embryonic stem (ES) cells and screened a quinazoline compound library for cardiomyogenic stimulators. Compound <B>62</B>, a 2,6-disubstituted 4-anilinoquinazoline derivative, was found to be a potent cardiomyogenic inducer of ES cells with a mechanism distinct from that of iressa.</P>
<p> [Full Paper]<br />Guofang Shen, Ying Hu, Jianwei Wu, Ke Jin, Danyan Zhu, Yandong Zhang, Yongping Yu, Yijia Lou<br /><i>ChemMedChem</i>, February 2, 2012, DOI: 10.1002/cmdc.201100603. <a href="http://dx.doi.org/10.1002/cmdc.201100603">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100593">
<title>Cytotoxic Salan&#x2013;Titanium(IV) Complexes: High Activity Toward a Range of Sensitive and Drug-Resistant Cell Lines, and Mechanistic Insights</title>
<link>http://dx.doi.org/10.1002/cmdc.201100593</link>
<dc:creator>Cesar M. Manna, Ori Braitbard, Esther Weiss, Jacob Hochman, Edit Y. Tshuva</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100593.gif" width="209" height="147" alt="Cytotoxic Salan&ndash;Titanium(IV) Complexes: High Activity Toward a Range of Sensitive and Drug-Resistant Cell Lines, and Mechanistic Insights" title="Cytotoxic Salan&ndash;Titanium(IV) Complexes: High Activity Toward a Range of Sensitive and Drug-Resistant Cell Lines, and Mechanistic Insights" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Titanic strength:</B> Salan&ndash;Ti<SUP>IV</SUP> complexes demonstrate high cytotoxicity toward a wide range of cancer cell lines, including cisplatin- and multi-drug-resistant lines, with marked selectivity for tumor tissue. These complexes are also highly robust; they retain activity after long-term pre-incubation in cell culture medium, and appear to induce p53-mediated cell-cycle arrest.</P>
<p> [Full Paper]<br />Cesar M. Manna, Ori Braitbard, Esther Weiss, Jacob Hochman, Edit Y. Tshuva<br /><i>ChemMedChem</i>, January 20, 2012, DOI: 10.1002/cmdc.201100593. <a href="http://dx.doi.org/10.1002/cmdc.201100593">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100589">
<title>Dual Dehydrosqualene/Squalene Synthase Inhibitors: Leads for Innate Immune System-Based Therapeutics</title>
<link>http://dx.doi.org/10.1002/cmdc.201100589</link>
<dc:creator>Fu-Yang Lin, Yonghui Zhang, Mary Hensler, Yi-Liang Liu, Ohn A. Chow, Wei Zhu, Ke Wang, Ran Pang, Wdee Thienphrapa, Victor Nizet, Eric Oldfield</dc:creator>
<dc:date>2012-01-30T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100589.gif" width="215" height="190" alt="Dual Dehydrosqualene/Squalene Synthase Inhibitors: Leads for Innate Immune System-Based Therapeutics" title="Dual Dehydrosqualene/Squalene Synthase Inhibitors: Leads for Innate Immune System-Based Therapeutics" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Double whammy!</B> Small molecules that inhibit <I>Staphylococcus aureus</I> dehydrosqualene synthase (CrtM) or host squalene synthase (SQS) are of interest as novel, innate immunity-based therapeutics, blocking virulence or stimulating antibacterial neutrophil extracellular trap (NET) formation. The discovery of leads that do both represents a new route to treating staph infections.</P>
<p> [Communication]<br />Fu-Yang Lin, Yonghui Zhang, Mary Hensler, Yi-Liang Liu, Ohn A. Chow, Wei Zhu, Ke Wang, Ran Pang, Wdee Thienphrapa, Victor Nizet, Eric Oldfield<br /><i>ChemMedChem</i>, January 30, 2012, DOI: 10.1002/cmdc.201100589. <a href="http://dx.doi.org/10.1002/cmdc.201100589">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100588">
<title>Preliminary Study of the Anticancer Applications of Mesoporous Materials Functionalized with the Natural Product Betulinic Acid</title>
<link>http://dx.doi.org/10.1002/cmdc.201100588</link>
<dc:creator>Sergio S&#xE1;nchez-Mu&#xF1;oz, Santiago G&#xF3;mez-Ruiz, Dami&#xE1;n P&#xE9;rez-Quintanilla, Sonia Morante-Zarcero, Isabel Sierra, Sanjiv Prashar, Reinhard Paschke, Goran N. Kalu&#x111;erovi&#x107;</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100588.gif" width="188" height="216" alt="Preliminary Study of the Anticancer Applications of Mesoporous Materials Functionalized with the Natural Product Betulinic Acid" title="Preliminary Study of the Anticancer Applications of Mesoporous Materials Functionalized with the Natural Product Betulinic Acid" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The perfect combination:</B> The combination of functionalized mesoporous materials such as MCM-41 with betulinic acid, a potent anticancer drug, led to novel drug delivery systems which may be useful in the future as adjuvant agents to avoid the recurrence of bone tumors on local implantations.</P>
<p> [Full Paper]<br />Sergio S&#xE1;nchez-Mu&#xF1;oz, Santiago G&#xF3;mez-Ruiz, Dami&#xE1;n P&#xE9;rez-Quintanilla, Sonia Morante-Zarcero, Isabel Sierra, Sanjiv Prashar, Reinhard Paschke, Goran N. Kalu&#x111;erovi&#x107;<br /><i>ChemMedChem</i>, January 25, 2012, DOI: 10.1002/cmdc.201100588. <a href="http://dx.doi.org/10.1002/cmdc.201100588">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100587">
<title>Pyrazinamide: A Frontline Drug Used for Tuberculosis. Molecular Mechanism of Action Resolved after 50 Years?</title>
<link>http://dx.doi.org/10.1002/cmdc.201100587</link>
<dc:creator>Alvin S. Kalinda, Courtney C. Aldrich</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100587.gif" width="167" height="109" alt="Pyrazinamide: A Frontline Drug Used for Tuberculosis. Molecular Mechanism of Action Resolved after 50 Years?" title="Pyrazinamide: A Frontline Drug Used for Tuberculosis. Molecular Mechanism of Action Resolved after 50 Years?" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Target acquired!</B> After 50 years of use, has the molecular mode of action finally been identified for pyrazinamide? Recently, inhibition of trans-translation in <I>Mycobacterium tuberculosis</I> was suggested as a novel mode of action for this important TB drug. The results of the study by Zhang et al., reported in <I>Science</I>, are highlighted here.</P>
<p> [Highlight]<br />Alvin S. Kalinda, Courtney C. Aldrich<br /><i>ChemMedChem</i>, January 13, 2012, DOI: 10.1002/cmdc.201100587. <a href="http://dx.doi.org/10.1002/cmdc.201100587">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100584">
<title>A Two-Step Strategy for Structure&#x2013;Activity Relationship Studies of N&lt;I&gt;-&lt;/I&gt;Methylated A&#x3B2;42 C-Terminal Fragments as A&#x3B2;42 Toxicity Inhibitors</title>
<link>http://dx.doi.org/10.1002/cmdc.201100584</link>
<dc:creator>Huiyuan Li, Reeve Zemel, Dahabada H. J. Lopes, Bernhard H. Monien, Gal Bitan</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100584.gif" width="446" height="81" alt="A Two-Step Strategy for Structure&ndash;Activity Relationship Studies of N-Methylated A&beta;42 C-Terminal Fragments as A&beta;42 Toxicity Inhibitors" title="A Two-Step Strategy for Structure&ndash;Activity Relationship Studies of N-Methylated A&beta;42 C-Terminal Fragments as A&beta;42 Toxicity Inhibitors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Step by Step:</B> A two-step <I>N-</I>methyl amino acid substitution method was used for a structure&ndash;activity relationship (SAR) study of A&beta;(31-42). This strategy provides a basis for the design of new peptidomimetic inhibitors with improved activity, physicochemical properties and metabolic stability.</P>
<p> [Full Paper]<br />Huiyuan Li, Reeve Zemel, Dahabada H. J. Lopes, Bernhard H. Monien, Gal Bitan<br /><i>ChemMedChem</i>, February 3, 2012, DOI: 10.1002/cmdc.201100584. <a href="http://dx.doi.org/10.1002/cmdc.201100584">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100579">
<title>In Silico Identification of an Interferon Inhibitor</title>
<link>http://dx.doi.org/10.1002/cmdc.201100579</link>
<dc:creator>Markus Kaiser, Christian Ottmann</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100579.gif" width="193" height="193" alt="In Silico Identification of an Interferon Inhibitor" title="In Silico Identification of an Interferon Inhibitor" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Inhibition of IFN&alpha;&ndash;IFNR:</B> Interferon (IFN) is an important signaling molecule and antiviral therapeutic agent. However, in certain diseases like type&nbsp;I diabetes, IFN action can be harmful. Schneider and co-workers recently reported the identification of the first IFN&alpha;&ndash;IFNR inhibitor via in silico screening, which binds to IFN&alpha; and impedes interferon signaling in cells.</P>
<p> [Highlight]<br />Markus Kaiser, Christian Ottmann<br /><i>ChemMedChem</i>, January 20, 2012, DOI: 10.1002/cmdc.201100579. <a href="http://dx.doi.org/10.1002/cmdc.201100579">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100578">
<title>Structure&#x2013;Activity Relationships for Negative Allosteric mGluR5 Modulators</title>
<link>http://dx.doi.org/10.1002/cmdc.201100578</link>
<dc:creator>Birgitte H. Kaae, Kasper Harps&#xF8;e, Trine Kvist, Jesper M. Mathiesen, Christina M&#xF8;lck, David Gloriam, Hermogenes N. Jimenez, Michelle A. Uberti, S&#xF8;ren M. Nielsen, Birgitte Nielsen, Hans Br&#xE4;uner-Osborne, Per Sauerberg, Rasmus P. Clausen, Ulf Madsen</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100578.gif" width="215" height="159" alt="Structure&ndash;Activity Relationships for Negative Allosteric mGluR5 Modulators" title="Structure&ndash;Activity Relationships for Negative Allosteric mGluR5 Modulators" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Exploring a dimeric approach:</B> The design and synthesis of 2-methyl-6-(phenylethynyl)pyridine (MPEP) analogues led to a potent and selective negative modulator of mGluR5. Compounds were characterized at mGluRs and iGluRs; binding and selectivity modes were investigated by homology modeling and docking studies.</P>
<p> [Full Paper]<br />Birgitte H. Kaae, Kasper Harps&#xF8;e, Trine Kvist, Jesper M. Mathiesen, Christina M&#xF8;lck, David Gloriam, Hermogenes N. Jimenez, Michelle A. Uberti, S&#xF8;ren M. Nielsen, Birgitte Nielsen, Hans Br&#xE4;uner-Osborne, Per Sauerberg, Rasmus P. Clausen, Ulf Madsen<br /><i>ChemMedChem</i>, January 20, 2012, DOI: 10.1002/cmdc.201100578. <a href="http://dx.doi.org/10.1002/cmdc.201100578">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100568">
<title>Chromenopyrazoles: Non-psychoactive and Selective CB&lt;sub&gt;1&lt;/sub&gt; Cannabinoid Agonists with Peripheral Antinociceptive Properties</title>
<link>http://dx.doi.org/10.1002/cmdc.201100568</link>
<dc:creator>Jose Cumella, Laura Hern&#xE1;ndez-Folgado, Rocio Gir&#xF3;n, Eva S&#xE1;nchez, Paula Morales, Dow P. Hurst, Maria G&#xF3;mez-Ca&#xF1;as, Maria G&#xF3;mez-Ruiz, Diana C. G. A. Pinto, Pilar Goya, Patricia H. Reggio, Mar&#xED;a Isabel Martin, Javier Fern&#xE1;ndez-Ruiz, Artur M. S. Silva, Nadine Jagerovic</dc:creator>
<dc:date>2012-02-02T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100568.gif" width="208" height="174" alt="Chromenopyrazoles: Non-psychoactive and Selective CB1 Cannabinoid Agonists with Peripheral Antinociceptive Properties" title="Chromenopyrazoles: Non-psychoactive and Selective CB1 Cannabinoid Agonists with Peripheral Antinociceptive Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Peripheral cannabinoid:</B> Chromenopyrazoles were identified as cannabinoid receptor ligands, and some compounds in the series were found to be selective agonists of the CB<sub>1</sub> receptor. Results of molecular modeling studies support this finding. Behavioral tests and peripheral pain assays carried out with the most effective agonist show peripheral analgesia without CNS-mediated effects.</P>
<p> [Full Paper]<br />Jose Cumella, Laura Hern&#xE1;ndez-Folgado, Rocio Gir&#xF3;n, Eva S&#xE1;nchez, Paula Morales, Dow P. Hurst, Maria G&#xF3;mez-Ca&#xF1;as, Maria G&#xF3;mez-Ruiz, Diana C. G. A. Pinto, Pilar Goya, Patricia H. Reggio, Mar&#xED;a Isabel Martin, Javier Fern&#xE1;ndez-Ruiz, Artur M. S. Silva, Nadine Jagerovic<br /><i>ChemMedChem</i>, February 2, 2012, DOI: 10.1002/cmdc.201100568. <a href="http://dx.doi.org/10.1002/cmdc.201100568">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100560">
<title>Fluorogenic Peptide-Based Substrates for Monitoring Thrombin Activity</title>
<link>http://dx.doi.org/10.1002/cmdc.201100560</link>
<dc:creator>Sander S. van Berkel, Bas van der Lee, Floris L. van Delft, Rob Wagenvoord, H. Coenraad Hemker, Floris P. J. T. Rutjes</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100560.gif" width="208" height="193" alt="Fluorogenic Peptide-Based Substrates for Monitoring Thrombin Activity" title="Fluorogenic Peptide-Based Substrates for Monitoring Thrombin Activity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>An eye on thrombin:</B> A series of fluorogenic peptidyl-AMC substrates were synthesized and subjected to a biological evaluation to determine their suitability in the thrombin generation test (TGT). Evaluation of the acquired thrombin generation curves showed that several of these substrates have excellent potential for replacement of the substrate in current use.</P>
<p> [Full Paper]<br />Sander S. van&#xA0;Berkel, Bas van&#xA0;der&#xA0;Lee, Floris L. van&#xA0;Delft, Rob Wagenvoord, H. Coenraad Hemker, Floris P. J. T. Rutjes<br /><i>ChemMedChem</i>, January 31, 2012, DOI: 10.1002/cmdc.201100560. <a href="http://dx.doi.org/10.1002/cmdc.201100560">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100559">
<title>Polycyclic Cage Structures as Lipophilic Scaffolds for Neuroactive Drugs</title>
<link>http://dx.doi.org/10.1002/cmdc.201100559</link>
<dc:creator>Jacques Joubert, Werner J. Geldenhuys, Cornelis J. Van der Schyf, Douglas W. Oliver, Hendrik Gert Kruger, Thavendran Govender, Sarel F. Malan</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100559.gif" width="127" height="198" alt="Polycyclic Cage Structures as Lipophilic Scaffolds for Neuroactive Drugs" title="Polycyclic Cage Structures as Lipophilic Scaffolds for Neuroactive Drugs" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Scaffolds for neuroprotection:</B> Less than five per cent of small-molecule drugs are able to cross the blood&ndash;brain barrier (BBB). Developments in the design of compounds incorporating lipophilic, polycyclic structures have been under intense investigation in recent years. Conjugation of privileged moieties and known drug structures to these polycyclic structures has enhanced the delivery of neuroactive drugs across the BBB with subsequent neuroprotective and/or neurorestorative activity.</P>
<p> [Minireview]<br />Jacques Joubert, Werner J. Geldenhuys, Cornelis J. Van&#xA0;der&#xA0;Schyf, Douglas W. Oliver, Hendrik Gert Kruger, Thavendran Govender, Sarel F. Malan<br /><i>ChemMedChem</i>, February 3, 2012, DOI: 10.1002/cmdc.201100559. <a href="http://dx.doi.org/10.1002/cmdc.201100559">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100546">
<title>Investigation of D&lt;sub&gt;1&lt;/sub&gt; Receptor&#x2013;Agonist Interactions and D&lt;sub&gt;1&lt;/sub&gt;/D&lt;sub&gt;2&lt;/sub&gt; Agonist Selectivity Using a Combination of Pharmacophore and Receptor Homology Modeling</title>
<link>http://dx.doi.org/10.1002/cmdc.201100546</link>
<dc:creator>Marcus Malo, Lars Brive, Kristina Luthman, Peder Svensson</dc:creator>
<dc:date>2012-02-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100546.gif" width="208" height="131" alt="Investigation of D1 Receptor&ndash;Agonist Interactions and D1/D2 Agonist Selectivity Using a Combination of Pharmacophore and Receptor Homology Modeling" title="Investigation of D1 Receptor&ndash;Agonist Interactions and D1/D2 Agonist Selectivity Using a Combination of Pharmacophore and Receptor Homology Modeling" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The delicate balance</B> between dopamine D<sub>1</sub> and D<sub>2</sub> agonism was investigated by using our combined receptor and pharmacophore modeling approach described in the preceding paper. Not only can the developed receptor models be used to understand the factors that determine receptor isoform selectivity, but also to design new dopamine receptor-selective agonists for use as potential therapeutic agents.</P>
<p> [Full Paper]<br />Marcus Malo, Lars Brive, Kristina Luthman, Peder Svensson<br /><i>ChemMedChem</i>, February 7, 2012, DOI: 10.1002/cmdc.201100546. <a href="http://dx.doi.org/10.1002/cmdc.201100546">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100545">
<title>Investigation of D&lt;sub&gt;2&lt;/sub&gt; Receptor&#x2013;Agonist Interactions Using a Combination of Pharmacophore and Receptor Homology Modeling</title>
<link>http://dx.doi.org/10.1002/cmdc.201100545</link>
<dc:creator>Marcus Malo, Lars Brive, Kristina Luthman, Peder Svensson</dc:creator>
<dc:date>2012-02-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100545.gif" width="207" height="164" alt="Investigation of D2 Receptor&ndash;Agonist Interactions Using a Combination of Pharmacophore and Receptor Homology Modeling" title="Investigation of D2 Receptor&ndash;Agonist Interactions Using a Combination of Pharmacophore and Receptor Homology Modeling" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The magic key</B> for dopamine D<sub>2</sub> receptor agonism was studied by using a combined receptor and pharmacophore modeling approach. All available experimental data, including a set of carefully selected active and inactive ligands, were used to identify the reasons behind selectivity and to pinpoint the specific ligand&ndash;receptor interactions made by D<sub>2</sub> agonists.</P>
<p> [Full Paper]<br />Marcus Malo, Lars Brive, Kristina Luthman, Peder Svensson<br /><i>ChemMedChem</i>, February 7, 2012, DOI: 10.1002/cmdc.201100545. <a href="http://dx.doi.org/10.1002/cmdc.201100545">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100538">
<title>8-Substituted 3-Arylcoumarins as Potent and Selective MAO-B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies</title>
<link>http://dx.doi.org/10.1002/cmdc.201100538</link>
<dc:creator>Dolores Vi&#xF1;a, Maria J. Matos, Giulio Ferino, Enzo Cadoni, Reyes Laguna, Fernanda Borges, Eugenio Uriarte, Lourdes Santana</dc:creator>
<dc:date>2012-01-27T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100538.gif" width="206" height="152" alt="8-Substituted 3-Arylcoumarins as Potent and Selective MAO-B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies" title="8-Substituted 3-Arylcoumarins as Potent and Selective MAO-B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>B-selective!</B> With the aim of finding new selective MAO-B inhibitors, herein we report the synthesis, in&nbsp;vitro evaluation, and a docking simulation of a new series of 3-arylcoumarins variously substituted at the 8-position as potential inhibitors of hMAO-A and B. Most of the studied compounds have high affinity and selectivity for hMAO-B, with IC<sub>50</sub> values in the low micro- to nanomolar range.</P>
<p> [Full Paper]<br />Dolores Vi&#xF1;a, Maria J. Matos, Giulio Ferino, Enzo Cadoni, Reyes Laguna, Fernanda Borges, Eugenio Uriarte, Lourdes Santana<br /><i>ChemMedChem</i>, January 27, 2012, DOI: 10.1002/cmdc.201100538. <a href="http://dx.doi.org/10.1002/cmdc.201100538">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100537">
<title>Arylpiperazine Dopamineric Ligands Protect Neuroblastoma Cells from Nitric Oxide (NO)-Induced Mitochondrial Damage and Apoptosis</title>
<link>http://dx.doi.org/10.1002/cmdc.201100537</link>
<dc:creator>Gordana Tovilovic, Nevena Zogovic, Ljubica Harhaji-Trajkovic, Maja Misirkic-Marjanovic, Kristina Janjetovic, Ljubica Vucicevic, Sladjana Kostic-Rajacic, Andre Schrattenholz, Aleksandra Isakovic, Vukic Soskic, Vladimir Trajkovic</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100537.gif" width="214" height="187" alt="Arylpiperazine Dopamineric Ligands Protect Neuroblastoma Cells from Nitric Oxide (NO)-Induced Mitochondrial Damage and Apoptosis" title="Arylpiperazine Dopamineric Ligands Protect Neuroblastoma Cells from Nitric Oxide (NO)-Induced Mitochondrial Damage and Apoptosis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Guarding the grey matter!</B> Arylpiperazine dopaminergic ligands protect neurons from nitric oxide cytotoxicity. Their ability to modulate cell survival signaling pathways, stabilize mitochondrial membrane, and ultimately prevent neuronal apoptosis, makes them plausible candidates for treatment of neurodegenerative diseases.</P>
<p> [Full Paper]<br />Gordana Tovilovic, Nevena Zogovic, Ljubica Harhaji-Trajkovic, Maja Misirkic-Marjanovic, Kristina Janjetovic, Ljubica Vucicevic, Sladjana Kostic-Rajacic, Andre Schrattenholz, Aleksandra Isakovic, Vukic Soskic, Vladimir Trajkovic<br /><i>ChemMedChem</i>, February 1, 2012, DOI: 10.1002/cmdc.201100537. <a href="http://dx.doi.org/10.1002/cmdc.201100537">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100533">
<title>The &#x3C3;-Hole Phenomenon of Halogen Atoms Forms the Structural Basis of the Strong Inhibitory Potency of C5 Halogen Substituted Glucopyranosyl Nucleosides towards Glycogen Phosphorylase&#xA0;b</title>
<link>http://dx.doi.org/10.1002/cmdc.201100533</link>
<dc:creator>Anastasia L. Kantsadi, Joseph M. Hayes, Stella Manta, Vicky T. Skamnaki, Christos Kiritsis, Anna-Maria G. Psarra, Zissis Koutsogiannis, Athina Dimopoulou, Stavroula Theofanous, Nikolaos Nikoleousakos, Panagiotis Zoumpoulakis, Maria Kontou, George Papadopoulos, Spyros E. Zographos, Dimitris Komiotis, Demetres D. Leonidas</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100533.gif" width="122" height="147" alt="The &sigma;-Hole Phenomenon of Halogen Atoms Forms the Structural Basis of the Strong Inhibitory Potency of C5 Halogen Substituted Glucopyranosyl Nucleosides towards Glycogen Phosphorylase&nbsp;b" title="The &sigma;-Hole Phenomenon of Halogen Atoms Forms the Structural Basis of the Strong Inhibitory Potency of C5 Halogen Substituted Glucopyranosyl Nucleosides towards Glycogen Phosphorylase&nbsp;b" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>On halogenated ground:</B> C5 halogen substituted glucopyranosyl nucleosides have been discovered as some of the most potent inhibitors of glycogen phosphorylase. The ability of the halogen atom to form intermolecular electrostatic interactions through the &sigma;-hole phenomenon rather than by steric effects alone is the structural basis behind their improved inhibitory potential over the unsubstituted ligand.</P>
<p> [Full Paper]<br />Anastasia L. Kantsadi, Joseph M. Hayes, Stella Manta, Vicky T. Skamnaki, Christos Kiritsis, Anna-Maria G. Psarra, Zissis Koutsogiannis, Athina Dimopoulou, Stavroula Theofanous, Nikolaos Nikoleousakos, Panagiotis Zoumpoulakis, Maria Kontou, George Papadopoulos, Spyros E. Zographos, Dimitris Komiotis, Demetres D. Leonidas<br /><i>ChemMedChem</i>, January 20, 2012, DOI: 10.1002/cmdc.201100533. <a href="http://dx.doi.org/10.1002/cmdc.201100533">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100531">
<title>Design, Synthesis, and Biological Activity of Hydroxamic Tertiary Amines as Histone Deacetylase Inhibitors</title>
<link>http://dx.doi.org/10.1002/cmdc.201100531</link>
<dc:creator>Stefania Terracciano, Maria Giovanna Chini, Raffaele Riccio, Ines Bruno, Giuseppe Bifulco</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100531.gif" width="209" height="167" alt="Design, Synthesis, and Biological Activity of Hydroxamic Tertiary Amines as Histone Deacetylase Inhibitors" title="Design, Synthesis, and Biological Activity of Hydroxamic Tertiary Amines as Histone Deacetylase Inhibitors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Linear thought process:</B> Non-peptide linear compounds equipped with hydroxamic groups as the metal binder were explored for their effect on histone deacetylase activity. Herein we report docking studies, synthesis, and biological evaluation of this new generation of hydroxamic tertiary amines.</P>
<p> [Full Paper]<br />Stefania Terracciano, Maria Giovanna Chini, Raffaele Riccio, Ines Bruno, Giuseppe Bifulco<br /><i>ChemMedChem</i>, January 25, 2012, DOI: 10.1002/cmdc.201100531. <a href="http://dx.doi.org/10.1002/cmdc.201100531">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100530">
<title>Diarylheterocycle Core Ring Features Effect in Selective COX-1 Inhibition</title>
<link>http://dx.doi.org/10.1002/cmdc.201100530</link>
<dc:creator>Maria Grazia Perrone, Paola Vitale, Paola Malerba, Angela Altomare, Rosanna Rizzi, Antonio Lavecchia, Carmen Di Giovanni, Ettore Novellino, Antonio Scilimati</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100530.gif" width="180" height="130" alt="Diarylheterocycle Core Ring Features Effect in Selective COX-1 Inhibition" title="Diarylheterocycle Core Ring Features Effect in Selective COX-1 Inhibition" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Getting to the core:</B> The role of the central nucleus in the diarylheterocycle COX-1 inhibitor class was investigated. We identified 5-(furan-2-yl)-1-(4-methoxyphenyl)-3-(trifluoromethyl)-1<I>H</I>-pyrazole (<B>17</B>) as a selective inhibitor of COX-1 activity. The results of molecular docking studies shed light the binding mode of <B>17</B> into the catalytic site of COX-1.</P>
<p> [Full Paper]<br />Maria Grazia Perrone, Paola Vitale, Paola Malerba, Angela Altomare, Rosanna Rizzi, Antonio Lavecchia, Carmen Di&#xA0;Giovanni, Ettore Novellino, Antonio Scilimati<br /><i>ChemMedChem</i>, January 25, 2012, DOI: 10.1002/cmdc.201100530. <a href="http://dx.doi.org/10.1002/cmdc.201100530">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100529">
<title>Discovery of Novel 2-&lt;I&gt;N&lt;/I&gt;-Aryl-Substituted Benzenesulfonamidoacetamides: Orally Bioavailable Tubulin Polymerization Inhibitors with Marked Antitumor Activities</title>
<link>http://dx.doi.org/10.1002/cmdc.201100529</link>
<dc:creator>Zulong Liu, Zuyu Zhou, Wei Tian, Xing Fan, Ding Xue, Long Yu, Qiang Yu, Ya-Qiu Long</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100529.gif" width="208" height="87" alt="Discovery of Novel 2-N-Aryl-Substituted Benzenesulfonamidoacetamides: Orally Bioavailable Tubulin Polymerization Inhibitors with Marked Antitumor Activities" title="Discovery of Novel 2-N-Aryl-Substituted Benzenesulfonamidoacetamides: Orally Bioavailable Tubulin Polymerization Inhibitors with Marked Antitumor Activities" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The latest and greatest:</B> Structural optimization of an in-house screening hit afforded a novel class of benzenesulfonamides as orally bioavailable and potent tubulin polymerization inhibitors. These compounds act as antimitotic agents and exhibit a tubulin binding mechanism similar to that of colchicine. The most potent analogues have in&nbsp;vivo antitumor efficacy and are able to circumvent P-glycoprotein-mediated multidrug resistance in tumor cells.</P>
<p> [Full Paper]<br />Zulong Liu, Zuyu Zhou, Wei Tian, Xing Fan, Ding Xue, Long Yu, Qiang Yu, Ya-Qiu Long<br /><i>ChemMedChem</i>, February 6, 2012, DOI: 10.1002/cmdc.201100529. <a href="http://dx.doi.org/10.1002/cmdc.201100529">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100528">
<title>Discovery of Selective Alpha&lt;sub&gt;2C&lt;/sub&gt; Adrenergic Receptor Agonists</title>
<link>http://dx.doi.org/10.1002/cmdc.201100528</link>
<dc:creator>Eric Jnoff, Bernard Christophe, Philippe Collart, Francis Coloretti, Aurel Debeuckelaere, Marc De Ryck, Bruno Fuks, Christophe Genicot, Michel Gillard, Michel Guyaux, Nathalie Price, Marie-Christine Vandergeten, C&#xE9;line Vermeiren</dc:creator>
<dc:date>2012-01-19T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100528.gif" width="118" height="42" alt="Discovery of Selective Alpha2C Adrenergic Receptor Agonists" title="Discovery of Selective Alpha2C Adrenergic Receptor Agonists" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Something to ease the pain:</B> Chemical modification of a 2-amino-oxazoline scaffold led to the identification of &alpha;<sub>2C</sub> adrenergic receptor (AR) agonists. These ligands were characterized by a dual &alpha;<sub>2C</sub>-AR agonist/&alpha;<sub>2A</sub>-AR antagonist profile. Structure&ndash;activity relationships were studied, and screening in anesthetized rats demonstrated a superior margin of safety for this class of compounds with respect to cardiovascular effects compared with nonselective &alpha;<sub>2</sub>-AR agonists.</P>
<p> [Communication]<br />Eric Jnoff, Bernard Christophe, Philippe Collart, Francis Coloretti, Aurel Debeuckelaere, Marc De&#xA0;Ryck, Bruno Fuks, Christophe Genicot, Michel Gillard, Michel Guyaux, Nathalie Price, Marie-Christine Vandergeten, C&#xE9;line Vermeiren<br /><i>ChemMedChem</i>, January 19, 2012, DOI: 10.1002/cmdc.201100528. <a href="http://dx.doi.org/10.1002/cmdc.201100528">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100522">
<title>Chiral Mercaptoacetamides Display Enantioselective Inhibition of Histone Deacetylase&#xA0;6 and Exhibit Neuroprotection in Cortical Neuron Models of Oxidative Stress</title>
<link>http://dx.doi.org/10.1002/cmdc.201100522</link>
<dc:creator>Jay H. Kalin, Hankun Zhang, Sophie Gaudrel-Grosay, Giulio Vistoli, Alan P. Kozikowski</dc:creator>
<dc:date>2012-01-10T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100522.gif" width="195" height="218" alt="Chiral Mercaptoacetamides Display Enantioselective Inhibition of Histone Deacetylase&nbsp;6 and Exhibit Neuroprotection in Cortical Neuron Models of Oxidative Stress" title="Chiral Mercaptoacetamides Display Enantioselective Inhibition of Histone Deacetylase&nbsp;6 and Exhibit Neuroprotection in Cortical Neuron Models of Oxidative Stress" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Isoform-selective</B> histone deacetylase (HDAC) inhibitors containing mercaptoacetamide zinc binding groups are known to be viable alternatives to the more traditional hydroxamic acid based inhibitors. Herein we demonstrate the HDAC6 enantioselectivity of &alpha;-methyl-substituted mercaptoacetamides and provide evidence to support their use as neuroprotective agents.</P>
<p> [Full Paper]<br />Jay H. Kalin, Hankun Zhang, Sophie Gaudrel-Grosay, Giulio Vistoli, Alan P. Kozikowski<br /><i>ChemMedChem</i>, January 10, 2012, DOI: 10.1002/cmdc.201100522. <a href="http://dx.doi.org/10.1002/cmdc.201100522">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100510">
<title>Discovery of 2-(2-Benzoxazoyl amino)-4-Aryl-5-Cyanopyrimidine as Negative Allosteric Modulators (NAMs) of Metabotropic Glutamate Receptor&#xA0;5 (mGlu&lt;sub&gt;5&lt;/sub&gt;): From an Artificial Neural Network Virtual Screen to an In Vivo Tool Compound</title>
<link>http://dx.doi.org/10.1002/cmdc.201100510</link>
<dc:creator>Ralf Mueller, Eric S. Dawson, Jens Meiler, Alice L. Rodriguez, Brian A. Chauder, Brittney S. Bates, Andrew S. Felts, Jeffrey P. Lamb, Usha N. Menon, Sataywan B. Jadhav, Alexander S. Kane, Carrie K. Jones, Karen J. Gregory, Colleen M. Niswender, P. Jeffrey Conn, Christopher M. Olsen, Danny G. Winder, Kyle A. Emmitte, Craig W. Lindsley</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100510.gif" width="154" height="91" alt="Discovery of 2-(2-Benzoxazoyl amino)-4-Aryl-5-Cyanopyrimidine as Negative Allosteric Modulators (NAMs) of Metabotropic Glutamate Receptor&nbsp;5 (mGlu5): From an Artificial Neural Network Virtual Screen to an In Vivo Tool Compound" title="Discovery of 2-(2-Benzoxazoyl amino)-4-Aryl-5-Cyanopyrimidine as Negative Allosteric Modulators (NAMs) of Metabotropic Glutamate Receptor&nbsp;5 (mGlu5): From an Artificial Neural Network Virtual Screen to an In Vivo Tool Compound" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>From ANNs to NAMs!</B> Data from an experimental metabotropic glutamate receptor&nbsp;5 (mGlu<sub>5</sub>) high-throughput screen (HTS) were employed to train artificial neural networks (ANNs) based on 345 confirmed negative allosteric modulators (NAMs) and 155&nbsp;774 inactive compounds. This effort identified two potent mGlu<sub>5</sub> NAMs with a unique chemotype. Optimization afforded a tool compound (shown), active in mouse models of anxiety and addiction.</P>
<p> [Communication]<br />Ralf Mueller, Eric S. Dawson, Jens Meiler, Alice L. Rodriguez, Brian A. Chauder, Brittney S. Bates, Andrew S. Felts, Jeffrey P. Lamb, Usha N. Menon, Sataywan B. Jadhav, Alexander S. Kane, Carrie K. Jones, Karen J. Gregory, Colleen M. Niswender, P. Jeffrey Conn, Christopher M. Olsen, Danny G. Winder, Kyle A. Emmitte, Craig W. Lindsley<br /><i>ChemMedChem</i>, January 20, 2012, DOI: 10.1002/cmdc.201100510. <a href="http://dx.doi.org/10.1002/cmdc.201100510">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100505">
<title>Novel 4-Amino Bis-pyridinium and Bis-quinolinium Derivatives as Choline Kinase Inhibitors with Antiproliferative Activity against the Human Breast Cancer SKBR-3 Cell Line</title>
<link>http://dx.doi.org/10.1002/cmdc.201100505</link>
<dc:creator>Ver&#xF3;nica G&#xF3;mez-P&#xE9;rez, Theresa McSorley, Wei Cun See Too, Manfred Konrad, Joaqu&#xED;n M. Campos</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100505.gif" width="207" height="152" alt="Novel 4-Amino Bis-pyridinium and Bis-quinolinium Derivatives as Choline Kinase Inhibitors with Antiproliferative Activity against the Human Breast Cancer SKBR-3 Cell Line" title="Novel 4-Amino Bis-pyridinium and Bis-quinolinium Derivatives as Choline Kinase Inhibitors with Antiproliferative Activity against the Human Breast Cancer SKBR-3 Cell Line" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Hitting the spot!</B> There is significant interest in the development of selective and potent choline kinase (ChoK) inhibitors for use as pharmacological tools. ChoK inhibitors with either bis-pyridinium or bis-quinolinium scaffolds exhibit mixed inhibition with a predominantly competitive component. The most active compounds have antiproliferative activities of ~1&nbsp;&mu;<span style="font-variant:small-caps">M</span> against the SKBR3 cell line and are much more potent than the choline homologue hemicholinium-3.</P>
<p> [Full Paper]<br />Ver&#xF3;nica G&#xF3;mez-P&#xE9;rez, Theresa McSorley, Wei Cun See&#xA0;Too, Manfred Konrad, Joaqu&#xED;n M. Campos<br /><i>ChemMedChem</i>, January 25, 2012, DOI: 10.1002/cmdc.201100505. <a href="http://dx.doi.org/10.1002/cmdc.201100505">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100504">
<title>Dipeptidyl Peptidase&#xA0;IV (DPPIV/CD26)-Based Prodrugs of Hydroxy-Containing Drugs</title>
<link>http://dx.doi.org/10.1002/cmdc.201100504</link>
<dc:creator>Alberto Diez-Torrubia, Silvia Cabrera, Anne-Marie Lambeir, Jan Balzarini, Mar&#xED;a-Jos&#xE9; Camarasa, Sonsoles Vel&#xE1;zquez</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100504.gif" width="211" height="119" alt="Dipeptidyl Peptidase&nbsp;IV (DPPIV/CD26)-Based Prodrugs of Hydroxy-Containing Drugs" title="Dipeptidyl Peptidase&nbsp;IV (DPPIV/CD26)-Based Prodrugs of Hydroxy-Containing Drugs" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Improve stability and solubility!</B> Tripeptide prodrugs of a variety of hydroxy-containing drugs exhibiting fair chemical stability are efficiently hydrolyzed by DPPIV/CD26 to ester valyl intermediates, which spontaneously release the parent drug. A number of these prodrugs have significantly higher water solubility than their poorly soluble parent compounds.</P>
<p> [Full Paper]<br />Alberto Diez-Torrubia, Silvia Cabrera, Anne-Marie Lambeir, Jan Balzarini, Mar&#xED;a-Jos&#xE9; Camarasa, Sonsoles Vel&#xE1;zquez<br /><i>ChemMedChem</i>, February 3, 2012, DOI: 10.1002/cmdc.201100504. <a href="http://dx.doi.org/10.1002/cmdc.201100504">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100499">
<title>Selective Agonists for Dopamine/Neurotensin Receptor Heterodimers</title>
<link>http://dx.doi.org/10.1002/cmdc.201100499</link>
<dc:creator>Susanne Koschatzky, Peter Gmeiner</dc:creator>
<dc:date>2011-12-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100499.gif" width="202" height="185" alt="Selective Agonists for Dopamine/Neurotensin Receptor Heterodimers" title="Selective Agonists for Dopamine/Neurotensin Receptor Heterodimers" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Select the right pair:</B> Radioligand binding studies of the physical interaction between co-expressed dopamine D<sub>2L</sub> or D<sub>3</sub> and neurotensin NTS<sub>1</sub> or NTS<sub>2</sub> receptors indicate substantial cross-inhibitory effects of both NTS<sub>1</sub> and NTS<sub>2</sub> receptor subtypes on the agonist binding of D<sub>2L</sub> or D<sub>3</sub> in the presence of neurotensin (NT). D<sub>3</sub>&ndash;NTS<sub>2</sub> co-expression gave a 20-fold decrease in affinity for biphenylcarboxamide <B>5</B> in the presence of NT.</P>
<p> [Full Paper]<br />Susanne Koschatzky, Peter Gmeiner<br /><i>ChemMedChem</i>, December 23, 2011, DOI: 10.1002/cmdc.201100499. <a href="http://dx.doi.org/10.1002/cmdc.201100499">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100469">
<title>A Benzopyrane Derivative as a P-Glycoprotein Stimulator: A Potential Agent to Decrease &#x3B2;-Amyloid Accumulation in Alzheimer&#x2019;s Disease</title>
<link>http://dx.doi.org/10.1002/cmdc.201100469</link>
<dc:creator>Marialessandra Contino, Mariangela Cantore, Elena Capparelli, Maria Grazia Perrone, Mauro Niso, Carmela Inglese, Francesco Berardi, Marcello Leopoldo, Roberto Perrone, Nicola Antonio Colabufo</dc:creator>
<dc:date>2011-12-23T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100469.gif" width="212" height="179" alt="A Benzopyrane Derivative as a P-Glycoprotein Stimulator: A Potential Agent to Decrease &beta;-Amyloid Accumulation in Alzheimer&rsquo;s Disease" title="A Benzopyrane Derivative as a P-Glycoprotein Stimulator: A Potential Agent to Decrease &beta;-Amyloid Accumulation in Alzheimer&rsquo;s Disease" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A simulating interaction:</B> The P-glycoprotein (P-gp) ligand <B>13</B> displays high P-gp interacting activity (EC<sub>50</sub>=2.90&nbsp;&mu;<span style="font-variant:small-caps">M</span>) and selectivity in tumor cell lines. Here, this promising compound was further evaluated ex vivo in an everted gut sac assay and found to behave as a P-gp stimulator, making this agent a potential lead for the development of new therapeutics to treat Alzheimer&#x27;s disease.</P>
<p> [Communication]<br />Marialessandra Contino, Mariangela Cantore, Elena Capparelli, Maria Grazia Perrone, Mauro Niso, Carmela Inglese, Francesco Berardi, Marcello Leopoldo, Roberto Perrone, Nicola Antonio Colabufo<br /><i>ChemMedChem</i>, December 23, 2011, DOI: 10.1002/cmdc.201100469. <a href="http://dx.doi.org/10.1002/cmdc.201100469">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100467">
<title>Synthesis, in&#xA0;vitro Cytotoxicity, and Interaction with DNA of Platinum(II) Complexes with &lt;I&gt;N&lt;/I&gt;-Monocycloalkyl Derivatives of 1&lt;I&gt;R&lt;/I&gt;,2&lt;I&gt;R&lt;/I&gt;-Diaminocyclohexane as Carrier Ligands</title>
<link>http://dx.doi.org/10.1002/cmdc.201100467</link>
<dc:creator>Yanyan Sun, Shaohua Gou, Fei Liu, Runting Yin, Lei Fang</dc:creator>
<dc:date>2012-01-13T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100467.gif" width="208" height="177" alt="Synthesis, in&nbsp;vitro Cytotoxicity, and Interaction with DNA of Platinum(II) Complexes with N-Monocycloalkyl Derivatives of 1R,2R-Diaminocyclohexane as Carrier Ligands" title="Synthesis, in&nbsp;vitro Cytotoxicity, and Interaction with DNA of Platinum(II) Complexes with N-Monocycloalkyl Derivatives of 1R,2R-Diaminocyclohexane as Carrier Ligands" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Platinum(II) complexes:</B> Oxaliplatin derivatives, especially <B>1&nbsp;f</B> and <B>2&nbsp;f</B>, show similar or superior cytotoxicity to oxaliplatin. The apoptotic mechanism of complex <B>2&nbsp;f</B> and its ability to cause S-phase cell-cycle arrest were determined by flow cytometry. This compound has the capacity to distort DNA through a binding mode distinct from that of oxaliplatin.</P>
<p> [Full Paper]<br />Yanyan Sun, Shaohua Gou, Fei Liu, Runting Yin, Lei Fang<br /><i>ChemMedChem</i>, January 13, 2012, DOI: 10.1002/cmdc.201100467. <a href="http://dx.doi.org/10.1002/cmdc.201100467">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100438">
<title>Huprine Derivatives as Sub-Nanomolar Human Acetylcholinesterase Inhibitors: From Rational Design to Validation by X-ray Crystallography</title>
<link>http://dx.doi.org/10.1002/cmdc.201100438</link>
<dc:creator>Cyril Ronco, Eug&#xE9;nie Carletti, Jacques-Philippe Colletier, Martin Weik, Florian Nachon, Ludovic Jean, Pierre-Yves Renard</dc:creator>
<dc:date>2011-11-04T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100438.gif" width="208" height="249" alt="Huprine Derivatives as Sub-Nanomolar Human Acetylcholinesterase Inhibitors: From Rational Design to Validation by X-ray Crystallography" title="Huprine Derivatives as Sub-Nanomolar Human Acetylcholinesterase Inhibitors: From Rational Design to Validation by X-ray Crystallography" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>This complete study</B>&mdash;from rational design to validation by X-ray crystallography&mdash;allowed us to discover two sub-nanomolar hAChE inhibitors (430 and 530&nbsp;p<span style="font-variant:small-caps">M</span>) grafted with an easily derivatized linker directed toward the AChE peripheral site. The crystal structure of mouse AChE in complex with compound <B>4</B> was solved and confirms the favorable position of the triazole in the active site gorge, paving the way for a new class of bifunctional ligands.</P>
<p> [Communication]<br />Cyril Ronco, Eug&#xE9;nie Carletti, Jacques-Philippe Colletier, Martin Weik, Florian Nachon, Ludovic Jean, Pierre-Yves Renard<br /><i>ChemMedChem</i>, November 4, 2011, DOI: 10.1002/cmdc.201100438. <a href="http://dx.doi.org/10.1002/cmdc.201100438">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100431">
<title>Why as a Medicinal Chemist I Am Not Optimistic about the Possibility of Finding, in a Reasonable Timeframe, Small-Molecule Drugs Capable of Curing the Evolution of Alzheimer&#x2019;s Disease</title>
<link>http://dx.doi.org/10.1002/cmdc.201100431</link>
<dc:creator>Jean-Louis Kraus</dc:creator>
<dc:date>2011-10-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p></p><p> [Viewpoint]<br />Jean-Louis Kraus<br /><i>ChemMedChem</i>, October 11, 2011, DOI: 10.1002/cmdc.201100431. <a href="http://dx.doi.org/10.1002/cmdc.201100431">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100423">
<title>High-Affinity, Selective &#x3C3; Ligands of the 1,2,3,4-Tetrahydro-1,4&#x27;-silaspiro[naphthalene-1,4&#x27;-piperidine] Type: Syntheses, Structures, and Pharmacological Properties</title>
<link>http://dx.doi.org/10.1002/cmdc.201100423</link>
<dc:creator>Reinhold Tacke, R&#xFC;diger Bertermann, Christian Burschka, Steffen D&#xF6;rrich, Markus Fischer, Barbara M&#xFC;ller, G&#xE9;raldine Meyerhans, Dirk Schepmann, Bernhard W&#xFC;nsch, Ingvar Arnason, Ragnar Bjornsson</dc:creator>
<dc:date>2011-11-11T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cmdc201100423.gif" width="155" height="158" alt="High-Affinity, Selective &sigma; Ligands of the 1,2,3,4-Tetrahydro-1,4&#x27;-silaspiro[naphthalene-1,4&#x27;-piperidine] Type: Syntheses, Structures, and Pharmacological Properties" title="High-Affinity, Selective &sigma; Ligands of the 1,2,3,4-Tetrahydro-1,4&#x27;-silaspiro[naphthalene-1,4&#x27;-piperidine] Type: Syntheses, Structures, and Pharmacological Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>C/Si switch:</B> We report the syntheses and pharmacological properties of novel silicon analogues of &sigma; ligands of the 1&#x27;-organyl-1,2,3,4-tetrahydrospiro[naphthalene-1,4&#x27;-piperidine] type. C/Si exchange leads to a moderate increase in &sigma;<sub>1</sub> receptor affinity and to a considerable improvement in &sigma;<sub>1</sub>/&sigma;<sub>2</sub> selectivity.</P>
<p> [Full Paper]<br />Reinhold Tacke, R&#xFC;diger Bertermann, Christian Burschka, Steffen D&#xF6;rrich, Markus Fischer, Barbara M&#xFC;ller, G&#xE9;raldine Meyerhans, Dirk Schepmann, Bernhard W&#xFC;nsch, Ingvar Arnason, Ragnar Bjornsson<br /><i>ChemMedChem</i>, November 11, 2011, DOI: 10.1002/cmdc.201100423. <a href="http://dx.doi.org/10.1002/cmdc.201100423">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103918">
<title>An Efficient Mixed-Ligand Pd Catalytic System to Promote C-N Coupling for the Synthesis of &lt;I&gt;N&lt;/I&gt;-Arylaminotriazole Nucleosides</title>
<link>http://dx.doi.org/10.1002/chem.201103918</link>
<dc:creator>Yuting Fan, Yi Xia, Jingjie Tang, Fabio Ziarelli, Fanqi Qu, Palma Rocchi, Juan L. Iovanna, Ling Peng</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103918.gif" width="437" height="156" alt="An Efficient Mixed-Ligand Pd Catalytic System to Promote C-N Coupling for the Synthesis of N-Arylaminotriazole Nucleosides" title="An Efficient Mixed-Ligand Pd Catalytic System to Promote C-N Coupling for the Synthesis of N-Arylaminotriazole Nucleosides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Make it unique!</B> A mixed-ligand system of Pd/Synphos/Xantphos promotes effective C-N coupling in the synthesis of various <I>N</I>-arylaminotriazole and <I>N</I>-arylaminopurine nucleoside analogues. This catalytic system is strikingly powerful and efficient, allowing for unparalleled substrate scope and high product yields as well as promotion of C-Cl bond activation for C-N coupling (see scheme).</P>
<p> [Communication]<br />Yuting Fan, Yi Xia, Jingjie Tang, Fabio Ziarelli, Fanqi Qu, Palma Rocchi, Juan L. Iovanna, Ling Peng<br /><i>Chem. Eur. J.</i>, January 20, 2012, DOI: 10.1002/chem.201103918. <a href="http://dx.doi.org/10.1002/chem.201103918">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103892">
<title>Cooperative Catalytic Reactions Using Distinct Transition-Metal Catalysts: Ruthenium- and Copper-Catalyzed Enantioselective Propargylic Alkylation</title>
<link>http://dx.doi.org/10.1002/chem.201103892</link>
<dc:creator>Masahiro Ikeda, Yoshihiro Miyake, Yoshiaki Nishibayashi</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103892.gif" width="212" height="187" alt="Cooperative Catalytic Reactions Using Distinct Transition-Metal Catalysts: Ruthenium- and Copper-Catalyzed Enantioselective Propargylic Alkylation" title="Cooperative Catalytic Reactions Using Distinct Transition-Metal Catalysts: Ruthenium- and Copper-Catalyzed Enantioselective Propargylic Alkylation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Homogeneous catalysis</B>: Highly enantioselective propargylic alkylations of propargylic alcohols with &beta;-ketoesters in the presence of a thiolate-bridged diruthenium complex and a copper complex are presented (see scheme). This methodology based on a cooperative catalytic system using distinct transition metals realizes a useful transformation that cannot be achieved by a single catalyst.</P>
<p> [Full Paper]<br />Masahiro Ikeda, Yoshihiro Miyake, Yoshiaki Nishibayashi<br /><i>Chem. Eur. J.</i>, February 1, 2012, DOI: 10.1002/chem.201103892. <a href="http://dx.doi.org/10.1002/chem.201103892">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103830">
<title>Unprecedented Organoimido-Derivatised Lacunary Polyoxometalates</title>
<link>http://dx.doi.org/10.1002/chem.201103830</link>
<dc:creator>Jian Hao, Jin Zhang, Panchao Yin, Zicheng Xiao, Fengping Xiao, Yongge Wei</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103830.gif" width="212" height="144" alt="Unprecedented Organoimido-Derivatised Lacunary Polyoxometalates" title="Unprecedented Organoimido-Derivatised Lacunary Polyoxometalates" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>An organoimido-substituted</B> monovacant hexamolybdate containing additional multidentate ligands and its phenylphosphonate derivative were both synthesized directly from an aromatic amine by using an <I>N</I>,<I>N</I>-dicyclohexylcarbodiimide (DCC) protocol. The inherent chirality of these compounds and their hydrophobic shells are pictured.</P>
<p> [Communication]<br />Jian Hao, Jin Zhang, Panchao Yin, Zicheng Xiao, Fengping Xiao, Yongge Wei<br /><i>Chem. Eur. J.</i>, February 1, 2012, DOI: 10.1002/chem.201103830. <a href="http://dx.doi.org/10.1002/chem.201103830">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103816">
<title>Enhancing Anisotropy Barriers of Dysprosium(III) Single-Ion Magnets</title>
<link>http://dx.doi.org/10.1002/chem.201103816</link>
<dc:creator>Gong-Jun Chen, Yun-Nan Guo, Jin-Lei Tian, Jinkui Tang, Wen Gu, Xin Liu, Shi-Ping Yan, Peng Cheng, Dai-Zheng Liao</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103816.gif" width="265" height="117" alt="Enhancing Anisotropy Barriers of Dysprosium(III) Single-Ion Magnets" title="Enhancing Anisotropy Barriers of Dysprosium(III) Single-Ion Magnets" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Magnetic personality</B>: The incorporation of a bulky auxiliary ligand in &beta;-diketone-based dysprosium(III) single-ion magnets (SIMs) remarkably increases the anisotropic barriers, representing a promising route toward the design of higher anisotropic barrier SIMs (see scheme).</P>
<p> [Communication]<br />Gong-Jun Chen, Yun-Nan Guo, Jin-Lei Tian, Jinkui Tang, Wen Gu, Xin Liu, Shi-Ping Yan, Peng Cheng, Dai-Zheng Liao<br /><i>Chem. Eur. J.</i>, February 3, 2012, DOI: 10.1002/chem.201103816. <a href="http://dx.doi.org/10.1002/chem.201103816">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103800">
<title>Synthesis of Optically Active Oxazoline Derivatives via Catalytic Asymmetric Desymmetrization of 1,3-Diols</title>
<link>http://dx.doi.org/10.1002/chem.201103800</link>
<dc:creator>Yutaro Tsuda, Masami Kuriyama, Osamu Onomura</dc:creator>
<dc:date>2012-02-01T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103800.gif" width="376" height="110" alt="Synthesis of Optically Active Oxazoline Derivatives via Catalytic Asymmetric Desymmetrization of 1,3-Diols" title="Synthesis of Optically Active Oxazoline Derivatives via Catalytic Asymmetric Desymmetrization of 1,3-Diols" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Chiral oxazolines</B>: A synthetic method to prepare optically active oxazolines through a copper-catalyzed asymmetric desymmetrization of 1,3-diols has been successfully developed. This reaction system tolerated a diverse range of substrates to give the desired oxazoline derivatives in good to excellent yields with high enantioselectivities (see scheme).</P>
<p> [Communication]<br />Yutaro Tsuda, Masami Kuriyama, Osamu Onomura<br /><i>Chem. Eur. J.</i>, February 1, 2012, DOI: 10.1002/chem.201103800. <a href="http://dx.doi.org/10.1002/chem.201103800">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103720">
<title>Simple Synthesis of Platinum Dendritic Aggregates Supported on Conductive Tungsten Oxide Nanowires as High-Performance Methanol Oxidation Electrocatalysts</title>
<link>http://dx.doi.org/10.1002/chem.201103720</link>
<dc:creator>Youngjin Ye, Jin Joo, Byungkwon Lim, Jinwoo Lee</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103720.gif" width="167" height="92" alt="Simple Synthesis of Platinum Dendritic Aggregates Supported on Conductive Tungsten Oxide Nanowires as High-Performance Methanol Oxidation Electrocatalysts" title="Simple Synthesis of Platinum Dendritic Aggregates Supported on Conductive Tungsten Oxide Nanowires as High-Performance Methanol Oxidation Electrocatalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Morphology-controlled Pt dendritic</B> aggregates supported on W<sub>18</sub>O<sub>49</sub> nanowires were fabricated by the simple colloidal method. The synthesized nanocatalysts exhibit strong catalytic activity toward methanol oxidation and high CO tolerance because of the highly branched structure of the dendritic Pt nanostructures and assistant catalytic activity of the tungsten oxide nanowires (see figure).</P>
<p> [Communication]<br />Youngjin Ye, Jin Joo, Byungkwon Lim, Jinwoo Lee<br /><i>Chem. Eur. J.</i>, February 3, 2012, DOI: 10.1002/chem.201103720. <a href="http://dx.doi.org/10.1002/chem.201103720">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103708">
<title>Morphing the Torsional Potential Energy Function from Local to Global Symmetry through a &#x3C0;&#xA0;Link: The Rotational Spectrum of &#x3B1;,&#x3B1;,&#x3B1;-Trifluoro-&lt;I&gt;p&lt;/I&gt;-tolualdehyde</title>
<link>http://dx.doi.org/10.1002/chem.201103708</link>
<dc:creator>Laura B. Favero, Jens-Uwe Grabow, Walther Caminati</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103708.gif" width="190" height="216" alt="Morphing the Torsional Potential Energy Function from Local to Global Symmetry through a &pi;&nbsp;Link: The Rotational Spectrum of &alpha;,&alpha;,&alpha;-Trifluoro-p-tolualdehyde" title="Morphing the Torsional Potential Energy Function from Local to Global Symmetry through a &pi;&nbsp;Link: The Rotational Spectrum of &alpha;,&alpha;,&alpha;-Trifluoro-p-tolualdehyde" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Dynamics and inertia</B>: The rotation of the CF<sub>3</sub> top in &alpha;,&alpha;,&alpha;-trifluorotoluene becomes considerably hindered by a <I>V</I><sub>3</sub> barrier in &alpha;,&alpha;,&alpha;-trifluoro-<I>p</I>-tolualdehyde. Situated in a local <I>V</I><sub>6</sub> environment, the <I>V</I><sub>3</sub> barrier is caused by the aldehyde group and communicated through the aromatic &pi;&nbsp;system. Quite dramatically, the ground state inertial defect jumps from &minus;1.271 to &minus;89.961&nbsp;u&Aring;<SUP>2</SUP>, thus reflecting the electronically induced rigidity (see figure).</P>
<p> [Communication]<br />Laura B. Favero, Jens-Uwe Grabow, Walther Caminati<br /><i>Chem. Eur. J.</i>, February 3, 2012, DOI: 10.1002/chem.201103708. <a href="http://dx.doi.org/10.1002/chem.201103708">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103649">
<title>Synthesis, Electrochemical Properties and Self-Assembly of a Proton-Conducting Core&#x2013;Shell Macromolecule</title>
<link>http://dx.doi.org/10.1002/chem.201103649</link>
<dc:creator>Meizhen Yin, Naiwen Kang, Guanglei Cui, Zhihong Liu, Feng Wang, Wantai Yang, Markus Klapper, Klaus M&#xFC;llen</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103649.gif" width="364" height="159" alt="Synthesis, Electrochemical Properties and Self-Assembly of a Proton-Conducting Core&ndash;Shell Macromolecule" title="Synthesis, Electrochemical Properties and Self-Assembly of a Proton-Conducting Core&ndash;Shell Macromolecule" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Let the protons flow</B>: The synthesis of a core&ndash;shell macromolecule bearing phosphonic acids is presented. The rigid central core serves as a scaffold to stabilize the flexible polymer shells. Pronounced proton conductivity is obtained under humidified conditions. The self-assembly of such dendritic macromolecules by electrostatic interactions on a modified gold substrate is investigated and characterized.</P>
<p> [Communication]<br />Meizhen Yin, Naiwen Kang, Guanglei Cui, Zhihong Liu, Feng Wang, Wantai Yang, Markus Klapper, Klaus M&#xFC;llen<br /><i>Chem. Eur. J.</i>, January 26, 2012, DOI: 10.1002/chem.201103649. <a href="http://dx.doi.org/10.1002/chem.201103649">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103601">
<title>Light-Harvesting Hybrid Assemblies</title>
<link>http://dx.doi.org/10.1002/chem.201103601</link>
<dc:creator>K. Venkata Rao, K. K. R. Datta, Muthusamy Eswaramoorthy, Subi. J. George</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103601.gif" width="389" height="107" alt="Light-Harvesting Hybrid Assemblies" title="Light-Harvesting Hybrid Assemblies" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Glowing hybrids:</B> An organic&ndash;inorganic approach has generated a variety of light-harvesting hybrid assemblies, with different physical nature based on their design (see scheme). We introduce these design concepts (covalent, semicovalent, and noncovalent approaches) involved in the synthesis of artificial photosynthetic hybrids (MOF=metal&ndash;organic framework; PMO=periodic mesoporous organosilica).</P>
<p> [Concept]<br />K. Venkata Rao, K. K. R. Datta, Muthusamy Eswaramoorthy, Subi. J. George<br /><i>Chem. Eur. J.</i>, January 31, 2012, DOI: 10.1002/chem.201103601. <a href="http://dx.doi.org/10.1002/chem.201103601">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103552">
<title>Intermolecular Communication on a Liposomal Membrane: Enzymatic Amplification of a Photonic Signal with a Gemini Peptide Lipid as a Membrane-Bound Artificial Receptor</title>
<link>http://dx.doi.org/10.1002/chem.201103552</link>
<dc:creator>Masaru Mukai, Kohei Maruo, Yoshihiro Sasaki, Jun-ichi Kikuchi</dc:creator>
<dc:date>2012-02-06T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103552.gif" width="391" height="96" alt="Intermolecular Communication on a Liposomal Membrane: Enzymatic Amplification of a Photonic Signal with a Gemini Peptide Lipid as a Membrane-Bound Artificial Receptor" title="Intermolecular Communication on a Liposomal Membrane: Enzymatic Amplification of a Photonic Signal with a Gemini Peptide Lipid as a Membrane-Bound Artificial Receptor" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><I><B>trans</B></I><B>-formers</B>: A supramolecular system that is capable of activating an enzyme through photoisomerization was constructed on a liposomal membrane. Quantitative evaluation of the present system by using CD and UV spectroscopy showed that enzyme activity was effectively regulated by the specific recognition of the photonic signal by the receptor and its response (see Scheme).</P>
<p> [Full Paper]<br />Masaru Mukai, Kohei Maruo, Yoshihiro Sasaki, Jun-ichi Kikuchi<br /><i>Chem. Eur. J.</i>, February 6, 2012, DOI: 10.1002/chem.201103552. <a href="http://dx.doi.org/10.1002/chem.201103552">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103530">
<title>A Concise Total Synthesis of Deoxyschizandrin and Exploration of Its Antiproliferative Effects and those of Structurally Related Derivatives</title>
<link>http://dx.doi.org/10.1002/chem.201103530</link>
<dc:creator>Shaojun Zheng, Sarah J. Aves, Luca Laraia, Warren R. J. D. Galloway, Kurt G. Pike, Wenjun Wu, David R. Spring</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103530.gif" width="351" height="125" alt="A Concise Total Synthesis of Deoxyschizandrin and Exploration of Its Antiproliferative Effects and those of Structurally Related Derivatives" title="A Concise Total Synthesis of Deoxyschizandrin and Exploration of Its Antiproliferative Effects and those of Structurally Related Derivatives" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A concise total</B> synthesis of the natural product deoxyschizandrin, based around a double organocuprate oxidation strategy, is reported. In addition, the results of biological studies exploring the ability of deoxyschizandrin and synthetic precursors lacking the medium ring biaryl unit to inhibit the proliferation of a human cancer cell line are presented.</P>
<p> [Full Paper]<br />Shaojun Zheng, Sarah J. Aves, Luca Laraia, Warren R. J. D. Galloway, Kurt G. Pike, Wenjun Wu, David R. Spring<br /><i>Chem. Eur. J.</i>, February 3, 2012, DOI: 10.1002/chem.201103530. <a href="http://dx.doi.org/10.1002/chem.201103530">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103527">
<title>Formation of a Hydrogen-Bonded Heptazine Framework by Self-Assembly of Melem into a Hexagonal Channel Structure</title>
<link>http://dx.doi.org/10.1002/chem.201103527</link>
<dc:creator>Sophia J. Makowski, Pia K&#xF6;stler, Wolfgang Schnick</dc:creator>
<dc:date>2012-02-07T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103527.gif" width="286" height="118" alt="Formation of a Hydrogen-Bonded Heptazine Framework by Self-Assembly of Melem into a Hexagonal Channel Structure" title="Formation of a Hydrogen-Bonded Heptazine Framework by Self-Assembly of Melem into a Hexagonal Channel Structure" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The</B> <I><B>s</B></I><B>-heptazine compound melem</B> C<sub>6</sub>N<sub>7</sub>(NH<sub>2</sub>)<sub>3</sub> assembles into a hydrogen-bonded hexagonal framework in hot aqueous solution (see figure). The structure exhibits infinite channels with diameter of 8.9&nbsp;&Aring; that are filled with crystal water. TG/DTA measurements, solid-state NMR spectroscopy, powder X-ray diffraction, and sorption measurements have been employed to investigate the thermal behavior of the material, the possibility of hydrolysis, and structural changes induced by dehydration.</P>
<p> [Full Paper]<br />Sophia J. Makowski, Pia K&#xF6;stler, Wolfgang Schnick<br /><i>Chem. Eur. J.</i>, February 7, 2012, DOI: 10.1002/chem.201103527. <a href="http://dx.doi.org/10.1002/chem.201103527">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103509">
<title>A Time-Resolved In Situ Quick-XAS Investigation of Thermal Activation of Fischer&#x2013;Tropsch Silica-Supported Cobalt Catalysts</title>
<link>http://dx.doi.org/10.1002/chem.201103509</link>
<dc:creator>Jingping Hong, Eric Marceau, Andrei Y. Khodakov, Anne Griboval-Constant, Camille La Fontaine, Val&#xE9;rie Briois</dc:creator>
<dc:date>2012-02-03T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103509.gif" width="206" height="159" alt="A Time-Resolved In Situ Quick-XAS Investigation of Thermal Activation of Fischer&ndash;Tropsch Silica-Supported Cobalt Catalysts" title="A Time-Resolved In Situ Quick-XAS Investigation of Thermal Activation of Fischer&ndash;Tropsch Silica-Supported Cobalt Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Quick X-ray absorption spectroscopy</B> (XAS) provides quantitative information about the composition of supported metal phases during catalyst activation. Decomposition of SiO<sub>2</sub>-supported cobalt nitrate in diluted NO leads to the rapid formation of cobalt(II) hydroxynitrates below 100&nbsp;&deg;C. Their decomposition starts progressively between 110 and 170&nbsp;&deg;C to give cobalt oxide nuclei, which contribute to the enhancement of the metal oxide dispersion (see figure).</P>
<p> [Communication]<br />Jingping Hong, Eric Marceau, Andrei Y. Khodakov, Anne Griboval-Constant, Camille La&#xA0;Fontaine, Val&#xE9;rie Briois<br /><i>Chem. Eur. J.</i>, February 3, 2012, DOI: 10.1002/chem.201103509. <a href="http://dx.doi.org/10.1002/chem.201103509">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103495">
<title>Highly Diastereoselective Construction of Fused Carbocycles from Cyclopropane-1,1-dicarboxylates and Cyclic Enol Silyl Ethers: Scope, Mechanism, and Origin of Diastereoselectivity</title>
<link>http://dx.doi.org/10.1002/chem.201103495</link>
<dc:creator>Jian-Ping Qu, Yong Liang, Hao Xu, Xiu-Li Sun, Zhi-Xiang Yu, Yong Tang</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103495.gif" width="301" height="91" alt="Highly Diastereoselective Construction of Fused Carbocycles from Cyclopropane-1,1-dicarboxylates and Cyclic Enol Silyl Ethers: Scope, Mechanism, and Origin of Diastereoselectivity" title="Highly Diastereoselective Construction of Fused Carbocycles from Cyclopropane-1,1-dicarboxylates and Cyclic Enol Silyl Ethers: Scope, Mechanism, and Origin of Diastereoselectivity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Cyclopropane rings true</B>: By selecting the appropriate substituents on the ester and silyl groups, fused cyclopentane derivatives with multiple contiguous stereocenters can be synthesized with excellent diastereoselectivity through Cu<SUP>II</SUP>/bisoxazoline-catalyzed intermolecular [3+2] cycloaddition reactions of cyclopropane-1,1-dicarboxylates and cyclic enol silyl ethers (see scheme).</P>
<p> [Communication]<br />Jian-Ping Qu, Yong Liang, Hao Xu, Xiu-Li Sun, Zhi-Xiang Yu, Yong Tang<br /><i>Chem. Eur. J.</i>, January 20, 2012, DOI: 10.1002/chem.201103495. <a href="http://dx.doi.org/10.1002/chem.201103495">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103479">
<title>Determination of the Absolute Configuration of Peptide Natural Products by Using Stable Isotope Labeling and Mass Spectrometry</title>
<link>http://dx.doi.org/10.1002/chem.201103479</link>
<dc:creator>Helge B. Bode, Daniela Reimer, Sebastian W. Fuchs, Ferdinand Kirchner, Christina Dauth, Carsten Kegler, Wolfram Lorenzen, Alexander O. Brachmann, Peter Gr&#xFC;n</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103479.gif" width="173" height="191" alt="Determination of the Absolute Configuration of Peptide Natural Products by Using Stable Isotope Labeling and Mass Spectrometry" title="Determination of the Absolute Configuration of Peptide Natural Products by Using Stable Isotope Labeling and Mass Spectrometry" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Game over&mdash;structure solved</B>: A combination of labeling experiments with mass spectrometry results in the reliable determination of the sum formula, the nature of the building blocks, and for peptide natural products also the determination of the absolute configuration as exemplified for the novel natural products GameXPeptide&nbsp;A&ndash;D (see scheme).</P>
<p> [Full Paper]<br />Helge B. Bode, Daniela Reimer, Sebastian W. Fuchs, Ferdinand Kirchner, Christina Dauth, Carsten Kegler, Wolfram Lorenzen, Alexander O. Brachmann, Peter Gr&#xFC;n<br /><i>Chem. Eur. J.</i>, January 20, 2012, DOI: 10.1002/chem.201103479. <a href="http://dx.doi.org/10.1002/chem.201103479">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103465">
<title>Photoreversible Supramolecular Polymerisation and Hierarchical Organization of Hydrogen-Bonded Supramolecular Co-polymers Composed of Diarylethenes and Oligothiophenes</title>
<link>http://dx.doi.org/10.1002/chem.201103465</link>
<dc:creator>Shiki Yagai, Keisuke Ohta, Marina Gushiken, Kazunori Iwai, Atsushi Asano, Shu Seki, Yoshihiro Kikkawa, Masakazu Morimoto, Akihide Kitamura, Takashi Karatsu</dc:creator>
<dc:date>2012-01-31T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103465.gif" width="308" height="56" alt="Photoreversible Supramolecular Polymerisation and Hierarchical Organization of Hydrogen-Bonded Supramolecular Co-polymers Composed of Diarylethenes and Oligothiophenes" title="Photoreversible Supramolecular Polymerisation and Hierarchical Organization of Hydrogen-Bonded Supramolecular Co-polymers Composed of Diarylethenes and Oligothiophenes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Designer photoresponsive assemblies</B>: Oligothiophenes and diarylethenes are held together by multiple hydrogen bonds, affording photoresponsive and electroacitve supramolecular copolymers. The co-polymer chains hierarchically organize into helical nanorods, which can be reversibly converted to small oligomeric species upon irradiation with UV and visible light (see figure).</P>
<p> [Full Paper]<br />Shiki Yagai, Keisuke Ohta, Marina Gushiken, Kazunori Iwai, Atsushi Asano, Shu Seki, Yoshihiro Kikkawa, Masakazu Morimoto, Akihide Kitamura, Takashi Karatsu<br /><i>Chem. Eur. J.</i>, January 31, 2012, DOI: 10.1002/chem.201103465. <a href="http://dx.doi.org/10.1002/chem.201103465">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103456">
<title>X-ray Crystallographic Proof of the Isomer &lt;I&gt;D&lt;/I&gt;&lt;sub&gt;2&lt;/sub&gt;-C&lt;sub&gt;84&lt;/sub&gt;(5) as Trifluoromethylated and Chlorinated Derivatives, C&lt;sub&gt;84&lt;/sub&gt;(CF&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;16&lt;/sub&gt;, C&lt;sub&gt;84&lt;/sub&gt;Cl&lt;sub&gt;20&lt;/sub&gt;, and C&lt;sub&gt;84&lt;/sub&gt;Cl&lt;sub&gt;32&lt;/sub&gt;</title>
<link>http://dx.doi.org/10.1002/chem.201103456</link>
<dc:creator>Shangfeng Yang, Chuanbao Chen, Tao Wei, Nadezhda B. Tamm, Erhard Kemnitz, Sergey I. Troyanov</dc:creator>
<dc:date>2012-01-26T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103456.gif" width="196" height="147" alt="X-ray Crystallographic Proof of the Isomer D2-C84(5) as Trifluoromethylated and Chlorinated Derivatives, C84(CF3)16, C84Cl20, and C84Cl32" title="X-ray Crystallographic Proof of the Isomer D2-C84(5) as Trifluoromethylated and Chlorinated Derivatives, C84(CF3)16, C84Cl20, and C84Cl32" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Minor isomer comes forward</B>: Minor isomer C<sub>84</sub>(5) has been captured by high temperature trifluoromethylation with CF<sub>3</sub>I and chlorination with VCl<sub>4</sub>. The compounds C<sub>84</sub>(CF<sub>3</sub>)<sub>16</sub>, C<sub>84</sub>Cl<sub>20</sub>, and C<sub>84</sub>(5)Cl<sub>32</sub> were investigated by X-ray crystallography providing the first direct proofs of the cage connectivity of <I>D</I><sub>2</sub>-C<sub>84</sub>(5). The <I>D</I><sub>2</sub>-C<sub>84</sub>(5)Cl<sub>32</sub> molecule (see figure; C grey, Cl green) contains two flattened, pyrene-like substructures on opposite poles of the cage resulting in its drum-like shape.</P>
<p> [Communication]<br />Shangfeng Yang, Chuanbao Chen, Tao Wei, Nadezhda B. Tamm, Erhard Kemnitz, Sergey I. Troyanov<br /><i>Chem. Eur. J.</i>, January 26, 2012, DOI: 10.1002/chem.201103456. <a href="http://dx.doi.org/10.1002/chem.201103456">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103435">
<title>An Approach to the Regioselective Diamination of Conjugated Di- and Trienes</title>
<link>http://dx.doi.org/10.1002/chem.201103435</link>
<dc:creator>Anton Lishchynskyi, Kilian Mu&#xF1;iz</dc:creator>
<dc:date>2012-01-25T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/chem201103435.gif" width="395" height="64" alt="An Approach to the Regioselective Diamination of Conjugated Di- and Trienes" title="An Approach to the Regioselective Diamination of Conjugated Di- and Trienes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>It&rsquo;s do or diaminate</B>: The selective diamination of 1,3-butadienes in the presence of hypervalent iodine reagents has been developed. This oxidation process proceeds with complete selectivity in favor of diamination. Depending on the substrate, it proceeds either with 1,2- or 1,4-regioselectivity (see scheme).</P>
<p> [Communication]<br />Anton Lishchynskyi, Kilian Mu&#xF1;iz<br /><i>Chem. Eur. J.</i>, January 25, 2012, DOI: 10.1002/chem.201103435. <a href="http://dx.doi.org/10.1002/chem.201103435">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103418">
<title>Pd-Catalyzed Reaction of Allyl Carbonate with Polyols: The Role of CO&lt;sub&gt;2&lt;/sub&gt; in Transesterification versus Etherification of Glycerol</title>
<link>http://dx.doi.org/10.1002/chem.201103418</link>
<dc:creator>Alvaro Gordillo, Guy C. Lloyd-Jones</dc:creator>
<dc:date>2012-01-20T:+05:00</dc:date>
<taxo:topics>
  <rdf:Bag>
  </rdf:Bag>
</taxo:topics>
<content:encoded><![CDATA[ <p><img src="htt
