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<title>News from European Journal of Inorganic Chemistry</title>
<link>http://doi.wiley.com/10.1002/(ISSN)1099-0682</link>
<description>News from the journal European Journal of Inorganic Chemistry</description>
<dc:language>en</dc:language>
<dc:rights>Copyright 2011, Wiley-VCH Verlag GmbH &#x26;amp; Co. KGaA</dc:rights>
<dc:date>2013-05-24T01:50:49Z</dc:date>
<dc:publisher>Wiley-VCH</dc:publisher>
<dc:creator>info@wiley-vch.de</dc:creator>
<dc:subject>Chemistry</dc:subject>
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<title>EurBest in EurJIC: Stabilized Germylenes Based on Diethylenetriamines and Related Diamines: Synthesis, Structures, and Chemical Properties</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18153.en.html</link>
<dc:date>2012-10-31T00:00:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200363.jpg" alt="EurBest in EurJIC: Stabilized Germylenes Based on Diethylenetriamines and Related Diamines: Synthesis, Structures, and Chemical Properties" align="left" hspace="5" vspace="5" border="0" /></p>A series of novel, low-valent germanium compounds have been obtained by the reaction of Ge[N(SiMe<sub>3</sub>)<sub>2</sub>]<sub>2</sub> with various diamines or by the metathesis reaction of [GeCl2⋅dioxane] with lithium amides. The oxidative insertion, [1+4] cycloaddition, and oxidation reactions of the synthesized germylenes were investigated. All the synthesized germylenes are monomeric.<br><br>Mengmeng Huang, Marina M. Kireenko, Kirill V. Zaitsev, Yuri F. Oprunenko, Andrei V. Churakov, Judith A. K. Howard, Elmira Kh. Lermontova, Denis Sorokin, Thomas Linder, Jörg Sundermeyer, Sergey S. Karlov and Galina S. Zaitseva<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200363">10.1002/ejic.201200363</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18152.en.html">
<title>EurBest in EurJIC: Tellurium&#x96;Nitrogen &#x3C0;-Heterocyclic Chemistry &#x96; Synthesis, Structure, and Reactivity Toward Halides and Pyridine of 3,4-Dicyano-1,2,5-telluradiazole</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18152.en.html</link>
<dc:date>2012-10-31T00:10:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200376.jpg" alt="EurBest in EurJIC: TelluriumNitrogen π-Heterocyclic Chemistry  Synthesis, Structure, and Reactivity Toward Halides and Pyridine of 3,4-Dicyano-1,2,5-telluradiazole" align="left" hspace="5" vspace="5" border="0" /></p>3,4-Dicyano-1,2,5-telluradiazole and its adducts with pyridine, chloride, and bromide ions have been isolated, and the supramolecular structures investigated by X-ray crystallography.<br><br>Nikolay A. Semenov, Nikolay A. Pushkarevsky, Jens Beckmann, Pamela Finke, Enno Lork, Rüdiger Mews, Irina Yu. Bagryanskaya, Yuri V. Gatilov, Sergey N. Konchenko, Vladimir G. Vasiliev and Andrey V. Zibarev<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200376">10.1002/ejic.201200376</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18085.en.html">
<title>EurBest in EurJIC: Zn-Mediated Synthesis of 3-Substituted Indoles Using a Three-Component Reaction Approach</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18085.en.html</link>
<dc:date>2012-10-19T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200150.jpg" alt="EurBest in EurJIC: Zn-Mediated Synthesis of 3-Substituted Indoles Using a Three-Component Reaction Approach" align="left" hspace="5" vspace="5" border="0" /></p>The Zn(salphen)-mediated synthesis of 3-substituted indoles by using a multicomponent reaction approach is reported. The reaction parameters were investigated and the selectivity for the 3-CR product was examined under various conditions. Selectivity for the target compound is significantly compromised by side-product formation due to in situ reaction of the intermediate species with malononitrile, which affords N-heterocyclic structures.<br><br>Daniele Anselmo, Eduardo C. Escudero-Adán, Marta Martínez Belmonte and Arjan W. Kleij<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200150">10.1002/ejic.201200150</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18084.en.html">
<title>EurBest in EurJIC: The Trifluoromethyl Group in Transition Metal Chemistry</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18084.en.html</link>
<dc:date>2012-10-19T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200620.jpg" alt="EurBest in EurJIC: The Trifluoromethyl Group in Transition Metal Chemistry" align="left" hspace="5" vspace="5" border="0" /></p>Definitely different: As the chemistry of trifluoromethylTM derivatives continues to develop, it becomes clearer that methyl and trifluoromethyl ligands (CH3 vs. CF3) exhibit more differences than similarities in their chemical behavior.<br><br>M. Angeles García-Monforte, Sonia Martínez-Salvador and Babil Menjón<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200620">10.1002/ejic.201200620</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18016.en.html">
<title>EurBest in EurJIC: Transition-Metal Complexes Containing the Dinucleating Tetra-N-Dentate 3,5-Bis(2-pyridyl)pyrazole (Hbpp) Ligand &#x96; A Robust Scaffold for Multiple Applications Including the Catalytic Oxidation of Water to Molecular Oxygen</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18016.en.html</link>
<dc:date>2012-10-09T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200661.jpg" alt="EurBest in EurJIC: Transition-Metal Complexes Containing the Dinucleating Tetra-N-Dentate 3,5-Bis(2-pyridyl)pyrazole (Hbpp) Ligand  A Robust Scaffold for Multiple Applications Including the Catalytic Oxidation of Water to Molecular Oxygen" align="left" hspace="5" vspace="5" border="0" /></p>A large diversity of transition-metal complexes bearing the dinucleating tetra-<i>N</i>-dentate ligand 3,5-bis(2-pyridyl)pyrazole (Hbpp) is described. Their applications in the field of catalysis as hydrogen-transfer, epoxidation, and water-oxidation catalysts are highlighted. Further, their applications in fundamental coordination chemistry are also discussed. <br><br>Jordi García-Antón, Roger Bofill, Lluís Escriche, Antoni Llobet and Xavier Sala<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200661">10.1002/ejic.201200661</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18015.en.html">
<title>EurBest in EurJIC: Crystalline Iron Oxohalide Nanotube Pea Pods</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/18015.en.html</link>
<dc:date>2012-10-09T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200205.jpg" alt="EurBest in EurJIC: Crystalline Iron Oxohalide Nanotube Pea Pods" align="left" hspace="5" vspace="5" border="0" /></p>Isostructural compounds Fe<sub>7</sub>Sb<sub>3</sub>(PO<sub>4</sub>)<sub>3</sub>O<sub>6</sub>Cl<sub>3</sub> and Fe<sub>7</sub>Sb<sub>3</sub>(PO<sub>4</sub>)<sub>3</sub>O<sub>6</sub>Br<sub>3</sub> are the first iron phosphates containing Sb<sup>III</sup>. Tubular Fe<sub>7</sub>(PO<sub>4</sub>)<sub>3</sub>O<sub>6</sub>X<sub>3</sub> units (X = Cl, Br) are linked by SbO<sub>4</sub> groups to build up a 3D framework. The Fe atoms are arranged to resemble an armchair-type (3,3) nanotube.<br><br>Iwan Zimmermann, Mats Johnsson and Sven Lidin<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200205">10.1002/ejic.201200205</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17934.en.html">
<title>EurBest in EurJIC: PtII and PdII Complexes with a trans-Chelating Bis(pyridyl) Ligand</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17934.en.html</link>
<dc:date>2012-09-18T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200442.jpg" alt="EurBest in EurJIC: PtII and PdII Complexes with a trans-Chelating Bis(pyridyl) Ligand" align="left" hspace="5" vspace="5" border="0" /></p>Pd<sup>II</sup> and Pt<sup>II</sup> complexes containing a <i>trans</i>-chelating bis(pyridyl) ligand bpib have been synthesised. The catalytic reactivity of bpib in Pd<sup>II</sup> for arene acetoxylation has been examined and compared with that of 2,2'-bipy. <br><br>Nan Wang, Theresa M. McCormick, Soo-Byung Ko and Suning Wang<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200442">10.1002/ejic.201200442</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17933.en.html">
<title>EurBest in EurJIC: Synthesis and Characterization of a (&#x3BC;-&#x3B7;2:&#x3B7;2-Peroxido)dicopper(II) Complex with N,N&#x27;,N&#x27;&#x27;-Triisopropyl-cis,cis-1,3,5-triaminocyclohexane (R3TACH, R = iPr): Selective Preparation of (&#x3BC;-&#x3B7;2:&#x3B7;2-Peroxido)dicopper(II) and Bis(&#x3BC;-oxido)dicopper(III) Species Regulated by Substituent Groups</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17933.en.html</link>
<dc:date>2012-09-18T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200228.jpg" alt="EurBest in EurJIC: Synthesis and Characterization of a (μ-η2:η2-Peroxido)dicopper(II) Complex with N,N',N''-Triisopropyl-cis,cis-1,3,5-triaminocyclohexane (R3TACH, R = iPr): Selective Preparation of (μ-η2:η2-Peroxido)dicopper(II) and Bis(μ-oxido)dicopper(III) Species Regulated by Substituent Groups" align="left" hspace="5" vspace="5" border="0" /></p>The selective preparation of (μ-η<sup>2</sup>:η<sup>2</sup>-peroxido)dicopper(II) and bis(μ-oxido)dicopper(III) species is regulated by the substituent groups of triaminocyclohexane derivative ligands. Their structural and spectroscopic features and reactivity are discussed. <br><br>Jun Matsumoto, Yuji Kajita and Hideki Masuda<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200228">10.1002/ejic.201200228</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17904.en.html">
<title>EurBest in EurJIC: The Simple Synthesis of Ferrocene Ligands from a Practitioner&#x27;s Perspective</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17904.en.html</link>
<dc:date>2012-09-11T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200540.jpg" alt="EurBest in EurJIC: The Simple Synthesis of Ferrocene Ligands from a Practitioner's Perspective" align="left" hspace="5" vspace="5" border="0" /></p>An overview is given on the synthesis of key precursors for use as ligands or building blocks in ferrocene chemistry. The review is a personal account detailing the reasons for synthetic routes that have been developed over 30 years. The focus is on the preparation of ferrocenylphosphanes; however, also included is a section on the preparation of compounds as precursors for material science. <br><br>Ian R. Butler<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200540">10.1002/ejic.201200540</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17903.en.html">
<title>EurBest in EurJIC: Spectroscopy and Photophysics in Cyclometalated RuII&#x96;Bis(bipyridyl) Complexes</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17903.en.html</link>
<dc:date>2012-09-11T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200460.jpg" alt="EurBest in EurJIC: Spectroscopy and Photophysics in Cyclometalated RuIIBis(bipyridyl) Complexes" align="left" hspace="5" vspace="5" border="0" /></p>Cyclometalated Ru<sup>II</sup> coordination compounds of the general formula [Ru(bpy)<sub>2</sub>(C∧N)]PF<sub>6</sub> {C∧N = 2-phenylpyridine (<b>1</b>), 2-(2,4-difluorophenyl)pyridine (<b>2</b>), 2-(4-methoxyphenyl)-5-methylpyridine (<b>3</b>), benzo[<i>h</i>]quinoline (<b>4</b>); bpy = 2,2'-bipyridine} have been synthesized, structurally and electrochemically characterized, and examined with spectroscopic techniques including ultrafast transient absorption. <br><br>Maria L. Muro-Small, James E. Yarnell, Catherine E. McCusker and Felix N. Castellano<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200460">10.1002/ejic.201200460</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17874.en.html">
<title>EurBest in EurJIC: Cavity Effect on Perrhenate Recognition by Polyammonium Cages</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17874.en.html</link>
<dc:date>2012-09-04T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200334.jpg" alt="EurBest in EurJIC: Cavity Effect on Perrhenate Recognition by Polyammonium Cages" align="left" hspace="5" vspace="5" border="0" /></p>The outstanding affinity of receptor <b>1</b>H<sub>6</sub><sup>6+</sup> towards ReO<sub>4</sub><sup></sup>, in an acidic water solution, opens new perspectives for the development of selective materials for the extraction and recovery of the perrhenate anion for clinical and environmental purposes. The formation of an inclusion complex, [<b>1</b>H<sub>6</sub>(ReO<sub>4</sub>)](CF<sub>3</sub>SO<sub>3</sub>)<sub>5</sub>, is confirmed by X-ray diffraction studies. <br><br>Valeria Amendola, Giancarla Alberti, Greta Bergamaschi, Raffaela Biesuz, Massimo Boiocchi, Stefania Ferrito and Franz-Peter Schmidtchen<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200334">10.1002/ejic.201200334</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17846.en.html">
<title>EurBest in EurJIC: Antiproliferative Activity of PtII Complexes with Carboxylated Phosphanes in Chelated or Ring-Opened Forms</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17846.en.html</link>
<dc:date>2012-08-29T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200282.jpg" alt="EurBest in EurJIC: Antiproliferative Activity of PtII Complexes with Carboxylated Phosphanes in Chelated or Ring-Opened Forms" align="left" hspace="5" vspace="5" border="0" /></p>The biological activity of four cisplatin-like Ptphosphane complexes has been tested. Some of the complexes can undergo intramolecular rearrangement by virtue of the functionalized phosphanes (fully opened/fully closed forms). The results show that only the opened forms exhibit moderate activity, which is substantially retained in the cisplatin-resistant cell lines. <br><br>Mauro Ravera, Elisabetta Gabano, Manuele Sardi, Elena Monti, Marzia B. Gariboldi and Domenico Osella<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200282">10.1002/ejic.201200282</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17845.en.html">
<title>EurBest in EurJIC: Coordination-Like Chemistry of Phosphinidenes by Phosphanes</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17845.en.html</link>
<dc:date>2012-08-29T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200273.jpg" alt="EurBest in EurJIC: Coordination-Like Chemistry of Phosphinidenes by Phosphanes" align="left" hspace="5" vspace="5" border="0" /></p>The coordination chemistry of neutral phosphane adducts of phosphinidenes (phosphanylidene-σ<sup>4</sup>-phosphoranes, also known as phospha-Wittig reagents, RP=PR<sub>3</sub>) is reviewed. <br><br>John D. Protasiewicz<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200273">10.1002/ejic.201200273</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17806.en.html">
<title>EurBest in EurJIC: pH-Dependent Imidazolato Bridge Formation in Dicopper Complexes: Magnetic, Electrochemical, and Catalytic Repercussions</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17806.en.html</link>
<dc:date>2012-08-21T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200167.jpg" alt="EurBest in EurJIC: pH-Dependent Imidazolato Bridge Formation in Dicopper Complexes: Magnetic, Electrochemical, and Catalytic Repercussions" align="left" hspace="5" vspace="5" border="0" /></p>The dicopper complexes of two dinucleating ligands undergo a strong antiferromagnetic coupling upon formation of an imidazolato bridge. UV/Vis and EPR spectroscopy as well as electrochemical studies confirmed the potentiometric solution speciation. <br><br>Inés Monte-Pérez, Ana M. Sosa, Sylvain Bernès, Núria Aliaga-Alcalde, Víctor M. Ugalde-Saldívar and Laura Gasque<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200167">10.1002/ejic.201200167</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17805.en.html">
<title>EurBest in EurJIC: Studies of the Electronic Properties of N-Heterocyclic Carbene Ligands in the Context of Homogeneous Catalysis and Bioorganometallic Chemistry</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17805.en.html</link>
<dc:date>2012-08-21T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200622.jpg" alt="EurBest in EurJIC: Studies of the Electronic Properties of N-Heterocyclic Carbene Ligands in the Context of Homogeneous Catalysis and Bioorganometallic Chemistry" align="left" hspace="5" vspace="5" border="0" /></p>Towards understanding the key attributes that define the influence of N-heterocyclic carbenes on catalysis, our efforts, involving combined experimental and computational approaches, in looking into a variety of catalytic and biomedical applications of these compounds are summarized. <br><br>Anuj Kumar and Prasenjit Ghosh<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200622">10.1002/ejic.201200622</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17764.en.html">
<title>EurBest in EurJIC: Layered Hydroxide&#x96;Porphyrin Hybrid Materials: Synthesis, Structure, and Properties</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17764.en.html</link>
<dc:date>2012-08-14T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200400.jpg" alt="EurBest in EurJIC: Layered HydroxidePorphyrin Hybrid Materials: Synthesis, Structure, and Properties" align="left" hspace="5" vspace="5" border="0" /></p>We provide a comprehensive overview of the synthesis and structural alignment of bulky porphyrin molecules in the interlayer space of layered hydroxideporphyrin hybrids. Emphasis is placed on the spectral and photophysical properties of intercalated porphyrins and phthalocyanines for photobactericidal purposes, catalysis, and sensing. <br><br>Jan Demel and Kamil Lang<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200400">10.1002/ejic.201200400</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17763.en.html">
<title>EurBest in EurJIC: Luminescence of ortho-Metalated Iridium Complexes Encapsulated in Zeolite Supercages by the Ship-in-a-Bottle Method</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17763.en.html</link>
<dc:date>2012-08-14T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200116.jpg" alt="EurBest in EurJIC: Luminescence of ortho-Metalated Iridium Complexes Encapsulated in Zeolite Supercages by the Ship-in-a-Bottle Method" align="left" hspace="5" vspace="5" border="0" /></p>Iridiumcarbon sigma bond formation in supercages of faujasite-type zeolites is achieved by using a microwave-assisted ship-in-a-bottle synthesis. The successive reaction of Ir<sup>III</sup> cations in the zeolite with two ligands leads to two types of complexes in the different supercages, and the emission from these Ir<sup>III</sup> complexes can be tuned in a range from blue to green. <br><br>Chen Xu, Dai Mochizuki, Yuta Hashimoto, Takehisa Honda, Yasunori Tsukahara, Tomohisa Yamauchi and Yuji Wada<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200116">10.1002/ejic.201200116</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17686.en.html">
<title>EurBest in EurJIC: A Comparative Study of Tricarbonylmanganese Photoactivatable CO Releasing Molecules (PhotoCORMs) by Using the Myoglobin Assay and Time-Resolved IR Spectroscopy</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17686.en.html</link>
<dc:date>2012-08-07T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200115.jpg" alt="EurBest in EurJIC: A Comparative Study of Tricarbonylmanganese Photoactivatable CO Releasing Molecules (PhotoCORMs) by Using the Myoglobin Assay and Time-Resolved IR Spectroscopy" align="left" hspace="5" vspace="5" border="0" /></p>CO-releasing molecules are interesting therapeutic agents that can deliver and release CO upon stimulation. Light triggers the release of CO in different complexes [LMn(CO)<sub>3</sub>]<sup>+</sup>, where L is an <i>N,N,N</i> ligand. Although different amounts of CO released per complex are observed by myoglobin assay, IR spectroscopic investigation of their solutions indicates loss of all CO ligands. <br><br>Wilhelm Huber, Rolf Linder, Johanna Niesel, Ulrich Schatzschneider, Bernhard Spingler and Peter C. Kunz<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200115">10.1002/ejic.201200115</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17678.en.html">
<title>EurBest in EurJIC: Rhenium(I) and Technetium(I) Tricarbonyl Complexes with [NSO]-Type Chelators: Synthesis, Structural Characterization, and Radiochemistry</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17678.en.html</link>
<dc:date>2012-08-07T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200056.jpg" alt="EurBest in EurJIC: Rhenium(I) and Technetium(I) Tricarbonyl Complexes with [NSO]-Type Chelators: Synthesis, Structural Characterization, and Radiochemistry" align="left" hspace="5" vspace="5" border="0" /></p><i>fac</i>-[Re(NSO)(CO)<sub>3</sub>] complexes were synthesized with varying chelate ring size and geometry. The order of complex formation preference is: linear (6,5-membered rings) > tripodal (6,5,7-membered rings) > linear (two six-membered rings). The analogous <i>fac</i>-[<sup>99m</sup>Tc(NSO)(CO)<sub>3</sub>] complexes were prepared in high yield and were stable in solution. <br><br>George Makris, Ourania Karagiorgou, Dionysia Papagiannopoulou, Angeliki Panagiotopoulou, Catherine P. Raptopoulou, Aris Terzis, Vassilis Psycharis, Maria Pelecanou, Ioannis Pirmettis and Minas S. Papadopoulos<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200056">10.1002/ejic.201200056</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17646.en.html">
<title>EurBest in EurJIC: Heterogeneous Bifunctional Metal/Acid Catalysts for Selective Chemical Processes</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17646.en.html</link>
<dc:date>2012-07-31T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200529.jpg" alt="EurBest in EurJIC: Heterogeneous Bifunctional Metal/Acid Catalysts for Selective Chemical Processes" align="left" hspace="5" vspace="5" border="0" /></p>Heterogeneous bifunctional catalysts containing metal and acid sites have great potential for the development of greener production processes, particularly for the preparation of fine chemicals. This review highlights the recent advancements and the most representative examples in the field. <br><br>Pierluigi Barbaro, Francesca Liguori, Noemi Linares and Carmen Moreno Marrodan<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200529">10.1002/ejic.201200529</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17628.en.html">
<title>EurBest in EurJIC: A Bombesin Copper Complex Based on a Bifunctional Cyclam Derivative</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17628.en.html</link>
<dc:date>2012-07-31T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200049.jpg" alt="EurBest in EurJIC: A Bombesin Copper Complex Based on a Bifunctional Cyclam Derivative" align="left" hspace="5" vspace="5" border="0" /></p>A new bombesin copper complex based on a bifunctional cyclam derivative was synthesized, characterized, and evaluated for its binding affinity to bombesin receptors through in vitro cell assays with PC-3 cells. <br><br>Christos C. Liolios, Christos Zikos, Eirini Fragogeorgi, Dimitra Benaki, Maria Pelecanou, Ioannis Pirmettis, Nikolaos Ioannidis, Yiannis Sanakis, Catherine P. Raptopoulou, Vassilis Psycharis, Aris Terzis, Frédéric Boschetti, Minas S. Papadopoulos, Gregory Sivolapenko and Alexandra D. Varvarigou<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200049">10.1002/ejic.201200049</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17631.en.html">
<title>EurBest in EurJIC: Developments in the Coordination Chemistry of Europium(II)</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17631.en.html</link>
<dc:date>2012-07-24T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200159.jpg" alt="EurBest in EurJIC: Developments in the Coordination Chemistry of Europium(II)" align="left" hspace="5" vspace="5" border="0" /></p>This review describes Eu<sup>2+</sup>-containing complexes reported in the 21st century with focus on the synthesis, reactivity, and application of these complexes. <br><br>Joel Garcia and Matthew J. Allen<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200159">10.1002/ejic.201200159</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17627.en.html">
<title>EurBest in EurJIC: Titration of Zr3(&#x3BC;-OH) Hydroxy Groups at the Cornerstones of Bulk MOF UiO-67, [Zr6O4(OH)4(biphenyldicarboxylate)6], and Their Reaction with [AuMe(PMe3)]</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17627.en.html</link>
<dc:date>2012-07-24T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200033.jpg" alt="EurBest in EurJIC: Titration of Zr3(μ-OH) Hydroxy Groups at the Cornerstones of Bulk MOF UiO-67, [Zr6O4(OH)4(biphenyldicarboxylate)6], and Their Reaction with [AuMe(PMe3)]" align="left" hspace="5" vspace="5" border="0" /></p>Thermally stable MOF UiO-67, [Zr<sub>6</sub>O<sub>4</sub>(OH)<sub>4</sub>(bpdc)<sub>6</sub>], is well-behaved chemically in the bulk: Cornerstone (μ<sub>3</sub>-OH) hydroxy groups react quantitatively with MeMgBr with stoichiometric release of methane. Post-synthetic modification with [AuMe(PMe<sub>3</sub>)] results in partial covalent grafting of the Au<sub>I</sub> center onto the cornerstone hydroxy groups. <br><br>Cherif Larabi and Elsje Alessandra Quadrelli<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200033">10.1002/ejic.201200033</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17487.en.html">
<title>EurBest in EurJIC: Metal Complexation of a D-Ribose-Based Ligand Decoded by Experimental and Theoretical Studies</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17487.en.html</link>
<dc:date>2012-06-26T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200322.jpg" alt="EurBest in EurJIC: Metal Complexation of a D-Ribose-Based Ligand Decoded by Experimental and Theoretical Studies" align="left" hspace="5" vspace="5" border="0" /></p>A new sugar-derived ligand, with its coordination site embedded in a pyranoside cycle in the chair conformation, has been designed. Its transition-metal complexes were characterized by experimental and complexation methods and revealed a dramatic impact of the preorganization and complementarity of the carbohydrate scaffold on the metal binding. <br><br>Federico Cisnetti, Jean-Didier Maréchal, Magali Nicaise, Régis Guillot, Michel Desmadril, François Lambert and Clotilde Policar<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200322">10.1002/ejic.201200322</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17486.en.html">
<title>EurBest in EurJIC: Hybrid Cage Compounds with Organic and Inorganic Building Blocks</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17486.en.html</link>
<dc:date>2012-06-26T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200384.jpg" alt="EurBest in EurJIC: Hybrid Cage Compounds with Organic and Inorganic Building Blocks" align="left" hspace="5" vspace="5" border="0" /></p>Empty and filled hybrid cage compounds with siloxane as well as ether units between four phosphorus bridge-head atoms were obtained from the deprotonation of the cyclic siloxadiphosphane [O(Si<i>i</i>Pr<sub>2</sub>)<sub>2</sub>PH]<sub>2</sub> and subsequent reaction with diiodo ethers. These compounds show very different coordination behaviour depending on the length of the ether chain and the metal cation used. <br><br>Andreas Kracke, Carsten von Hänisch and Nina Kramer<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200384">10.1002/ejic.201200384</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17469.en.html">
<title>EurBest in EurJIC: Microwave-Assisted Synthesis of (N-Heterocyclic carbene)MCl Complexes of Group 11 Metals</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17469.en.html</link>
<dc:date>2012-06-19T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200248.jpg" alt="EurBest in EurJIC: Microwave-Assisted Synthesis of (N-Heterocyclic carbene)MCl Complexes of Group 11 Metals" align="left" hspace="5" vspace="5" border="0" /></p>The use of microwave heating for the direct synthesis of (NHC)MCl complexes (NHC = N-heterocyclic carbene; M = Cu, Ag, Au) in very short reaction times is presented. Comparable or better yields than those reported by using conventional heating can be obtained with this protocol. <br><br>Brant Landers and Oscar Navarro<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200248">10.1002/ejic.201200248</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17468.en.html">
<title>EurBest in EurJIC: Synthesis and Spectroscopic Characterisation of a Heterodinuclear Iron(III)-Copper(II) Complex Based on an Asymmetric Dinucleating Ligand System</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17468.en.html</link>
<dc:date>2012-06-19T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200156.jpg" alt="EurBest in EurJIC: Synthesis and Spectroscopic Characterisation of a Heterodinuclear Iron(III)-Copper(II) Complex Based on an Asymmetric Dinucleating Ligand System" align="left" hspace="5" vspace="5" border="0" /></p>The synthesis of a new asymmetric dinucleating ligand FloH, designed with two sets of metal ion binding groups suited to selective complexation, is reported. The site-directed generation of a heterodinuclear Fe<sup>III</sup>Cu<sup>II</sup> complex is performed in highyield and purity by using FloH. <br><br>Florian Heims, Valeriu Mereacre, Antonella Ciancetta, Stefan Mebs, Annie K. Powell, Claudio Greco and Kallol Ray<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200156">10.1002/ejic.201200156</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17437.en.html">
<title>EurBest in EurJIC: Isolated Silver Intermediate of Gold Precatalyst Activation</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17437.en.html</link>
<dc:date>2012-06-12T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200327.jpg" alt="EurBest in EurJIC: Isolated Silver Intermediate of Gold Precatalyst Activation" align="left" hspace="5" vspace="5" border="0" /></p>The reaction of AgSbF<sub>6</sub> with the gold chloride complex of the extremely bulky N-heterocyclic carbene ligand IPr** (simplified in the figure) revealed a silver cation coordinated to a single AuCl fragment  an intermediate proposed for most gold-catalyzed organic transformations. <br><br>Simone G. Weber, Frank Rominger and Bernd F. Straub<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200327">10.1002/ejic.201200327</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17436.en.html">
<title>EurBest in EurJIC: Cobalt(II) Complexes Bearing a Bulky N-Heterocyclic Carbene for Catalysis of Kumada&#x96;Tamao&#x96;Corriu Cross-Coupling Reactions of Aryl Halides</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17436.en.html</link>
<dc:date>2012-06-12T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200095.jpg" alt="EurBest in EurJIC: Cobalt(II) Complexes Bearing a Bulky N-Heterocyclic Carbene for Catalysis of KumadaTamaoCorriu Cross-Coupling Reactions of Aryl Halides" align="left" hspace="5" vspace="5" border="0" /></p>A series of cobalt(II) dimeric tetrahedral (30e) complexes were obtained in good yields and were transformed into the monomeric forms with pyridine. These complexes were characterized by SQUID, XPS, UV/Vis spectroscopy, elemental analysis, and X-ray crystallography, and were found to have high catalytic activity for KumadaTamaoCorriu cross-coupling reactions of aryl halides. <br><br>Kouki Matsubara, Tsukasa Sueyasu, Mariko Esaki, Aya Kumamoto, Shinya Nagao, Hitomi Yamamoto, Yuji Koga, Satoshi Kawata and Taisuke Matsumoto<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200095">10.1002/ejic.201200095</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17430.en.html">
<title>EurBest in EurJIC: 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://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17430.en.html</link>
<dc:date>2012-06-06T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201101292.jpg" alt="EurBest in EurJIC: Single-Strand Molecular Wheels and Coordination Polymers in Copper(II) Benzoate Chemistry by the Employment of α-Benzoin Oxime and Azides: Synthesis, Structures, and Magnetic Characterization" align="left" hspace="5" vspace="5" border="0" /></p>The reaction illustrated gives the decanuclear complexes [Cu<sub>10</sub>(bzox)<sub>10</sub>(DMF)<sub>4</sub>] and [Cu<sub>10</sub>(bzox)<sub>10</sub>] (bzoxH<sub>2</sub> = α-benzoin oxime, DMF = <i>N</i>,<i>N</i>-dimethylformamide), which have a single-strand wheel topology, and the 1D chain [Cu(N<sub>3</sub>)(O<sub>2</sub>CPh)(MeOH)]<sub><i>n</i></sub>. The Cu<sub>10</sub> clusters are both antiferromagnetically coupled with <i>S</i> = 0 ground states, whereas the 1D chain consists of ferromagnetically coupled <i>S</i> = 1/2 Cu<sup>II</sup> ions. <br><br>Theocharis C. Stamatatos, Gina Vlahopoulou, Catherine P. Raptopoulou, Vassilis Psycharis, Albert Escuer, George Christou and Spyros P. Perlepes<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201101292">10.1002/ejic.201101292</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17428.en.html">
<title>EurBest in EurJIC: Porous Silica-Based Mixed Oxides with Basic Organic Sites</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17428.en.html</link>
<dc:date>2012-06-05T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200088.jpg" alt="EurBest in EurJIC: Porous Silica-Based Mixed Oxides with Basic Organic Sites" align="left" hspace="5" vspace="5" border="0" /></p>Porous, organically modified silica-based mixed oxides were prepared by sol-gel processing of organotrialkoxysilanes with bridging amono groups and metal chlorides. Materials with ordered porosity and uniform mesopores were obtained with metal proportions up to about 20 %. <br><br>Jasmin Geserick, Sarah Meyer, Michael Puchberger, Silvia Pabisch, Herwig Peterlik, Ole Bethge, Emmerich Bertagnolli and Ulrich Schubert<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200088">10.1002/ejic.201200088</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17427.en.html">
<title>EurBest in EurJIC: Copper Complexes of &#x93;Superpodal&#x94; Amine Ligands and Reactivity Studies towards Dioxygen</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17427.en.html</link>
<dc:date>2012-06-05T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201101265.jpg" alt="EurBest in EurJIC: Copper Complexes of Superpodal Amine Ligands and Reactivity Studies towards Dioxygen" align="left" hspace="5" vspace="5" border="0" /></p>Copper(I/II) complexes of varying nuclearity have been obtained with a series of tetrapodal pentadentate N-donor ligands. <br><br>Anna Jozwiuk, E. Alper Ünal, Stefan Leopold, John P. Boyd, Marco Haryono, Nadine Kurowski, Francisco Velazquez Escobar, Peter Hildebrandt, Jochen Lach, Frank W. Heinemann, Dennis Wiedemann, Elisabeth Irran and Andreas Grohmann<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201101265">10.1002/ejic.201101265</a><br>]]></content:encoded>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17337.en.html">
<title>EurBest in EurJIC: FeIII Spin-Crossover Complexes with Photoisomerizable Ligands: Experimental and Theoretical Studies on the Ligand-Driven Light-Induced Spin Change Effect</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17337.en.html</link>
<dc:date>2012-05-22T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201101227.jpg" alt="EurBest in EurJIC: FeIII Spin-Crossover Complexes with Photoisomerizable Ligands: Experimental and Theoretical Studies on the Ligand-Driven Light-Induced Spin Change Effect" align="left" hspace="5" vspace="5" border="0" /></p>[Fe(salten)(3-azpy)]BPh<sub>4</sub> (<b>1</b>) and [Fe(salten)(4-azpy)]BPh<sub>4</sub> (<b>2</b>) have been synthesized and characterized [salten = 4-azaheptamethylene-1,7-bis(salicylideneiminate), azpy = phenylazopyridine]. Both exhibit a low to high spin transition in the solid state and are predominantly high spin in solution. <i>cistrans</i> isomerization of coordinated azpy leaves their spin equilibria almost unaffected. <br><br>Alexander Bannwarth, Sven Olaf Schmidt, Gerhard Peters, Frank D. Sönnichsen, Wulf Thimm, Rainer Herges and Felix Tuczek<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201101227">10.1002/ejic.201101227</a><br>]]></content:encoded>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17336.en.html">
<title>EurBest in EurJIC: Rhodium Nanoparticles from Dirhodium(II) Ethylene Glycol Tetracarboxylates</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17336.en.html</link>
<dc:date>2012-05-22T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201101424.jpg" alt="EurBest in EurJIC: Rhodium Nanoparticles from Dirhodium(II) Ethylene Glycol Tetracarboxylates" align="left" hspace="5" vspace="5" border="0" /></p>Rh<sup>II</sup> carboxylates [Rh<sub>2</sub>{O<sub>2</sub>CCH<sub>2</sub>(OCH<sub>2</sub>CH<sub>2</sub>)<sub>2</sub>OCH<sub>3</sub>}<sub>4</sub>]<sub><i>n</i></sub> and [Rh<sub>2</sub>{O<sub>2</sub>CCH<sub>2</sub>(OCH<sub>2</sub>CH<sub>2</sub>)<sub>2</sub>OCH<sub>3</sub>}<sub>4</sub>(PPh<sub>3</sub>)] featuring ethylene glycol chains were prepared and used to generate rhodium nanoparticles using the alcohol-reducing process. Nanoparticle sizes between (3.0±0.4) and (3.9±0.4) nm were obtained. <br><br>André Tuchscherer, Rico Packheiser, Tobias Rüffer, Herbert Schletter, Michael Hietschold and Heinrich Lang<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201101424">10.1002/ejic.201101424</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17303.en.html">
<title>EurBest in EurJIC: Bio-Metallodendrimers &#x96; Emerging Strategies in Metal-Based Drug Design</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17303.en.html</link>
<dc:date>2012-05-16T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200161.jpg" alt="EurBest in EurJIC: Bio-Metallodendrimers  Emerging Strategies in Metal-Based Drug Design" align="left" hspace="5" vspace="5" border="0" /></p>The use of metallodendrimers is fast becoming an attractive strategy in the design of a new class of metal-based biomolecules. This review surveys illustrative examples of these multivalent biologically active molecules as metal-based drugs and as agents for biosensing, photothermal and photodynamic therapy. <br><br>Preshendren Govender, Bruno Therrien and Gregory S. Smith<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200161">10.1002/ejic.201200161</a><br>]]></content:encoded>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17298.en.html">
<title>EurBest in EurJIC: Magnetoluminescent Agents for Dual MRI and Time-Gated Fluorescence Imaging</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17298.en.html</link>
<dc:date>2012-05-15T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201200045.jpg" alt="EurBest in EurJIC: Magnetoluminescent Agents for Dual MRI and Time-Gated Fluorescence Imaging" align="left" hspace="5" vspace="5" border="0" /></p>The synthesis and characterization of Fe<sub>3</sub>O<sub>4</sub>@Tb-DOTAm-(acetylene)<sub>3</sub> and Fe<sub>3</sub>O<sub>4</sub>@Tb-DOTAm-(Phen)<sub>3</sub>, two magnetoluminescent agents for dual imaging by MRI and confocal imaging are presented. The nanoparticles are characterized by high transverse and longitudinal relaxivities and long luminescence lifetimes ideal for time-gated spectroscopy. <br><br>Eric D. Smolensky, Yue Zhou and Valérie C. Pierre<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201200045">10.1002/ejic.201200045</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17297.en.html">
<title>EurBest in EurJIC: Synthesis, Reactivity and Ring-Opening Polymerization of a Tin-Bridged ansa-Cycloheptatrienyl-Cyclopentadienyl Titanium Sandwich Complex</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17297.en.html</link>
<dc:date>2012-05-15T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201101339.jpg" alt="EurBest in EurJIC: Synthesis, Reactivity and Ring-Opening Polymerization of a Tin-Bridged ansa-Cycloheptatrienyl-Cyclopentadienyl Titanium Sandwich Complex" align="left" hspace="5" vspace="5" border="0" /></p>The synthesis of a <i>t</i>Bu<sub>2</sub>Sn-bridged <i>ansa</i>-cycloheptatrienyl-cyclopentadienyl titanium sandwich complex is presented. As a result of its tilted structure, this strained stanna[1]troticenophane is easily converted into poly(troticenylstannanes) by ring-opening polymerization and undergoes regioselective insertion of platinum(0) into the <i>ipso</i>-C<sub>7</sub>H<sub>6</sub>Sn bond upon reaction with [Pt(PEt<sub>3</sub>)<sub>3</sub>].<br><br>Alain C. Tagne Kuate, Constantin G. Daniliuc, Peter G. Jones and Matthias Tamm<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201101339">10.1002/ejic.201101339</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17281.en.html">
<title>EurBest in EurJIC: Spectroscopic Evidence in Solid and Solution of a Discrete Copper(I) Tetrahedral Complex Dimer Supported by Supramolecular Interactions</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17281.en.html</link>
<dc:date>2012-05-08T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201101356.jpg" alt="EurBest in EurJIC: Spectroscopic Evidence in Solid and Solution of a Discrete Copper(I) Tetrahedral Complex Dimer Supported by Supramolecular Interactions" align="left" hspace="5" vspace="5" border="0" /></p>The self-association in a tetrahedral [Cu(<i>N</i>-{4-nitrophenyl}pyridine-2-yl-methanimine)(PPh<sub>3</sub>)Br] complex is reported. Experimental evidence for the dimerization in solution of this complex was obtained by NMR techniques. The dimer linked by noncovalent interactions has a close similarity to that in the crystalline packing. The thermodynamic parameters obtained by VT-<sup>1</sup>H NMR suggest that this process is enthalpy driven.<br><br>Danilo H. Jara, Luis Lemus, Liliana Farías, Eleonora Freire, Ricardo Baggio and Juan Guerrero<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201101356">10.1002/ejic.201101356</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17280.en.html">
<title>EurBest in EurJIC: Design, Testing and Kinetic Analysis of Bulky Monodentate Phosphorus Ligands in the Mizoroki&#x96;Heck Reaction</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17280.en.html</link>
<dc:date>2012-05-08T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201101271.jpg" alt="EurBest in EurJIC: Design, Testing and Kinetic Analysis of Bulky Monodentate Phosphorus Ligands in the MizorokiHeck Reaction" align="left" hspace="5" vspace="5" border="0" /></p>Bulky monodentate phosphoramidites give very fast palladium catalysts for the MizorokiHeck arylation with migratory insertion as rate-limiting step. <br><br>Deborah L. Dodds, Maarten D. K. Boele, Gino P. F. van Strijdonck, Johannes G. de Vries, Piet W. N. M. van Leeuwen and Paul C. J. Kamer<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201101271">10.1002/ejic.201101271</a>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17255.en.html">
<title>EurBest in EurJIC: Ruthenium Acetate Complexes as Versatile Probes of Metal&#x96;Ligand Interactions: Insight into the Ligand Effects of Vinylidene, Carbene, Carbonyl, Nitrosyl and Isocyanide</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17255.en.html</link>
<dc:date>2012-04-30T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201100931.jpg" alt="EurBest in EurJIC: Ruthenium Acetate Complexes as Versatile Probes of MetalLigand Interactions: Insight into the Ligand Effects of Vinylidene, Carbene, Carbonyl, Nitrosyl and Isocyanide" align="left" hspace="5" vspace="5" border="0" /></p>The complex <i>cis</i>-[Ru(κ<sup>2</sup>-OAc)<sub>2</sub>(PPh<sub>3</sub>)<sub>2</sub>] acts as a precursor for the formation of the complexes <i>trans</i>-[Ru(κ<sup>1</sup>-OAc)(κ<sup>2</sup>-OAc)L(PPh<sub>3</sub>)<sub>2</sub>] where L is a two-electron donor, σ-donor/π-acceptor ligand. The structural and spectroscopic data of these species provide insight into the relative electron demand of the ligands L. <br><br>Christine E. Welby, Thomas O. Eschemann, Christopher A. Unsworth, Elizabeth J. Smith, Robert J. Thatcher, Adrian C. Whitwood and Jason M. Lynam<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201100931">10.1002/ejic.201100931</a><br>]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17254.en.html">
<title>EurBest in EurJIC: Chelating C4-Bound Imidazolylidene Complexes through Oxidative Addition of Imidazolium Salts to Palladium(0)</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0682/homepage/news/17254.en.html</link>
<dc:date>2012-04-30T00:10:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ejic-201100940.jpg" alt="EurBest in EurJIC: Chelating C4-Bound Imidazolylidene Complexes through Oxidative Addition of Imidazolium Salts to Palladium(0)" align="left" hspace="5" vspace="5" border="0" /></p>Oxidative addition of 4-iodoimidazolium salts to low-valent palladium(0) provides access to abnormal NHCpalladium complexes without requiring protection of the C2 position. Hence, this site is available for further functionalisation which allows, for example, dimetallic complexes to be prepared. <br><br>Anneke Krüger, Evelyne Kluser, Helge Müller-Bunz, Antonia Neels and Martin Albrecht<br>DOI: <a href = "http://doi.wiley.com/10.1002/ejic.201100940">10.1002/ejic.201100940</a><br>]]></content:encoded>
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</rdf:RDF>