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<title>ChemPlusChem</title>
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<description>News and current content from the journal ChemPlusChem</description>
<dc:language>en</dc:language>
<dc:rights>Copyright 2010, Wiley-VCH</dc:rights>
<dc:date>2011-10-09T00:00:00+02:00</dc:date>
<dc:publisher>Wiley-VCH</dc:publisher>
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<dc:subject>Chemistry</dc:subject>
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<rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201300067" />
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300120">
<title>Synthesis, Self-Assembly, and Electrocatalysis of Polyallylamine-Functionalized Platinum Nanocubes</title>
<link>http://dx.doi.org/10.1002/cplu.201300120</link>
<dc:creator>Gengtao Fu, Ruopeng Zhao, Linfei Ding, Lin Tao, Jun Lin, Yu Chen, Yawen Tang, Yiming Zhou, Tianhong Lu</dc:creator>
<dc:date>2013-05-22T14:40+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300120.gif" width="292" height="132" alt="Synthesis, Self-Assembly, and Electrocatalysis of Polyallylamine-Functionalized Platinum Nanocubes" title="Synthesis, Self-Assembly, and Electrocatalysis of Polyallylamine-Functionalized Platinum Nanocubes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The title composite</B> was prepared and self-assembled on carbon nanotubes (CNTs). Even after cleaning with UV/Ozone and electrochemical methods, the residual polyallylamine strongly influences the electronic structure of Pt. The resultant Pt-NC/CNT nanohybrid shows superior electrochemical activity and stability towards the oxygen reduction reaction in H<sub>2</sub>SO<sub>4</sub> solutions compared with commercial Pt/C catalyst.</P>
<p> [Communication]<br />Gengtao Fu, Ruopeng Zhao, Linfei Ding, Lin Tao, Jun Lin, Yu Chen, Yawen Tang, Yiming Zhou, Tianhong Lu<br /><i>ChemPlusChem</i>, May 22, 2013, DOI: 10.1002/cplu.201300120. <a href="http://dx.doi.org/10.1002/cplu.201300120">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300083">
<title>Facile Synthesis of Phosphate-Functionalized MWCNT–TiO&lt;sub&gt;2&lt;/sub&gt; Nanocomposites as Efficient Photocatalysts and Insights into the Roles of Nanostructured Carbon</title>
<link>http://dx.doi.org/10.1002/cplu.201300083</link>
<dc:creator>Zhijun Li, Lumei He, Liqiang Jing, Jingsheng Lin, Yunbo Luan</dc:creator>
<dc:date>2013-05-17T11:41+05:00</dc:date>
<taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300083.gif" width="433" height="99" alt="Facile Synthesis of Phosphate-Functionalized MWCNT&ndash;TiO2 Nanocomposites as Efficient Photocatalysts and Insights into the Roles of Nanostructured Carbon" title="Facile Synthesis of Phosphate-Functionalized MWCNT&ndash;TiO2 Nanocomposites as Efficient Photocatalysts and Insights into the Roles of Nanostructured Carbon" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Pollutant breakdown</B>: As depicted, the photogenerated electrons of TiO<sub>2</sub> transfer to the multiwalled carbon nanotube (MWCNT) and are captured by adsorbed O<sub>2</sub>. Phosphate functionalization of MWCNTs promotes O<sub>2</sub> adsorption to improve photogenerated charge separation of the resulting MWCNT&ndash;TiO<sub>2</sub> composite.</P>
<p> [Full Paper]<br />Zhijun Li, Lumei He, Liqiang Jing, Jingsheng Lin, Yunbo Luan<br /><i>ChemPlusChem</i>, May 17, 2013, DOI: 10.1002/cplu.201300083. <a href="http://dx.doi.org/10.1002/cplu.201300083">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300110">
<title>Is There B-N Bond-Length Alternation in 1,2:3,4:5,6-Tris(biphenylylene)borazines?</title>
<link>http://dx.doi.org/10.1002/cplu.201300110</link>
<dc:creator>Matthias Müller, Cäcilia Maichle-Mössmer, Peter Sirsch, Holger F. Bettinger</dc:creator>
<dc:date>2013-05-17T11:40+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300110.gif" width="139" height="134" alt="Is There B-N Bond-Length Alternation in 1,2:3,4:5,6-Tris(biphenylylene)borazines?" title="Is There B-N Bond-Length Alternation in 1,2:3,4:5,6-Tris(biphenylylene)borazines?" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>All things being equal</B>: The electrophilic aromatic bromination of 1,2:3,4:5,6-tris(biphenylylene)borazine yields the tribromo derivative that has only small bond-length alternation (BLA) according to X-ray crystallography and state-of-the art computations (see scheme). A re-investigation of the structure of the parent 1,2:3,4:5,6-tris(biphenylylene)borazine compound by experiment and theory reveals positional disorder of the borazine core.</P>
<p> [Full Paper]<br />Matthias M&#xFC;ller, C&#xE4;cilia Maichle-M&#xF6;ssmer, Peter Sirsch, Holger F. Bettinger<br /><i>ChemPlusChem</i>, May 17, 2013, DOI: 10.1002/cplu.201300110. <a href="http://dx.doi.org/10.1002/cplu.201300110">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/19176.en.html">
<title>ChemPlusChem 5/2013: Like Oil and Water</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/19176.en.html</link>
<dc:date>2013-05-16T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cplu_5.png" alt="ChemPlusChem 5/2013: Like Oil and Water" align="left" hspace="5" vspace="5" border="0" /></p><!-- module_2 --><p>In the cover article, Martin Pumera et al. use <a href="http://onlinelibrary.wiley.com/doi/10.1002/cplu.201300011/abstract" target="_blank">self-propelled biocompatible capsules</a> loaded with various surfactants and compared their influence upon movement of oil droplets. Their findings are expected to have great impact on potential applications of such capsules for environmental clean-up. Also, a report on <a href="http://onlinelibrary.wiley.com/doi/10.1002/cplu.201300044/abstract" target="_blank">visualizing hyperconjugation</a> through UV-photoelectron spectroscopy is outlined by Vladimir Ya. Lee et al. Meanwhile, Pierre Fr&#xE8;re et al. describe the synthesis as well as the optical, theoretical, electrochemical, X-ray, and electrical characteristics of <a href="http://onlinelibrary.wiley.com/doi/10.1002/cplu.201300037/abstract" target="_blank">new thiophene/furan-capped co-oligomers for organic field-effect transistors</a>.</p><p><a href="http://onlinelibrary.wiley.com/doi/10.1002/cplu.v78.5/issuetoc" target="_blank">Browse Issue 5/2013 now</a></p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300113">
<title>Synthesis, Structure, and Halo-, Photo-, and Thermochromism Properties of 5-Azotriazolyl Salicylic Acid and Its Cd&lt;SUP&gt;II&lt;/SUP&gt; Complex</title>
<link>http://dx.doi.org/10.1002/cplu.201300113</link>
<dc:creator>Jiao-Min Lin, Meng Yang, Yan-Xuan Qiu, Wen-Bin Chen, Hua Yan, Fei-Xian Gao, Zhen-Jie OuYang, Wen Dong, Tong-Chun Kuang</dc:creator>
<dc:date>2013-05-13T16:35+05:00</dc:date>
<taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300113.gif" width="367" height="137" alt="Synthesis, Structure, and Halo-, Photo-, and Thermochromism Properties of 5-Azotriazolyl Salicylic Acid and Its CdII Complex" title="Synthesis, Structure, and Halo-, Photo-, and Thermochromism Properties of 5-Azotriazolyl Salicylic Acid and Its CdII Complex" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>No two ways about it</B>: Two photo- and thermoisomeric compounds of [(H<sub>3</sub>ATSA)]&middot;2&nbsp;H<sub>2</sub>O and [Cd<sub>2</sub>(H<sub>2</sub>ATSA)<sub>4</sub>]&middot;13&nbsp;H<sub>2</sub>O have been prepared and their optical properties investigated as well as simulated by DFT and TDDFT calculations (see figure). The multiple chromic properties of these compounds may be exploited to create new photoactive devices.</P>
<p> [Full Paper]<br />Jiao-Min Lin, Meng Yang, Yan-Xuan Qiu, Wen-Bin Chen, Hua Yan, Fei-Xian Gao, Zhen-Jie OuYang, Wen Dong, Tong-Chun Kuang<br /><i>ChemPlusChem</i>, May 13, 2013, DOI: 10.1002/cplu.201300113. <a href="http://dx.doi.org/10.1002/cplu.201300113">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300135">
<title>Versatile Fluorescent Conjugated Polyelectrolyte-Capped Mesoporous Silica Nanoparticles for Controlled Drug Delivery and Imaging</title>
<link>http://dx.doi.org/10.1002/cplu.201300135</link>
<dc:creator>Fang Pu, Xia Liu, Xinjian Yang, Zhen Liu, Jinsong Ren, Shu Wang, Xiaogang Qu</dc:creator>
<dc:date>2013-05-13T16:34+05:00</dc:date>
<taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300135.gif" width="388" height="139" alt="Versatile Fluorescent Conjugated Polyelectrolyte-Capped Mesoporous Silica Nanoparticles for Controlled Drug Delivery and Imaging" title="Versatile Fluorescent Conjugated Polyelectrolyte-Capped Mesoporous Silica Nanoparticles for Controlled Drug Delivery and Imaging" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Luminescent cap</B>: The properties of a fluorescent conjugated polyelectrolyte and mesoporous silica nanoparticles have been combined to prepare a pH-controlled drug delivery and cellular imaging system by using a simple and general method (see scheme). The fluorescent conjugated polyelectrolyte was used as both the capping agent and the imaging probe with low cytotoxicity. It is a promising candidate for simultaneous diagnostics and therapeutics.</P>
<p> [Full Paper]<br />Fang Pu, Xia Liu, Xinjian Yang, Zhen Liu, Jinsong Ren, Shu Wang, Xiaogang Qu<br /><i>ChemPlusChem</i>, May 13, 2013, DOI: 10.1002/cplu.201300135. <a href="http://dx.doi.org/10.1002/cplu.201300135">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300036">
<title>9-Fluorenone-2-Carboxylic Acid as a Scaffold for Tubulin Interacting Compounds</title>
<link>http://dx.doi.org/10.1002/cplu.201300036</link>
<dc:creator>Francesco Calogero, Stella Borrelli, Gaetano Speciale, Michael S. Christodoulou, Daniele Cartelli, Dario Ballinari, Francesco Sola, Clara Albanese, Antonella Ciavolella, Daniele Passarella, Graziella Cappelletti, Stefano Pieraccini, Maurizio Sironi</dc:creator>
<dc:date>2013-05-13T16:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300036.gif" width="212" height="176" alt="9-Fluorenone-2-Carboxylic Acid as a Scaffold for Tubulin Interacting Compounds" title="9-Fluorenone-2-Carboxylic Acid as a Scaffold for Tubulin Interacting Compounds" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Tubulin as the target</B>: The introduction of a hydrophobic group at position&nbsp;7 of 9-fluorenone-2-carboxylic acid (see structure) generates new tubulin binders, the design of which is suggested by modeling studies. The antiproliferative activity on two different cell lines, fluorescent microscopy, flow cytometry, and sedimentation assay tests confirmed the supposed mechanism.</P>
<p> [Full Paper]<br />Francesco Calogero, Stella Borrelli, Gaetano Speciale, Michael S. Christodoulou, Daniele Cartelli, Dario Ballinari, Francesco Sola, Clara Albanese, Antonella Ciavolella, Daniele Passarella, Graziella Cappelletti, Stefano Pieraccini, Maurizio Sironi<br /><i>ChemPlusChem</i>, May 13, 2013, DOI: 10.1002/cplu.201300036. <a href="http://dx.doi.org/10.1002/cplu.201300036">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300133">
<title>One-pot Synthesis of Mesoporous TiO&lt;sub&gt;2&lt;/sub&gt; from Self-Assembled Sol Particles and Its Application as Mesoscopic Photoanodes of Dye-Sensitized Solar Cells</title>
<link>http://dx.doi.org/10.1002/cplu.201300133</link>
<dc:creator>Min Zhang, Keyou Yan, Wei Han, Shihe Yang</dc:creator>
<dc:date>2013-05-09T07:54+05:00</dc:date>
<taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300133.gif" width="251" height="141" alt="One-pot Synthesis of Mesoporous TiO2 from Self-Assembled Sol Particles and Its Application as Mesoscopic Photoanodes of Dye-Sensitized Solar Cells" title="One-pot Synthesis of Mesoporous TiO2 from Self-Assembled Sol Particles and Its Application as Mesoscopic Photoanodes of Dye-Sensitized Solar Cells" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Highly crystalline mesoporous TiO<sub>2</sub></B> was synthesized by a one-pot strategy that combines advantages of the St&ouml;ber, surfactant-templated, and hydrothermal methods (see figure; ACAC=acetyl acetone, IPA=isopropanol, TIP=titanium isopropoxide). The resulting photoanodes showed much higher efficiency because of extended electron lifetime related to the mesoporous structure confinement effect and accelerated electron transport.</P>
<p> [Full Paper]<br />Min Zhang, Keyou Yan, Wei Han, Shihe Yang<br /><i>ChemPlusChem</i>, May 09, 2013, DOI: 10.1002/cplu.201300133. <a href="http://dx.doi.org/10.1002/cplu.201300133">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300086">
<title>Multifunctional Macrocyclic Receptors as Templates for Aromatic Amino Acids: A Rare Example of a Highly Selective Multi-Input Multi-Output Chemo-“Logic Gate”</title>
<link>http://dx.doi.org/10.1002/cplu.201300086</link>
<dc:creator>Caterina Fraschetti, Antonello Filippi, Maria Elisa Crestoni, Tadashi Ema, Maurizio Speranza</dc:creator>
<dc:date>2013-05-06T12:34+05:00</dc:date>
<taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300086.gif" width="264" height="81" alt="Multifunctional Macrocyclic Receptors as Templates for Aromatic Amino Acids: A Rare Example of a Highly Selective Multi-Input Multi-Output Chemo-&ldquo;Logic Gate&rdquo;" title="Multifunctional Macrocyclic Receptors as Templates for Aromatic Amino Acids: A Rare Example of a Highly Selective Multi-Input Multi-Output Chemo-&ldquo;Logic Gate&rdquo;" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A logical choice</B>: Proton-bound complexes between aromatic amino acids and a chiral multifunctional macrocycle, shown in green in the figure, behave as selective multi-input multi-output devices (&ldquo;logic gates&rdquo;) which, in the presence of an amine, may or may not release the amino acid depending on its configuration and basicity of the amine.</P>
<p> [Full Paper]<br />Caterina Fraschetti, Antonello Filippi, Maria Elisa Crestoni, Tadashi Ema, Maurizio Speranza<br /><i>ChemPlusChem</i>, May 06, 2013, DOI: 10.1002/cplu.201300086. <a href="http://dx.doi.org/10.1002/cplu.201300086">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300063">
<title>Silver-Containing Ionic Liquids with Alkylamine Ligands</title>
<link>http://dx.doi.org/10.1002/cplu.201300063</link>
<dc:creator>Daphne Depuydt, Neil R. Brooks, Stijn Schaltin, Luc Van Meervelt, Jan Fransaer, Koen Binnemans</dc:creator>
<dc:date>2013-05-06T12:32+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300063.gif" width="165" height="157" alt="Silver-Containing Ionic Liquids with Alkylamine Ligands" title="Silver-Containing Ionic Liquids with Alkylamine Ligands" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>All that glitters is not gold</B>: Thermally stable liquid metal salts have been synthesised by using readily available organic amine ligands and silver bis(trifluoromethylsulfonyl)imide. These compounds are useful for the electrodeposition of metallic silver with high deposition rates (see picture).</P>
<p> [Full Paper]<br />Daphne Depuydt, Neil R. Brooks, Stijn Schaltin, Luc Van&#xA0;Meervelt, Jan Fransaer, Koen Binnemans<br /><i>ChemPlusChem</i>, May 06, 2013, DOI: 10.1002/cplu.201300063. <a href="http://dx.doi.org/10.1002/cplu.201300063">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300042">
<title>Recognition of a Bromide Ion by the Protonated Form of 2-(1&lt;I&gt;H&lt;/I&gt;-Imidazol-2-ylthio)-3-methylnaphthalene-1,4-dione</title>
<link>http://dx.doi.org/10.1002/cplu.201300042</link>
<dc:creator>Bigyan R. Jali, Jubaraj B. Baruah</dc:creator>
<dc:date>2013-05-03T16:05+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300042.gif" width="294" height="113" alt="Recognition of a Bromide Ion by the Protonated Form of 2-(1H-Imidazol-2-ylthio)-3-methylnaphthalene-1,4-dione" title="Recognition of a Bromide Ion by the Protonated Form of 2-(1H-Imidazol-2-ylthio)-3-methylnaphthalene-1,4-dione" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Caught in a bind</B>: A fluorescence emission study on the interactions of various mineral acids reveals that a bromide ion is recognized by the protonated form of 2-(1<I>H</I>-imidazole-2-ylthio)-3-methylnaphthalene-1,4-dione; this is attributed to the formation of the enol form of the corresponding bromide salt in solution (see picture).</P>
<p> [Full Paper]<br />Bigyan R. Jali, Jubaraj B. Baruah<br /><i>ChemPlusChem</i>, May 03, 2013, DOI: 10.1002/cplu.201300042. <a href="http://dx.doi.org/10.1002/cplu.201300042">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300035">
<title>Liquid Phase Isobutane/2-Butene Alkylation Promoted by Hydrogen Chloride Using Lewis Acidic Ionic Liquids</title>
<link>http://dx.doi.org/10.1002/cplu.201300035</link>
<dc:creator>Ferdinand Pöhlmann, Lisa Schilder, Wolfgang Korth, Andreas Jess</dc:creator>
<dc:date>2013-05-03T16:04+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300035.gif" width="216" height="180" alt="Liquid Phase Isobutane/2-Butene Alkylation Promoted by Hydrogen Chloride Using Lewis Acidic Ionic Liquids " title="Liquid Phase Isobutane/2-Butene Alkylation Promoted by Hydrogen Chloride Using Lewis Acidic Ionic Liquids " style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>High-octane action</B>: Isobutane/2-butene alkylation was achieved using an hydrogen chloride gas-promoted, chloroaluminate ionic liquid catalyst in a discontinuous stirred tank reactor. Introducing the HCl additive led to high activity and selectivity in the production of desired trimethylpentanes (TMPs); figure also shows undesired secondary products (C<sub>5</sub>-C<sub>7</sub>, dimethylhexanes (DMHs), C<sub>9+</sub>). Additionally, deactivation of the ionic liquid catalyst was easily avoided.</P>
<p> [Full Paper]<br />Ferdinand P&#xF6;hlmann, Lisa Schilder, Wolfgang Korth, Andreas Jess<br /><i>ChemPlusChem</i>, May 03, 2013, DOI: 10.1002/cplu.201300035. <a href="http://dx.doi.org/10.1002/cplu.201300035">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300057">
<title>Structure and Reactivity of the Glutathione Radical Cation: Radical Rearrangement from the Cysteine Sulfur to the Glutamic Acid α-Carbon Atom</title>
<link>http://dx.doi.org/10.1002/cplu.201300057</link>
<dc:creator>Sandra Osburn, Giel Berden, Jos Oomens, Kerim Gulyuz, Nick C. Polfer, Richard A. J. O’Hair, Victor Ryzhov</dc:creator>
<dc:date>2013-05-02T18:35+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300057.gif" width="192" height="193" alt="Structure and Reactivity of the Glutathione Radical Cation: Radical Rearrangement from the Cysteine Sulfur to the Glutamic Acid &alpha;-Carbon Atom" title="Structure and Reactivity of the Glutathione Radical Cation: Radical Rearrangement from the Cysteine Sulfur to the Glutamic Acid &alpha;-Carbon Atom" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Totally radical</B>: Gas-phase ion&ndash;molecule reactions were used to observe a radical rearrangement in the radical cation of glutathione (see scheme). This rearrangement proceeded from sulfur to the glutamic acid &alpha;-carbon atom, which was confirmed by infrared multiple photon dissociation (IRMPD) spectroscopy in two different IR regions (1000&ndash;1800 and 2800&ndash;3700&nbsp;cm<SUP>&minus;1</SUP>) and DFT calculations.</P>
<p> [Full Paper]<br />Sandra Osburn, Giel Berden, Jos Oomens, Kerim Gulyuz, Nick C. Polfer, Richard A. J. O&#x2019;Hair, Victor Ryzhov<br /><i>ChemPlusChem</i>, May 02, 2013, DOI: 10.1002/cplu.201300057. <a href="http://dx.doi.org/10.1002/cplu.201300057">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300105">
<title>Mesostructured Dihydroxy-Functionalized Guanidinium-Based Polyoxometalate with Enhanced Heterogeneous Catalytic Activity in Epoxidation</title>
<link>http://dx.doi.org/10.1002/cplu.201300105</link>
<dc:creator>Guojian Chen, Yu Zhou, Pingping Zhao, Zhouyang Long, Jun Wang</dc:creator>
<dc:date>2013-04-26T14:58+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300105.gif" width="214" height="198" alt="Mesostructured Dihydroxy-Functionalized Guanidinium-Based Polyoxometalate with Enhanced Heterogeneous Catalytic Activity in Epoxidation" title="Mesostructured Dihydroxy-Functionalized Guanidinium-Based Polyoxometalate with Enhanced Heterogeneous Catalytic Activity in Epoxidation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>IL effects</B>: A self-assembled mesoporous polyoxometalate (POM) with coral-shaped morphology was obtained by pairing Keggin POM anions with newly designed dihydroxy-tethered guanidinium cations of an ionic liquid (IL). Enhancement of the heterogeneous catalytic activity in epoxidation is explained by a unique substrate&ndash;solvent&ndash;catalyst synergistic mechanism (see figure).</P>
<p> [Full Paper]<br />Guojian Chen, Yu Zhou, Pingping Zhao, Zhouyang Long, Jun Wang<br /><i>ChemPlusChem</i>, Apr 26, 2013, DOI: 10.1002/cplu.201300105. <a href="http://dx.doi.org/10.1002/cplu.201300105">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300095">
<title>Controlled Synthesis of Manganese Oxyhydroxide Nanotubes: Implications for High-Efficiency Supercapacitors</title>
<link>http://dx.doi.org/10.1002/cplu.201300095</link>
<dc:creator>Hui Teng Tan, Xianhong Rui, Wenhui Shi, Chen Xu, Hong Yu, Harry E. Hoster, Qingyu Yan</dc:creator>
<dc:date>2013-04-24T08:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300095.gif" width="214" height="195" alt="Controlled Synthesis of Manganese Oxyhydroxide Nanotubes: Implications for High-Efficiency Supercapacitors" title="Controlled Synthesis of Manganese Oxyhydroxide Nanotubes: Implications for High-Efficiency Supercapacitors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Nothing on the inside</B>: The unique structural properties of MnOOH nanotubes endow them with excellent electrochemical characteristics in terms of the specific capacitance, energy, and power densities (see figure). Furthermore, hybridizing graphite felt (GF) with MnOOH species using the binder-free concept enables them to be used as flexible supercapacitor electrodes.</P>
<p> [Full Paper]<br />Hui Teng Tan, Xianhong Rui, Wenhui Shi, Chen Xu, Hong Yu, Harry E. Hoster, Qingyu Yan<br /><i>ChemPlusChem</i>, Apr 24, 2013, DOI: 10.1002/cplu.201300095. <a href="http://dx.doi.org/10.1002/cplu.201300095">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300047">
<title>Extraction of Noble and Rare-Earth Metals from Aqueous Solutions by DNA Cross-Linked Hydrogels</title>
<link>http://dx.doi.org/10.1002/cplu.201300047</link>
<dc:creator>Yuko Maeda, Anatoly Zinchenko, Larisa I. Lopatina, Vladimir G. Sergeyev, Shizuaki Murata</dc:creator>
<dc:date>2013-04-22T16:22+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300047.gif" width="447" height="87" alt="Extraction of Noble and Rare-Earth Metals from Aqueous Solutions by DNA Cross-Linked Hydrogels" title="Extraction of Noble and Rare-Earth Metals from Aqueous Solutions by DNA Cross-Linked Hydrogels" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Treasure trove</B>: A method for the extraction of noble and rare-earth metals by a DNA cross-linked hydrogel, based on high DNA affinity to these elements, is described (see picture). The hydrogel is promising in applications for metal accumulation and recycling.</P>
<p> [Communication]<br />Yuko Maeda, Anatoly Zinchenko, Larisa I. Lopatina, Vladimir G. Sergeyev, Shizuaki Murata<br /><i>ChemPlusChem</i>, Apr 22, 2013, DOI: 10.1002/cplu.201300047. <a href="http://dx.doi.org/10.1002/cplu.201300047">Read article.</a></p> ]]>
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</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/19069.en.html">
<title>VIP: Liquid Phase Isobutane/2-Butene Alkylation Using Hydrogen-Chloride-Promoted Lewis Acidic Ionic Liquids</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/19069.en.html</link>
<dc:date>2013-04-19T00:00:00+02:00</dc:date>
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<![CDATA[<!-- module_2 --><p>F. P&#xF6;hlmann, L. Schilder, W. Korth, A. Jess*</p><p>In isobutane/butene alkylation, chloroaluminate ionic liquid catalysts (CAIL) ([BMIM]Cl/AlCl<sub>3</sub>, <i>x</i><sub>AlCl3</sub>=0.64) deactivate fast with time on stream with respect to activity and selectivity. Hence, it is crucial to find promising co-catalysts to stop the deactivation process. So, the effect of anhydrous hydrogen chloride gas (HCl) was studied in a batch reactor. This gaseous co-catalyst leads to an increased reaction rate and improves the yield of trimethylpentanes, the primarily desired high-octane compounds of alkylation. Moreover, already deactivated CAIL catalysts are reactivated by gaseous HCl. As a consequence the deactivation of the CAIL catalyst can be suppressed completely.</p><!-- DOI: 10.1002/cplu.201300035-->]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300067">
<title>Water-Soluble Palladium Click Chelating Complex: An Efficient and Reusable Precatalyst for Suzuki–Miyaura and Hiyama Reactions in Water</title>
<link>http://dx.doi.org/10.1002/cplu.201300067</link>
<dc:creator>Fanzhen Kong, Chunshan Zhou, Jinyun Wang, Zhangyu Yu, Ruihu Wang</dc:creator>
<dc:date>2013-04-18T16:09+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300067.gif" width="288" height="165" alt="Water-Soluble Palladium Click Chelating Complex: An Efficient and Reusable Precatalyst for Suzuki&ndash;Miyaura and Hiyama Reactions in Water" title="Water-Soluble Palladium Click Chelating Complex: An Efficient and Reusable Precatalyst for Suzuki&ndash;Miyaura and Hiyama Reactions in Water" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>In complete control</B>: A water-soluble palladium(II) click chelating complex serves as an efficient precursor for the formation of palladium nanoparticles (NPs; see picture). Excellent catalytic performances are achieved in Suzuki&ndash;Miyaura and Hiyama cross-coupling reactions in water.</P>
<p> [Full Paper]<br />Fanzhen Kong, Chunshan Zhou, Jinyun Wang, Zhangyu Yu, Ruihu Wang<br /><i>ChemPlusChem</i>, Apr 18, 2013, DOI: 10.1002/cplu.201300067. <a href="http://dx.doi.org/10.1002/cplu.201300067">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300068">
<title>Physical Properties and Structural Characterization of Ionic Liquids and Solid Electrolytes Utilizing the Carbamoylcyano(nitroso)methanide Anion</title>
<link>http://dx.doi.org/10.1002/cplu.201300068</link>
<dc:creator>Judith Janikowski, Mohd R. Razali, Craig M. Forsyth, Kate M. Nairn, Stuart R. Batten, Douglas R. MacFarlane, Jennifer M. Pringle</dc:creator>
<dc:date>2013-04-16T15:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300068.gif" width="274" height="119" alt="Physical Properties and Structural Characterization of Ionic Liquids and Solid Electrolytes Utilizing the Carbamoylcyano(nitroso)methanide Anion" title="Physical Properties and Structural Characterization of Ionic Liquids and Solid Electrolytes Utilizing the Carbamoylcyano(nitroso)methanide Anion" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Plastic fantastic</B>: The first use of the carbamoylcyano(nitroso)methanide anion for the synthesis of ionic liquids produces crystal structures that depend strongly on the nature of the cation. The organic ionic plastic crystals made using this anion display good solid-state ionic conductivities, consistent with the increasing interest in this type of material as new solid-state electrolytes.</P>
<p> [Full Paper]<br />Judith Janikowski, Mohd R. Razali, Craig M. Forsyth, Kate M. Nairn, Stuart R. Batten, Douglas R. MacFarlane, Jennifer M. Pringle<br /><i>ChemPlusChem</i>, Apr 16, 2013, DOI: 10.1002/cplu.201300068. <a href="http://dx.doi.org/10.1002/cplu.201300068">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300046">
<title>Preparation and Separation of Telechelic Carborane-Containing Poly(ethylene glycol)s</title>
<link>http://dx.doi.org/10.1002/cplu.201300046</link>
<dc:creator>Pavel Matejíček, Mariusz Uchman, Martin Lepšík, Martin Srnec, Jiří Zedník, Petr Kozlík, Kveta Kalíková</dc:creator>
<dc:date>2013-04-16T15:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300046.gif" width="215" height="124" alt="Preparation and Separation of Telechelic Carborane-Containing Poly(ethylene glycol)s" title="Preparation and Separation of Telechelic Carborane-Containing Poly(ethylene glycol)s" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Off the PEG</B>: The first example of thiol/ene coupling of carboranes leads to telechelic poly(ethylene glycol)s (PEGs, see figure). The radical stability and the reaction mechanism have been checked by quantum chemical calculations. The raw products are separated by advanced chromatography techniques.</P>
<p> [Full Paper]<br />Pavel Matej&#xED;&#x10D;ek, Mariusz Uchman, Martin Lep&#x161;&#xED;k, Martin Srnec, Ji&#x159;&#xED; Zedn&#xED;k, Petr Kozl&#xED;k, Kveta Kal&#xED;kov&#xE1;<br /><i>ChemPlusChem</i>, Apr 16, 2013, DOI: 10.1002/cplu.201300046. <a href="http://dx.doi.org/10.1002/cplu.201300046">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300092">
<title>Experimental and Theoretical Studies on the Controlled Synthesis of Alkali-Metal-Doped Rare-Earth Oxysulfide Nanocrystals</title>
<link>http://dx.doi.org/10.1002/cplu.201300092</link>
<dc:creator>Tao Zhang, Jun Gu, Yi Ding, Ya-Wen Zhang, Chun-Hua Yan</dc:creator>
<dc:date>2013-04-16T15:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300092.gif" width="167" height="168" alt="Experimental and Theoretical Studies on the Controlled Synthesis of Alkali-Metal-Doped Rare-Earth Oxysulfide Nanocrystals" title="Experimental and Theoretical Studies on the Controlled Synthesis of Alkali-Metal-Doped Rare-Earth Oxysulfide Nanocrystals" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Making a difference</B>: The doping alkali metal (Li, Na, K) was demonstrated to affect the size, morphology, composition, crystallinity, and luminescence properties of RE<sub>2</sub>O<sub>2</sub>S (RE=rare earth) ultrathin nanoplates (see figure) synthesized through thermolysis of metal acetylacetonates in hot surfactant in the presence of sublimed sulfur, as confirmed by both controlled experiments and first-principles calculations.</P>
<p> [Full Paper]<br />Tao Zhang, Jun Gu, Yi Ding, Ya-Wen Zhang, Chun-Hua Yan<br /><i>ChemPlusChem</i>, Apr 16, 2013, DOI: 10.1002/cplu.201300092. <a href="http://dx.doi.org/10.1002/cplu.201300092">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300091">
<title>Dual Control of Interparticle Forces in Assembly of Gold Nanoparticles</title>
<link>http://dx.doi.org/10.1002/cplu.201300091</link>
<dc:creator>Bo Hu, Xian Cao, Peng Zhang</dc:creator>
<dc:date>2013-04-16T15:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300091.gif" width="437" height="135" alt="Dual Control of Interparticle Forces in Assembly of Gold Nanoparticles" title="Dual Control of Interparticle Forces in Assembly of Gold Nanoparticles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Dual control</B> on the self-assembly process of gold nanoparticles by two factors, thiol-containing biomolecules and ionic strength of dielectric medium, has been developed, resulting in the collective effects and an interesting quasi-stable state (see figure).</P>
<p> [Full Paper]<br />Bo Hu, Xian Cao, Peng Zhang<br /><i>ChemPlusChem</i>, Apr 16, 2013, DOI: 10.1002/cplu.201300091. <a href="http://dx.doi.org/10.1002/cplu.201300091">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300015">
<title>Nickel Phosphite Superstructures Assembled by Nanotubes: Original Application for Effective Electrode Materials of Supercapacitors</title>
<link>http://dx.doi.org/10.1002/cplu.201300015</link>
<dc:creator>Huan Pang, Chengzhen Wei, Yahui Ma, Shanshan Zhao, Guochang Li, Jiangshan Zhang, Jing Chen, Sujuan Li</dc:creator>
<dc:date>2013-04-16T15:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300015.gif" width="157" height="157" alt="Nickel Phosphite Superstructures Assembled by Nanotubes: Original Application for Effective Electrode Materials of Supercapacitors" title="Nickel Phosphite Superstructures Assembled by Nanotubes: Original Application for Effective Electrode Materials of Supercapacitors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The bigger the better</B>: Nickel phosphite superstructures (see picture) assembled by nanotubes are successfully applied as electrochemical supercapacitors with good specific capacitances (1876&nbsp;F&nbsp;g<SUP>&minus;1</SUP> at 0.625&nbsp;A&nbsp;g<SUP>&minus;1</SUP>), good rate capabilities, and excellent cycling properties (95&nbsp;% of the initial specific capacitance at 6.25&nbsp;A&nbsp;g<SUP>&minus;1</SUP> after 2000&nbsp;cycles).</P>
<p> [Full Paper]<br />Huan Pang, Chengzhen Wei, Yahui Ma, Shanshan Zhao, Guochang Li, Jiangshan Zhang, Jing Chen, Sujuan Li<br /><i>ChemPlusChem</i>, Apr 16, 2013, DOI: 10.1002/cplu.201300015. <a href="http://dx.doi.org/10.1002/cplu.201300015">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300090">
<title>Micro- and Mesoporous Polycyanurate Networks Based on Triangular Units</title>
<link>http://dx.doi.org/10.1002/cplu.201300090</link>
<dc:creator>Hao Yu, Changjiang Shen, Zhonggang Wang</dc:creator>
<dc:date>2013-04-15T14:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300090.gif" width="212" height="142" alt="Micro- and Mesoporous Polycyanurate Networks Based on Triangular Units" title="Micro- and Mesoporous Polycyanurate Networks Based on Triangular Units" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Three sides to the story</B>: Microporous and mesoporous polycyanurate networks were synthesized by means of thermal self-cyclotrimerization from two triangular cyanate resin monomers, 1,3,5-tri(4-cyanatophenyl)benzene and 1,3,5-tricyanatobenzene, respectively (see scheme). The adsorptions of CO<sub>2</sub>, H<sub>2</sub>, benzene, <I>n</I>-hexane, and water vapors were investigated.</P>
<p> [Full Paper]<br />Hao Yu, Changjiang Shen, Zhonggang Wang<br /><i>ChemPlusChem</i>, Apr 15, 2013, DOI: 10.1002/cplu.201300090. <a href="http://dx.doi.org/10.1002/cplu.201300090">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300017">
<title>One-Pot Synthesis of Palladium Hollow Nanospheres and Their Enhanced Electrocatalytic Properties</title>
<link>http://dx.doi.org/10.1002/cplu.201300017</link>
<dc:creator>Liu Yang, Zhicheng Li, Xiaofeng Lu, Yan Tong, Guangdi Nie, Ce Wang</dc:creator>
<dc:date>2013-04-15T14:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300017.gif" width="404" height="106" alt="One-Pot Synthesis of Palladium Hollow Nanospheres and Their Enhanced Electrocatalytic Properties" title="One-Pot Synthesis of Palladium Hollow Nanospheres and Their Enhanced Electrocatalytic Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>One for all</B>: Pd hollow nanospheres (PHNs) have been synthesized by a one-pot route using a RB-PdCl<sub>4</sub><SUP>2&minus;</SUP> complex (RB=rhodamine&nbsp;B) formed by an electrostatic interaction as sacrificial template (see scheme). The as-prepared materials exhibit enhanced electrocatalytic properties in fuel cells.</P>
<p> [Full Paper]<br />Liu Yang, Zhicheng Li, Xiaofeng Lu, Yan Tong, Guangdi Nie, Ce Wang<br /><i>ChemPlusChem</i>, Apr 15, 2013, DOI: 10.1002/cplu.201300017. <a href="http://dx.doi.org/10.1002/cplu.201300017">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201300041">
<title>Free-Standing Ultrathin Cobalt Nanosheets Synthesized by Means of In Situ Reduction and Interface-Directed Assembly and Their Magnetic Properties</title>
<link>http://dx.doi.org/10.1002/cplu.201300041</link>
<dc:creator>Shichao Du, Zhiyu Ren, Yang Qu, Jian-qiang Wang, Lingjun Kong, Keying Shi, Buhe Bateer, Honggang Fu</dc:creator>
<dc:date>2013-04-12T08:37+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cplu201300041.gif" width="436" height="125" alt="Free-Standing Ultrathin Cobalt Nanosheets Synthesized by Means of In Situ Reduction and Interface-Directed Assembly and Their Magnetic Properties" title="Free-Standing Ultrathin Cobalt Nanosheets Synthesized by Means of In Situ Reduction and Interface-Directed Assembly and Their Magnetic Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Making a stand</B>: By means of in situ reduction and self-assembly at an unconventional liquid&ndash;liquid interface, free-standing ultrathin cobalt nanosheets (CoNs) consisting of nanosized Co clusters were successfully synthesized (see figure). The as-prepared CoNs display ferromagnetic behavior and a large thermal irreversibility. This strategy has been used also in the synthesis of Fe and Ni nanosheets.</P>
<p> [Communication]<br />Shichao Du, Zhiyu Ren, Yang Qu, Jian-qiang Wang, Lingjun Kong, Keying Shi, Buhe Bateer, Honggang Fu<br /><i>ChemPlusChem</i>, Apr 12, 2013, DOI: 10.1002/cplu.201300041. <a href="http://dx.doi.org/10.1002/cplu.201300041">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/18849.en.html">
<title>Poster Prize at SupraChem 2013</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/18849.en.html</link>
<dc:date>2013-02-18T00:00:00+01:00</dc:date>
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<![CDATA[<!-- module_2 --><p>Wiley-VCH was pleased to sponsored the best poster prize at <a href="http://www.uni-muenster.de/Suprachem2013/index.php">SupraChem 2013</a> held in M&#xFC;nster last week. The worthy winner is Malte Hansen from Burkhard K&#xF6;nig&#x92;s group based at the University of Regensburg for the poster titled &#x93;Photocatalytic Water Oxidation with Ruthenium-Complex-Functionalized Vesicles&#x94;. Congratulations to the winner.</p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/18372.en.html">
<title>Poster Prizes at ElecMol′12</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/18372.en.html</link>
<dc:date>2012-12-13T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/elecmol.png" alt="Poster Prizes at ElecMol&#x2032;12" align="left" hspace="5" vspace="5" border="0" /></p><!-- module_2 --><p>Wiley-VCH was pleased to sponsored eight poster prizes at the 6th International Meeting on Molecular Electronics (<a href="http://www.elecmol.com/" target="_blank">ElecMol&#x2032;12</a>), which was recently held in Grenoble (France). The prizes were awarded by the <i>ChemPubSoc Europe</i> journals <i>ChemPlusChem</i>, <i>Chemistry-A European Journal</i>, and <i>ChemPhysChem</i>.</p><p>The worthy winners  singled out by the jury were <b>Tiphaine Bourgeteau</b> from Serge Palacin&#x92;s group, <b>Vincent Derycke</b>, <b>Sebastien Haar</b> from Paolo Samori&#x92;s group, <b>Dipankar Kalita</b> from Nedjma Bendiab&#x92;s group, <b>Kazuaki Hiroki</b>, <b>Giuseppe Tarabella</b> from Salvatore Iannota&#x92;s group, <b>Tino Wagner</b> from Andreas Stemmer&#x92;s group, and <b>Silvia Zanetti</b> from Bernard Doudin&#x92;s group. Congratulations to all the winners.</p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/17811.en.html">
<title>EUCheMS Lectureship for Nazario Martín</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/17811.en.html</link>
<dc:date>2012-08-22T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/Martin.png" alt="EUCheMS Lectureship for Nazario Mart&#xED;n" align="left" hspace="5" vspace="5" border="0" /></p>Nazario Mart&#xED;n (Universidad Complutense de Madrid and the Madrid Institute for Advanced Studies in Nanoscience, IMDEA) has been awarded a 2012 EuCheMS Lectureship. This award is given every year to outstanding chemists from European countries and aims to promote scientific cooperation among chemists in Europe. His lecture is expected to be delivered at the 2013 European Symposium on Organic Chemistry.</p><p>Nazario Mart&#xED;n studied at the Universidad Complutense de Madrid (UCM), where he earned a PhD in 1984 and was mentored by Carlos Seoane and Jos&#xE9; L. Soto. After a year working at the pharmaceutical company Juste S.A.Q.F., he returned to the UCM in 1985 and was promoted to associate professor in 1989 and to full professor in 2001. Mart&#xED;n was President of the Spanish Royal Society of Chemistry (RSEQ) from 2006--2012, and he contributed to the creation of the IMDEA, where he has been Vice-Director since 2007. Mart&#xED;n&#xB4;s research interests include the molecular and supramolecular chemistry of carbon nanostructures involving electron-transfer processes and photovoltaics. His most recent publication outlines the synthesis and electronic properties of <a href="http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201200115/abstract" target="_blank">&#x3C0;-extended tetrathiafulvalenes</a>. Mart&#xED;n is on the International Advisory Boards of <i>ChemPlusChem</i> and <i>ChemSusChem</i>.</p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cplu.201190001">
<title>ChemPlusChem – A Genuinely Multidisciplinary Journal of Chemistry &amp; Materials</title>
<link>http://dx.doi.org/10.1002/cplu.201190001</link>
<dc:date>2012-05-21T09:33+05:00</dc:date>
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<![CDATA[ <p></p><p> [Call for Papers]<br /><br /><i>ChemPlusChem</i>, May 21, 2012, DOI: 10.1002/cplu.201190001. <a href="http://dx.doi.org/10.1002/cplu.201190001">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/17544.en.html">
<title>The Launch of ChemPlus Chem – The Board's View</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506/homepage/news/17544.en.html</link>
<dc:date>2011-10-09T00:00:00+02:00</dc:date>
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<![CDATA[<p><img height="80" alt="" src="http://www.wiley-vch.de/vch/journals/2688/team/hocek.jpg" style="float:left;" width="50" /><i>ChemPlusChem</i> is the first genuinely multidisciplinary chemistry journal. Editorial Board Co-Chairman <b>Michal Hocek</b> explains: "Research in chemical and molecular sciences is becoming more and more complex and inter- and multidisciplinary and also its impact in physical, biological and material sciences is rapidly growing. Typically nowadays projects involve synthesis of compounds, catalysis, spectroscopy, crystallography, biological evaluations, physical measurements, and/or material studies".</p><p style="clear:both;margin-top:10px;"><img src="http://www.wiley-vch.de/vch/journals/2688/team/driess.jpg" alt="" width="50" style="float:left;" border="0" height="80" />"To be an active part of crossdisciplinary research can be a tremendous &#x27;catalyst&#x27; to boost creativity in chemistry and in turn to convince colleagues from other disciplines to interconnect with the beauty and power of chemistry," said <b>Matthias Driess</b> from the Technische Universit&#xE4;t Berlin and Co-chair of <i>ChemPlusChem</i>. "The launch of <i>ChemPlusChem</i> will be of benefit to all crossdisciplinary researchers and will ensure that fruitful scientific collaborations keep heading in the right direction."</p> <p style="clear:both;margin-top:10px;">Co-Chair <img src="http://www.wiley-vch.de/vch/journals/2688/team/sommerdijk.jpg" alt="" width="50" style="float:left;" border="0" height="80" /><b>Nico Sommerdijk</b> (Technische Universiteit Eindhoven) adds: "Great inventions almost always are the product of multidisciplinary research! There is a great need for a chemistry journal that is able to review and publish creative studies that bring together contributions from many areas of research. I think <i>ChemPlusChem</i> will be that journal." </p><p style="clear:both;margin-top:10px;"><a href="http://dx.doi.org/10.1002/cplu.201100057">Learn more</a> from the Editorial in the inaugural issue.</p><p><a href="http://www.wiley.com/trackthrough?urlcode=468090">Enjoy free trial access</a> until September.</p>]]>
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