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<title>News from ChemCatChem</title>
<link>http://doi.wiley.com/10.1002/(ISSN)1867-3899</link>
<description>News from the journal ChemCatChem</description>
<dc:language>en</dc:language>
<dc:rights>Copyright 2011, Wiley-VCH Verlag GmbH &#x26;amp; Co. KGaA</dc:rights>
<dc:date>2013-05-19T22:37:26Z</dc:date>
<dc:publisher>Wiley-VCH</dc:publisher>
<dc:creator>info@wiley-vch.de</dc:creator>
<dc:subject>Chemistry</dc:subject>
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<title>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>
<content:encoded><![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 -->]]></content:encoded>
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<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>
<content:encoded><![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>]]></content:encoded>
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<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>
<content:encoded><![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>]]></content:encoded>
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