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<dc:date>2013-04-16T00:00:00+02:00</dc:date>
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<title>Insight into the Mechanism of the Preferential Oxidation of Carbon Monoxide by Using Isotope-Modulated Excitation IR Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cctc.201300172</link>
<dc:creator>Nobutaka Maeda, Fabian Meemken, Alfons Baiker</dc:creator>
<dc:date>2013-05-16T14:40+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300172.gif" width="216" height="179" alt="Insight into the Mechanism of the Preferential Oxidation of Carbon Monoxide by Using Isotope-Modulated Excitation IR Spectroscopy" title="Insight into the Mechanism of the Preferential Oxidation of Carbon Monoxide by Using Isotope-Modulated Excitation IR Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>DRIFTing through time:</B> Modulation excitation in&nbsp;situ diffuse-reflectance IR Fourier transform (DRIFT) spectroscopy with periodic isotopic perturbation (D<sub>2</sub> and <SUP>13</SUP>CO) has been applied to elucidate the pathway for the preferential oxidation of carbon monoxide (PROX) over a commercial Pt/alumina catalyst. The time- and phase-domain IR spectra suggest a water-assisted pathway for the preferential oxidation reaction.</P>
<p> [Communication]<br />Nobutaka Maeda, Fabian Meemken, Alfons Baiker<br /><i>ChemCatChem</i>, May 16, 2013, DOI: 10.1002/cctc.201300172. <a href="http://dx.doi.org/10.1002/cctc.201300172">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300054">
<title>A Microfluidic System for the Continuous Recycling of Unmodified Homogeneous Palladium Catalysts through Liquid/Liquid Phase Separation</title>
<link>http://dx.doi.org/10.1002/cctc.201300054</link>
<dc:creator>Pengfei Li, Jason S. Moore , Klavs F. Jensen</dc:creator>
<dc:date>2013-05-16T14:40+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300054.gif" width="216" height="145" alt="A Microfluidic System for the Continuous Recycling of Unmodified Homogeneous Palladium Catalysts through Liquid/Liquid Phase Separation" title="A Microfluidic System for the Continuous Recycling of Unmodified Homogeneous Palladium Catalysts through Liquid/Liquid Phase Separation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A parting of the waves:</B> A prototype microflow system for the continuous recycling of homogeneous catalysts through liquid/liquid phase separation was developed and its effectiveness demonstrated in a challenging palladium-catalyzed hydroxylation reaction. The unmodified catalyst is recycled under standard reaction conditions by using a combination of chemical and engineering methods.</P>
<p> [Communication]<br />Pengfei Li, Jason S. Moore&#xA0;, Klavs F. Jensen<br /><i>ChemCatChem</i>, May 16, 2013, DOI: 10.1002/cctc.201300054. <a href="http://dx.doi.org/10.1002/cctc.201300054">Read article.</a></p> ]]>
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<title>A Recyclable “Boomerang” Linear Polystyrene-Stabilized Pd Nanoparticles for the Suzuki Coupling Reaction of Aryl Chlorides in Water</title>
<link>http://dx.doi.org/10.1002/cctc.201300204</link>
<dc:creator>Atsushi Ohtaka, Erina Sakaguchi, Tomohiro Yamaguchi, Go Hamasaka, Yasuhiro Uozumi, Osamu Shimomura, Ryôki Nomura</dc:creator>
<dc:date>2013-05-16T14:39+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300204.gif" width="215" height="174" alt="A Recyclable &ldquo;Boomerang&rdquo; Linear Polystyrene-Stabilized Pd Nanoparticles for the Suzuki Coupling Reaction of Aryl Chlorides in Water" title="A Recyclable &ldquo;Boomerang&rdquo; Linear Polystyrene-Stabilized Pd Nanoparticles for the Suzuki Coupling Reaction of Aryl Chlorides in Water" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Boomerang! It keeps coming back!</B> The reversible transfer of Pd species between water (reaction medium) and polystyrene (polymer support) was confirmed for Suzuki coupling reaction of aryl chloride with arylboronic acid in the presence of tetrabutylammonium bromide. No clear change in particle size was observed by TEM after re-stabilization of the Pd species on linear polystyrene.</P>
<p> [Communication]<br />Atsushi Ohtaka, Erina Sakaguchi, Tomohiro Yamaguchi, Go Hamasaka, Yasuhiro Uozumi, Osamu Shimomura, Ry&#xF4;ki Nomura<br /><i>ChemCatChem</i>, May 16, 2013, DOI: 10.1002/cctc.201300204. <a href="http://dx.doi.org/10.1002/cctc.201300204">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300157">
<title>Interfacial Engineering of Platinum Catalysts for Fuel Cells: Methanol Oxidation is Dramatically Improved by Polymer Coating on a Platinum Catalyst</title>
<link>http://dx.doi.org/10.1002/cctc.201300157</link>
<dc:creator>Tsuyohiko Fujigaya, Minoru Okamoto, Kazuya Matsumoto, Kenji Kaneko, Naotoshi Nakashima</dc:creator>
<dc:date>2013-05-16T14:39+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300157.gif" width="196" height="151" alt="Interfacial Engineering of Platinum Catalysts for Fuel Cells: Methanol Oxidation is Dramatically Improved by Polymer Coating on a Platinum Catalyst" title="Interfacial Engineering of Platinum Catalysts for Fuel Cells: Methanol Oxidation is Dramatically Improved by Polymer Coating on a Platinum Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>All coated up:</B> Platinum nanoparticles loaded on multiwalled carbon nanotubes (MWNTs) are coated with pyridine-containing polybenzimidazole (PyPBI). Interestingly, although a slight decrease in the accessibility of methanol is observed after coating, the methanol oxidation activity of Pt dramatically improves after coating with PyPBI.</P>
<p> [Communication]<br />Tsuyohiko Fujigaya, Minoru Okamoto, Kazuya Matsumoto, Kenji Kaneko, Naotoshi Nakashima<br /><i>ChemCatChem</i>, May 16, 2013, DOI: 10.1002/cctc.201300157. <a href="http://dx.doi.org/10.1002/cctc.201300157">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300075">
<title>Electrocatalytic Reduction of Nitrate on a Pt Electrode Modified by p-Block Metal Adatoms in Acid Solution</title>
<link>http://dx.doi.org/10.1002/cctc.201300075</link>
<dc:creator>Jian Yang, Federico Calle-Vallejo, Matteo Duca, Marc T. M. Koper</dc:creator>
<dc:date>2013-05-16T14:39+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300075.gif" width="215" height="178" alt="Electrocatalytic Reduction of Nitrate on a Pt Electrode Modified by p-Block Metal Adatoms in Acid Solution" title="Electrocatalytic Reduction of Nitrate on a Pt Electrode Modified by p-Block Metal Adatoms in Acid Solution" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Some metals do it better:</B> Polycrystalline platinum electrodes are modified with p-block elements and their abilities for nitrate reduction to volatile nitrogen oxides in perchloric and sulfuric acid solutions investigated. Online electrochemical mass spectrometry is used to detect volatile products on the electrode surface and DFT calculations give insight into the nature of the promoting action.</P>
<p> [Full Paper]<br />Jian Yang, Federico Calle-Vallejo, Matteo Duca, Marc T. M. Koper<br /><i>ChemCatChem</i>, May 16, 2013, DOI: 10.1002/cctc.201300075. <a href="http://dx.doi.org/10.1002/cctc.201300075">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300310">
<title>German Catalysis, Celebrated in Weimar</title>
<link>http://dx.doi.org/10.1002/cctc.201300310</link>
<dc:creator>Marc Armbrüster, Malte Behrens, Barthel Engendahl, Mehtap Oezaslan, Marcus Rose, Christoph Sprung</dc:creator>
<dc:date>2013-05-14T11:37+05:00</dc:date>
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</taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300310.gif" width="157" height="187" alt="German Catalysis, Celebrated in Weimar" title="German Catalysis, Celebrated in Weimar" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Catalysis, reloaded:</B> At the 46th annual meeting of the German Catalysis Society, hosted by DECHEMA, 300 researchers presented innovative catalytic systems and concepts, with overlaps between homogeneous, heterogeneous, and biocatalysis described in many cases. The conference, attended by over 500 participants, was also an excellent forum for nano-, electro-, and photocatalysis, with a strong industrial focus.</P>
<p> [Conference Report]<br />Marc Armbr&#xFC;ster, Malte Behrens, Barthel Engendahl, Mehtap Oezaslan, Marcus Rose, Christoph Sprung<br /><i>ChemCatChem</i>, May 14, 2013, DOI: 10.1002/cctc.201300310. <a href="http://dx.doi.org/10.1002/cctc.201300310">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200953">
<title>Towards Physical Descriptors of Active and Selective Catalysts for the Oxidation of &lt;I&gt;n&lt;/I&gt;-Butane to Maleic Anhydride</title>
<link>http://dx.doi.org/10.1002/cctc.201200953</link>
<dc:creator>Maik Eichelbaum, Robert Glaum, Michael Hävecker, Knut Wittich, Christian Heine, Heiner Schwarz, Cornelia-Katharina Dobner, Cathrin Welker-Nieuwoudt, Annette Trunschke, Robert Schlögl</dc:creator>
<dc:date>2013-05-14T11:37+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200953.gif" width="443" height="120" alt="Towards Physical Descriptors of Active and Selective Catalysts for the Oxidation of n-Butane to Maleic Anhydride" title="Towards Physical Descriptors of Active and Selective Catalysts for the Oxidation of n-Butane to Maleic Anhydride" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Charge transport matters:</B> The gas-phase response of the electrical conductivity, measured contact-free with the in&nbsp;situ microwave cavity perturbation technique, is studied for vanadium(III), (IV), and (V) phosphorus oxide catalysts under selective <I>n</I>-butane oxidation conditions. The deduced surface&ndash;bulk charge transport properties of the samples provide a fingerprint for the activity and selectivity in the demanding selective oxidation that requires a 14&nbsp;e<SUP>&minus;</SUP> transfer per catalytic cycle.</P>
<p> [Full Paper]<br />Maik Eichelbaum, Robert Glaum, Michael H&#xE4;vecker, Knut Wittich, Christian Heine, Heiner Schwarz, Cornelia-Katharina Dobner, Cathrin Welker-Nieuwoudt, Annette Trunschke, Robert Schl&#xF6;gl<br /><i>ChemCatChem</i>, May 14, 2013, DOI: 10.1002/cctc.201200953. <a href="http://dx.doi.org/10.1002/cctc.201200953">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300033">
<title>Mechanistic Study of Ethanol Dehydrogenation over Silica-Supported Silver</title>
<link>http://dx.doi.org/10.1002/cctc.201300033</link>
<dc:creator>Vitaly L. Sushkevich, Irina I. Ivanova, Esben Taarning</dc:creator>
<dc:date>2013-05-13T16:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300033.gif" width="216" height="185" alt="Mechanistic Study of Ethanol Dehydrogenation over Silica-Supported Silver" title="Mechanistic Study of Ethanol Dehydrogenation over Silica-Supported Silver" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Every mechanism should have a silver lining:</B> Ethanol is selectively converted into acetaldehyde over Ag supported on silica. The Ag particles and SiOH groups of silica act in a complementary manner in a concerted mechanism, which is proposed based on in&nbsp;situ FTIR spectroscopic studies and kinetic experiments with specifically deuterated ethanol. The proposed mechanism shows the way for the design of efficient supported Ag catalysts.</P>
<p> [Full Paper]<br />Vitaly L. Sushkevich, Irina I. Ivanova, Esben Taarning<br /><i>ChemCatChem</i>, May 13, 2013, DOI: 10.1002/cctc.201300033. <a href="http://dx.doi.org/10.1002/cctc.201300033">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200895">
<title>Sulfur Promotion in Conjugated Isomerization of Safflower Oil over Bifunctional Structured Rh/SBA-15 Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201200895</link>
<dc:creator>Nasima Chorfa, Safia Hamoudi, Joseph Arul, Khaled Belkacemi</dc:creator>
<dc:date>2013-05-13T16:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200895.gif" width="171" height="196" alt="Sulfur Promotion in Conjugated Isomerization of Safflower Oil over Bifunctional Structured Rh/SBA-15 Catalysts" title="Sulfur Promotion in Conjugated Isomerization of Safflower Oil over Bifunctional Structured Rh/SBA-15 Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>And they were all yellow:</B> The sulfur-promoted formation of conjugated linoleic acid isomers during the combined hydrogenation and directed isomerization of safflower oil can be explained mechanistically through the preferable formation of the more nucleophilic rhodium sulfide (Rh-SH) over that of the hydride (Rh-H). The Rh-SH species could induce more easily the addition and elimination steps for the double-bond conjugation of linoleic acid.</P>
<p> [Full Paper]<br />Nasima Chorfa, Safia Hamoudi, Joseph Arul, Khaled Belkacemi<br /><i>ChemCatChem</i>, May 13, 2013, DOI: 10.1002/cctc.201200895. <a href="http://dx.doi.org/10.1002/cctc.201200895">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300155">
<title>Alloyed Ultrathin Nanowires: A New Choice in Electrocatalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201300155</link>
<dc:creator>Hui-Hui Li, Chun-Hua Cui, Shu-Hong Yu</dc:creator>
<dc:date>2013-05-09T07:53+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300155.gif" width="197" height="196" alt="Alloyed Ultrathin Nanowires: A New Choice in Electrocatalysts" title="Alloyed Ultrathin Nanowires: A New Choice in Electrocatalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Skinnier than a supermodel:</B> There will be an optimal size for ultrathin alloyed nanowires (NWs) as electrocatalysts. The ultrathin size of the NWs maximizes the surface area and utilization of precious metals, thereby lowering the precious metals loading and reducing the cost while increasing their electroactivity and stability.</P>
<p> [Highlight]<br />Hui-Hui Li, Chun-Hua Cui, Shu-Hong Yu<br /><i>ChemCatChem</i>, May 09, 2013, DOI: 10.1002/cctc.201300155. <a href="http://dx.doi.org/10.1002/cctc.201300155">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300140">
<title>Tandem Synthesis of N-Alkylated Amides from Aldoximes and Alcohols by Using a Ru/Ir Dual-Catalyst System</title>
<link>http://dx.doi.org/10.1002/cctc.201300140</link>
<dc:creator>Feng Li, Panpan Qu, Juan Ma, Xiaoyuan Zou, Chunlou Sun</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/cctc201300140.gif" width="216" height="170" alt="Tandem Synthesis of N-Alkylated Amides from Aldoximes and Alcohols by Using a Ru/Ir Dual-Catalyst System" title="Tandem Synthesis of N-Alkylated Amides from Aldoximes and Alcohols by Using a Ru/Ir Dual-Catalyst System" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>In the same boat:</B> Tandem rearrangement/N-alkylation reactions in the presence of a Ru/Ir dual-catalyst system affords the desired N-alkylated amines in good-to-excellent yields with no intermediate amides or over-alkylated N,N-dialkylated amides. This environmentally friendly tandem reaction employs readily available starting materials, affords excellent selectivities for the N-alkylated amides, and shows high atom efficiency.</P>
<p> [Communication]<br />Feng Li, Panpan Qu, Juan Ma, Xiaoyuan Zou, Chunlou Sun<br /><i>ChemCatChem</i>, May 06, 2013, DOI: 10.1002/cctc.201300140. <a href="http://dx.doi.org/10.1002/cctc.201300140">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300136">
<title>Reversible Hydrogenation–Oxidative Dehydrogenation of Quinolines over a Highly Active Pt Nanowire Catalyst under Mild Conditions</title>
<link>http://dx.doi.org/10.1002/cctc.201300136</link>
<dc:creator>Danhua Ge, Lei Hu, Jiaqing Wang, Xingming Li, Fenqiang Qi, Jianmei Lu, Xueqin Cao, Hongwei Gu</dc:creator>
<dc:date>2013-05-06T12:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300136.gif" width="215" height="154" alt="Reversible Hydrogenation&ndash;Oxidative Dehydrogenation of Quinolines over a Highly Active Pt Nanowire Catalyst under Mild Conditions" title="Reversible Hydrogenation&ndash;Oxidative Dehydrogenation of Quinolines over a Highly Active Pt Nanowire Catalyst under Mild Conditions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Over the wire and back again:</B> The reversible hydrogenation&ndash;oxidative dehydrogenation of quinolines is reported by using Pt nanowire (NW) as the catalyst under mild reaction conditions. Pt NW shows high activity and selectivity in the hydrogenation of quinolines under H<sub>2</sub> pressure (1&nbsp;bar=100&nbsp;kPa), and these hydrogenation products can be easily oxidized under the same conditions in an atmosphere of oxygen (1&nbsp;bar) or in air.</P>
<p> [Communication]<br />Danhua Ge, Lei Hu, Jiaqing Wang, Xingming Li, Fenqiang Qi, Jianmei Lu, Xueqin Cao, Hongwei Gu<br /><i>ChemCatChem</i>, May 06, 2013, DOI: 10.1002/cctc.201300136. <a href="http://dx.doi.org/10.1002/cctc.201300136">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200908">
<title>Pd Ultra-Small Clusters as Precursors for Silica-Encapsulated Pd Nanoreactors: Highly Sinter-Resistant Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201200908</link>
<dc:creator>Anupam Samanta, R. Nandini Devi</dc:creator>
<dc:date>2013-05-06T12:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200908.gif" width="216" height="104" alt="Pd Ultra-Small Clusters as Precursors for Silica-Encapsulated Pd Nanoreactors: Highly Sinter-Resistant Catalysts" title="Pd Ultra-Small Clusters as Precursors for Silica-Encapsulated Pd Nanoreactors: Highly Sinter-Resistant Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The silica sphere is your oyster:</B> Water-dispersible ultra-small clusters of Pd are synthesized by using a quaternary ammonium thiol as the protecting ligand. Further calcination and removal of organics leads to nanoreactors with individual Pd particles encapsulated within porous silica spheres that exhibit excellent catalytic activity and thermal stability.</P>
<p> [Full Paper]<br />Anupam Samanta, R. Nandini Devi<br /><i>ChemCatChem</i>, May 06, 2013, DOI: 10.1002/cctc.201200908. <a href="http://dx.doi.org/10.1002/cctc.201200908">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300097">
<title>Optimizing the Structure of 4-Dialkylamino-α,α-diarylprolinol Ethers as Catalysts for the Enantioselective Cyclopropanation of α,β-Unsaturated Aldehydes in Water</title>
<link>http://dx.doi.org/10.1002/cctc.201300097</link>
<dc:creator>Jose I. Martínez, Efraim Reyes, Uxue Uria, Luisa Carrillo, Jose L. Vicario</dc:creator>
<dc:date>2013-05-06T12:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300097.gif" width="390" height="105" alt="Optimizing the Structure of 4-Dialkylamino-&alpha;,&alpha;-diarylprolinol Ethers as Catalysts for the Enantioselective Cyclopropanation of &alpha;,&beta;-Unsaturated Aldehydes in Water" title="Optimizing the Structure of 4-Dialkylamino-&alpha;,&alpha;-diarylprolinol Ethers as Catalysts for the Enantioselective Cyclopropanation of &alpha;,&beta;-Unsaturated Aldehydes in Water" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Be water my friend:</B> A new family of chiral diarylprolinol-type organocatalysts with improved performances in conjugate addition reactions in water and proceeding under the iminium activation manifold were studied. Once the optimized catalyst structure had been found, it proved its efficiency in the catalytic enantioselective cyclopropanation of &alpha;,&beta;-unsaturated aldehydes using water as the only reaction medium.</P>
<p> [Full Paper]<br />Jose I. Mart&#xED;nez, Efraim Reyes, Uxue Uria, Luisa Carrillo, Jose L. Vicario<br /><i>ChemCatChem</i>, May 06, 2013, DOI: 10.1002/cctc.201300097. <a href="http://dx.doi.org/10.1002/cctc.201300097">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300166">
<title>Direct Synthesis of Phenol from Benzene and O&lt;sub&gt;2&lt;/sub&gt;, Regulated by NH&lt;sub&gt;3&lt;/sub&gt; on Pt/β and Pt-Re/ZSM-5 Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201300166</link>
<dc:creator>Linsheng Wang, Sadaaki Yamamoto, Sachin Malwadkar, Shin-ichi Nagamatsu, Takehiko Sasaki, Kenichiro Hayashizaki, Mizuki Tada, Yasuhiro Iwasawa</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/cctc201300166.gif" width="216" height="188" alt="Direct Synthesis of Phenol from Benzene and O2, Regulated by NH3 on Pt/&beta; and Pt-Re/ZSM-5 Catalysts" title="Direct Synthesis of Phenol from Benzene and O2, Regulated by NH3 on Pt/&beta; and Pt-Re/ZSM-5 Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Best director:</B> The direct synthesis of phenol from benzene and O<sub>2</sub> was performed with 78&ndash;94&nbsp;% selectivity on Pt/&beta; and Pt-Re/ZSM-5 catalysts, regulated by NH<sub>3</sub> (See figure, (1)). An alternating process (see figure, (2)-1 and (2)-2) afforded the selective synthesis of phenol with 83&ndash;99.8&nbsp;% selectivity, whilst minimizing the consumption of NH<sub>3</sub>.</P>
<p> [Communication]<br />Linsheng Wang, Sadaaki Yamamoto, Sachin Malwadkar, Shin-ichi Nagamatsu, Takehiko Sasaki, Kenichiro Hayashizaki, Mizuki Tada, Yasuhiro Iwasawa<br /><i>ChemCatChem</i>, May 03, 2013, DOI: 10.1002/cctc.201300166. <a href="http://dx.doi.org/10.1002/cctc.201300166">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200948">
<title>Synthesis of Fragrance Compounds from Biorenewables: Tandem Hydroformylation–Acetalization of Bicyclic Monoterpenes</title>
<link>http://dx.doi.org/10.1002/cctc.201200948</link>
<dc:creator>Marina C. de Freitas, Camila G. Vieira, Eduardo N. dos Santos, Elena V. Gusevskaya</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/cctc201200948.gif" width="448" height="115" alt="Synthesis of Fragrance Compounds from Biorenewables: Tandem Hydroformylation&ndash;Acetalization of Bicyclic Monoterpenes" title="Synthesis of Fragrance Compounds from Biorenewables: Tandem Hydroformylation&ndash;Acetalization of Bicyclic Monoterpenes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The sweet smell of success:</B> Bicyclic monoterpenes, cheap biomass-based substrates available from coniferous trees, can be transformed into valuable fragrance compounds through an efficient tandem catalytic process by using a Rh catalyst and environmentally friendly ethanol as a solvent.</P>
<p> [Full Paper]<br />Marina C. de&#xA0;Freitas, Camila G. Vieira, Eduardo N. dos&#x2002;Santos, Elena V. Gusevskaya<br /><i>ChemCatChem</i>, May 03, 2013, DOI: 10.1002/cctc.201200948. <a href="http://dx.doi.org/10.1002/cctc.201200948">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300143">
<title>Dendrimer-Encapsulated Bimetallic Pt-Ni Nanoparticles as Highly Efficient Catalysts for Hydrogen Generation from Chemical Hydrogen Storage Materials</title>
<link>http://dx.doi.org/10.1002/cctc.201300143</link>
<dc:creator>Kengo Aranishi, Ashish Kumar Singh, Qiang Xu</dc:creator>
<dc:date>2013-05-03T16:03+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300143.gif" width="216" height="129" alt="Dendrimer-Encapsulated Bimetallic Pt-Ni Nanoparticles as Highly Efficient Catalysts for Hydrogen Generation from Chemical Hydrogen Storage Materials" title="Dendrimer-Encapsulated Bimetallic Pt-Ni Nanoparticles as Highly Efficient Catalysts for Hydrogen Generation from Chemical Hydrogen Storage Materials" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>I feel it in my dendrimers...</B> Bimetallic Pt-Ni dendrimer-encapsulated nanoparticles (DENs) with different Pt/Ni ratios are synthesized through the co-complexation of Pt<SUP>2+</SUP> and Ni<SUP>2+</SUP> cations to the internal tertiary amine of the dendrimer followed by coreduction by NaBH<sub>4</sub>. The Pt-Ni DENs show high catalytic activities in hydrous hydrazine decomposition and ammonia borane hydrolysis.</P>
<p> [Full Paper]<br />Kengo Aranishi, Ashish Kumar Singh, Qiang Xu<br /><i>ChemCatChem</i>, May 03, 2013, DOI: 10.1002/cctc.201300143. <a href="http://dx.doi.org/10.1002/cctc.201300143">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200914">
<title>On the Nature of Selective Palladium-Based Nanoparticles on Nitrogen-Doped Carbon Nanotubes for the Direct Synthesis of H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;</title>
<link>http://dx.doi.org/10.1002/cctc.201200914</link>
<dc:creator>S. Abate, M. Freni, R. Arrigo, M. E. Schuster, S. Perathoner, G. Centi</dc:creator>
<dc:date>2013-05-02T18:27+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200914.gif" width="216" height="216" alt="On the Nature of Selective Palladium-Based Nanoparticles on Nitrogen-Doped Carbon Nanotubes for the Direct Synthesis of H2O2" title="On the Nature of Selective Palladium-Based Nanoparticles on Nitrogen-Doped Carbon Nanotubes for the Direct Synthesis of H2O2" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Caps off to gold:</B> High selectivities (&gt;95&nbsp;%) are obtained if Pd nanoparticles are covered with an organic capping agent, the removal of which during the reaction leads to a decrease in selectivity. With Au, the intrinsic reaction rate decreases but selectivity is better after the removal of the capping agent. The presence of Au creates small Pd terraces fully covered with chemisorbed O<sub>2</sub>; H<sub>2</sub>O<sub>2</sub> synthesis occurs at the perimeter of these terraces.</P>
<p> [Full Paper]<br />S. Abate, M. Freni, R. Arrigo, M. E. Schuster, S. Perathoner, G. Centi<br /><i>ChemCatChem</i>, May 02, 2013, DOI: 10.1002/cctc.201200914. <a href="http://dx.doi.org/10.1002/cctc.201200914">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300082">
<title>Novel Catalyst Design by using Cisplatin To Covalently Anchor Catalytically Active Copper Complexes to DNA</title>
<link>http://dx.doi.org/10.1002/cctc.201300082</link>
<dc:creator>Lorina Gjonaj, Gerard Roelfes</dc:creator>
<dc:date>2013-05-02T18:26+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300082.gif" width="447" height="173" alt="Novel Catalyst Design by using Cisplatin To Covalently Anchor Catalytically Active Copper Complexes to DNA" title="Novel Catalyst Design by using Cisplatin To Covalently Anchor Catalytically Active Copper Complexes to DNA" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Anchored to DNA:</B> Covalent anchoring of catalytically active complexes to DNA is achieved through a tethered cisplatin moiety. The resulting DNA-based catalysts give good enantiomeric excess values in the catalyzed Diels&ndash;Alder and Friedel&ndash;Crafts alkylation reactions.</P>
<p> [Communication]<br />Lorina Gjonaj, Gerard Roelfes<br /><i>ChemCatChem</i>, May 02, 2013, DOI: 10.1002/cctc.201300082. <a href="http://dx.doi.org/10.1002/cctc.201300082">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300064">
<title>On the Unique Reactivity of Pd(OAc)&lt;sub&gt;2&lt;/sub&gt; with Organic Azides: Expedient Synthesis of Nitriles and Imines</title>
<link>http://dx.doi.org/10.1002/cctc.201300064</link>
<dc:creator>Laura Martínez-Sarti, Silvia Díez-González</dc:creator>
<dc:date>2013-05-01T21:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300064.gif" width="214" height="107" alt="On the Unique Reactivity of Pd(OAc)2 with Organic Azides: Expedient Synthesis of Nitriles and Imines" title="On the Unique Reactivity of Pd(OAc)2 with Organic Azides: Expedient Synthesis of Nitriles and Imines" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>As good as it gets:</B> Pd(OAc)<sub>2</sub> is a highly efficient catalyst for the transformation of primary azides into nitriles or imines under neutral, technical-grade conditions, with unprecedented selectivities.</P>
<p> [Communication]<br />Laura Mart&#xED;nez-Sarti, Silvia D&#xED;ez-Gonz&#xE1;lez<br /><i>ChemCatChem</i>, May 01, 2013, DOI: 10.1002/cctc.201300064. <a href="http://dx.doi.org/10.1002/cctc.201300064">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300009">
<title>Highly Porous Organic Polymer containing Free –CO&lt;sub&gt;2&lt;/sub&gt;H Groups: A Convenient Carbocatalyst for Indole C-H Activation at Room Temperature</title>
<link>http://dx.doi.org/10.1002/cctc.201300009</link>
<dc:creator>Arindam Modak, John Mondal, Asim Bhaumik</dc:creator>
<dc:date>2013-05-01T13:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300009.gif" width="446" height="122" alt="Highly Porous Organic Polymer containing Free &ndash;CO2H Groups: A Convenient Carbocatalyst for Indole C-H Activation at Room Temperature" title="Highly Porous Organic Polymer containing Free &ndash;CO2H Groups: A Convenient Carbocatalyst for Indole C-H Activation at Room Temperature" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Rich in more ways than one:</B> High surface area &ndash;CO<sub>2</sub>H rich organic polymer have been designed, which acts as an excellent carbocatalyst in a series of indole 3-substitution reactions at room temperature.</P>
<p> [Communication]<br />Arindam Modak, John Mondal, Asim Bhaumik<br /><i>ChemCatChem</i>, May 01, 2013, DOI: 10.1002/cctc.201300009. <a href="http://dx.doi.org/10.1002/cctc.201300009">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300072">
<title>Activity, Recyclability, and Stability of Lipases Immobilized on Oil-Filled Spherical Silica Nanoparticles with Different Silica Shell Structures</title>
<link>http://dx.doi.org/10.1002/cctc.201300072</link>
<dc:creator>Yasutaka Kuwahara, Takato Yamanishi, Takashi Kamegawa, Kohsuke Mori, Hiromi Yamashita</dc:creator>
<dc:date>2013-04-29T16:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300072.gif" width="447" height="107" alt="Activity, Recyclability, and Stability of Lipases Immobilized on Oil-Filled Spherical Silica Nanoparticles with Different Silica Shell Structures" title="Activity, Recyclability, and Stability of Lipases Immobilized on Oil-Filled Spherical Silica Nanoparticles with Different Silica Shell Structures" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Trapped oil:</B> <I>Candida antarctica</I> lipase&nbsp;A is immobilized on oil-filled spherical silica nanoparticles with different silica shell structures through an anionic surfactant-induced self-assembly approach (see scheme) with ethanol as a cosolvent. The entrapped enzymes mostly retain their activities and exhibit recyclability and thermal and chemical stability, depending on the thickness and pore characteristics of the silica shells. TEOS=Tetraethoxyorthosilicate, APTES=3-aminopropyl triethoxysilane.</P>
<p> [Full Paper]<br />Yasutaka Kuwahara, Takato Yamanishi, Takashi Kamegawa, Kohsuke Mori, Hiromi Yamashita<br /><i>ChemCatChem</i>, Apr 29, 2013, DOI: 10.1002/cctc.201300072. <a href="http://dx.doi.org/10.1002/cctc.201300072">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300029">
<title>Revealing the Atomic Structure of Intermetallic GaPd&lt;sub&gt;2&lt;/sub&gt; Nanocatalysts by using Aberration-Corrected Scanning Transmission Electron Microscopy</title>
<link>http://dx.doi.org/10.1002/cctc.201300029</link>
<dc:creator>Rowan Leary, Francisco de la Peña, Jonathan S. Barnard, Yuan Luo, Marc Armbrüster, John Meurig Thomas, Paul A. Midgley</dc:creator>
<dc:date>2013-04-29T16:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300029.gif" width="215" height="194" alt="Revealing the Atomic Structure of Intermetallic GaPd2 Nanocatalysts by using Aberration-Corrected Scanning Transmission Electron Microscopy" title="Revealing the Atomic Structure of Intermetallic GaPd2 Nanocatalysts by using Aberration-Corrected Scanning Transmission Electron Microscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A clear view in a dark field:</B> The annular dark-field imaging mode and electron energy-loss spectroscopy were used to provide directly interpretable imaging and chemical analysis of GaPd<sub>2</sub> nanocatalysts, revealing intricacies of the &ldquo;nano-sized&rdquo; intermetallic compound that are intriguing from both a crystallographic and catalytic perspective.</P>
<p> [Full Paper]<br />Rowan Leary, Francisco de&#xA0;la&#xA0;Pe&#xF1;a, Jonathan S. Barnard, Yuan Luo, Marc Armbr&#xFC;ster, John Meurig&#xA0;Thomas, Paul A. Midgley<br /><i>ChemCatChem</i>, Apr 29, 2013, DOI: 10.1002/cctc.201300029. <a href="http://dx.doi.org/10.1002/cctc.201300029">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899/homepage/news/19116.en.html">
<title>VIP: Ag/AgBr-Grafted Graphite-like Carbon Nitride with Enhanced Plasmonic Photocatalytic Activity Under Visible Light</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899/homepage/news/19116.en.html</link>
<dc:date>2013-04-29T00:00:00+02:00</dc:date>
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<![CDATA[<p>Yang-Sen Xu, Wei-De Zhang*</p>
<br><p>Ag/AgBr-grafted graphite-like carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) was constructed by in situ photoreduction of AgBr/g-C<sub>3</sub>N<sub>4</sub> hybrid prepared by using the deposition-precipitation method. Compared with bare g-C<sub>3</sub>N<sub>4</sub> and Ag/AgBr nanoparticles, a 28-fold and 6-fold enhancement in the degradation rate toward rhodamine B is observed over the Ag/AgBr/g-C<sub>3</sub>N<sub>4</sub> hybrid under visible light irradiation, respectively. This study provides new insight into the development of highly efficient and stable g-C<sub>3</sub>N<sub>4</sub>-based plasmonic photocatalysts and facilitates their practical applications in environmental issues.</p><p>Coming soon.</p><!-- DOI: 10.1002/cctc.201300144 --><!-- A300144 -->]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200883">
<title>Some Turning Points in the Chemical Electron Microscopic Study of Heterogeneous Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201200883</link>
<dc:creator>John Meurig Thomas, Caterina Ducati, Rowan Leary, Paul A. Midgley</dc:creator>
<dc:date>2013-04-25T15:32+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200883.gif" width="215" height="194" alt="Some Turning Points in the Chemical Electron Microscopic Study of Heterogeneous Catalysts" title="Some Turning Points in the Chemical Electron Microscopic Study of Heterogeneous Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Half a century, take a bow to the pavilion:</B> Over the past 50&nbsp;years or so, electron microscopy has become an invaluable technique for the study of solid catalysts. We recount some of the most important developments, including early high-resolution studies, insights obtained using aberration-corrected optics, recent advances in electron tomography, time-resolved electron microscopy, and precession electron diffraction.</P>
<p> [Essay]<br />John Meurig Thomas, Caterina Ducati, Rowan Leary, Paul A. Midgley<br /><i>ChemCatChem</i>, Apr 25, 2013, DOI: 10.1002/cctc.201200883. <a href="http://dx.doi.org/10.1002/cctc.201200883">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899/homepage/news/19105.en.html">
<title>VIP: Hydroxynitrile lyases do not catalyse a promiscuous addition of cyanide to imines</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899/homepage/news/19105.en.html</link>
<dc:date>2013-04-25T00:00:00+02:00</dc:date>
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<![CDATA[<p>Guzman Torrelo, Jianfeng Jin, and Ulf Hanefeld*</p>
<br>
<br><p>Ten years ago, it was reported that hydroxynitrile lyase (HNL) from defatted almond meal shows catalytic promiscuity in the addition of cyanide to imines. Here we provide experimental evidence that this addition occurs in a non-enzymatic reaction, and two structurally different HNLs do not catalyse this reaction.</p>
<br><!-- DOI: 10.1002/cctc.201200804 -->
<br><p>Received November 08, 2012, DOI: 10.1002/cctc.201200804</p>
<br>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300050">
<title>Isatin as a Strategic Motif for Asymmetric Catalysis</title>
<link>http://dx.doi.org/10.1002/cctc.201300050</link>
<dc:creator>Somayeh Mohammadi, Roghayeh Heiran, Raquel P. Herrera, Eugenia Marqués-López</dc:creator>
<dc:date>2013-04-24T08:37+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300050.gif" width="216" height="215" alt="Isatin as a Strategic Motif for Asymmetric Catalysis" title="Isatin as a Strategic Motif for Asymmetric Catalysis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Strategic move:</B> Isatin as a core structure has inspired the development of useful catalytic strategies to give access to interesting molecular architectures with biological activity.</P>
<p> [Minireview]<br />Somayeh Mohammadi, Roghayeh Heiran, Raquel P. Herrera, Eugenia Marqu&#xE9;s-L&#xF3;pez<br /><i>ChemCatChem</i>, Apr 24, 2013, DOI: 10.1002/cctc.201300050. <a href="http://dx.doi.org/10.1002/cctc.201300050">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300099">
<title>Synthesis of 2,5-Diarylpyrroles by Ligand-Free Palladium-Catalyzed CH Activation of Pyrroles in Ionic Liquids</title>
<link>http://dx.doi.org/10.1002/cctc.201300099</link>
<dc:creator>Peter Ehlers, Andranik Petrosyan, Jens Baumgard, Stefan Jopp, Norbert Steinfeld, Tariel V. Ghochikyan, Ashot S. Saghyan, Christine Fischer, Peter Langer</dc:creator>
<dc:date>2013-04-24T08:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300099.gif" width="215" height="169" alt="Synthesis of 2,5-Diarylpyrroles by Ligand-Free Palladium-Catalyzed CH Activation of Pyrroles in Ionic Liquids" title="Synthesis of 2,5-Diarylpyrroles by Ligand-Free Palladium-Catalyzed CH Activation of Pyrroles in Ionic Liquids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>No ligand, no problem:</B> Diarylpyrroles are synthesized through palladium-catalyzed CH activation and arylation in tetrabutylammonium acetate as an ionic solvent, allowing for a ligand-free catalysis with simple palladium salts or polyvinylpyrrolidone-stabilized palladium nanoparticles.</P>
<p> [Full Paper]<br />Peter Ehlers, Andranik Petrosyan, Jens Baumgard, Stefan Jopp, Norbert Steinfeld, Tariel V. Ghochikyan, Ashot S. Saghyan, Christine Fischer, Peter Langer<br /><i>ChemCatChem</i>, Apr 24, 2013, DOI: 10.1002/cctc.201300099. <a href="http://dx.doi.org/10.1002/cctc.201300099">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200880">
<title>A Study of Commercial Nanoparticulate γ-Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; Catalyst Supports</title>
<link>http://dx.doi.org/10.1002/cctc.201200880</link>
<dc:creator>Yahaya Rozita, Rik Brydson, Tim P. Comyn, Andrew J. Scott, Chris Hammond, Andy Brown, Sandra Chauruka, Ali Hassanpour, Neil P. Young, Angus I. Kirkland, Hidetaka Sawada, Ron I. Smith</dc:creator>
<dc:date>2013-04-24T08:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200880.gif" width="212" height="167" alt="A Study of Commercial Nanoparticulate &gamma;-Al2O3 Catalyst Supports" title="A Study of Commercial Nanoparticulate &gamma;-Al2O3 Catalyst Supports" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>New insights into familiar supports:</B> We investigate a range of commercially available &gamma;-Al<sub>2</sub>O<sub>3</sub> powders by using a combination of integrated experimental techniques such as XRD, neutron powder diffraction, and TEM. Most of the &gamma;-Al<sub>2</sub>O<sub>3</sub> powders studied comprised a significant proportion of cubeoctahedral nanoparticles containing numerous steps on the {1&nbsp;1&nbsp;1}-type aluminum cation-rich surface facets.</P>
<p> [Full Paper]<br />Yahaya Rozita, Rik Brydson, Tim P. Comyn, Andrew J. Scott, Chris Hammond, Andy Brown, Sandra Chauruka, Ali Hassanpour, Neil P. Young, Angus I. Kirkland, Hidetaka Sawada, Ron I. Smith<br /><i>ChemCatChem</i>, Apr 24, 2013, DOI: 10.1002/cctc.201200880. <a href="http://dx.doi.org/10.1002/cctc.201200880">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300052">
<title>One-Pot Production of Enantiopure Alkylamines and Arylalkylamines of Opposite Chirality Catalyzed by ω-Transaminase</title>
<link>http://dx.doi.org/10.1002/cctc.201300052</link>
<dc:creator>Eul-Soo Park, M. Shaheer Malik, Joo-Young Dong, Jong-Shik Shin</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/cctc201300052.gif" width="445" height="119" alt="One-Pot Production of Enantiopure Alkylamines and Arylalkylamines of Opposite Chirality Catalyzed by &omega;-Transaminase" title="One-Pot Production of Enantiopure Alkylamines and Arylalkylamines of Opposite Chirality Catalyzed by &omega;-Transaminase" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Looking for favors:</B> The thermodynamically favorable asymmetric amination of alkyl ketones was catalyzed by &omega;-transaminase with racemic arylalkylamines as an amine donor, thus affording enantiopure alkylamines and arylalkylamines of opposite chirality.</P>
<p> [Communication]<br />Eul-Soo Park, M. Shaheer Malik, Joo-Young Dong, Jong-Shik Shin<br /><i>ChemCatChem</i>, Apr 22, 2013, DOI: 10.1002/cctc.201300052. <a href="http://dx.doi.org/10.1002/cctc.201300052">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300032">
<title>Ligand-Free Copper-Catalyzed Coupling of Phenols with Nitroarenes by using a Metal–Organic Framework as a Robust and Recoverable Catalyst</title>
<link>http://dx.doi.org/10.1002/cctc.201300032</link>
<dc:creator>Nam T. S. Phan, Tung T. Nguyen, Vu T. Nguyen, Khoa D. Nguyen</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/cctc201300032.gif" width="447" height="116" alt="Ligand-Free Copper-Catalyzed Coupling of Phenols with Nitroarenes by using a Metal&ndash;Organic Framework as a Robust and Recoverable Catalyst" title="Ligand-Free Copper-Catalyzed Coupling of Phenols with Nitroarenes by using a Metal&ndash;Organic Framework as a Robust and Recoverable Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Catalytic MOF:</B> A highly porous metal&ndash;organic framework Cu<sub>2</sub>(BDC)<sub>2</sub>(DABCO) (H<sub>2</sub>BDC=1,4-benzenedicarboxylic acid, DABCO=1,4-diazabicyclo[2.2.2]octane) was synthesized and used as an efficient recyclable heterogeneous catalyst for the coupling reaction of phenols with nitroarenes to form diaryl ethers without using a ligand.</P>
<p> [Full Paper]<br />Nam T. S. Phan, Tung T. Nguyen, Vu T. Nguyen, Khoa D. Nguyen<br /><i>ChemCatChem</i>, Apr 22, 2013, DOI: 10.1002/cctc.201300032. <a href="http://dx.doi.org/10.1002/cctc.201300032">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200904">
<title>Electrocatalytic Reduction of Carbon Dioxide to Carbon Monoxide by a Polymerized Film of an Alkynyl-Substituted Rhenium(I) Complex</title>
<link>http://dx.doi.org/10.1002/cctc.201200904</link>
<dc:creator>Engelbert Portenkirchner, Jacek Gasiorowski, Kerstin Oppelt, Stefanie Schlager, Clemens Schwarzinger, Helmut Neugebauer, Günther Knör, Niyazi Serdar Sariciftci</dc:creator>
<dc:date>2013-04-19T12:33+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200904.gif" width="215" height="172" alt="Electrocatalytic Reduction of Carbon Dioxide to Carbon Monoxide by a Polymerized Film of an Alkynyl-Substituted Rhenium(I) Complex" title="Electrocatalytic Reduction of Carbon Dioxide to Carbon Monoxide by a Polymerized Film of an Alkynyl-Substituted Rhenium(I) Complex" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Electrocatalytic reduction:</B> The alkynyl-substituted Re<SUP>I</SUP> complex [Re(5,5&#x27;-bisphenylethynyl-2,2&#x27;-bipyridyl)(CO)<sub>3</sub>Cl] was immobilized by electropolymerization onto a Pt-plate electrode. The polymerized film exhibited electrocatalytic activity for the reduction of CO<sub>2</sub> to CO.</P>
<p> [Full Paper]<br />Engelbert Portenkirchner, Jacek Gasiorowski, Kerstin Oppelt, Stefanie Schlager, Clemens Schwarzinger, Helmut Neugebauer, G&#xFC;nther Kn&#xF6;r, Niyazi Serdar Sariciftci<br /><i>ChemCatChem</i>, Apr 19, 2013, DOI: 10.1002/cctc.201200904. <a href="http://dx.doi.org/10.1002/cctc.201200904">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300123">
<title>“Imprinting” Catalytically Active Pd Nanoparticles onto Ionic-Liquid-Modified Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; Supports</title>
<link>http://dx.doi.org/10.1002/cctc.201300123</link>
<dc:creator>Leandro Luza, Aitor Gual, Dario Eberhardt, Sérgio R. Teixeira, Sandra S. X. Chiaro, Jairton Dupont</dc:creator>
<dc:date>2013-04-18T16:07+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300123.gif" width="216" height="129" alt="&ldquo;Imprinting&rdquo; Catalytically Active Pd Nanoparticles onto Ionic-Liquid-Modified Al2O3 Supports" title="&ldquo;Imprinting&rdquo; Catalytically Active Pd Nanoparticles onto Ionic-Liquid-Modified Al2O3 Supports" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Going against tradition:</B> Uniformly distributed Pd nanoparticles on imidazolium-ionic-liquid-modified Al<sub>2</sub>O<sub>3</sub> surfaces are prepared by a top down approach by using a new sputtering chamber. The hydrogenation of 1,3-cyclohexadiene is used to probe the surface properties of these new Pd nanoparticles.</P>
<p> [Full Paper]<br />Leandro Luza, Aitor Gual, Dario Eberhardt, S&#xE9;rgio R. Teixeira, Sandra S. X. Chiaro, Jairton Dupont<br /><i>ChemCatChem</i>, Apr 18, 2013, DOI: 10.1002/cctc.201300123. <a href="http://dx.doi.org/10.1002/cctc.201300123">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300039">
<title>Selective Hydrogenation of Nitroaromatic Compounds with a Nickel-Oxide-Supported Nano-Palladium Catalyst under Ambient Reaction Conditions</title>
<link>http://dx.doi.org/10.1002/cctc.201300039</link>
<dc:creator>Huimin Yang, Xinjiang Cui, Youquan Deng, Feng Shi</dc:creator>
<dc:date>2013-04-18T16:07+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300039.gif" width="445" height="131" alt="Selective Hydrogenation of Nitroaromatic Compounds with a Nickel-Oxide-Supported Nano-Palladium Catalyst under Ambient Reaction Conditions" title="Selective Hydrogenation of Nitroaromatic Compounds with a Nickel-Oxide-Supported Nano-Palladium Catalyst under Ambient Reaction Conditions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Very supportive:</B> An active nickel-oxide-supported nano-palladium catalyst, Pd/NiO-M, promotes the selective hydrogenation of nitroaromatic compounds into anilines under ambient conditions. The catalyst was recovered and reused without deactivation.</P>
<p> [Communication]<br />Huimin Yang, Xinjiang Cui, Youquan Deng, Feng Shi<br /><i>ChemCatChem</i>, Apr 18, 2013, DOI: 10.1002/cctc.201300039. <a href="http://dx.doi.org/10.1002/cctc.201300039">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200912">
<title>Synthesis of Chiral Ligands with Multiple Stereogenic Centers and Their Application in Titanium(IV)-Catalyzed Enantioselective Desymmetrization of &lt;I&gt;meso-&lt;/I&gt;Epoxides</title>
<link>http://dx.doi.org/10.1002/cctc.201200912</link>
<dc:creator>Manish Kumar, Rukhsana I. Kureshy, Debashis Ghosh, Noor-ul H. Khan, Sayed H. R. Abdi, Hari C. Bajaj</dc:creator>
<dc:date>2013-04-18T16:06+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200912.gif" width="214" height="132" alt="Synthesis of Chiral Ligands with Multiple Stereogenic Centers and Their Application in Titanium(IV)-Catalyzed Enantioselective Desymmetrization of meso-Epoxides" title="Synthesis of Chiral Ligands with Multiple Stereogenic Centers and Their Application in Titanium(IV)-Catalyzed Enantioselective Desymmetrization of meso-Epoxides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Chiral ligands</B> with diverse stereogenic centers from diastereomeric combinations of aminoalcohol functionalities with (<I>R</I>)- and (<I>S</I>)-1,1-binaphthol are prepared. In asymmetric ring-opening reactions, catalytically active Ti complexes are generated in&nbsp;situ in the presence of water. <I>syn-beta</I>-Amino alcohols of <I>meso-</I>stilbene oxide with (1<I>S,</I>2<I>S</I>) and (1<I>R,</I>2<I>R</I>) configuration are produced in excellent yields (&gt;98&nbsp;%) and enantioselectivities (<I>ee&gt;</I>99&nbsp;%) at room temperature.</P>
<p> [Full Paper]<br />Manish Kumar, Rukhsana I. Kureshy, Debashis Ghosh, Noor-ul H. Khan, Sayed H. R. Abdi, Hari C. Bajaj<br /><i>ChemCatChem</i>, Apr 18, 2013, DOI: 10.1002/cctc.201200912. <a href="http://dx.doi.org/10.1002/cctc.201200912">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300092">
<title>Binuclear Cooperative Catalysts for the Hydrogenation and Hydroformylation of Olefins</title>
<link>http://dx.doi.org/10.1002/cctc.201300092</link>
<dc:creator>Dennis G. H. Hetterscheid, Samir H. Chikkali, Bas de Bruin, Joost N. H. Reek</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/cctc201300092.gif" width="198" height="187" alt="Binuclear Cooperative Catalysts for the Hydrogenation and Hydroformylation of Olefins" title="Binuclear Cooperative Catalysts for the Hydrogenation and Hydroformylation of Olefins" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Let&rsquo;s cooperate!</B> Cooperative bimetallic catalysis plays an important role in bioenzymatic conversions, and numerous examples are reported in (bio)inorganic and organic chemistry. In organometallic chemistry, this type of catalysis is rare. Here, the concept of cooperative binuclear substrate activation in hydrogenation and hydroformylation reactions is discussed.</P>
<p> [Minireview]<br />Dennis G. H. Hetterscheid, Samir H. Chikkali, Bas de&#xA0;Bruin, Joost N. H. Reek<br /><i>ChemCatChem</i>, Apr 16, 2013, DOI: 10.1002/cctc.201300092. <a href="http://dx.doi.org/10.1002/cctc.201300092">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300037">
<title>Gd&lt;sub&gt;2&lt;/sub&gt;Ti&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt;/In&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;: Efficient Visible-Light-Driven Heterojunction-Based Composite Photocatalysts for Hydrogen Production</title>
<link>http://dx.doi.org/10.1002/cctc.201300037</link>
<dc:creator>Amtul Nashim , Satyabadi Martha, K. M. Parida</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/cctc201300037.gif" width="214" height="162" alt="Gd2Ti2O7/In2O3: Efficient Visible-Light-Driven Heterojunction-Based Composite Photocatalysts for Hydrogen Production" title="Gd2Ti2O7/In2O3: Efficient Visible-Light-Driven Heterojunction-Based Composite Photocatalysts for Hydrogen Production" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Let there be hydrogen:</B> The collection of photogenerated charge carriers on different photocatalytic surfaces enhances the activity of heterojunction-based Gd<sub>2</sub>Ti<sub>2</sub>O<sub>7</sub>/In<sub>2</sub>O<sub>3</sub> composites for hydrogen production.</P>
<p> [Full Paper]<br />Amtul Nashim&#xA0;, Satyabadi Martha, K. M. Parida&#xA0;<br /><i>ChemCatChem</i>, Apr 16, 2013, DOI: 10.1002/cctc.201300037. <a href="http://dx.doi.org/10.1002/cctc.201300037">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200862">
<title>Selective Gas-Phase Oxidation of Alcohols over Nanoporous Silver</title>
<link>http://dx.doi.org/10.1002/cctc.201200862</link>
<dc:creator>Zhiwen Li, Junling Xu, Xiaohu Gu, Kang Wang, Wenhui Wang, Xiaomei Zhang, Zhonghua Zhang, Yi Ding</dc:creator>
<dc:date>2013-04-16T15:29+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200862.gif" width="215" height="174" alt="Selective Gas-Phase Oxidation of Alcohols over Nanoporous Silver" title="Selective Gas-Phase Oxidation of Alcohols over Nanoporous Silver" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Hi ho silver lining:</B> Dealloyed nanoporous silver showed high activity and selectivity for the partial oxidation of MeOH into formaldehyde and of several primary and secondary aliphatic alcohols into their corresponding aldehydes or ketones.</P>
<p> [Communication]<br />Zhiwen Li, Junling Xu, Xiaohu Gu, Kang Wang, Wenhui Wang, Xiaomei Zhang, Zhonghua Zhang, Yi Ding<br /><i>ChemCatChem</i>, Apr 16, 2013, DOI: 10.1002/cctc.201200862. <a href="http://dx.doi.org/10.1002/cctc.201200862">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899/homepage/news/19053.en.html">
<title>VIP: Electrocatalytic reduction of nitrate on a Pt electrode modified by p-block metal adatoms in acid solution</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899/homepage/news/19053.en.html</link>
<dc:date>2013-04-16T00:00:00+02:00</dc:date>
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<![CDATA[<p>Jian Yang, Federico Calle-Vallejo, Matteo Duca, Marc T.M. Koper*</p>
<br><p>The electrocatalytic reduction of nitrate on platinum was studied in the presence of a large variety of p-block metal promoters, in perchloric and sulfuric acidic media. Tin is the most active promoter, yielding volatile reaction products such as nitrous oxide and nitric oxide. Density functional theory calculations indicate that tin hydroxide  adsorbed on the platinum surface enhances the nitrate adsorption and thereby increases the reduction activity.</p>
<br><!-- DOI: 10.1002/cctc.201300075 -->
<br><p>Received January 28, 2013, DOI: 10.1002/cctc.201200616</p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300063">
<title>A Monovacant Lacunary Silicotungstate as an Efficient Heterogeneous Catalyst for Dehydration of Primary Amides to Nitriles</title>
<link>http://dx.doi.org/10.1002/cctc.201300063</link>
<dc:creator>Shintaro Itagaki, Keigo Kamata, Kazuya Yamaguchi, Noritaka Mizuno</dc:creator>
<dc:date>2013-04-15T14:09+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300063.gif" width="439" height="104" alt="A Monovacant Lacunary Silicotungstate as an Efficient Heterogeneous Catalyst for Dehydration of Primary Amides to Nitriles" title="A Monovacant Lacunary Silicotungstate as an Efficient Heterogeneous Catalyst for Dehydration of Primary Amides to Nitriles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Acting up with nitriles:</B> A monovacant lacunary silicotungstate, TBA<sub>4</sub>[<I>&alpha;</I>-H<sub>4</sub>SiW<sub>11</sub>O<sub>39</sub>] (<B>I</B>) could act as an efficient heterogeneous catalyst for dehydration of primary amides. Various kinds of primary amides, including benzylic, double bond-containing, heteroaromatic, and aliphatic could be converted into the corresponding nitriles in moderate to excellent yields.</P>
<p> [Communication]<br />Shintaro Itagaki, Keigo Kamata, Kazuya Yamaguchi, Noritaka Mizuno<br /><i>ChemCatChem</i>, Apr 15, 2013, DOI: 10.1002/cctc.201300063. <a href="http://dx.doi.org/10.1002/cctc.201300063">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300010">
<title>CNT-Supported Mo&lt;sub&gt;&lt;I&gt;x&lt;/I&gt;&lt;/sub&gt;C Catalysts: Effect of Loading and Carburization Parameters</title>
<link>http://dx.doi.org/10.1002/cctc.201300010</link>
<dc:creator>Benjamin Frank, Klaus Friedel, Frank Girgsdies, Xing Huang, Robert Schlögl, Annette Trunschke</dc:creator>
<dc:date>2013-04-15T14:09+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300010.gif" width="216" height="216" alt="CNT-Supported MoxC Catalysts: Effect of Loading and Carburization Parameters" title="CNT-Supported MoxC Catalysts: Effect of Loading and Carburization Parameters" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Reducing to the essential:</B> The synthesis of carbon nanotube-supported &alpha;-MoC and &beta;-Mo<sub>2</sub>C nanoparticles can be controlled by the carburization conditions used. The effects of molybdenum loading, heating rate of carburization, and carburization atmosphere on the catalytic performance of resulting molybdenum carbide catalysts in the steam reforming of methanol are discussed.</P>
<p> [Full Paper]<br />Benjamin Frank, Klaus Friedel, Frank Girgsdies, Xing Huang, Robert Schl&#xF6;gl, Annette Trunschke<br /><i>ChemCatChem</i>, Apr 15, 2013, DOI: 10.1002/cctc.201300010. <a href="http://dx.doi.org/10.1002/cctc.201300010">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200936">
<title>Terpene-Derived Bifunctional Thioureas in Asymmetric Organocatalysis</title>
<link>http://dx.doi.org/10.1002/cctc.201200936</link>
<dc:creator>Senthil Narayanaperumal, Daniel G. Rivera, Rodrigo C. Silva, Márcio W. Paixão</dc:creator>
<dc:date>2013-04-15T14:09+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200936.gif" width="212" height="212" alt="Terpene-Derived Bifunctional Thioureas in Asymmetric Organocatalysis" title="Terpene-Derived Bifunctional Thioureas in Asymmetric Organocatalysis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>From pine resin to catalyst:</B> The easily available rosin diterpene abietic acid has been transformed into a unique class of bifunctional thiourea catalysts that can also incorporate further substituents, thereby enabling either Lewis base or enamine activation modes. Their application in a wide range of stereoselective transformations has revealed the positive effect of this chiral and rigid skeleton on the catalytic performance of these hybrid thioureas.</P>
<p> [Review]<br />Senthil Narayanaperumal, Daniel G. Rivera, Rodrigo C. Silva, M&#xE1;rcio W. Paix&#xE3;o<br /><i>ChemCatChem</i>, Apr 15, 2013, DOI: 10.1002/cctc.201200936. <a href="http://dx.doi.org/10.1002/cctc.201200936">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200863">
<title>On-Chip Catalytic Microreactors for Modern Catalysis Research</title>
<link>http://dx.doi.org/10.1002/cctc.201200863</link>
<dc:creator>Bin-Bin Xu, Yong-Lai Zhang, Shu Wei, Hong Ding, Hong-Bo Sun</dc:creator>
<dc:date>2013-04-15T14:09+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200863.gif" width="446" height="113" alt="On-Chip Catalytic Microreactors for Modern Catalysis Research" title="On-Chip Catalytic Microreactors for Modern Catalysis Research" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Great expectations for microreactors:</B> We highlight the importance of on-chip catalytic microreactors for catalysis research. New approaches to the fabrication of on-chip catalytic microreactors and their integration with multifunctional components are introduced. It is believed that on-chip catalytic microreactors could become a highly efficient experimental platform for modern catalysis.</P>
<p> [Concept]<br />Bin-Bin Xu, Yong-Lai Zhang, Shu Wei, Hong Ding, Hong-Bo Sun<br /><i>ChemCatChem</i>, Apr 15, 2013, DOI: 10.1002/cctc.201200863. <a href="http://dx.doi.org/10.1002/cctc.201200863">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300129">
<title>Ship in a Bottle: In&#160;situ Confined Growth of Complex Yolk-shell Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201300129</link>
<dc:creator>James Goebl, Yadong Yin</dc:creator>
<dc:date>2013-04-15T14:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300129.gif" width="216" height="127" alt="Ship in a Bottle: In&nbsp;situ Confined Growth of Complex Yolk-shell Catalysts" title="Ship in a Bottle: In&nbsp;situ Confined Growth of Complex Yolk-shell Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Ship in a Bottle:</B> The confined synthesis of binary anisotropic nanoparticle catalysts within a hollow support allows for the creation of highly complex new catalyst architectures.</P>
<p> [Highlight]<br />James Goebl, Yadong Yin<br /><i>ChemCatChem</i>, Apr 15, 2013, DOI: 10.1002/cctc.201300129. <a href="http://dx.doi.org/10.1002/cctc.201300129">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200960">
<title>Dimensional Effects in the Carbidization of Supported Iron Nanoparticles</title>
<link>http://dx.doi.org/10.1002/cctc.201200960</link>
<dc:creator>Petr A. Chernavskii, Vladimir I. Zaikovskii, Galina V. Pankina, Andrei Y. Khodakov</dc:creator>
<dc:date>2013-04-15T14:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200960.gif" width="215" height="134" alt="Dimensional Effects in the Carbidization of Supported Iron Nanoparticles" title="Dimensional Effects in the Carbidization of Supported Iron Nanoparticles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Iron-clad results:</B> The effect of nanoparticle size on the kinetics of iron carbidization on silica-supported catalysts was studied by using an in&nbsp;situ magnetic method combined with simultaneous analysis of the reaction products. The activation energy of carbide formation in both CO and syngas grew with a decrease in the particle size of iron: Smaller iron carbide particles (<I>d</I>=9&nbsp;nm) appear to be less stable than their larger counterparts.</P>
<p> [Communication]<br />Petr A. Chernavskii, Vladimir I. Zaikovskii, Galina V. Pankina, Andrei Y. Khodakov<br /><i>ChemCatChem</i>, Apr 15, 2013, DOI: 10.1002/cctc.201200960. <a href="http://dx.doi.org/10.1002/cctc.201200960">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200700">
<title>Catalysis of Enantioselective Strecker Reaction in the Synthesis of &lt;span style="font-variant:small-caps"&gt;D&lt;/span&gt;-Homophenylalanine Using Recyclable, Chiral, Macrocyclic Mn&lt;SUP&gt;III&lt;/SUP&gt;–Salen Complexes</title>
<link>http://dx.doi.org/10.1002/cctc.201200700</link>
<dc:creator>S. Saravanan, Noor-ul H. Khan, Prasanta K. Bera, Rukhsana I. Kureshy, Sayed H. R. Abdi, Prathibha Kumari, Hari C. Bajaj</dc:creator>
<dc:date>2013-04-12T08:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200700.gif" width="214" height="138" alt="Catalysis of Enantioselective Strecker Reaction in the Synthesis of D-Homophenylalanine Using Recyclable, Chiral, Macrocyclic MnIII&ndash;Salen Complexes " title="Catalysis of Enantioselective Strecker Reaction in the Synthesis of D-Homophenylalanine Using Recyclable, Chiral, Macrocyclic MnIII&ndash;Salen Complexes " style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Salen away to sea:</B> A convenient approach to the asymmetric Strecker reaction was established by synthesizing chiral, mono- and dinuclear, macrocyclic Mn<SUP>III</SUP>&ndash;salen complexes possessing achiral and chiral linkers. These complexes showed very good catalytic ability for the enantioselevtive Strecker reaction of aldimines.</P>
<p> [Full Paper]<br />S. Saravanan, Noor-ul H. Khan, Prasanta K. Bera, Rukhsana I. Kureshy, Sayed H. R. Abdi, Prathibha Kumari, Hari C. Bajaj<br /><i>ChemCatChem</i>, Apr 12, 2013, DOI: 10.1002/cctc.201200700. <a href="http://dx.doi.org/10.1002/cctc.201200700">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300028">
<title>Asymmetric Biocatalytic Cannizzaro-Type Reaction</title>
<link>http://dx.doi.org/10.1002/cctc.201300028</link>
<dc:creator>Christiane Wuensch, Horst Lechner, Silvia M. Glueck, Klaus Zangger, Mélanie Hall, Kurt Faber</dc:creator>
<dc:date>2013-04-12T08:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300028.gif" width="214" height="142" alt="Asymmetric Biocatalytic Cannizzaro-Type Reaction" title="Asymmetric Biocatalytic Cannizzaro-Type Reaction" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Blowing out of disproportion:</B> Alcohol dehydrogenases were found to catalyze a bio-Cannizzaro-type reaction. The disproportionation of various aldehydes into their corresponding alcohols and carboxylic acids was achieved in a redox-neutral process. The asymmetric variant proceeded with high stereoselectivities.</P>
<p> [Communication]<br />Christiane Wuensch, Horst Lechner, Silvia M. Glueck, Klaus Zangger, M&#xE9;lanie Hall, Kurt Faber<br /><i>ChemCatChem</i>, Apr 12, 2013, DOI: 10.1002/cctc.201300028. <a href="http://dx.doi.org/10.1002/cctc.201300028">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200942">
<title>Catalytic Dehydrogenative Amide and Ester Formation with Rhenium–Triphos Complexes</title>
<link>http://dx.doi.org/10.1002/cctc.201200942</link>
<dc:creator>P. Philipp M. Schleker, Roman Honeker, Jürgen Klankermayer, Walter Leitner</dc:creator>
<dc:date>2013-04-11T09:01+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200942.gif" width="446" height="102" alt="Catalytic Dehydrogenative Amide and Ester Formation with Rhenium&ndash;Triphos Complexes" title="Catalytic Dehydrogenative Amide and Ester Formation with Rhenium&ndash;Triphos Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>[Re]ad all about it:</B> The first examples of the rhenium-catalyzed dehydrogenative formation of amides and esters with the highly active ReH<sub>5</sub>(triphos) complex is demonstrated. The addition of a tertiary amine additive improves the selectivity and the stability of the catalyst in the formation of esters from primary alcohols.</P>
<p> [Communication]<br />P. Philipp M. Schleker, Roman Honeker, J&#xFC;rgen Klankermayer, Walter Leitner<br /><i>ChemCatChem</i>, Apr 11, 2013, DOI: 10.1002/cctc.201200942. <a href="http://dx.doi.org/10.1002/cctc.201200942">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200839">
<title>Catalytic Hydrogenation of CO&lt;sub&gt;2&lt;/sub&gt; to Formic Acid with Silica-Tethered Iridium Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201200839</link>
<dc:creator>Zheng Xu, Nicholas D. McNamara, Gregory T. Neumann, William F. Schneider, Jason C. Hicks</dc:creator>
<dc:date>2013-04-11T09:01+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200839.gif" width="215" height="176" alt="Catalytic Hydrogenation of CO2 to Formic Acid with Silica-Tethered Iridium Catalysts" title="Catalytic Hydrogenation of CO2 to Formic Acid with Silica-Tethered Iridium Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Tetherball:</B> A heterogeneous, mesoporous silica-tethered iridium catalyst (Ir-PN/SBA-15) containing a bidentate iminophosphine ligand is synthesized for the hydrogenation of CO<sub>2</sub> to formic acid in aqueous solution. This new recyclable catalyst exhibits high activities to formic acid production under mild conditions [60&nbsp;&deg;C, 4.0&nbsp;MPa total pressure (H<sub>2</sub>/CO<sub>2</sub>=1:1)].</P>
<p> [Communication]<br />Zheng Xu, Nicholas D. McNamara, Gregory T. Neumann, William F. Schneider, Jason C. Hicks<br /><i>ChemCatChem</i>, Apr 11, 2013, DOI: 10.1002/cctc.201200839. <a href="http://dx.doi.org/10.1002/cctc.201200839">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300005">
<title>Enhancement of Catalytic Activities of Octahedral Molecular Sieve Manganese Oxide for Total and Preferential CO Oxidation through Vanadium Ion Framework Substitution</title>
<link>http://dx.doi.org/10.1002/cctc.201300005</link>
<dc:creator>Homer C. Genuino, Yongtao Meng, Dayton T. Horvath, Chung-Hao Kuo, Mohammad S. Seraji, Aimee M. Morey, Raymond L. Joesten, Steven L. Suib</dc:creator>
<dc:date>2013-04-11T09:00+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300005.gif" width="443" height="124" alt="Enhancement of Catalytic Activities of Octahedral Molecular Sieve Manganese Oxide for Total and Preferential CO Oxidation through Vanadium Ion Framework Substitution" title="Enhancement of Catalytic Activities of Octahedral Molecular Sieve Manganese Oxide for Total and Preferential CO Oxidation through Vanadium Ion Framework Substitution" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Doping for better performance</B>: Vanadium ions substituted into the framework of octahedral molecular sieve manganese oxide nanomaterials through a simple reflux method significantly improved the catalytic activity for total and preferential carbon monoxide oxidation.</P>
<p> [Full Paper]<br />Homer C. Genuino, Yongtao Meng, Dayton T. Horvath, Chung-Hao Kuo, Mohammad S. Seraji, Aimee M. Morey, Raymond L. Joesten, Steven L. Suib<br /><i>ChemCatChem</i>, Apr 11, 2013, DOI: 10.1002/cctc.201300005. <a href="http://dx.doi.org/10.1002/cctc.201300005">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200877">
<title>On the Use of Seawater as Reaction Media for Large-Scale Applications in Biorefineries</title>
<link>http://dx.doi.org/10.1002/cctc.201200877</link>
<dc:creator>Pablo Domínguez de María</dc:creator>
<dc:date>2013-04-11T09:00+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200877.gif" width="212" height="159" alt="On the Use of Seawater as Reaction Media for Large-Scale Applications in Biorefineries" title="On the Use of Seawater as Reaction Media for Large-Scale Applications in Biorefineries" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Seawater and biorefineries:</B> Many biorefinery-oriented methods can be performed in seawater, which enables the use of nonpotable water resources for biomass (e.g., algae) valorization. Provided that adequate waste(sea)water treatments are implemented, the use of seawater may enable the local delivery of chemicals and biofuels for coastal regions.</P>
<p> [Concept]<br />Pablo Dom&#xED;nguez&#xA0;de&#xA0;Mar&#xED;a<br /><i>ChemCatChem</i>, Apr 11, 2013, DOI: 10.1002/cctc.201200877. <a href="http://dx.doi.org/10.1002/cctc.201200877">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200758">
<title>Immobilizing Carbon Nanotubes on SiC Foam as a Monolith Catalyst for Oxidative Dehydrogenation Reactions</title>
<link>http://dx.doi.org/10.1002/cctc.201200758</link>
<dc:creator>Hua Yuan, Zhenhua Sun, Hongyang Liu, Bingsen Zhang, Chunlin Chen, Haihua Wang, Zhenming Yang, Jinsong Zhang, Fei Wei, Dang Sheng Su</dc:creator>
<dc:date>2013-04-11T09:00+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200758.gif" width="215" height="119" alt="Immobilizing Carbon Nanotubes on SiC Foam as a Monolith Catalyst for Oxidative Dehydrogenation Reactions" title="Immobilizing Carbon Nanotubes on SiC Foam as a Monolith Catalyst for Oxidative Dehydrogenation Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Foam party:</B> A new method is reported for the immobilization of carbon nanotubes (CNTs) onto silicon carbide foam to afford a CNT/SiC monolith catalyst for sustainable chemistry applications. The as-synthesized monolith displayed good stability and high catalytic performance in the oxidative dehydrogenation (ODH) of 1-butene into butadiene.</P>
<p> [Communication]<br />Hua Yuan, Zhenhua Sun, Hongyang Liu, Bingsen Zhang, Chunlin Chen, Haihua Wang, Zhenming Yang, Jinsong Zhang, Fei Wei, Dang Sheng Su<br /><i>ChemCatChem</i>, Apr 11, 2013, DOI: 10.1002/cctc.201200758. <a href="http://dx.doi.org/10.1002/cctc.201200758">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200954">
<title>Imidazolium-Based Organic–Inorganic Hybrid Silica as a Functional Platform Dramatically Boosts Chiral Organometallics Performance in Asymmetric Catalysis</title>
<link>http://dx.doi.org/10.1002/cctc.201200954</link>
<dc:creator>Daquan Xia, Tanyu Cheng, Wei Xiao, Ketang Liu, Zhaoliang Wang, Guohua Liu, Hexing Li, Wei Wang</dc:creator>
<dc:date>2013-04-10T15:39+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200954.gif" width="442" height="187" alt="Imidazolium-Based Organic&ndash;Inorganic Hybrid Silica as a Functional Platform Dramatically Boosts Chiral Organometallics Performance in Asymmetric Catalysis" title="Imidazolium-Based Organic&ndash;Inorganic Hybrid Silica as a Functional Platform Dramatically Boosts Chiral Organometallics Performance in Asymmetric Catalysis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A phase-transfer featured</B>, imidazolium-based, organic&ndash;inorganic hybrid silica as a functional platform, is used to develop a bifunctionalized heterogeneous catalyst that displays comparable or higher catalytic activity and enantioselectivity than its homogeneous counterpart in asymmetric transformations. This hybrid silica also boosts asymmetric catalysis and can be recovered conveniently and reused without affecting its catalytic efficiency.</P>
<p> [Full Paper]<br />Daquan Xia, Tanyu Cheng, Wei Xiao, Ketang Liu, Zhaoliang Wang, Guohua Liu, Hexing Li, Wei Wang<br /><i>ChemCatChem</i>, Apr 10, 2013, DOI: 10.1002/cctc.201200954. <a href="http://dx.doi.org/10.1002/cctc.201200954">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200887">
<title>Light-Induced Reduction of Cuprous Oxide in an Environmental Transmission Electron Microscope</title>
<link>http://dx.doi.org/10.1002/cctc.201200887</link>
<dc:creator>Filippo Cavalca, Anders B. Laursen, Jakob B. Wagner, Christian D. Damsgaard, Ib Chorkendorff, Thomas W. Hansen</dc:creator>
<dc:date>2013-04-10T15:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200887.gif" width="212" height="211" alt="Light-Induced Reduction of Cuprous Oxide in an Environmental Transmission Electron Microscope" title="Light-Induced Reduction of Cuprous Oxide in an Environmental Transmission Electron Microscope" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Illuminating photocatalysis:</B> Exposing cuprous oxide to light in an aqueous environment causes reduction to metallic copper. Using a combination of imaging, diffraction, and spectroscopy new insight into the reduction mechanism has been obtained.</P>
<p> [Full Paper]<br />Filippo Cavalca, Anders B. Laursen, Jakob B. Wagner, Christian D. Damsgaard, Ib Chorkendorff, Thomas W. Hansen<br /><i>ChemCatChem</i>, Apr 10, 2013, DOI: 10.1002/cctc.201200887. <a href="http://dx.doi.org/10.1002/cctc.201200887">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200875">
<title>Three Carbons for Complexity! Recent Developments of Palladium-Catalyzed Reactions of Allenes</title>
<link>http://dx.doi.org/10.1002/cctc.201200875</link>
<dc:creator>Tilman Lechel, Fabian Pfrengle, Hans-Ulrich Reissig, Reinhold Zimmer</dc:creator>
<dc:date>2013-04-09T14:41+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200875.gif" width="215" height="158" alt="Three Carbons for Complexity! Recent Developments of Palladium-Catalyzed Reactions of Allenes" title="Three Carbons for Complexity! Recent Developments of Palladium-Catalyzed Reactions of Allenes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Complexity at its best!</B> This review summarizes the latest advances in the field of allenes for their applications as substrates in palladium-catalyzed reactions. The progress in the field of allene chemistry is amazing and covers a plethora of products ranging from simple acyclic compounds to complex molecule architectures and natural products.</P>
<p> [Review]<br />Tilman Lechel, Fabian Pfrengle, Hans-Ulrich Reissig, Reinhold Zimmer<br /><i>ChemCatChem</i>, Apr 09, 2013, DOI: 10.1002/cctc.201200875. <a href="http://dx.doi.org/10.1002/cctc.201200875">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300021">
<title>Encapsulation of an Olefin Metathesis Catalyst in the Nanocages of SBA-1: Facile Preparation, High Encapsulation Efficiency, and High Activity</title>
<link>http://dx.doi.org/10.1002/cctc.201300021</link>
<dc:creator>Hengquan Yang, Zhancheng Ma, Ting Zhou, Wenjuan Zhang, Jianbin Chao, Yong Qin</dc:creator>
<dc:date>2013-04-09T14:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300021.gif" width="170" height="165" alt="Encapsulation of an Olefin Metathesis Catalyst in the Nanocages of SBA-1: Facile Preparation, High Encapsulation Efficiency, and High Activity" title="Encapsulation of an Olefin Metathesis Catalyst in the Nanocages of SBA-1: Facile Preparation, High Encapsulation Efficiency, and High Activity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Reaction in a cage:</B> 2nd generation Hoveyda&ndash;Grubbs catalyst was effectively encapsulated in the nanocages of a mesoporous material SBA-1 through a simple post-reduction of the pore size. This solid catalyst showed an activity comparable to its homogeneous counterpart in olefin metathesis reaction and more sensitive temperature effects than the homogeneous counterpart. This catalyst can be recycled seven times without significant Ru leaching.</P>
<p> [Full Paper]<br />Hengquan Yang, Zhancheng Ma, Ting Zhou, Wenjuan Zhang, Jianbin Chao, Yong Qin<br /><i>ChemCatChem</i>, Apr 09, 2013, DOI: 10.1002/cctc.201300021. <a href="http://dx.doi.org/10.1002/cctc.201300021">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300006">
<title>Zeolite Catalyzed Transformation of Carbohydrates to Alkyl Levulinates</title>
<link>http://dx.doi.org/10.1002/cctc.201300006</link>
<dc:creator>Shumugavel Saravanamurugan, Anders Riisager</dc:creator>
<dc:date>2013-04-09T14:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300006.gif" width="214" height="187" alt="Zeolite Catalyzed Transformation of Carbohydrates to Alkyl Levulinates" title="Zeolite Catalyzed Transformation of Carbohydrates to Alkyl Levulinates" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Caught in an acid trap!</B> Zeolites with moderate acidity are demonstrated to be versatile and reusable solid-acid catalysts for the transformation of biomass derived carbohydrates to alkyl levulinates in alcohol solvents. In short-chained alcohols it proved possible to obtain significantly higher yields of alkyl levulinates, than what is achievable of levulinic acid in analogous reactions performed in water.</P>
<p> [Communication]<br />Shumugavel Saravanamurugan, Anders Riisager<br /><i>ChemCatChem</i>, Apr 09, 2013, DOI: 10.1002/cctc.201300006. <a href="http://dx.doi.org/10.1002/cctc.201300006">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200922">
<title>Mesoporous Gallosilicate with 3&#160;D Architecture as a Robust Energy-Efficient Heterogeneous Catalyst for Diphenylmethane Production</title>
<link>http://dx.doi.org/10.1002/cctc.201200922</link>
<dc:creator>Chokkalingam Anand, Stalin Joseph, Geoffrey Lawrence, Dattatray S. Dhawale, Md. Abdul Wahab, Jin-Ho Choy, Ajayan Vinu</dc:creator>
<dc:date>2013-04-09T14:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200922.gif" width="216" height="194" alt="Mesoporous Gallosilicate with 3&nbsp;D Architecture as a Robust Energy-Efficient Heterogeneous Catalyst for Diphenylmethane Production" title="Mesoporous Gallosilicate with 3&nbsp;D Architecture as a Robust Energy-Efficient Heterogeneous Catalyst for Diphenylmethane Production" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>3&nbsp;D architecture:</B> We report the preparation and catalytic activity of 3&nbsp;D mesoporous gallosilicate with <I>Ia3d</I> symmetry (GaKIT-6) and different gallium content, which show a high activity even at reaction temperature as low as 313&nbsp;K, as well as a high benzyl chloride (BC) conversion and diphenylmethane (DPM) selectivity. The GaKIT-6 catalysts are found to be not only highly active but also stable and recyclable.</P>
<p> [Full Paper]<br />Chokkalingam Anand, Stalin Joseph, Geoffrey Lawrence, Dattatray S. Dhawale, Md. Abdul Wahab, Jin-Ho Choy, Ajayan Vinu<br /><i>ChemCatChem</i>, Apr 09, 2013, DOI: 10.1002/cctc.201200922. <a href="http://dx.doi.org/10.1002/cctc.201200922">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300080">
<title>A Ruthenium Catalyst with Simple Triphenylphosphane for the Enantioselective Hydrogenation of Aromatic Ketones</title>
<link>http://dx.doi.org/10.1002/cctc.201300080</link>
<dc:creator>Han Zhou, Hanmin Huang</dc:creator>
<dc:date>2013-04-08T15:51+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300080.gif" width="447" height="84" alt="A Ruthenium Catalyst with Simple Triphenylphosphane for the Enantioselective Hydrogenation of Aromatic Ketones" title="A Ruthenium Catalyst with Simple Triphenylphosphane for the Enantioselective Hydrogenation of Aromatic Ketones" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Keep it simple:</B> An efficient Ru catalyst constructed from simple and commercially available triphenylphosphane and enantiopure (1<I>S</I>,1&#x27;<I>S</I>)-1,1&#x27;-biisoindoline (BIDN) was applied to the asymmetric hydrogenation of aromatic ketones. A range of simple aromatic ketones could be hydrogenated with good to excellent enantioselectivities (up to 95&nbsp;% <I>ee</I>).</P>
<p> [Full Paper]<br />Han Zhou, Hanmin Huang<br /><i>ChemCatChem</i>, Apr 08, 2013, DOI: 10.1002/cctc.201300080. <a href="http://dx.doi.org/10.1002/cctc.201300080">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200742">
<title>Microwave-Assisted Ethanol Reduction as a New Method for the Preparation of Highly Active and Stable CNT-Supported PtRu Electrocatalysts for Methanol Oxidation</title>
<link>http://dx.doi.org/10.1002/cctc.201200742</link>
<dc:creator>Abu Bakr Ahmed Amine Nassr, Michael Bron</dc:creator>
<dc:date>2013-04-08T15:51+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200742.gif" width="173" height="82" alt="Microwave-Assisted Ethanol Reduction as a New Method for the Preparation of Highly Active and Stable CNT-Supported PtRu Electrocatalysts for Methanol Oxidation" title="Microwave-Assisted Ethanol Reduction as a New Method for the Preparation of Highly Active and Stable CNT-Supported PtRu Electrocatalysts for Methanol Oxidation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Microwaves assist everything!</B> A facile microwave-assisted synthesis route for the preparation of PtRu/carbon nanotube electrocatalysts is presented, in which an ethanol/water mixture is used as a solvent/reducing agent. The prepared catalysts are highly active in methanol electrooxidation. After reduction at higher temperatures, the degree of alloying and catalyst stability are enhanced.</P>
<p> [Full Paper]<br />Abu Bakr Ahmed Amine Nassr, Michael Bron<br /><i>ChemCatChem</i>, Apr 08, 2013, DOI: 10.1002/cctc.201200742. <a href="http://dx.doi.org/10.1002/cctc.201200742">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200876">
<title>Enhancing Biocatalysis: The Case of Unfolded Cytochrome&#160;&lt;I&gt;c&lt;/I&gt; Immobilized on Kaolinite</title>
<link>http://dx.doi.org/10.1002/cctc.201200876</link>
<dc:creator>Elena Castellini, Carlo Augusto Bortolotti, Giulia Di Rocco, Fabrizio Bernini, Antonio Ranieri</dc:creator>
<dc:date>2013-04-05T14:22+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200876.gif" width="216" height="128" alt="Enhancing Biocatalysis: The Case of Unfolded Cytochrome&nbsp;c Immobilized on Kaolinite" title="Enhancing Biocatalysis: The Case of Unfolded Cytochrome&nbsp;c Immobilized on Kaolinite" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Enhanced catalysis!</B> Urea-unfolded wild-type cytochrome&nbsp;<I>c</I> and its variants immobilized on kaolinite show peroxidase activity that is significantly higher than that of the folded wild-type protein. The accessibility of the substrate to the metal center and the influence of strategic amino acidic residues on the surface of the protein are discussed. This approach sheds light on the factors affecting the catalytic activity of a new versatile biocatalytic interface.</P>
<p> [Communication]<br />Elena Castellini, Carlo Augusto Bortolotti, Giulia Di&#xA0;Rocco, Fabrizio Bernini, Antonio Ranieri<br /><i>ChemCatChem</i>, Apr 05, 2013, DOI: 10.1002/cctc.201200876. <a href="http://dx.doi.org/10.1002/cctc.201200876">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200692">
<title>Enantioselective Intramolecular 1,5-Hydride Transfer/Cyclization through the Direct Functionalization of C(sp&lt;SUP&gt;3&lt;/SUP&gt;)-H Bonds Adjacent to a Heteroatom: From Nitrogen to Oxygen</title>
<link>http://dx.doi.org/10.1002/cctc.201200692</link>
<dc:creator>Min Wang</dc:creator>
<dc:date>2013-04-05T14:22+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200692.gif" width="446" height="109" alt="Enantioselective Intramolecular 1,5-Hydride Transfer/Cyclization through the Direct Functionalization of C(sp3)-H Bonds Adjacent to a Heteroatom: From Nitrogen to Oxygen" title="Enantioselective Intramolecular 1,5-Hydride Transfer/Cyclization through the Direct Functionalization of C(sp3)-H Bonds Adjacent to a Heteroatom: From Nitrogen to Oxygen" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Direct and effective:</B> the asymmetric catalytic 1,5-hydride transfer/cyclization, internal redox process, has recently been reported. This transformation is an effective method to functionalization of sp<SUP>3</SUP>-C-H bond adjacent to heteroatom.</P>
<p> [Highlight]<br />Min Wang<br /><i>ChemCatChem</i>, Apr 05, 2013, DOI: 10.1002/cctc.201200692. <a href="http://dx.doi.org/10.1002/cctc.201200692">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300045">
<title>Atomic Resolution Analysis of Microporous Titanosilicate ETS-10 through Aberration Corrected STEM Imaging</title>
<link>http://dx.doi.org/10.1002/cctc.201300045</link>
<dc:creator>Alvaro Mayoral, Joaquin Coronas, Clara Casado, Carlos Tellez, Isabel Díaz</dc:creator>
<dc:date>2013-04-04T15:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300045.gif" width="447" height="103" alt="Atomic Resolution Analysis of Microporous Titanosilicate ETS-10 through Aberration Corrected STEM Imaging" title="Atomic Resolution Analysis of Microporous Titanosilicate ETS-10 through Aberration Corrected STEM Imaging" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>It&#x27;s all your fault!</B> Microporous titanosilicate ETS-10 crystals have been analyzed by advanced electron microscopy techniques. With the last generation of spherical aberration corrected electron microscopes, truly atomic resolution images have been recorded. Owing to the extremely high-resolution images that have been obtained, the multiple defects (stacking faults, lack of porosity and &ldquo;double-pores&rdquo;) present in this type of material can be analyzed in great detail.</P>
<p> [Communication]<br />Alvaro Mayoral, Joaquin Coronas, Clara Casado, Carlos Tellez, Isabel D&#xED;az<br /><i>ChemCatChem</i>, Apr 04, 2013, DOI: 10.1002/cctc.201300045. <a href="http://dx.doi.org/10.1002/cctc.201300045">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200889">
<title>KOH Activation of Thermally Modified Carbon as a Support of Ru Catalysts for Ammonia Synthesis</title>
<link>http://dx.doi.org/10.1002/cctc.201200889</link>
<dc:creator>Bingyu Lin, Kemei Wei, Jun Ni, Jianxin Lin</dc:creator>
<dc:date>2013-04-04T15:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200889.gif" width="215" height="143" alt="KOH Activation of Thermally Modified Carbon as a Support of Ru Catalysts for Ammonia Synthesis" title="KOH Activation of Thermally Modified Carbon as a Support of Ru Catalysts for Ammonia Synthesis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Activated carbon:</B> Thermally modified carbon can be activated by KOH treatment and the quantity of the surface groups and the textural properties can be controlled by changing the treatment conditions, which improved the dispersion of Ru particles. The difference in the amount of surface functional groups and the size of Ru particles affected the catalytic activity of Ru catalysts in the synthesis of ammonia.</P>
<p> [Full Paper]<br />Bingyu Lin, Kemei Wei, Jun Ni, Jianxin Lin<br /><i>ChemCatChem</i>, Apr 04, 2013, DOI: 10.1002/cctc.201200889. <a href="http://dx.doi.org/10.1002/cctc.201200889">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200879">
<title>Catalyst Development for CO&lt;sub&gt;2&lt;/sub&gt; Hydrogenation to Fuels</title>
<link>http://dx.doi.org/10.1002/cctc.201200879</link>
<dc:creator>Uwe Rodemerck, Martin Holena, Edmund Wagner, Quido Smejkal, Axel Barkschat, Manfred Baerns</dc:creator>
<dc:date>2013-04-04T15:29+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200879.gif" width="214" height="174" alt="Catalyst Development for CO2 Hydrogenation to Fuels" title="Catalyst Development for CO2 Hydrogenation to Fuels" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Fuel for thought:</B> New active and selective catalyst compositions for hydrogenation of CO<sub>2</sub> to mainly fuel-type higher hydrocarbons were developed by application of an evolutionary strategy. A detailed study of the reaction conditions revealed that modified Fe catalysts supported on TiO<sub>2</sub> resulted in high selectivities even at high CO<sub>2</sub> conversions.</P>
<p> [Full Paper]<br />Uwe Rodemerck, Martin Holena, Edmund Wagner, Quido Smejkal, Axel Barkschat, Manfred Baerns<br /><i>ChemCatChem</i>, Apr 04, 2013, DOI: 10.1002/cctc.201200879. <a href="http://dx.doi.org/10.1002/cctc.201200879">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200837">
<title>Unsaturated NHC Complexes Immobilized by the Backbone: Synthesis and Application</title>
<link>http://dx.doi.org/10.1002/cctc.201200837</link>
<dc:creator>Peng Li, Wolfgang A. Herrmann, Fritz E. Kühn</dc:creator>
<dc:date>2013-04-03T14:16+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200837.gif" width="215" height="92" alt="Unsaturated NHC Complexes Immobilized by the Backbone: Synthesis and Application" title="Unsaturated NHC Complexes Immobilized by the Backbone: Synthesis and Application" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Flex that backbone!</B> An SBA-15-supported rhodium&ndash;<I>N</I>-heterocyclic carbene (NHC) catalytic complex shows good activity and stability in hydrogenation reactions. Compared to conventional immobilized unsaturated NHC carbene complexes, Rh-NHC is connected to the SBA-15 surface by a linker originating from the backbone of the unsaturated NHC ligand. The catalyst structure maintains two unchanged &ldquo;wing-tip&rdquo; ligands on the supported NHC.</P>
<p> [Full Paper]<br />Peng Li, Wolfgang A. Herrmann, Fritz E. K&#xFC;hn<br /><i>ChemCatChem</i>, Apr 03, 2013, DOI: 10.1002/cctc.201200837. <a href="http://dx.doi.org/10.1002/cctc.201200837">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300034">
<title>Nickel Catalyst Boosts Solar Hydrogen Generation of CdSe Nanocrystals</title>
<link>http://dx.doi.org/10.1002/cctc.201300034</link>
<dc:creator>Gongming Wang, Yat Li</dc:creator>
<dc:date>2013-04-03T14:15+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300034.gif" width="196" height="163" alt="Nickel Catalyst Boosts Solar Hydrogen Generation of CdSe Nanocrystals" title="Nickel Catalyst Boosts Solar Hydrogen Generation of CdSe Nanocrystals" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The sun has got his hat on!</B> A simple, robust and highly active nickel complex catalyst was reported for photo-generation of hydrogen. The Ni catalyst modified CdSe nanocrystal system achieved a benchmark turnover frequency of &gt;600&nbsp;000 and extraordinary longevity of 360&nbsp;h.</P>
<p> [Highlight]<br />Gongming Wang, Yat Li<br /><i>ChemCatChem</i>, Apr 03, 2013, DOI: 10.1002/cctc.201300034. <a href="http://dx.doi.org/10.1002/cctc.201300034">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300084">
<title>Superior Catalytic Performance of Mesoporous Zeolite TS-1 for the Oxidation of Bulky Organic Sulfides</title>
<link>http://dx.doi.org/10.1002/cctc.201300084</link>
<dc:creator>Zhenzhen Kang, Guoyong Fang, Qingping Ke, Jianbo Hu, Tiandi Tang</dc:creator>
<dc:date>2013-04-02T12:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300084.gif" width="213" height="182" alt="Superior Catalytic Performance of Mesoporous Zeolite TS-1 for the Oxidation of Bulky Organic Sulfides" title="Superior Catalytic Performance of Mesoporous Zeolite TS-1 for the Oxidation of Bulky Organic Sulfides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Rich man, pore man:</B> A facile and universal route to mesoporous zeolite TS-1 (MTS-1) is reported. Compared with mesoporous-free TS-1, the MTS-1 zeolite shows extraordinarily catalytic activity and highly controllable chemoselectivity for the oxidation of sulfides into sulfoxides or sulfones. Based on the catalytic data, the Ti-hydroperoxo (&eta;<SUP>2</SUP>) group is proposed to be the active site for the oxidation of sulfides into sulfoxides and sulfones.</P>
<p> [Communication]<br />Zhenzhen Kang, Guoyong Fang, Qingping Ke, Jianbo Hu, Tiandi Tang<br /><i>ChemCatChem</i>, Apr 02, 2013, DOI: 10.1002/cctc.201300084. <a href="http://dx.doi.org/10.1002/cctc.201300084">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200871">
<title>Redesign of a Phenylalanine Aminomutase into a Phenylalanine Ammonia Lyase</title>
<link>http://dx.doi.org/10.1002/cctc.201200871</link>
<dc:creator>Sebastian Bartsch, Gjalt G. Wybenga, Maaike Jansen, Matthew M. Heberling, Bian Wu, Bauke W. Dijkstra, Dick B. Janssen</dc:creator>
<dc:date>2013-04-02T12:07+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200871.gif" width="439" height="116" alt="Redesign of a Phenylalanine Aminomutase into a Phenylalanine Ammonia Lyase" title="Redesign of a Phenylalanine Aminomutase into a Phenylalanine Ammonia Lyase" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The lid dictates:</B> An aminomutase was converted into an ammonia lyase by a rational single-point mutation that destabilizes the closed conformation of the lid covering the active site. The resulting aromatic &beta;-amino acid converting lyase exhibited significantly increased reaction rates (44-fold) and was applied in a preparative-scale asymmetric amination reaction and in kinetic resolution for the production of &beta;-phenylalanine.</P>
<p> [Full Paper]<br />Sebastian Bartsch, Gjalt G. Wybenga, Maaike Jansen, Matthew M. Heberling, Bian Wu, Bauke W. Dijkstra, Dick B. Janssen<br /><i>ChemCatChem</i>, Apr 02, 2013, DOI: 10.1002/cctc.201200871. <a href="http://dx.doi.org/10.1002/cctc.201200871">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200966">
<title>Oxidative Dehydrogenation of Ethane: Common Principles and Mechanistic Aspects</title>
<link>http://dx.doi.org/10.1002/cctc.201200966</link>
<dc:creator>Christian A. Gärtner, André C. van Veen, Johannes A. Lercher</dc:creator>
<dc:date>2013-04-02T12:02+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200966.gif" width="215" height="129" alt="Oxidative Dehydrogenation of Ethane: Common Principles and Mechanistic Aspects" title="Oxidative Dehydrogenation of Ethane: Common Principles and Mechanistic Aspects" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A great suC=Cess:</B> The oxidative dehydrogenation (ODH) of ethane is a process that enables the production of ethene with high selectivities. Different catalysts and reactor configurations have been developed for this process. This Review focuses on the mechanistic aspects of heterogeneously catalyzed ODH reactions and the main features and common principles of this reaction are discussed.</P>
<p> [Review]<br />Christian A. G&#xE4;rtner, Andr&#xE9; C. van&#xA0;Veen, Johannes A. Lercher<br /><i>ChemCatChem</i>, Apr 02, 2013, DOI: 10.1002/cctc.201200966. <a href="http://dx.doi.org/10.1002/cctc.201200966">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200592">
<title>Biorelevant Metals in Sustainable Metal Catalysis—A Survey</title>
<link>http://dx.doi.org/10.1002/cctc.201200592</link>
<dc:creator>Michael S. Holzwarth, Bernd Plietker</dc:creator>
<dc:date>2013-03-28T13:55+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200592.gif" width="196" height="192" alt="Biorelevant Metals in Sustainable Metal Catalysis&mdash;A Survey" title="Biorelevant Metals in Sustainable Metal Catalysis&mdash;A Survey" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Nature&rsquo;s metals:</B> For a wide range of catalytic transformations, the nature of the catalyst has to be considered when evaluating the necessary steps to take academic research to industrial application. Herein we survey state of the art progress in sustainable metal catalysis, that is, catalytic reactions performed with inexpensive biorelevant metals such as B, Mg, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Mo, Se, Si, and W.</P>
<p> [Review]<br />Michael S. Holzwarth, Bernd Plietker<br /><i>ChemCatChem</i>, Mar 28, 2013, DOI: 10.1002/cctc.201200592. <a href="http://dx.doi.org/10.1002/cctc.201200592">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300015">
<title>Asymmetric Allylic Alkylation of Alkene through Direct C (sp&lt;SUP&gt;3&lt;/SUP&gt;)-H Functionalization</title>
<link>http://dx.doi.org/10.1002/cctc.201300015</link>
<dc:creator>Guihua Chen, Kang Chen, Zhang-Jie Shi</dc:creator>
<dc:date>2013-03-28T13:48+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300015.gif" width="447" height="98" alt="Asymmetric Allylic Alkylation of Alkene through Direct C (sp3)-H Functionalization" title="Asymmetric Allylic Alkylation of Alkene through Direct C (sp3)-H Functionalization" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Put your Trost in this reaction:</B> The first catalytic asymmetric Tsuji&ndash;Trost reaction via allylic C-H activation was realized using a new class of chiral phosphoramidite ligands. This work represents a considerable breakthrough in palladium catalyzed asymmetric allylic C-H alkylations.</P>
<p> [Highlight]<br />Guihua Chen, Kang Chen, Zhang-Jie Shi<br /><i>ChemCatChem</i>, Mar 28, 2013, DOI: 10.1002/cctc.201300015. <a href="http://dx.doi.org/10.1002/cctc.201300015">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200824">
<title>Efficient Hydrodeoxygenation of Aliphatic Ketones over an Alkali-Treated Ni/HZSM-5 Catalyst</title>
<link>http://dx.doi.org/10.1002/cctc.201200824</link>
<dc:creator>Xiangjin Kong, Weichi Lai, Jun Tian, Yang Li, Xilong Yan, Ligong Chen</dc:creator>
<dc:date>2013-03-28T13:48+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200824.gif" width="216" height="80" alt="Efficient Hydrodeoxygenation of Aliphatic Ketones over an Alkali-Treated Ni/HZSM-5 Catalyst" title="Efficient Hydrodeoxygenation of Aliphatic Ketones over an Alkali-Treated Ni/HZSM-5 Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Alkaline support:</B> The hydrodeoxygenation of aliphatic ketones is studied in a fixed-bed reactor by using cyclohexanone as a model substrate. Alkali-treated Ni/HZSM-5 exhibits excellent performance for this reaction.</P>
<p> [Full Paper]<br />Xiangjin Kong, Weichi Lai, Jun Tian, Yang Li, Xilong Yan, Ligong Chen<br /><i>ChemCatChem</i>, Mar 28, 2013, DOI: 10.1002/cctc.201200824. <a href="http://dx.doi.org/10.1002/cctc.201200824">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200860">
<title>One-Pot, Two-Step Protocol for the Catalytic Asymmetric Synthesis of Optically Active N,O- and O,O-Acetals</title>
<link>http://dx.doi.org/10.1002/cctc.201200860</link>
<dc:creator>M. Fatih Polat, Lara Hettmanczyk, Wei Zhang, Zoltan Szabo, Johan Franzén</dc:creator>
<dc:date>2013-03-28T13:47+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200860.gif" width="386" height="95" alt="One-Pot, Two-Step Protocol for the Catalytic Asymmetric Synthesis of Optically Active N,O- and O,O-Acetals" title="One-Pot, Two-Step Protocol for the Catalytic Asymmetric Synthesis of Optically Active N,O- and O,O-Acetals" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>N,O problem:</B> An asymmetric catalytic one-pot N,O- and O,O-acetalization cascade is presented. This strategy is based on catalytic asymmetric conjugate addition and subsequent acid-catalyzed acetal formation that allows efficient and fast construction of functionalized dioxabicyclo- and oxaazabicyclo[3.3.1]nonane structures that are important motifs in several natural products and pharmaceutically interesting compounds.</P>
<p> [Communication]<br />M. Fatih Polat, Lara Hettmanczyk, Wei Zhang, Zoltan Szabo, Johan Franz&#xE9;n<br /><i>ChemCatChem</i>, Mar 28, 2013, DOI: 10.1002/cctc.201200860. <a href="http://dx.doi.org/10.1002/cctc.201200860">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200825">
<title>Oxidation of 1,2-Cyclohexanediol to Adipic Acid with Oxygen: A Study Into Selectivity-Affecting Parameters</title>
<link>http://dx.doi.org/10.1002/cctc.201200825</link>
<dc:creator>Elena Rozhko, Katerina Raabova, Francesco Macchia, Andrea Malmusi, Paolo Righi, Pasquale Accorinti, Stefano Alini, Pierpaolo Babini, Giuseppina Cerrato, Maela Manzoli, Fabrizio Cavani</dc:creator>
<dc:date>2013-03-27T12:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200825.gif" width="216" height="141" alt="Oxidation of 1,2-Cyclohexanediol to Adipic Acid with Oxygen: A Study Into Selectivity-Affecting Parameters" title="Oxidation of 1,2-Cyclohexanediol to Adipic Acid with Oxygen: A Study Into Selectivity-Affecting Parameters" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The synthesis of adipic acid</B> through aerobic oxidative cleavage of <I>trans</I>-1,2-cyclohexanediol is investigated under basic and acid conditions. In the former case, supported Ru(OH)<sub>3</sub> catalysts are active but poorly selective, owing to side reactions starting from the key reaction intermediate 1,2-cyclohexanedione. Under acidic conditions, Keggin polyoxometalates are selective to adipic acid, but this then reacts with the unconverted reactant to yield esters.</P>
<p> [Full Paper]<br />Elena Rozhko, Katerina Raabova, Francesco Macchia, Andrea Malmusi, Paolo Righi, Pasquale Accorinti, Stefano Alini, Pierpaolo Babini, Giuseppina Cerrato, Maela Manzoli, Fabrizio Cavani<br /><i>ChemCatChem</i>, Mar 27, 2013, DOI: 10.1002/cctc.201200825. <a href="http://dx.doi.org/10.1002/cctc.201200825">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200759">
<title>Maximizing Activity and Stability by Turning Gold Catalysis Upside Down: Oxide Particles on Nanoporous Gold</title>
<link>http://dx.doi.org/10.1002/cctc.201200759</link>
<dc:creator>Andre Wichmann, Arne Wittstock, Kristian Frank, Monika M. Biener, Björn Neumann, Lutz Mädler, Jürgen Biener, Andreas Rosenauer, Marcus Bäumer</dc:creator>
<dc:date>2013-03-27T12:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200759.gif" width="192" height="180" alt="Maximizing Activity and Stability by Turning Gold Catalysis Upside Down: Oxide Particles on Nanoporous Gold" title="Maximizing Activity and Stability by Turning Gold Catalysis Upside Down: Oxide Particles on Nanoporous Gold" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Gold goes upside down:</B> A highly active and stable gold catalyst is generated by the deposition of metal oxide particles on a monolithic, high-surface area gold support. The catalyst combines exceptional activity for CO oxidation and NO reduction at low temperatures and unprecedented stability at several hundred degrees Celsius. This novel catalyst design opens up applications such as in exhaust gas control.</P>
<p> [Full Paper]<br />Andre Wichmann, Arne Wittstock, Kristian Frank, Monika M. Biener, Bj&#xF6;rn Neumann, Lutz M&#xE4;dler, J&#xFC;rgen Biener, Andreas Rosenauer, Marcus B&#xE4;umer<br /><i>ChemCatChem</i>, Mar 27, 2013, DOI: 10.1002/cctc.201200759. <a href="http://dx.doi.org/10.1002/cctc.201200759">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300031">
<title>Direct C-H bond Arylation in Water Promoted by (O,O)- and (O,N)-Chelate Ruthenium(II) Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201300031</link>
<dc:creator>Keisham S. Singh, Pierre H. Dixneuf</dc:creator>
<dc:date>2013-03-25T06:51+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300031.gif" width="399" height="99" alt="Direct C-H bond Arylation in Water Promoted by (O,O)- and (O,N)-Chelate Ruthenium(II) Catalysts" title="Direct C-H bond Arylation in Water Promoted by (O,O)- and (O,N)-Chelate Ruthenium(II) Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Two strong arms to hold the catalyst:</B> (O,O) and (O,N)-chelate ruthenium(II) complexes obtained from kojic acid or glycine are efficient catalysts for the (hetero)arylation of C<sub>sp<SUP>2</SUP></sub>-H bonds if associated to potassium pivalate. Moreover, the catalysts operate in water</P>
<p> [Communication]<br />Keisham S. Singh, Pierre H. Dixneuf<br /><i>ChemCatChem</i>, Mar 25, 2013, DOI: 10.1002/cctc.201300031. <a href="http://dx.doi.org/10.1002/cctc.201300031">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200760">
<title>Effects of La, Ce, and Y Oxides on SnO&lt;sub&gt;2&lt;/sub&gt; Catalysts for CO and CH&lt;sub&gt;4&lt;/sub&gt; Oxidation</title>
<link>http://dx.doi.org/10.1002/cctc.201200760</link>
<dc:creator>Xianglan Xu, Rongbin Zhang, Xianrong Zeng, Xue Han, Yucheng Li, Yang Liu, Xiang Wang</dc:creator>
<dc:date>2013-03-25T06:51+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200760.gif" width="215" height="162" alt="Effects of La, Ce, and Y Oxides on SnO2 Catalysts for CO and CH4 Oxidation" title="Effects of La, Ce, and Y Oxides on SnO2 Catalysts for CO and CH4 Oxidation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Good news for doping</B>: Ce cations can be doped into the lattice of SnO<sub>2</sub> to form solid-solution structures, which results in catalysts with improved activity and stability. However, La and Y cations react with SnO<sub>2</sub> to form very stable pyrochlores, Sn<sub>2</sub>La<sub>2</sub>O<sub>7</sub> and Sn<sub>2</sub>Y<sub>2</sub>O<sub>7</sub>, which have a decreased catalytic activity.</P>
<p> [Full Paper]<br />Xianglan Xu, Rongbin Zhang, Xianrong Zeng, Xue Han, Yucheng Li, Yang Liu, Xiang Wang<br /><i>ChemCatChem</i>, Mar 25, 2013, DOI: 10.1002/cctc.201200760. <a href="http://dx.doi.org/10.1002/cctc.201200760">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200944">
<title>Mechanistic Investigations of a Stable, Highly Active, Extremely Sterically Shielded Molecular Gold Catalyst</title>
<link>http://dx.doi.org/10.1002/cctc.201200944</link>
<dc:creator>Simone G. Weber, David Zahner, Frank Rominger, Bernd F. Straub</dc:creator>
<dc:date>2013-03-25T06:50+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200944.gif" width="211" height="150" alt="Mechanistic Investigations of a Stable, Highly Active, Extremely Sterically Shielded Molecular Gold Catalyst" title="Mechanistic Investigations of a Stable, Highly Active, Extremely Sterically Shielded Molecular Gold Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Deeply buried but very vivid:</B> An unprecedented combination of high activity, stability, selectivity, and Lewis acidity as well as mechanistic insight is provided by the gold bistriflimide complex of an IPr** N-heterocyclic carbene ancillary ligand with its record buried volume.</P>
<p> [Full Paper]<br />Simone G. Weber, David Zahner, Frank Rominger, Bernd F. Straub<br /><i>ChemCatChem</i>, Mar 25, 2013, DOI: 10.1002/cctc.201200944. <a href="http://dx.doi.org/10.1002/cctc.201200944">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200913">
<title>Interplay Between Bromine and Iodine in Oxidative Dehydrogenation</title>
<link>http://dx.doi.org/10.1002/cctc.201200913</link>
<dc:creator>Kunlun Ding, Horia Metiu, Galen D. Stucky</dc:creator>
<dc:date>2013-03-25T06:50+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200913.gif" width="196" height="208" alt="Interplay Between Bromine and Iodine in Oxidative Dehydrogenation" title="Interplay Between Bromine and Iodine in Oxidative Dehydrogenation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A single pass to the goal:</B> A single-pass C<sub>3</sub>H<sub>6</sub>+C<sub>3</sub>H<sub>7</sub>X yield above 80&nbsp;% was achieved in propane oxidative dehydrogenation using bromine and iodine together as oxidants. This dual-halogen process is promising for the synthesis of many other unsaturated hydrocarbons, including olefins, diolefins, and aromatics.</P>
<p> [Full Paper]<br />Kunlun Ding, Horia Metiu, Galen D. Stucky<br /><i>ChemCatChem</i>, Mar 25, 2013, DOI: 10.1002/cctc.201200913. <a href="http://dx.doi.org/10.1002/cctc.201200913">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200867">
<title>Palladium-Catalysed Regioselective Direct Arylations of Heteroarenes by Bromobenzamides: Direct Synthesis of Heteroaryl Benzamides</title>
<link>http://dx.doi.org/10.1002/cctc.201200867</link>
<dc:creator>Lu Chen, Christian Bruneau, Pierre H. Dixneuf, Henri Doucet</dc:creator>
<dc:date>2013-03-25T06:50+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200867.gif" width="215" height="153" alt="Palladium-Catalysed Regioselective Direct Arylations of Heteroarenes by Bromobenzamides: Direct Synthesis of Heteroaryl Benzamides" title="Palladium-Catalysed Regioselective Direct Arylations of Heteroarenes by Bromobenzamides: Direct Synthesis of Heteroaryl Benzamides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A new sensation in direct arylation</B>: In the presence of KOAc, the Pd-catalyzed direct heteroarylation of 2- or 4-bromobenzamides with heteroarenes proceeds without the formation of C-N or C-C bonds by the coupling of two bromobenzamides. With 4-bromobenzamides, both primary and tertiary amides can be employed, whereas only tertiary 2-bromobenzamides were reactive. The nature of the heteroarene had a moderate influence on the reaction. DMAc=<I>N</I>,<I>N</I>-dimethylacetamide.</P>
<p> [Full Paper]<br />Lu Chen, Christian Bruneau, Pierre H. Dixneuf, Henri Doucet<br /><i>ChemCatChem</i>, Mar 25, 2013, DOI: 10.1002/cctc.201200867. <a href="http://dx.doi.org/10.1002/cctc.201200867">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200743">
<title>Platinum(II) Catalyzed Enantioselective Cycloisomerizations of 3-Hydroxylated 1,5-Enynes</title>
<link>http://dx.doi.org/10.1002/cctc.201200743</link>
<dc:creator>Yang Zhang, Hélène Jullien, Delphine Brissy, Pascal Retailleau, Arnaud Voituriez, Angela Marinetti</dc:creator>
<dc:date>2013-03-25T06:41+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200743.gif" width="437" height="105" alt="Platinum(II) Catalyzed Enantioselective Cycloisomerizations of 3-Hydroxylated 1,5-Enynes" title="Platinum(II) Catalyzed Enantioselective Cycloisomerizations of 3-Hydroxylated 1,5-Enynes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The cycloisomerization of 1,5-enynes</B> with hydroxyl functions at their propargylic positions was investigated by using NHC-based platinacyclic phosphoramidite complexes as the chiral catalysts. The (<I>R</I>)-Monophos complexes display good catalytic activity in mild conditions. They afford the desired bicyclo[3.1.0]hexan-3-ones in up to 81&nbsp;% <I>ee</I> from enynes with aryl-substituted alkyne functions.</P>
<p> [Full Paper]<br />Yang Zhang, H&#xE9;l&#xE8;ne Jullien, Delphine Brissy, Pascal Retailleau, Arnaud Voituriez, Angela Marinetti<br /><i>ChemCatChem</i>, Mar 25, 2013, DOI: 10.1002/cctc.201200743. <a href="http://dx.doi.org/10.1002/cctc.201200743">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200660">
<title>Dye Degradation by Layer-by-Layer Immobilised Peroxidase/Redox Mediator Systems</title>
<link>http://dx.doi.org/10.1002/cctc.201200660</link>
<dc:creator>Raffaele Saladino, Melissa Guazzaroni, Claudia Crestini, Marcello Crucianelli</dc:creator>
<dc:date>2013-03-25T06:41+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200660.gif" width="212" height="137" alt="Dye Degradation by Layer-by-Layer Immobilised Peroxidase/Redox Mediator Systems" title="Dye Degradation by Layer-by-Layer Immobilised Peroxidase/Redox Mediator Systems" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Environmentally benign bio-catalysts:</B> The role of a poly-electrolyte coating in the immobilisation of peroxidases was studied. Efficient yields for the degradation of several dyes were obtained with H<sub>2</sub>O<sub>2</sub> in the presence of different redox mediators. Generally, azo dyes were degraded with higher yields.</P>
<p> [Full Paper]<br />Raffaele Saladino, Melissa Guazzaroni, Claudia Crestini, Marcello Crucianelli<br /><i>ChemCatChem</i>, Mar 25, 2013, DOI: 10.1002/cctc.201200660. <a href="http://dx.doi.org/10.1002/cctc.201200660">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200872">
<title>Quantitative &lt;I&gt;Z&lt;/I&gt;-Contrast Imaging of Supported Metal Complexes and Clusters—A Gateway to Understanding Catalysis on the Atomic Scale</title>
<link>http://dx.doi.org/10.1002/cctc.201200872</link>
<dc:creator>Nigel D. Browning, Ceren Aydin, Jing Lu, Apoorva Kulkarni, Norihiko L. Okamoto, Volkan Ortalan, Bryan W. Reed, Alper Uzun, Bruce C. Gates</dc:creator>
<dc:date>2013-03-20T16:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200872.gif" width="212" height="127" alt="Quantitative Z-Contrast Imaging of Supported Metal Complexes and Clusters&mdash;A Gateway to Understanding Catalysis on the Atomic Scale" title="Quantitative Z-Contrast Imaging of Supported Metal Complexes and Clusters&mdash;A Gateway to Understanding Catalysis on the Atomic Scale" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Pinpointing catalytic sites:</B> <I>Z</I>-contrast imaging in an aberration-corrected scanning transmission electron microscope is used to reveal the size, shape, and composition of supported metal complexes. In tandem with spectroscopic techniques, the structure of these complexes can be fully resolved on the atomic scale.</P>
<p> [Full Paper]<br />Nigel D. Browning, Ceren Aydin, Jing Lu, Apoorva Kulkarni, Norihiko L. Okamoto, Volkan Ortalan, Bryan W. Reed, Alper Uzun, Bruce C. Gates<br /><i>ChemCatChem</i>, Mar 20, 2013, DOI: 10.1002/cctc.201200872. <a href="http://dx.doi.org/10.1002/cctc.201200872">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300043">
<title>Manipulation of the Reducibility of Ceria-Supported Au Catalysts by Interface Engineering</title>
<link>http://dx.doi.org/10.1002/cctc.201300043</link>
<dc:creator>Lei Wang, Gang Lu, Dan Yang, Jin Wang, Zhibin Zhu, Zhixiang Wang, Kebin Zhou</dc:creator>
<dc:date>2013-03-19T06:54+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300043.gif" width="196" height="195" alt="Manipulation of the Reducibility of Ceria-Supported Au Catalysts by Interface Engineering" title="Manipulation of the Reducibility of Ceria-Supported Au Catalysts by Interface Engineering" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Baby face:</B> Interface engineering of ceria-supported Au catalysts was achieved by a combination of DFT calculations and synthetic techniques. The reducibility of the Au/ceria catalysts was determined by the interfacial -Au-O-Ce<sub><I>n</I></sub>- structures.</P>
<p> [Communication]<br />Lei Wang, Gang Lu, Dan Yang, Jin Wang, Zhibin Zhu, Zhixiang Wang, Kebin Zhou<br /><i>ChemCatChem</i>, Mar 19, 2013, DOI: 10.1002/cctc.201300043. <a href="http://dx.doi.org/10.1002/cctc.201300043">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200687">
<title>Unusually High Activity of Pt Islands on Rh(1&#160;1&#160;1) Electrodes for Ethanol Oxidation</title>
<link>http://dx.doi.org/10.1002/cctc.201200687</link>
<dc:creator>Vinicius Del Colle, Vitali Grozovski, Enrique Herrero, Juan M. Feliu</dc:creator>
<dc:date>2013-03-19T06:52+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200687.gif" width="309" height="98" alt="Unusually High Activity of Pt Islands on Rh(1&nbsp;1&nbsp;1) Electrodes for Ethanol Oxidation" title="Unusually High Activity of Pt Islands on Rh(1&nbsp;1&nbsp;1) Electrodes for Ethanol Oxidation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Dream island</B>: Monoatomic, high-platinum islands deposited on a Rh(1&nbsp;1&nbsp;1) electrode have an electrocatalytic activity for ethanol oxidation that is 20&nbsp;times higher than that measured on platinum electrodes. On these islands, CO<sub>2</sub> and acetic acid are the final products.</P>
<p> [Communication]<br />Vinicius Del Colle, Vitali Grozovski, Enrique Herrero, Juan M. Feliu<br /><i>ChemCatChem</i>, Mar 19, 2013, DOI: 10.1002/cctc.201200687. <a href="http://dx.doi.org/10.1002/cctc.201200687">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200751">
<title>Proton Shuttle Mechanism in the Transition State of Lipase-Catalyzed N-Acylation of Amino Alcohols</title>
<link>http://dx.doi.org/10.1002/cctc.201200751</link>
<dc:creator>Per-Olof Syrén, Florian Le Joubioux, Yesmine Ben Henda, Thierry Maugard, Karl Hult, Marianne Graber</dc:creator>
<dc:date>2013-03-19T03:49+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200751.gif" width="212" height="168" alt="Proton Shuttle Mechanism in the Transition State of Lipase-Catalyzed N-Acylation of Amino Alcohols" title="Proton Shuttle Mechanism in the Transition State of Lipase-Catalyzed N-Acylation of Amino Alcohols" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Tetrahedra prevailing:</B> An increased reaction rate for lipase-catalyzed N-acylation of amino alcohols and related compounds can be explained by a hydrogen shuttle mechanism that avoids nitrogen inversion in the transition state and favors a tetrahedral intermediate for facile amide bond synthesis.</P>
<p> [Full Paper]<br />Per-Olof Syr&#xE9;n, Florian Le&#xA0;Joubioux, Yesmine Ben&#xA0;Henda, Thierry Maugard, Karl Hult, Marianne Graber<br /><i>ChemCatChem</i>, Mar 19, 2013, DOI: 10.1002/cctc.201200751. <a href="http://dx.doi.org/10.1002/cctc.201200751">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200769">
<title>Synthesis of Pt/C Catalysts through Reductive Deposition: Ways of Tuning Catalytic Properties</title>
<link>http://dx.doi.org/10.1002/cctc.201200769</link>
<dc:creator>Ksenia M. Kaprielova, Igor I. Ovchinnikov, Olga A. Yakovina, Alexander S. Lisitsyn</dc:creator>
<dc:date>2013-03-18T09:25+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200769.gif" width="216" height="180" alt="Synthesis of Pt/C Catalysts through Reductive Deposition: Ways of Tuning Catalytic Properties" title="Synthesis of Pt/C Catalysts through Reductive Deposition: Ways of Tuning Catalytic Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Get all you wished for:</B> This study reveals new capabilities of reductive deposition as a method for the preparation of Pt-on-carbon catalysts. It enables one to avoid confinement of Pt nanoparticles in narrow pores, to adjust the particle size to optimum for the reaction of interest, to obtain various types of Pt distribution over the support, and to influence catalytic properties by simple means.</P>
<p> [Full Paper]<br />Ksenia M. Kaprielova, Igor I. Ovchinnikov, Olga A. Yakovina, Alexander S. Lisitsyn<br /><i>ChemCatChem</i>, Mar 18, 2013, DOI: 10.1002/cctc.201200769. <a href="http://dx.doi.org/10.1002/cctc.201200769">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200923">
<title>Painting Anatase (TiO&lt;sub&gt;2&lt;/sub&gt;) Nanocrystals on Long Nanofibers to Prepare Photocatalysts with Large Active Surface for Dye Degradation and Organic Synthesis</title>
<link>http://dx.doi.org/10.1002/cctc.201200923</link>
<dc:creator>Zhanfeng Zheng, Jian Zhao, Hongwei Liu, Jiangwen Liu, Arixin Bo, Huaiyong Zhu</dc:creator>
<dc:date>2013-03-14T06:41+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200923.gif" width="384" height="130" alt="Painting Anatase (TiO2) Nanocrystals on Long Nanofibers to Prepare Photocatalysts with Large Active Surface for Dye Degradation and Organic Synthesis" title="Painting Anatase (TiO2) Nanocrystals on Long Nanofibers to Prepare Photocatalysts with Large Active Surface for Dye Degradation and Organic Synthesis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A porous paint:</B> Anatase nanocrystals with large surface areas that were painted on the surface of titanate nanofibers bonded solidly. This process generated a superior active surface for photocatalytic reactions, either serving as the photocatalyst or Au catalyst support.</P>
<p> [Full Paper]<br />Zhanfeng Zheng, Jian Zhao, Hongwei Liu, Jiangwen Liu, Arixin Bo, Huaiyong Zhu<br /><i>ChemCatChem</i>, Mar 14, 2013, DOI: 10.1002/cctc.201200923. <a href="http://dx.doi.org/10.1002/cctc.201200923">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200799">
<title>Rh&lt;sub&gt;1&lt;/sub&gt;/γ-Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; Single-Atom Catalysis of O&lt;sub&gt;2&lt;/sub&gt; Activation and CO Oxidation: Mechanism, Effects of Hydration, Oxidation State, and Cluster Size</title>
<link>http://dx.doi.org/10.1002/cctc.201200799</link>
<dc:creator>Tushar K. Ghosh, Nisanth N. Nair</dc:creator>
<dc:date>2013-03-14T03:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200799.gif" width="214" height="93" alt="Rh1/&gamma;-Al2O3 Single-Atom Catalysis of O2 Activation and CO Oxidation: Mechanism, Effects of Hydration, Oxidation State, and Cluster Size" title="Rh1/&gamma;-Al2O3 Single-Atom Catalysis of O2 Activation and CO Oxidation: Mechanism, Effects of Hydration, Oxidation State, and Cluster Size" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Be small and neutral!</B> O<sub>2</sub> activation and CO oxidation with Rh<sub>1</sub> and Rh<sub>6</sub> supported on &gamma;-Al<sub>2</sub>O<sub>3</sub> are investigated here through ab&nbsp;initio molecular dynamics techniques. Simulation finds that reactivity varies as Rh<SUP>0</SUP>&gt;Rh<SUP>I</SUP>&gt;Rh<sub>6</sub>.</P>
<p> [Full Paper]<br />Tushar K. Ghosh, Nisanth N. Nair<br /><i>ChemCatChem</i>, Mar 14, 2013, DOI: 10.1002/cctc.201200799. <a href="http://dx.doi.org/10.1002/cctc.201200799">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200691">
<title>Improved &lt;I&gt;para&lt;/I&gt;-Xylene Selectivity in &lt;I&gt;meta-&lt;/I&gt;Xylene Isomerization Over ZSM-5 Crystals with Relatively Long &lt;I&gt;b&lt;/I&gt;-Axis Length</title>
<link>http://dx.doi.org/10.1002/cctc.201200691</link>
<dc:creator>Yan Liu, Xiaozhao Zhou, Xinmei Pang, Yinying Jin, Xiangju Meng, Xiaoming Zheng, Xionghou Gao, Feng-Shou Xiao</dc:creator>
<dc:date>2013-03-14T03:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200691.gif" width="215" height="189" alt="Improved para-Xylene Selectivity in meta-Xylene Isomerization Over ZSM-5 Crystals with Relatively Long b-Axis Length" title="Improved para-Xylene Selectivity in meta-Xylene Isomerization Over ZSM-5 Crystals with Relatively Long b-Axis Length" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Join the chain gang:</B> Chain-like ZSM-5 crystals that are synthesized in the presence of starch show higher <I>p</I>-xylene selectivity in <I>m</I>-xylene isomerization than normal, mesoporous, and sheet-like ZSM-5 crystals.</P>
<p> [Full Paper]<br />Yan Liu, Xiaozhao Zhou, Xinmei Pang, Yinying Jin, Xiangju Meng, Xiaoming Zheng, Xionghou Gao, Feng-Shou Xiao<br /><i>ChemCatChem</i>, Mar 14, 2013, DOI: 10.1002/cctc.201200691. <a href="http://dx.doi.org/10.1002/cctc.201200691">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200770">
<title>Efficient Synthesis of Cyclic Carbonates by Mg&lt;SUP&gt;II&lt;/SUP&gt;/Phosphine-Catalyzed Coupling Reactions of Carbon Dioxide and Epoxides</title>
<link>http://dx.doi.org/10.1002/cctc.201200770</link>
<dc:creator>Yiping Ren, Jae-Jin Shim</dc:creator>
<dc:date>2013-03-14T03:27+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200770.gif" width="429" height="97" alt="Efficient Synthesis of Cyclic Carbonates by MgII/Phosphine-Catalyzed Coupling Reactions of Carbon Dioxide and Epoxides" title="Efficient Synthesis of Cyclic Carbonates by MgII/Phosphine-Catalyzed Coupling Reactions of Carbon Dioxide and Epoxides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Green synthesis of cyclic carbonates:</B> Magnesium(II)/phosphine complexes are developed for the synthesis of cyclic carbonates through the coupling of epoxides and carbon dioxide. Various cyclic carbonates are prepared in excellent yields under extremely mild, solvent-free conditions at relatively low temperatures and pressures. The catalyst system shows excellent recyclability, and the cyclic carbonates can be separated easily.</P>
<p> [Communication]<br />Yiping Ren, Jae-Jin Shim<br /><i>ChemCatChem</i>, Mar 14, 2013, DOI: 10.1002/cctc.201200770. <a href="http://dx.doi.org/10.1002/cctc.201200770">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200718">
<title>Methylated β-Cyclodextrin-Capped Ruthenium Nanoparticles: Synthesis Strategies, Characterization, and Application in Hydrogenation Reactions</title>
<link>http://dx.doi.org/10.1002/cctc.201200718</link>
<dc:creator>Nguyet Trang Thanh Chau, Soraya Handjani, Jean-Paul Guegan, Miguel Guerrero, Eric Monflier, Karine Philippot, Audrey Denicourt-Nowicki, Alain Roucoux</dc:creator>
<dc:date>2013-03-14T03:27+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200718.gif" width="377" height="93" alt="Methylated &beta;-Cyclodextrin-Capped Ruthenium Nanoparticles: Synthesis Strategies, Characterization, and Application in Hydrogenation Reactions" title="Methylated &beta;-Cyclodextrin-Capped Ruthenium Nanoparticles: Synthesis Strategies, Characterization, and Application in Hydrogenation Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Supramolecular nanocatalysts!</B> Ruthenium nanoparticles stabilized by methylated &beta;-cyclodextrins in water can be prepared using either a one-pot or a cascade reduction process (see picture). This preparation of nanoparticles can be used for the hydrogenation of arenes in biphasic media.</P>
<p> [Full Paper]<br />Nguyet Trang Thanh Chau, Soraya Handjani, Jean-Paul Guegan, Miguel Guerrero, Eric Monflier, Karine Philippot, Audrey Denicourt-Nowicki, Alain Roucoux<br /><i>ChemCatChem</i>, Mar 14, 2013, DOI: 10.1002/cctc.201200718. <a href="http://dx.doi.org/10.1002/cctc.201200718">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200724">
<title>Advanced Core–Shell Nanoparticle Catalysts for Efficient Organic Transformations</title>
<link>http://dx.doi.org/10.1002/cctc.201200724</link>
<dc:creator>Takato Mitsudome, Kiyotomi Kaneda</dc:creator>
<dc:date>2013-03-14T03:26+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200724.gif" width="210" height="140" alt="Advanced Core&ndash;Shell Nanoparticle Catalysts for Efficient Organic Transformations" title="Advanced Core&ndash;Shell Nanoparticle Catalysts for Efficient Organic Transformations" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Straight to the core of the matter:</B> Recent progress in conceptual designs of state-of-the-art core&ndash;shell nanostructured catalysts with active species in the core is reviewed. The core&ndash;shell catalysts possess multifunctions and show unique catalysis for efficient organic transformations.</P>
<p> [Minireview]<br />Takato Mitsudome, Kiyotomi Kaneda<br /><i>ChemCatChem</i>, Mar 14, 2013, DOI: 10.1002/cctc.201200724. <a href="http://dx.doi.org/10.1002/cctc.201200724">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200665">
<title>Knowledge Extraction from Catalysis of the Past: A Case of Selective CO Oxidation over Noble Metal Catalysts between 2000 and 2012</title>
<link>http://dx.doi.org/10.1002/cctc.201200665</link>
<dc:creator>M. Erdem Günay, Ramazan Yildirim</dc:creator>
<dc:date>2013-03-14T03:25+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200665.gif" width="202" height="196" alt="Knowledge Extraction from Catalysis of the Past: A Case of Selective CO Oxidation over Noble Metal Catalysts between 2000 and 2012" title="Knowledge Extraction from Catalysis of the Past: A Case of Selective CO Oxidation over Noble Metal Catalysts between 2000 and 2012" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Extracting knowledge from past data:</B> A simple method is designed by using various data mining tools, such as decision trees, clustering techniques, and artificial neural networks, to extract valuable knowledge from the experimental data for selective CO oxidation in the literature; this way, some useful trends, rules, and correlations, which are not easily comprehensible to the naked eye, are deduced systematically.</P>
<p> [Full Paper]<br />M. Erdem G&#xFC;nay, Ramazan Yildirim<br /><i>ChemCatChem</i>, Mar 14, 2013, DOI: 10.1002/cctc.201200665. <a href="http://dx.doi.org/10.1002/cctc.201200665">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200433">
<title>Fischer–Tropsch Synthesis Over Cobalt Supported On Silica-Incorporated Mesoporous Carbon</title>
<link>http://dx.doi.org/10.1002/cctc.201200433</link>
<dc:creator>Prashant R. Karandikar, Jo-Yong Park, Yun-Jo Lee, Ki-Won Jun, Kyoung-Su Ha, Geun Jae Kwak, Hae-Gu Park, Joo Yeong Cheon</dc:creator>
<dc:date>2013-03-14T03:25+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200433.gif" width="333" height="70" alt="Fischer&ndash;Tropsch Synthesis Over Cobalt Supported On Silica-Incorporated Mesoporous Carbon" title="Fischer&ndash;Tropsch Synthesis Over Cobalt Supported On Silica-Incorporated Mesoporous Carbon" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>CSI: Carbon&ndash;Silica Investigations:</B> The incorporation of silica in the porous carbon framework modifies the surface chemistry of the hydrophobic support through oxygenated functional groups, resulting in preferential Co adsorption in the vicinity of silica. This encouraged greater dispersion and reducibility of cobalt than seen for carbon-supported cobalt catalysts. The deactivation of cobalt over carbon supported catalyst is reduced by the hybridization of carbon using silica particles.</P>
<p> [Full Paper]<br />Prashant R. Karandikar, Jo-Yong Park, Yun-Jo Lee, Ki-Won Jun, Kyoung-Su Ha, Geun Jae Kwak, Hae-Gu Park, Joo Yeong Cheon<br /><i>ChemCatChem</i>, Mar 14, 2013, DOI: 10.1002/cctc.201200433. <a href="http://dx.doi.org/10.1002/cctc.201200433">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200906">
<title>Enantioselective Synthesis of N-Substituted Aspartic Acids Using an Engineered Variant of Methylaspartate Ammonia Lyase</title>
<link>http://dx.doi.org/10.1002/cctc.201200906</link>
<dc:creator>Vinod Puthan Veetil, Hans Raj, Marianne de Villiers, Pieter G. Tepper, Frank J. Dekker, Wim J. Quax, Gerrit J. Poelarends</dc:creator>
<dc:date>2013-03-07T15:14+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200906.gif" width="432" height="89" alt="Enantioselective Synthesis of N-Substituted Aspartic Acids Using an Engineered Variant of Methylaspartate Ammonia Lyase" title="Enantioselective Synthesis of N-Substituted Aspartic Acids Using an Engineered Variant of Methylaspartate Ammonia Lyase" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Unnatural reactions:</B> We report the synthesis of a large variety of N-substituted aspartic acids by addition of structurally diverse amines to fumaric acid; the reactions are catalyzed by a previously engineered variant of methylaspartate ammonia lyase. The additions are highly enantioselective and yield only the <span style="font-variant:small-caps">L</span> enantiomers of the corresponding amino acid products (&gt;99&nbsp;%&nbsp;<I>ee</I>).</P>
<p> [Communication]<br />Vinod Puthan&#xA0;Veetil, Hans Raj, Marianne de&#xA0;Villiers, Pieter G. Tepper, Frank J. Dekker, Wim J. Quax, Gerrit J. Poelarends<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201200906. <a href="http://dx.doi.org/10.1002/cctc.201200906">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200744">
<title>Hydroformylation of 1-Dodecene with Water-Soluble Rhodium Catalysts with Bidentate Ligands in Multiphase Systems</title>
<link>http://dx.doi.org/10.1002/cctc.201200744</link>
<dc:creator>Tobias Hamerla, Anke Rost, Yasemin Kasaka, Reinhard Schomäcker</dc:creator>
<dc:date>2013-03-07T15:14+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200744.gif" width="214" height="145" alt="Hydroformylation of 1-Dodecene with Water-Soluble Rhodium Catalysts with Bidentate Ligands in Multiphase Systems" title="Hydroformylation of 1-Dodecene with Water-Soluble Rhodium Catalysts with Bidentate Ligands in Multiphase Systems" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Third phase for the catalyst:</B> A hydrophilic metal&ndash;ligand complex formed from the precursor [Rh(acac)(CO)<sub>2</sub>] and the bidentate ligand SulfoXantPhos (see picture) was found to be a suitable candidate as a catalyst complex for the hydroformylation of 1-dodecene in multiphase systems formulated from water, 1-dodecene, and a nonionic surfactant.</P>
<p> [Full Paper]<br />Tobias Hamerla, Anke Rost, Yasemin Kasaka, Reinhard Schom&#xE4;cker<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201200744. <a href="http://dx.doi.org/10.1002/cctc.201200744">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200670">
<title>X-Ray Imaging of SAPO-34 Molecular Sieves at the Nanoscale: Influence of Steaming on the Methanol-to-Hydrocarbons Reaction</title>
<link>http://dx.doi.org/10.1002/cctc.201200670</link>
<dc:creator>Luis R. Aramburo, Javier Ruiz-Martínez, Linn Sommer, Bjørnar Arstad, Robison Buitrago-Sierra, Antonio Sepúlveda-Escribano, Henny W. Zandbergen, Unni Olsbye, Frank M. F. de Groot, Bert M. Weckhuysen</dc:creator>
<dc:date>2013-03-07T15:14+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200670.gif" width="212" height="149" alt="X-Ray Imaging of SAPO-34 Molecular Sieves at the Nanoscale: Influence of Steaming on the Methanol-to-Hydrocarbons Reaction" title="X-Ray Imaging of SAPO-34 Molecular Sieves at the Nanoscale: Influence of Steaming on the Methanol-to-Hydrocarbons Reaction" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Full steam ahead:</B> In&nbsp;situ scanning transmission X-ray microscopy has been used in combination with catalytic testing and bulk characterization methods to study the effect of a hydrothermal treatment on the reactivity and stability of H-SAPO-34 during the methanol-to-hydrocarbons reaction.</P>
<p> [Full Paper]<br />Luis R. Aramburo, Javier Ruiz-Mart&#xED;nez, Linn Sommer, Bj&#xF8;rnar Arstad, Robison Buitrago-Sierra, Antonio Sep&#xFA;lveda-Escribano, Henny W. Zandbergen, Unni Olsbye, Frank M. F. de&#xA0;Groot, Bert M. Weckhuysen<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201200670. <a href="http://dx.doi.org/10.1002/cctc.201200670">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200658">
<title>Enhancing the Electrocatalytic Activity of Pt–Pd Catalysts by Introducing Porous Architectures</title>
<link>http://dx.doi.org/10.1002/cctc.201200658</link>
<dc:creator>Xiangheng Niu, Hongli Zhao, Chen Chen, Minbo Lan</dc:creator>
<dc:date>2013-03-07T15:14+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200658.gif" width="214" height="139" alt="Enhancing the Electrocatalytic Activity of Pt&ndash;Pd Catalysts by Introducing Porous Architectures" title="Enhancing the Electrocatalytic Activity of Pt&ndash;Pd Catalysts by Introducing Porous Architectures" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>When the bubble bursts:</B> Remarkable enhancement of the electrocatalytic activity of Pt&ndash;Pd catalysts was achieved by introducing porous architectures with three-dimensional dendritic microstructures, which were fabricated in&nbsp;situ by means of a novel periodic hydrogen-evolution-assisted electrodeposition strategy (see scheme). The resulting catalyst exhibited significantly improved catalytic properties for glucose electrooxidation.</P>
<p> [Full Paper]<br />Xiangheng Niu, Hongli Zhao, Chen Chen, Minbo Lan<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201200658. <a href="http://dx.doi.org/10.1002/cctc.201200658">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200850">
<title>Design and Application of a Hybrid Material Featuring Well-Defined, Tuneable Grafting Sites for Supported Catalysis.</title>
<link>http://dx.doi.org/10.1002/cctc.201200850</link>
<dc:creator>Nicolas Popoff, Jeff Espinas, Jérémie Pelletier, Kai C. Szeto, Jean Thivolle-Cazat, Laurent Delevoye, Régis M. Gauvin, Mostafa Taoufik</dc:creator>
<dc:date>2013-03-07T15:13+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200850.gif" width="212" height="161" alt="Design and Application of a Hybrid Material Featuring Well-Defined, Tuneable Grafting Sites for Supported Catalysis." title="Design and Application of a Hybrid Material Featuring Well-Defined, Tuneable Grafting Sites for Supported Catalysis." style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>To tether a tungsten:</B> A hybrid material, featuring single-site phenolic functionalities on a silica surface was developed and subsequently used to tether a tungstenocarbyne complex. Drastic improvements in terms of activity and stability in propene metathesis were observed with respect to the silica counterpart. Further tuning of the spacer moiety with fluorine atoms led to additional significant improvements in activity.</P>
<p> [Full Paper]<br />Nicolas Popoff, Jeff Espinas, J&#xE9;r&#xE9;mie Pelletier, Kai C. Szeto, Jean Thivolle-Cazat, Laurent Delevoye, R&#xE9;gis M. Gauvin, Mostafa Taoufik<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201200850. <a href="http://dx.doi.org/10.1002/cctc.201200850">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200833">
<title>Influence of the Precipitation Method on Acid–Base-Catalyzed Reactions over Mg–Zr Mixed Oxides</title>
<link>http://dx.doi.org/10.1002/cctc.201200833</link>
<dc:creator>Joseph T. Kozlowski, Malte Behrens, Robert Schlögl, Robert J. Davis</dc:creator>
<dc:date>2013-03-07T15:13+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200833.gif" width="215" height="168" alt="Influence of the Precipitation Method on Acid&ndash;Base-Catalyzed Reactions over Mg&ndash;Zr Mixed Oxides" title="Influence of the Precipitation Method on Acid&ndash;Base-Catalyzed Reactions over Mg&ndash;Zr Mixed Oxides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>It never rains but it precipitates:</B> Mixed oxides of Zr and Mg are prepared by two precipitation methods to investigate the promotional effect of ZrO<sub>2</sub> on MgO for dehydration, dehydrogenation, aldolization, and transesterification. The oxide catalysts are characterized by adsorption microcalorimetry, electron microscopy, and X-ray diffraction, and results are correlated to catalytic performance.</P>
<p> [Full Paper]<br />Joseph T. Kozlowski, Malte Behrens, Robert Schl&#xF6;gl, Robert J. Davis<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201200833. <a href="http://dx.doi.org/10.1002/cctc.201200833">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200890">
<title>Lipase-Catalyzed Stereoselective Cross-Aldol Reaction Promoted by Water</title>
<link>http://dx.doi.org/10.1002/cctc.201200890</link>
<dc:creator>Zong-Bo Xie, Na Wang, Long-Hua Zhou, Fang Wan, Ting He, Zhang-Gao Le, Xiao-Qi Yu</dc:creator>
<dc:date>2013-03-07T15:12+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200890.gif" width="431" height="112" alt="Lipase-Catalyzed Stereoselective Cross-Aldol Reaction Promoted by Water" title="Lipase-Catalyzed Stereoselective Cross-Aldol Reaction Promoted by Water" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Lip synthing</B>: A lipase-catalyzed, green, and efficient approach for the cross-aldol reaction promoted by water with high yield and good stereoselectivity is described.</P>
<p> [Full Paper]<br />Zong-Bo Xie, Na Wang, Long-Hua Zhou, Fang Wan, Ting He, Zhang-Gao Le, Xiao-Qi Yu<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201200890. <a href="http://dx.doi.org/10.1002/cctc.201200890">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200854">
<title>Superior Performance of Fe(BTC) With Respect to Other Metal-Containing Solids in the &lt;I&gt;N&lt;/I&gt;-Hydroxyphthalimide-Promoted Heterogeneous Aerobic Oxidation of Cycloalkanes</title>
<link>http://dx.doi.org/10.1002/cctc.201200854</link>
<dc:creator>Yusuke Mikami, Amarajothi Dhakshinamoorthy, Mercedes Alvaro, Hermenegildo Garcia</dc:creator>
<dc:date>2013-03-07T15:12+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200854.gif" width="213" height="139" alt="Superior Performance of Fe(BTC) With Respect to Other Metal-Containing Solids in the N-Hydroxyphthalimide-Promoted Heterogeneous Aerobic Oxidation of Cycloalkanes" title="Superior Performance of Fe(BTC) With Respect to Other Metal-Containing Solids in the N-Hydroxyphthalimide-Promoted Heterogeneous Aerobic Oxidation of Cycloalkanes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Aerobic oxidation:</B> The <I>N</I>-hydroxyphthalimide (NHPI)-promoted aerobic oxidation of cycloalkanes can be performed by supporting NHPI on high-surface-area solids. Of the materials tested, NHPI incorporated onto commercially available Fe(BTC) (BTC=1,3,5-benzenetricarboxylate) appears to be most efficient due to the balance of high combined selectivity toward &ndash;ol/-one products and conversion.</P>
<p> [Full Paper]<br />Yusuke Mikami, Amarajothi Dhakshinamoorthy, Mercedes Alvaro, Hermenegildo Garcia<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201200854. <a href="http://dx.doi.org/10.1002/cctc.201200854">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300041">
<title>Minimizing the Formation of Coke and Methane on Co Nanoparticles in Steam Reforming of Biomass-Derived Oxygenates</title>
<link>http://dx.doi.org/10.1002/cctc.201300041</link>
<dc:creator>Junming Sun, Donghai Mei, Ayman M. Karim, Abhaya K. Datye, Yong Wang</dc:creator>
<dc:date>2013-03-07T15:11+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300041.gif" width="214" height="132" alt="Minimizing the Formation of Coke and Methane on Co Nanoparticles in Steam Reforming of Biomass-Derived Oxygenates" title="Minimizing the Formation of Coke and Methane on Co Nanoparticles in Steam Reforming of Biomass-Derived Oxygenates" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Small and active:</B> Co nanoparticles supported on graphitized activated carbon are highly stable and selective for acetone steam reforming. DFT calculations were performed to analyze the reaction mechanism. The present work provides insight into the rational design of catalysts that can selectively oxidize species arising from C-C bond cleavage of biomass-derived oxygenates to maximize H<sub>2</sub> selectivity and minimize the formation of coke and methane.</P>
<p> [Communication]<br />Junming Sun, Donghai Mei, Ayman M. Karim, Abhaya K. Datye, Yong Wang<br /><i>ChemCatChem</i>, Mar 07, 2013, DOI: 10.1002/cctc.201300041. <a href="http://dx.doi.org/10.1002/cctc.201300041">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200792">
<title>Copper-Catalyzed Synthesis of α-Aryl Ketones by Metal–Organic Framework MOF-199 as an Efficient Heterogeneous Catalyst</title>
<link>http://dx.doi.org/10.1002/cctc.201200792</link>
<dc:creator>Nam T. S. Phan, Tung T. Nguyen, Phuong Ho, Khoa D. Nguyen</dc:creator>
<dc:date>2013-03-06T12:58+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200792.gif" width="214" height="168" alt="Copper-Catalyzed Synthesis of &alpha;-Aryl Ketones by Metal&ndash;Organic Framework MOF-199 as an Efficient Heterogeneous Catalyst" title="Copper-Catalyzed Synthesis of &alpha;-Aryl Ketones by Metal&ndash;Organic Framework MOF-199 as an Efficient Heterogeneous Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>MOF-199</B> exhibits high activity in the C-arylation reaction of aryl iodides and acetylacetone to form &alpha;-aryl ketones. The catalyst can be facilely separated and be reused without significant degradation in catalytic activity.</P>
<p> [Full Paper]<br />Nam T. S. Phan, Tung T. Nguyen, Phuong Ho, Khoa D. Nguyen<br /><i>ChemCatChem</i>, Mar 06, 2013, DOI: 10.1002/cctc.201200792. <a href="http://dx.doi.org/10.1002/cctc.201200792">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200810">
<title>An Atomic Scale View of Methanol Reactivity at the Cu(1&#160;1&#160;1)/CuO&lt;sub&gt;&lt;I&gt;x&lt;/I&gt;&lt;/sub&gt; Interface</title>
<link>http://dx.doi.org/10.1002/cctc.201200810</link>
<dc:creator>Timothy J. Lawton, Georgios Kyriakou, Ashleigh E. Baber, E. Charles H. Sykes</dc:creator>
<dc:date>2013-03-06T12:57+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200810.gif" width="214" height="103" alt="An Atomic Scale View of Methanol Reactivity at the Cu(1&nbsp;1&nbsp;1)/CuOx Interface" title="An Atomic Scale View of Methanol Reactivity at the Cu(1&nbsp;1&nbsp;1)/CuOx Interface" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Methanol all around the perimeter:</B> The interaction and reaction of methanol on a catalytically relevant Cu/CuO<sub><I>x</I></sub> interface has been studied at the atomic scale with scanning tunneling microscopy.</P>
<p> [Full Paper]<br />Timothy J. Lawton, Georgios Kyriakou, Ashleigh E. Baber, E. Charles H. Sykes<br /><i>ChemCatChem</i>, Mar 06, 2013, DOI: 10.1002/cctc.201200810. <a href="http://dx.doi.org/10.1002/cctc.201200810">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200721">
<title>Mechanistic Insights into the Reduction of Carbon Dioxide with Silanes over N-Heterocyclic Carbene Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201200721</link>
<dc:creator>Siti Nurhanna Riduan, Jackie Y. Ying, Yugen Zhang</dc:creator>
<dc:date>2013-03-06T12:57+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200721.gif" width="424" height="128" alt="Mechanistic Insights into the Reduction of Carbon Dioxide with Silanes over N-Heterocyclic Carbene Catalysts" title="Mechanistic Insights into the Reduction of Carbon Dioxide with Silanes over N-Heterocyclic Carbene Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Which silane reacts first?</B> Experimental results and DFT calculations of the N-heterocyclic carbene catalyzed reduction of carbon dioxide to methanol with silanes indicated that the overall process involved a three-step cascade reaction with the first hydrosilylation as the rate-determining step (see picture). This mechanism explains the pathway to the methoxide end product and the high hydrogen transfer yield.</P>
<p> [Full Paper]<br />Siti Nurhanna Riduan, Jackie Y. Ying, Yugen Zhang<br /><i>ChemCatChem</i>, Mar 06, 2013, DOI: 10.1002/cctc.201200721. <a href="http://dx.doi.org/10.1002/cctc.201200721">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201300014">
<title>Cationic-Rhodium-Catalyzed Kinetic Resolution of Allylic Alcohols through a Redox Isomerization Reaction in a Noncoordinating Solvent</title>
<link>http://dx.doi.org/10.1002/cctc.201300014</link>
<dc:creator>Kai Ren, Lei Zhang, Bei Hu, Mengmeng Zhao, Yahui Tu, Xiaomin Xie, Tony Y. Zhang, Zhaoguo Zhang</dc:creator>
<dc:date>2013-03-02T01:32+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201300014.gif" width="293" height="88" alt="Cationic-Rhodium-Catalyzed Kinetic Resolution of Allylic Alcohols through a Redox Isomerization Reaction in a Noncoordinating Solvent" title="Cationic-Rhodium-Catalyzed Kinetic Resolution of Allylic Alcohols through a Redox Isomerization Reaction in a Noncoordinating Solvent" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>On the [Rh]oad again:</B> A series of optically pure allylic alcohols is obtained through the Rh/BINAP-catalyzed redox isomerization of racemic allylic alcohols. An improved system involves the use of cationic rhodium and a noncoordinating solvent, in which aromatic and aliphatic allylic alcohols are effectively resolved with <I>k</I><sub>f</sub>/<I>k</I><sub>s</sub> (<I>k</I><sub>f</sub>=rate of fast reaction, <I>k</I><sub>s</sub>=rate of slow reaction) values up to 24.</P>
<p> [Communication]<br />Kai Ren, Lei Zhang, Bei Hu, Mengmeng Zhao, Yahui Tu, Xiaomin Xie, Tony Y. Zhang, Zhaoguo Zhang<br /><i>ChemCatChem</i>, Mar 02, 2013, DOI: 10.1002/cctc.201300014. <a href="http://dx.doi.org/10.1002/cctc.201300014">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200614">
<title>Compositional and Morphological Changes of Ordered Pt&lt;sub&gt;&lt;I&gt;x&lt;/I&gt;&lt;/sub&gt;Fe&lt;sub&gt;&lt;I&gt;y&lt;/I&gt;&lt;/sub&gt;/C Oxygen Electroreduction Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201200614</link>
<dc:creator>Liang Chen, Mickey C. Y. Chan, Feihong Nan, Christina Bock, Gianluigi A. Botton, Patrick H. J. Mercier, Barry R. MacDougall</dc:creator>
<dc:date>2013-03-02T01:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200614.gif" width="214" height="199" alt="Compositional and Morphological Changes of Ordered PtxFey/C Oxygen Electroreduction Catalysts" title="Compositional and Morphological Changes of Ordered PtxFey/C Oxygen Electroreduction Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Pulling the platinum card:</B> Changes in the O<sub>2</sub> reduction (ORR) activity and the structure of carbon-supported Pt<sub><I>x</I></sub>Fe<sub><I>y</I></sub> catalysts upon electrochemical stress testing are investigated. The dissolution of Pt induced by potential cycling clearly contributes to the observed decrease in the Pt surface area and mass ORR activity for the Pt<sub><I>x</I></sub>Fe<sub><I>y</I></sub>/C catalysts.</P>
<p> [Full Paper]<br />Liang Chen, Mickey C. Y. Chan, Feihong Nan, Christina Bock, Gianluigi A. Botton, Patrick H. J. Mercier, Barry R. MacDougall<br /><i>ChemCatChem</i>, Mar 02, 2013, DOI: 10.1002/cctc.201200614. <a href="http://dx.doi.org/10.1002/cctc.201200614">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200606">
<title>Laccase-Catalyzed C-S and C-C Coupling for a One-Pot Synthesis of 1,4-Naphthoquinone Sulfides and 1,4-Naphthoquinone Sulfide Dimers</title>
<link>http://dx.doi.org/10.1002/cctc.201200606</link>
<dc:creator>Kevin W. Wellington, Gregory E. R. Gordon, Lindelani A. Ndlovu, Paul Steenkamp</dc:creator>
<dc:date>2013-03-02T01:29+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200606.gif" width="215" height="169" alt="Laccase-Catalyzed C-S and C-C Coupling for a One-Pot Synthesis of 1,4-Naphthoquinone Sulfides and 1,4-Naphthoquinone Sulfide Dimers" title="Laccase-Catalyzed C-S and C-C Coupling for a One-Pot Synthesis of 1,4-Naphthoquinone Sulfides and 1,4-Naphthoquinone Sulfide Dimers" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A beautiful couple:</B> Oxidative C-S and C-C bond formation with aryl and alkyl thiols is catalyzed under mild conditions in a reaction vessel open to air at pH&nbsp;4.5 in the presence of a commercial laccase (Novozym 51003 or Suberase) and a cosolvent (DMF) to afford 1,4-naphthoquinone sulfides. Although both monothiolation and dithiolation of the 1,4-naphthohydroquinone are accomplished, the latter is favored.</P>
<p> [Full Paper]<br />Kevin W. Wellington, Gregory E. R. Gordon, Lindelani A. Ndlovu, Paul Steenkamp<br /><i>ChemCatChem</i>, Mar 02, 2013, DOI: 10.1002/cctc.201200606. <a href="http://dx.doi.org/10.1002/cctc.201200606">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200662">
<title>Isolation, Characterization, and Identification of Catalytically Active Species in the MoO&lt;sub&gt;3&lt;/sub&gt;/SiO&lt;sub&gt;2&lt;/sub&gt; Catalyst during Solid Acid Catalyzed Reactions</title>
<link>http://dx.doi.org/10.1002/cctc.201200662</link>
<dc:creator>Trupti V. Kotbagi, Ankush V. Biradar, Shubhangi B. Umbarkar, Mohan K. Dongare</dc:creator>
<dc:date>2013-03-01T03:57+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200662.gif" width="212" height="158" alt="Isolation, Characterization, and Identification of Catalytically Active Species in the MoO3/SiO2 Catalyst during Solid Acid Catalyzed Reactions" title="Isolation, Characterization, and Identification of Catalytically Active Species in the MoO3/SiO2 Catalyst during Solid Acid Catalyzed Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Water is beneficial, too!</B> The MoO<sub>3</sub>/SiO<sub>2</sub> catalyst with very high acidity is prepared by the sol&ndash;gel process, and its characterization reveals the in&nbsp;situ formation of reduced silicomolybdic acid on silica nanoparticles in the presence of water, which acts as catalytically active species that dissolves in the reaction medium and gives high activity responsible for the esterification of ethanol and acetic acid.</P>
<p> [Full Paper]<br />Trupti V. Kotbagi, Ankush V. Biradar, Shubhangi B. Umbarkar, Mohan K. Dongare<br /><i>ChemCatChem</i>, Mar 01, 2013, DOI: 10.1002/cctc.201200662. <a href="http://dx.doi.org/10.1002/cctc.201200662">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200804">
<title>Hydroxynitrile Lyases Do Not Catalyse the Promiscuous Addition of Cyanide to Imines</title>
<link>http://dx.doi.org/10.1002/cctc.201200804</link>
<dc:creator>Guzman Torrelo, Jianfeng Jin, Ulf Hanefeld</dc:creator>
<dc:date>2013-02-28T21:52+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200804.gif" width="391" height="124" alt="Hydroxynitrile Lyases Do Not Catalyse the Promiscuous Addition of Cyanide to Imines" title="Hydroxynitrile Lyases Do Not Catalyse the Promiscuous Addition of Cyanide to Imines" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Blank reaction:</B> Ten years ago, it was reported that hydroxynitrile lyase (HNL) from defatted almond meal shows catalytic promiscuity in the addition of cyanide to imines. Here we provide experimental evidence that this addition occurs in a non-enzymatic reaction, and two structurally different HNLs do not catalyse this reaction.</P>
<p> [Communication]<br />Guzman Torrelo, Jianfeng Jin, Ulf Hanefeld<br /><i>ChemCatChem</i>, Feb 28, 2013, DOI: 10.1002/cctc.201200804. <a href="http://dx.doi.org/10.1002/cctc.201200804">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200762">
<title>Mechanistic Insight into Catalytic Oxidation of Ammonia on Clean, O- and OH-Assisted Ir(1&#160;1&#160;1) Surfaces</title>
<link>http://dx.doi.org/10.1002/cctc.201200762</link>
<dc:creator>Xiaoqing Lu, Zhigang Deng, Ka-Shing Chau, Longfei Li, Zengqiang Wen, Wenyue Guo, Chi-Man Lawrence Wu</dc:creator>
<dc:date>2013-02-25T09:27+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200762.gif" width="432" height="120" alt="Mechanistic Insight into Catalytic Oxidation of Ammonia on Clean, O- and OH-Assisted Ir(1&nbsp;1&nbsp;1) Surfaces" title="Mechanistic Insight into Catalytic Oxidation of Ammonia on Clean, O- and OH-Assisted Ir(1&nbsp;1&nbsp;1) Surfaces" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Surface coverage reveals all:</B> Catalytic oxidation mechanisms of NH<sub><I>x</I></sub> (<I>x</I>=1&ndash;3) on an Ir(1&nbsp;1&nbsp;1) surface with O and OH oxidizing agents are investigated by using DFT calculations. Reactions proceed via NH<sub>3</sub>+O&rarr;NH<sub>2</sub>+OH, NH<sub>2</sub>+OH&rarr;NH+H<sub>2</sub>O, and NH+OH&rarr;N+H<sub>2</sub>O, followed by N-N and/or N-O recombination reactions. Promotional effects of O and OH are elucidated by energy barrier analysis; relationships between final product selectivity, O and N coverage, and reaction temperature are analyzed.</P>
<p> [Full Paper]<br />Xiaoqing Lu, Zhigang Deng, Ka-Shing Chau, Longfei Li, Zengqiang Wen, Wenyue Guo, Chi-Man Lawrence Wu<br /><i>ChemCatChem</i>, Feb 25, 2013, DOI: 10.1002/cctc.201200762. <a href="http://dx.doi.org/10.1002/cctc.201200762">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200675">
<title>Effect of Noble Metals on the Strength of Brønsted Acid Sites in Bifunctional Zeolites</title>
<link>http://dx.doi.org/10.1002/cctc.201200675</link>
<dc:creator>Dominic Santi, Sandra Rabl, Vincenzo Calemma, Michael Dyballa, Michael Hunger, Jens Weitkamp</dc:creator>
<dc:date>2013-02-25T09:27+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200675.gif" width="215" height="166" alt="Effect of Noble Metals on the Strength of Br&oslash;nsted Acid Sites in Bifunctional Zeolites" title="Effect of Noble Metals on the Strength of Br&oslash;nsted Acid Sites in Bifunctional Zeolites" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Noble metals change everything:</B> The introduction of noble metals (M) into zeolites causes a decrease in the strength of Br&oslash;nsted acid sites (Si(OH)Al). This effect is because of charge transfer between the noble metal and the support-framework oxygen atoms, which affects the OH bond strength in the Si(OH)Al groups.</P>
<p> [Full Paper]<br />Dominic Santi, Sandra Rabl, Vincenzo Calemma, Michael Dyballa, Michael Hunger, Jens Weitkamp<br /><i>ChemCatChem</i>, Feb 25, 2013, DOI: 10.1002/cctc.201200675. <a href="http://dx.doi.org/10.1002/cctc.201200675">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200955">
<title>Atomic-Scale Probing the Priority of Oxidation Sites of an Organic Molecule Adsorbed at the Cu-O/Cu(1&#160;1&#160;0) Interface</title>
<link>http://dx.doi.org/10.1002/cctc.201200955</link>
<dc:creator>Kai Sheng, Huihui Kong, Zhiwen Li, Chi Zhang, Qiang Sun, Qinggang Tan, Yunxiang Pan, Aiguo Hu, Wei Xu</dc:creator>
<dc:date>2013-02-23T03:29+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200955.gif" width="195" height="191" alt="Atomic-Scale Probing the Priority of Oxidation Sites of an Organic Molecule Adsorbed at the Cu-O/Cu(1&nbsp;1&nbsp;0) Interface" title="Atomic-Scale Probing the Priority of Oxidation Sites of an Organic Molecule Adsorbed at the Cu-O/Cu(1&nbsp;1&nbsp;0) Interface" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Adsorbent with four binding modes:</B> The interface between metal and oxides is considered to play a key role in redox reactions. A combination of STM imaging and DFT calculations provided direct evidence at the atomic scale that the interface of Cu-O/Cu(1&nbsp;1&nbsp;0) is the most favorable site for the adsorption and activation of an organic, multifunctional molecule.</P>
<p> [Full Paper]<br />Kai Sheng, Huihui Kong, Zhiwen Li, Chi Zhang, Qiang Sun, Qinggang Tan, Yunxiang Pan, Aiguo Hu, Wei Xu<br /><i>ChemCatChem</i>, Feb 23, 2013, DOI: 10.1002/cctc.201200955. <a href="http://dx.doi.org/10.1002/cctc.201200955">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200709">
<title>Biocatalytic Methods for C-C Bond Formation</title>
<link>http://dx.doi.org/10.1002/cctc.201200709</link>
<dc:creator>Kateryna Fesko, Mandana Gruber-Khadjawi</dc:creator>
<dc:date>2013-02-21T17:14+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200709.gif" width="392" height="96" alt="Biocatalytic Methods for C-C Bond Formation" title="Biocatalytic Methods for C-C Bond Formation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>One plus One makes One:</B> This review describes the latest results regarding optimizations and applications of the novel as well as known enzymes for carbon-carbon bond formation.</P>
<p> [Review]<br />Kateryna Fesko, Mandana Gruber-Khadjawi<br /><i>ChemCatChem</i>, Feb 21, 2013, DOI: 10.1002/cctc.201200709. <a href="http://dx.doi.org/10.1002/cctc.201200709">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200818">
<title>Ruthenium(II)-Phosphite Complexes as Catalysts for the Hydrogenation of Carbon Dioxide</title>
<link>http://dx.doi.org/10.1002/cctc.201200818</link>
<dc:creator>Keven Muller, Yu Sun, Werner R. Thiel</dc:creator>
<dc:date>2013-02-21T17:11+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200818.gif" width="163" height="176" alt="Ruthenium(II)-Phosphite Complexes as Catalysts for the Hydrogenation of Carbon Dioxide" title="Ruthenium(II)-Phosphite Complexes as Catalysts for the Hydrogenation of Carbon Dioxide" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Ru(II) for the home team:</B> Ruthenium complexes of simple and cheap phosphite ligands give high activities in the hydrogenation of carbon dioxide under supercritical conditions. The activities correlate well with the steric demand of the substituents.</P>
<p> [Communication]<br />Keven Muller, Yu Sun, Werner R. Thiel<br /><i>ChemCatChem</i>, Feb 21, 2013, DOI: 10.1002/cctc.201200818. <a href="http://dx.doi.org/10.1002/cctc.201200818">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200644">
<title>Diastereodivergent Processes in Palladium-Catalyzed Allylic Alkylation</title>
<link>http://dx.doi.org/10.1002/cctc.201200644</link>
<dc:creator>Maria Teresa Oliveira, Davide Audisio, Supaporn Niyomchon, Nuno Maulide</dc:creator>
<dc:date>2013-02-21T17:11+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200644.gif" width="216" height="159" alt="Diastereodivergent Processes in Palladium-Catalyzed Allylic Alkylation" title="Diastereodivergent Processes in Palladium-Catalyzed Allylic Alkylation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Lost identity:</B> Pd-catalyzed asymmetric allylic alkylation allows the quantitative deracemization of chiral substrates. The reaction can be diastereodivergent if multiple diastereomers of the product are possible and if a specific process offers the ability to generate each of them. Herein, the advances made in this field are summarized and novel diastereodivergent deracemization and diastereodivergent de-epimerization concepts are introduced and discussed.</P>
<p> [Concept]<br />Maria Teresa Oliveira, Davide Audisio, Supaporn Niyomchon, Nuno Maulide<br /><i>ChemCatChem</i>, Feb 21, 2013, DOI: 10.1002/cctc.201200644. <a href="http://dx.doi.org/10.1002/cctc.201200644">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200712">
<title>From Oxide-Supported Palladium to Intermetallic Palladium Phases: Consequences for Methanol Steam Reforming</title>
<link>http://dx.doi.org/10.1002/cctc.201200712</link>
<dc:creator>Harald Lorenz, Christoph Rameshan, Thomas Bielz, Norbert Memmel, Werner Stadlmayr, Lukas Mayr, Qian Zhao, Soipatta Soisuwan, Bernhard Klötzer, Simon Penner</dc:creator>
<dc:date>2013-02-20T16:16+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200712.gif" width="216" height="181" alt="From Oxide-Supported Palladium to Intermetallic Palladium Phases: Consequences for Methanol Steam Reforming" title="From Oxide-Supported Palladium to Intermetallic Palladium Phases: Consequences for Methanol Steam Reforming" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Steam powered:</B> Recent work towards unraveling the CO<sub>2</sub> selectivity of a number of unsupported and supported Pd-X intermetallic compounds (X=Zn, Ga, In, Sn, and Ge) is reviewed and the importance of bifunctional synergy between the catalyst constituents for establishing a state of pronounced CO<sub>2</sub> selectivity is highlighted.</P>
<p> [Minireview]<br />Harald Lorenz, Christoph Rameshan, Thomas Bielz, Norbert Memmel, Werner Stadlmayr, Lukas Mayr, Qian Zhao, Soipatta Soisuwan, Bernhard Kl&#xF6;tzer, Simon Penner<br /><i>ChemCatChem</i>, Feb 20, 2013, DOI: 10.1002/cctc.201200712. <a href="http://dx.doi.org/10.1002/cctc.201200712">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200916">
<title>Synthesis of Cyclic Carbonates from Epoxides and CO&lt;sub&gt;2&lt;/sub&gt; under Mild Conditions Using a Simple, Highly Efficient Niobium-Based Catalyst</title>
<link>http://dx.doi.org/10.1002/cctc.201200916</link>
<dc:creator>Antoine Monassier, Valerio D’Elia, Mirza Cokoja, Hailin Dong, Jérémie D. A. Pelletier, Jean-Marie Basset, Fritz E. Kühn</dc:creator>
<dc:date>2013-02-20T16:14+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200916.gif" width="215" height="140" alt="Synthesis of Cyclic Carbonates from Epoxides and CO2 under Mild Conditions Using a Simple, Highly Efficient Niobium-Based Catalyst" title="Synthesis of Cyclic Carbonates from Epoxides and CO2 under Mild Conditions Using a Simple, Highly Efficient Niobium-Based Catalyst" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Like a sore thumb:</B> Niobium stands out among neighboring transition metals for its catalytic performance in the synthesis of cyclic carbonates. Readily available NbCl<sub>5</sub> is a very efficient catalyst for the preparation of industrially relevant carbonates at ambient temperature, low CO<sub>2</sub> pressure, and low concentrations. DMAP=<I>N</I>,<I>N</I>-dimethylaminopyridine.</P>
<p> [Communication]<br />Antoine Monassier, Valerio D&#x2019;Elia, Mirza Cokoja, Hailin Dong, J&#xE9;r&#xE9;mie D. A. Pelletier, Jean-Marie Basset, Fritz E. K&#xFC;hn<br /><i>ChemCatChem</i>, Feb 20, 2013, DOI: 10.1002/cctc.201200916. <a href="http://dx.doi.org/10.1002/cctc.201200916">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200598">
<title>Support effects in a Rh diamine complex heterogenized on carbon materials</title>
<link>http://dx.doi.org/10.1002/cctc.201200598</link>
<dc:creator>C. C. Gheorghiu, C. Salinas Martínez de Lecea, M. C. Román Martínez</dc:creator>
<dc:date>2013-02-19T17:54+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200598.gif" width="216" height="207" alt="Support effects in a Rh diamine complex heterogenized on carbon materials" title="Support effects in a Rh diamine complex heterogenized on carbon materials" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A nosy partner:</B> Partial complex reduction during hydrogenation reactions was observed in carbon xerogels supports leading to a catalytic activity enhancement. Selectivity to an intermediate product can be modulated by the mesopore size of the support.</P>
<p> [Full Paper]<br />C. C. Gheorghiu, C. Salinas&#xA0;Mart&#xED;nez&#xA0;de&#xA0;Lecea, M. C. Rom&#xE1;n&#xA0;Mart&#xED;nez<br /><i>ChemCatChem</i>, Feb 19, 2013, DOI: 10.1002/cctc.201200598. <a href="http://dx.doi.org/10.1002/cctc.201200598">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200629">
<title>AgBr Nanocrystals from Plates to Cubes and Their Photocatalytic Properties</title>
<link>http://dx.doi.org/10.1002/cctc.201200629</link>
<dc:creator>Hua Wang, Yang Liu, Pengfei Hu, Liang He, Jinghong Li, Lin Guo</dc:creator>
<dc:date>2013-02-19T03:26+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200629.gif" width="214" height="129" alt="AgBr Nanocrystals from Plates to Cubes and Their Photocatalytic Properties" title="AgBr Nanocrystals from Plates to Cubes and Their Photocatalytic Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Crystal evolution:</B> AgBr nanocrystals, evolving from plates through truncated cubes and finally to regular cubes, corresponding to a progressive shrinkage of exposed {1&nbsp;1&nbsp;1} facets and enlargement of exposed {1&nbsp;0&nbsp;0} facets, are prepared and their growth mechanism investigated. These nanocrystals exhibit facet-dependent photocatalytic properties.</P>
<p> [Full Paper]<br />Hua Wang, Yang Liu, Pengfei Hu, Liang He, Jinghong Li, Lin Guo<br /><i>ChemCatChem</i>, Feb 19, 2013, DOI: 10.1002/cctc.201200629. <a href="http://dx.doi.org/10.1002/cctc.201200629">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200582">
<title>Hydrodeoxygenation of Phenol and Derivatives over an Ionic Liquid-Like Copolymer Stabilized Nanocatalyst in Aqueous Media</title>
<link>http://dx.doi.org/10.1002/cctc.201200582</link>
<dc:creator>Jinzhu Chen, Jing Huang, Limin Chen, Longlong Ma, Tiejun Wang, Uzma I. Zakai</dc:creator>
<dc:date>2013-02-18T21:32+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200582.gif" width="214" height="186" alt="Hydrodeoxygenation of Phenol and Derivatives over an Ionic Liquid-Like Copolymer Stabilized Nanocatalyst in Aqueous Media" title="Hydrodeoxygenation of Phenol and Derivatives over an Ionic Liquid-Like Copolymer Stabilized Nanocatalyst in Aqueous Media" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Bio-oil to fuels:</B> Highly selective hydrodeoxygenation of phenolic bio-oil related phenols to alkanes is achieved in aqueous media over a dual-functional catalyst system consisting of water-soluble ionic liquid-like copolymer (A)-stabilized nanocatalysts and a mineral acid. HDO=hydrodeoxygenation.</P>
<p> [Full Paper]<br />Jinzhu Chen, Jing Huang, Limin Chen, Longlong Ma, Tiejun Wang, Uzma I. Zakai<br /><i>ChemCatChem</i>, Feb 18, 2013, DOI: 10.1002/cctc.201200582. <a href="http://dx.doi.org/10.1002/cctc.201200582">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200896">
<title>Confinement Effect on Ag Clusters in the Channels of Well-Ordered Mesoporous TiO&lt;sub&gt;2&lt;/sub&gt; and their Enhanced Photocatalytic Performance</title>
<link>http://dx.doi.org/10.1002/cctc.201200896</link>
<dc:creator>Ting Li, Wei Zhou, Jianqiang Wang, Yang Qu, Chungui Tian, Kai Pan, Guohui Tian, Honggang Fu</dc:creator>
<dc:date>2013-02-18T20:09+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200896.gif" width="215" height="229" alt="Confinement Effect on Ag Clusters in the Channels of Well-Ordered Mesoporous TiO2 and their Enhanced Photocatalytic Performance" title="Confinement Effect on Ag Clusters in the Channels of Well-Ordered Mesoporous TiO2 and their Enhanced Photocatalytic Performance" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Pug-walls:</B> The confinement effect of ordered mesoporous TiO<sub>2</sub> results in the formation of highly dispersed Ag clusters with strong interactions between the clusters and the pore walls. The mesoporous Ag/TiO<sub>2</sub> composite exhibits excellent photocatalytic activity under UV/Vis light, owing to the Schottky barrier favoring the separation of photogenerated electron/hole pairs and to surface plasmon resonance, thus improving photocatalytic performance.</P>
<p> [Communication]<br />Ting Li, Wei Zhou, Jianqiang Wang, Yang Qu, Chungui Tian, Kai Pan, Guohui Tian, Honggang Fu<br /><i>ChemCatChem</i>, Feb 18, 2013, DOI: 10.1002/cctc.201200896. <a href="http://dx.doi.org/10.1002/cctc.201200896">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200711">
<title>Phosphite-Thiazoline versus Phosphite-Oxazoline for Pd-Catalyzed Allylic Substitution Reactions: A Case for Comparison</title>
<link>http://dx.doi.org/10.1002/cctc.201200711</link>
<dc:creator>Javier Mazuela, Oscar Pàmies, Montserrat Diéguez</dc:creator>
<dc:date>2013-02-12T09:32+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200711.gif" width="212" height="192" alt="Phosphite-Thiazoline versus Phosphite-Oxazoline for Pd-Catalyzed Allylic Substitution Reactions: A Case for Comparison" title="Phosphite-Thiazoline versus Phosphite-Oxazoline for Pd-Catalyzed Allylic Substitution Reactions: A Case for Comparison" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Come together, right now, over</B> <I><B>ee</B></I><B>:</B> Through the combination of substrates with phosphite-oxazoline or phosphite-thiazoline ligands, we identify one of the few catalytic systems that provide high regio- and enantioselectivities in both enantiomers of the alkylation product for a wide range of hindered and unhindered mono-, di-, and trisubstituted substrates with several carbon nucleophiles.</P>
<p> [Full Paper]<br />Javier Mazuela, Oscar P&#xE0;mies, Montserrat Di&#xE9;guez<br /><i>ChemCatChem</i>, Feb 12, 2013, DOI: 10.1002/cctc.201200711. <a href="http://dx.doi.org/10.1002/cctc.201200711">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200894">
<title>Lignin-Based Green Catalyst for the Chemical Fixation of Carbon Dioxide with Epoxides To Form Cyclic Carbonates under Solvent-Free Conditions</title>
<link>http://dx.doi.org/10.1002/cctc.201200894</link>
<dc:creator>Zhilian Wu, Haibo Xie, Xue Yu, Enhui Liu</dc:creator>
<dc:date>2013-02-12T09:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200894.gif" width="215" height="170" alt="Lignin-Based Green Catalyst for the Chemical Fixation of Carbon Dioxide with Epoxides To Form Cyclic Carbonates under Solvent-Free Conditions" title="Lignin-Based Green Catalyst for the Chemical Fixation of Carbon Dioxide with Epoxides To Form Cyclic Carbonates under Solvent-Free Conditions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Fixated on CO<sub>2</sub>:</B> Lignin, the second most-abundant biorenewable polymer on our planet, was successfully used as a catalyst in the presence of KI in the cycloaddition of CO<sub>2</sub> with a series of epoxides. This method represents an integrated and ideal green process for the utilization of &ldquo;carbon-neutral&rdquo; resources.</P>
<p> [Communication]<br />Zhilian Wu, Haibo Xie, Xue Yu, Enhui Liu<br /><i>ChemCatChem</i>, Feb 12, 2013, DOI: 10.1002/cctc.201200894. <a href="http://dx.doi.org/10.1002/cctc.201200894">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200650">
<title>Direct Nucleophilic Substitution of Free Allylic Alcohols in Water Catalyzed by FeCl&lt;sub&gt;3&lt;/sub&gt;·6&#160;H&lt;sub&gt;2&lt;/sub&gt;O: Which is the Real Catalyst?</title>
<link>http://dx.doi.org/10.1002/cctc.201200650</link>
<dc:creator>Paz Trillo, Alejandro Baeza, Carmen Nájera</dc:creator>
<dc:date>2013-02-12T09:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200650.gif" width="212" height="171" alt="Direct Nucleophilic Substitution of Free Allylic Alcohols in Water Catalyzed by FeCl3&middot;6&nbsp;H2O: Which is the Real Catalyst?" title="Direct Nucleophilic Substitution of Free Allylic Alcohols in Water Catalyzed by FeCl3&middot;6&nbsp;H2O: Which is the Real Catalyst?" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Taking a leaf out of the green book:</B> The use of FeCl<sub>3</sub><B>&middot;</B>6&nbsp;H<sub>2</sub>O as an efficient water-compatible catalyst for the allylic substitution of free alcohols is disclosed. This inexpensive, low-toxic, and easily accessible Fe<SUP>III</SUP> salt used as the catalyst in a process conducted in pure water as the solvent represents an environmentally friendly alternative to previously reported methods and allows the introduction of a broad range of nitrogenated and carbon nucleophiles.</P>
<p> [Full Paper]<br />Paz Trillo, Alejandro Baeza, Carmen N&#xE1;jera<br /><i>ChemCatChem</i>, Feb 12, 2013, DOI: 10.1002/cctc.201200650. <a href="http://dx.doi.org/10.1002/cctc.201200650">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200684">
<title>In&#160;Situ Fabrication of Ag/Ag&lt;sub&gt;3&lt;/sub&gt;PO&lt;sub&gt;4&lt;/sub&gt;/Graphene Triple Heterostructure Visible-Light Photocatalyst through Graphene-Assisted Reduction Strategy</title>
<link>http://dx.doi.org/10.1002/cctc.201200684</link>
<dc:creator>Baojiang Jiang, Yanhui Wang, Jian-Qiang Wang, Chungui Tian, Wenjun Li, Qingmao Feng, Qingjiang Pan, Honggang Fu</dc:creator>
<dc:date>2013-02-11T09:00+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200684.gif" width="215" height="212" alt="In&nbsp;Situ Fabrication of Ag/Ag3PO4/Graphene Triple Heterostructure Visible-Light Photocatalyst through Graphene-Assisted Reduction Strategy" title="In&nbsp;Situ Fabrication of Ag/Ag3PO4/Graphene Triple Heterostructure Visible-Light Photocatalyst through Graphene-Assisted Reduction Strategy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Triple chase!</B> The Ag/Ag<sub>3</sub>PO<sub>4</sub>/graphene triple heterostructure composites are fabricated through the redox reaction between Ag<SUP>+</SUP> and graphene. The triple heterostructure can improve the charge separation rate under visible-light irradiation. Simultaneously, photocorrosion can be inhibited effectively, which leads to the high structural stability. Thus, the novel Ag/Ag<sub>3</sub>PO<sub>4</sub>/graphene triple heterostructure demonstrates improved photocatalytic activity and structural stability under visible-light irradiation.</P>
<p> [Full Paper]<br />Baojiang Jiang, Yanhui Wang, Jian-Qiang Wang, Chungui Tian, Wenjun Li, Qingmao Feng, Qingjiang Pan, Honggang Fu<br /><i>ChemCatChem</i>, Feb 11, 2013, DOI: 10.1002/cctc.201200684. <a href="http://dx.doi.org/10.1002/cctc.201200684">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200730">
<title>Cyclopalladated Arylimine Self-Assembly Films for Suzuki Reaction</title>
<link>http://dx.doi.org/10.1002/cctc.201200730</link>
<dc:creator>Na Zhao, Tiesheng Li, Zhen Zhai, Jingjing Qiu, Wenjian Xu, Hui Liu, Yangjie Wu</dc:creator>
<dc:date>2013-02-11T08:59+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200730.gif" width="215" height="153" alt="Cyclopalladated Arylimine Self-Assembly Films for Suzuki Reaction" title="Cyclopalladated Arylimine Self-Assembly Films for Suzuki Reaction" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Cyclos and cycles:</B> Cyclopalladated arylimine complexes are immobilized on solid slides and characterized. The heterogeneous catalyst obtained exhibits 10&nbsp;times the catalytic performance of its homogeneous counterpart. None of the reactions require the use of ligands, air isolation, or assistant solvents. The catalysts are run for 8&nbsp;cycles without deactivation. A Suzuki reaction mechanism is proposed.</P>
<p> [Full Paper]<br />Na Zhao, Tiesheng Li, Zhen Zhai, Jingjing Qiu, Wenjian Xu, Hui Liu, Yangjie Wu<br /><i>ChemCatChem</i>, Feb 11, 2013, DOI: 10.1002/cctc.201200730. <a href="http://dx.doi.org/10.1002/cctc.201200730">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200620">
<title>Control of the Interphases Formation Degree in Co&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;/ZnO Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201200620</link>
<dc:creator>Fernando Rubio-Marcos, Vanesa Calvino-Casilda, Miguel A. Bañares, José F. Fernandez</dc:creator>
<dc:date>2013-02-07T13:55+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200620.gif" width="216" height="155" alt="Control of the Interphases Formation Degree in Co3O4/ZnO Catalysts" title="Control of the Interphases Formation Degree in Co3O4/ZnO Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Keep dry and carry on:</B> ZnO supported Co<sub>3</sub>O<sub>4</sub> nanoparticles are highly active in the transformation of renewable materials through carbonylation of glycerol by urea. The activity of the catalyst is modulated by interaction of the nanoparticles with the ZnO support, which depends on the preparation stage. The Co<sub>3</sub>O<sub>4</sub>/ZnO catalyst system prepared by a dry mixing method at room temperature is very promising for this reaction.</P>
<p> [Full Paper]<br />Fernando Rubio-Marcos, Vanesa Calvino-Casilda, Miguel A. Ba&#xF1;ares, Jos&#xE9; F. Fernandez<br /><i>ChemCatChem</i>, Feb 07, 2013, DOI: 10.1002/cctc.201200620. <a href="http://dx.doi.org/10.1002/cctc.201200620">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200618">
<title>Surface Segregation of Pd from TiO&lt;sub&gt;2&lt;/sub&gt;-Supported AuPd Nanoalloys under CO Oxidation Conditions Observed In&#160;situ by ETEM and DRIFTS</title>
<link>http://dx.doi.org/10.1002/cctc.201200618</link>
<dc:creator>Laurent Delannoy, Suzanne Giorgio, Jean Gabriel Mattei, Claude R. Henry, Nadia El Kolli, Christophe Méthivier, Catherine Louis</dc:creator>
<dc:date>2013-02-07T13:55+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200618.gif" width="216" height="211" alt="Surface Segregation of Pd from TiO2-Supported AuPd Nanoalloys under CO Oxidation Conditions Observed In&nbsp;situ by ETEM and DRIFTS" title="Surface Segregation of Pd from TiO2-Supported AuPd Nanoalloys under CO Oxidation Conditions Observed In&nbsp;situ by ETEM and DRIFTS" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Gold Ghost in the Shell:</B> Surface Pd segregation is observed upon exposure of bimetallic AuPd nanoparticles to a CO+O<sub>2</sub> reaction mixture. The process was scrutinized by means of two in&nbsp;situ techniques, environmental high-resolution electron microscopy (ETEM) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS).</P>
<p> [Full Paper]<br />Laurent Delannoy, Suzanne Giorgio, Jean Gabriel Mattei, Claude R. Henry, Nadia El&#xA0;Kolli, Christophe M&#xE9;thivier, Catherine Louis<br /><i>ChemCatChem</i>, Feb 07, 2013, DOI: 10.1002/cctc.201200618. <a href="http://dx.doi.org/10.1002/cctc.201200618">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200643">
<title>Deactivation Pathways of the Catalytic Activity of Metal–Organic Frameworks in Condensation Reactions</title>
<link>http://dx.doi.org/10.1002/cctc.201200643</link>
<dc:creator>Maksym Opanasenko, Amarajothi Dhakshinamoorthy, Jiří Čejka, Hermenegildo Garcia</dc:creator>
<dc:date>2013-02-05T15:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200643.gif" width="392" height="71" alt="Deactivation Pathways of the Catalytic Activity of Metal&ndash;Organic Frameworks in Condensation Reactions" title="Deactivation Pathways of the Catalytic Activity of Metal&ndash;Organic Frameworks in Condensation Reactions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>What is the poison?</B> Three different condensation reactions were chosen as model reaction to determine the nature of the poisons causing structural instability (see picture), and varied product selectivity for two related metal&ndash;organic framework catalysts, Fe(BTC) and synthetic MIL-100(Fe). Undesired intermediates or byproducts were found to block the pores, whereas phenolic substrates could substitute the metal ligands thus destabilizing the catalyst structure.</P>
<p> [Full Paper]<br />Maksym Opanasenko, Amarajothi Dhakshinamoorthy, Ji&#x159;&#xED; &#x10C;ejka, Hermenegildo Garcia<br /><i>ChemCatChem</i>, Feb 05, 2013, DOI: 10.1002/cctc.201200643. <a href="http://dx.doi.org/10.1002/cctc.201200643">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200603">
<title>Aerobic Liquid-Phase Oxidation of Ethylbenzene to Acetophenone Catalyzed by Carbon Nanotubes</title>
<link>http://dx.doi.org/10.1002/cctc.201200603</link>
<dc:creator>Jin Luo, Feng Peng, Hao Yu, Hongjuan Wang, Wenxu Zheng</dc:creator>
<dc:date>2013-01-30T05:39+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200603.gif" width="216" height="115" alt="Aerobic Liquid-Phase Oxidation of Ethylbenzene to Acetophenone Catalyzed by Carbon Nanotubes" title="Aerobic Liquid-Phase Oxidation of Ethylbenzene to Acetophenone Catalyzed by Carbon Nanotubes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Carbon nanotubes (CNTs) as a metal-free catalyst</B> exhibited high activity and excellent stability for the aerobic oxidation of ethylbenzene (EB) to acetophenone (AcPO) in the liquid phase. The results demonstrated that the CNTs played an important role in the decomposition of 1-phenylethyl hydroperoxide (PEHP) and contributed to the production of AcPO.</P>
<p> [Full Paper]<br />Jin Luo, Feng Peng, Hao Yu, Hongjuan Wang, Wenxu Zheng<br /><i>ChemCatChem</i>, Jan 30, 2013, DOI: 10.1002/cctc.201200603. <a href="http://dx.doi.org/10.1002/cctc.201200603">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200757">
<title>Selective Production of Aromatics from Alkylfurans over Solid Acid Catalysts</title>
<link>http://dx.doi.org/10.1002/cctc.201200757</link>
<dc:creator>Dong Wang, Christian M. Osmundsen, Esben Taarning, James A. Dumesic</dc:creator>
<dc:date>2013-01-30T05:38+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200757.gif" width="312" height="69" alt="Selective Production of Aromatics from Alkylfurans over Solid Acid Catalysts" title="Selective Production of Aromatics from Alkylfurans over Solid Acid Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Aroma all around!</B> Benzene, toluene, and <I>p</I>-xylene are produced by the reaction of ethylene with furan, 2-methylfuran, and 2,5-dimethylfuran over WO<sub><I>x</I></sub>&ndash;ZrO<sub>2</sub> catalysts at 523&nbsp;K in yields of 18, 34, and 80&nbsp;%, respectively.</P>
<p> [Full Paper]<br />Dong Wang, Christian M. Osmundsen, Esben Taarning, James A. Dumesic<br /><i>ChemCatChem</i>, Jan 30, 2013, DOI: 10.1002/cctc.201200757. <a href="http://dx.doi.org/10.1002/cctc.201200757">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200578">
<title>Copper-Incorporated Porous Polydivinylbenzene as Efficient and Recyclable Heterogeneous Catalyst in Ullmann Biaryl Ether Coupling</title>
<link>http://dx.doi.org/10.1002/cctc.201200578</link>
<dc:creator>Liang Wang, Jian Zhang, Jing Sun, Longfeng Zhu, Haiyan Zhang, Fujian Liu, Dafang Zheng, Xiangju Meng, Xiaodong Shi, Feng-Shou Xiao</dc:creator>
<dc:date>2013-01-25T16:42+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200578.gif" width="215" height="152" alt="Copper-Incorporated Porous Polydivinylbenzene as Efficient and Recyclable Heterogeneous Catalyst in Ullmann Biaryl Ether Coupling" title="Copper-Incorporated Porous Polydivinylbenzene as Efficient and Recyclable Heterogeneous Catalyst in Ullmann Biaryl Ether Coupling" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Recycling at its best:</B> A copper-incorporated porous, Schiff base-modified polydivinylbenzene is an effective heterogeneous catalyst for the Ullmann coupling reaction. The porous, solid-supported catalysts have excellent reactivity and can be readily recycled with a slight decrease in catalyst reactivity, rendering them practical heterogeneous catalysts that best reproduce the homogeneous catalyst reactivity.</P>
<p> [Full Paper]<br />Liang Wang, Jian Zhang, Jing Sun, Longfeng Zhu, Haiyan Zhang, Fujian Liu, Dafang Zheng, Xiangju Meng, Xiaodong Shi, Feng-Shou Xiao<br /><i>ChemCatChem</i>, Jan 25, 2013, DOI: 10.1002/cctc.201200578. <a href="http://dx.doi.org/10.1002/cctc.201200578">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200630">
<title>Rhodium-Catalyzed Homogeneous and Aqueous Biphasic Hydroformylation of the Acrolein Acetal 2-Vinyl-5-Methyl-1,3-Dioxane</title>
<link>http://dx.doi.org/10.1002/cctc.201200630</link>
<dc:creator>Jérémy Ternel, Jean-Luc Dubois, Jean-Luc Couturier, Eric Monflier, Jean-François Carpentier</dc:creator>
<dc:date>2013-01-21T16:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200630.gif" width="215" height="166" alt="Rhodium-Catalyzed Homogeneous and Aqueous Biphasic Hydroformylation of the Acrolein Acetal 2-Vinyl-5-Methyl-1,3-Dioxane" title="Rhodium-Catalyzed Homogeneous and Aqueous Biphasic Hydroformylation of the Acrolein Acetal 2-Vinyl-5-Methyl-1,3-Dioxane" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Ligands of mass formylation:</B> The acetal VMD derived from acrolein and MPD is hydroformylated with rhodium catalysts under homogeneous conditions with perfect chemoselectivity for the aldehydes. Diphosphine ligands with a narrow bite angle (&asymp;85&deg;), such as dppe, favor the branched aldehyde with selectivities up to 78&nbsp;%, whereas those with a large bite angle (&asymp;110&deg;), such as xantphos, produce the linear aldehyde with up to 91&nbsp;% selectivity.</P>
<p> [Full Paper]<br />J&#xE9;r&#xE9;my Ternel, Jean-Luc Dubois, Jean-Luc Couturier, Eric Monflier, Jean-Fran&#xE7;ois Carpentier<br /><i>ChemCatChem</i>, Jan 21, 2013, DOI: 10.1002/cctc.201200630. <a href="http://dx.doi.org/10.1002/cctc.201200630">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200654">
<title>Optimum Energy-Dispersive X-Ray Spectroscopy Elemental Mapping for Advanced Catalytic Materials</title>
<link>http://dx.doi.org/10.1002/cctc.201200654</link>
<dc:creator>Bingsen Zhang, Wei Zhang, Lidong Shao, Dang Sheng Su</dc:creator>
<dc:date>2013-01-11T15:50+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200654.gif" width="216" height="212" alt="Optimum Energy-Dispersive X-Ray Spectroscopy Elemental Mapping for Advanced Catalytic Materials" title="Optimum Energy-Dispersive X-Ray Spectroscopy Elemental Mapping for Advanced Catalytic Materials" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>EDX marks the spot:</B> STEM-EDX mapping is a highly useful tool for studying advanced catalytic materials. Beam intensity and dwell time can be adjusted to an optimum balance for obtaining an unambiguously elemental map.</P>
<p> [Communication]<br />Bingsen Zhang, Wei Zhang, Lidong Shao, Dang Sheng Su<br /><i>ChemCatChem</i>, Jan 11, 2013, DOI: 10.1002/cctc.201200654. <a href="http://dx.doi.org/10.1002/cctc.201200654">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200617">
<title>Asymmetric Cyanoethoxy Carbonylation Reaction of Aldehydes Catalyzed by a Ti&lt;SUP&gt;IV&lt;/SUP&gt; Macrocyclic Complex: An Efficient Synthetic Protocol for β-Blocker and α&lt;sub&gt;1&lt;/sub&gt;-Adrenergic Receptor Agonists</title>
<link>http://dx.doi.org/10.1002/cctc.201200617</link>
<dc:creator>Arghya Sadhukhan, Manoj K. Choudhary, Noor-ul H. Khan, Rukhsana I. Kureshy, Sayed H. R. Abdi, Hari C. Bajaj</dc:creator>
<dc:date>2013-01-09T16:37+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200617.gif" width="215" height="195" alt="Asymmetric Cyanoethoxy Carbonylation Reaction of Aldehydes Catalyzed by a TiIV Macrocyclic Complex: An Efficient Synthetic Protocol for &beta;-Blocker and &alpha;1-Adrenergic Receptor Agonists" title="Asymmetric Cyanoethoxy Carbonylation Reaction of Aldehydes Catalyzed by a TiIV Macrocyclic Complex: An Efficient Synthetic Protocol for &beta;-Blocker and &alpha;1-Adrenergic Receptor Agonists" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A crown of titanium:</B> A new class of chiral macrocyclic Ti<SUP>IV</SUP>&ndash;salen complexes are efficient, recyclable, and scalable catalysts for the asymmetric addition of ethyl cyanoformate to aldehydes, which is useful for the synthesis of bioactive compounds. The figure shows the best-performing ligand with two salen units linked flexibly in a crown ether-like motif.</P>
<p> [Full Paper]<br />Arghya Sadhukhan, Manoj K. Choudhary, Noor-ul H. Khan, Rukhsana I. Kureshy, Sayed H. R. Abdi, Hari C. Bajaj<br /><i>ChemCatChem</i>, Jan 09, 2013, DOI: 10.1002/cctc.201200617. <a href="http://dx.doi.org/10.1002/cctc.201200617">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200595">
<title>Organometallic Catalysts for Use in a Fuel Cell</title>
<link>http://dx.doi.org/10.1002/cctc.201200595</link>
<dc:creator>Takahiro Matsumoto, Kyoungmok Kim, Hidetaka Nakai, Takashi Hibino, Seiji Ogo</dc:creator>
<dc:date>2013-01-09T16:37+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200595.gif" width="215" height="180" alt="Organometallic Catalysts for Use in a Fuel Cell" title="Organometallic Catalysts for Use in a Fuel Cell" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Running rings around fuel cells:</B> The performance of a fuel cell is increased by using organometallic catalysis. An organometallic [Ni<SUP>II</SUP>Ru<SUP>IV</SUP>] peroxo catalyst functions as the cathode catalyst in a fuel cell with a much greater efficiency than our previous systems. The organometallic catalyst acts in both solid and solution phases and allows for observation of the mechanism, providing opportunity for further improvement.</P>
<p> [Full Paper]<br />Takahiro Matsumoto, Kyoungmok Kim, Hidetaka Nakai, Takashi Hibino, Seiji Ogo<br /><i>ChemCatChem</i>, Jan 09, 2013, DOI: 10.1002/cctc.201200595. <a href="http://dx.doi.org/10.1002/cctc.201200595">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200648">
<title>From Regioselective Condensation to Regioselective N-Alkylation: A Novel and Environmentally Benign Strategy for the Synthesis of &lt;I&gt;N&lt;/I&gt;,&lt;I&gt;N&lt;/I&gt;'-Alkyl Aryl Ureas and &lt;I&gt;N&lt;/I&gt;,&lt;I&gt;N&lt;/I&gt;'-Dialkyl Ureas</title>
<link>http://dx.doi.org/10.1002/cctc.201200648</link>
<dc:creator>Feng Li, Chunlou Sun, Haixia Shan, Xiaoyuan Zou, Jianjiang Xie</dc:creator>
<dc:date>2013-01-09T16:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200648.gif" width="413" height="91" alt="From Regioselective Condensation to Regioselective N-Alkylation: A Novel and Environmentally Benign Strategy for the Synthesis of N,N&#x27;-Alkyl Aryl Ureas and N,N&#x27;-Dialkyl Ureas" title="From Regioselective Condensation to Regioselective N-Alkylation: A Novel and Environmentally Benign Strategy for the Synthesis of N,N&#x27;-Alkyl Aryl Ureas and N,N&#x27;-Dialkyl Ureas" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Watch out, the borrowers are about!</B> <I>N</I>,<I>N</I>&#x27;-alkyl aryl ureas and <I>N</I>,<I>N</I>&#x27;-dialkyl ureas were synthesized by a transition metal-catalyzed regioselective N3-alkylation of the N-monosubstituted ureas with alcohols. This opens up the design of regioselective N-alkylation of amines with alcohols based on the regioselective condensation of amines with aldehydes, facilitating the progress of the &ldquo;hydrogen autotransfer&rdquo; (or &ldquo;hydrogen-borrowing&rdquo;)</P>
<p> [Full Paper]<br />Feng Li, Chunlou Sun, Haixia Shan, Xiaoyuan Zou, Jianjiang Xie<br /><i>ChemCatChem</i>, Jan 09, 2013, DOI: 10.1002/cctc.201200648. <a href="http://dx.doi.org/10.1002/cctc.201200648">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cctc.201200535">
<title>Carbon-Supported Gold Nanocatalysts: Shape Effect in the Selective Glycerol Oxidation</title>
<link>http://dx.doi.org/10.1002/cctc.201200535</link>
<dc:creator>Di Wang, Alberto Villa, Dangsheng Su, Laura Prati, Robert Schlögl</dc:creator>
<dc:date>2012-11-30T15:21+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cctc201200535.gif" width="215" height="184" alt="Carbon-Supported Gold Nanocatalysts: Shape Effect in the Selective Glycerol Oxidation" title="Carbon-Supported Gold Nanocatalysts: Shape Effect in the Selective Glycerol Oxidation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Order, order!</B> More ordered graphitic layers on the supporting carbon nanofibers surface led to Au particles bonded through their {1&nbsp;1&nbsp;1} plane, exhibiting more facet area. This catalyst presented higher selectivity toward C-C bond cleavage in the liquid-phase oxidation of glycerol.</P>
<p> [Full Paper]<br />Di Wang, Alberto Villa, Dangsheng Su, Laura Prati, Robert Schl&#xF6;gl<br /><i>ChemCatChem</i>, Nov 30, 2012, DOI: 10.1002/cctc.201200535. <a href="http://dx.doi.org/10.1002/cctc.201200535">Read article.</a></p> ]]>
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