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<dc:date>2012-04-23T00:00:00+02:00</dc:date>
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<title>Watching, Contemplating, or Analyzing?</title>
<link>http://dx.doi.org/10.1002/cphc.201300439</link>
<dc:date>2013-05-17T11:39+05:00</dc:date>
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<![CDATA[ <p></p><p> [News]<br /><br /><i>ChemPhysChem</i>, May 17, 2013, DOI: 10.1002/cphc.201300439. <a href="http://dx.doi.org/10.1002/cphc.201300439">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300234">
<title>A Versatile Approach towards the Compaction, Decompaction, and Immobilization of DNA at Interfaces by Using Cyclodextrins</title>
<link>http://dx.doi.org/10.1002/cphc.201300234</link>
<dc:creator>Alfredo González-Pérez, Juan M. Ruso</dc:creator>
<dc:date>2013-05-17T11:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300234.gif" width="200" height="126" alt="A Versatile Approach towards the Compaction, Decompaction, and Immobilization of DNA at Interfaces by Using Cyclodextrins" title="A Versatile Approach towards the Compaction, Decompaction, and Immobilization of DNA at Interfaces by Using Cyclodextrins" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Die another DNA:</B> The decompaction of the DNA/hexadecyltrimethylammonium bromide (CTAB) complex is strongly influenced by the concentration of &beta;-cyclodextrin (CD) and by the reaction temperature, owing to a subtle balance between the hydration of the complex and the lower compressibility of the native structures. Moreover, the formation of self-assembled layers of &beta;-CD/CTAB complexes on glass or mica surfaces facilitates the immobilization of DNA, either in its coil or globule conformations (see picture).</P>
<p> [Article]<br />Alfredo Gonz&#xE1;lez-P&#xE9;rez, Juan M. Ruso<br /><i>ChemPhysChem</i>, May 17, 2013, DOI: 10.1002/cphc.201300234. <a href="http://dx.doi.org/10.1002/cphc.201300234">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300122">
<title>Photoinduced Biphasic Hydrogen Evolution: Decamethylosmocene as a Light-Driven Electron Donor</title>
<link>http://dx.doi.org/10.1002/cphc.201300122</link>
<dc:creator>Peiyu Ge, Astrid J. Olaya, Micheál D. Scanlon, Imren Hatay Patir, Heron Vrubel, Hubert H. Girault</dc:creator>
<dc:date>2013-05-17T11:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300122.gif" width="196" height="176" alt="Photoinduced Biphasic Hydrogen Evolution: Decamethylosmocene as a Light-Driven Electron Donor" title="Photoinduced Biphasic Hydrogen Evolution: Decamethylosmocene as a Light-Driven Electron Donor" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A weak but productive donor:</B> Mechanistic and kinetic insights into light-driven biphasic hydrogen evolution in the presence of the weak electron donor decamethylosmocene , which on white-light illumination produces an excited-state species that can reduce organically solubilized protons (see picture), are obtained by gas chromatographic, cyclic voltammetric, and UV/Vis and <SUP>1</SUP>H&nbsp;NMR spectroscopic analysis.</P>
<p> [Article]<br />Peiyu Ge, Astrid J. Olaya, Miche&#xE1;l D. Scanlon, Imren Hatay&#xA0;Patir, Heron Vrubel, Hubert H. Girault<br /><i>ChemPhysChem</i>, May 17, 2013, DOI: 10.1002/cphc.201300122. <a href="http://dx.doi.org/10.1002/cphc.201300122">Read article.</a></p> ]]>
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</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201201013">
<title>Direct Observation of the Electroadsorptive Effect on Ultrathin Films for Microsensor and Catalytic-Surface Control</title>
<link>http://dx.doi.org/10.1002/cphc.201201013</link>
<dc:creator>Theodor Doll, Juan J. Velasco-Velez , Dirk Rosenthal, Jonathan Avila , Victor Fuenzalida</dc:creator>
<dc:date>2013-05-17T11:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201201013.gif" width="212" height="94" alt="Direct Observation of the Electroadsorptive Effect on Ultrathin Films for Microsensor and Catalytic-Surface Control" title="Direct Observation of the Electroadsorptive Effect on Ultrathin Films for Microsensor and Catalytic-Surface Control" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Time-series XPS measurements</B> in combination with conductivity analysis on the adsorption of NO<sub>2</sub>/O<sub>2</sub> on compact and porous SnO<sub>2</sub> thin films (see picture) allow for the direct observation of the electroadsorptive effect. Diffusion of NO<sub><I>x</I></sub> species to the surface during the experiment is clearly seen for the porous layers.</P>
<p> [Article]<br />Theodor Doll, Juan J. Velasco-Velez&#xA0;, Dirk Rosenthal, Jonathan Avila&#xA0;, Victor Fuenzalida<br /><i>ChemPhysChem</i>, May 17, 2013, DOI: 10.1002/cphc.201201013. <a href="http://dx.doi.org/10.1002/cphc.201201013">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300029">
<title>A Chemical Lift-off Process: Removing Non-Specific Adsorption in an Electrochemical Epstein–Barr Virus Immunoassay</title>
<link>http://dx.doi.org/10.1002/cphc.201300029</link>
<dc:creator>Lutz Stratmann, Magdalena Gebala, Wolfgang Schuhmann</dc:creator>
<dc:date>2013-05-16T14:35+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300029.gif" width="404" height="134" alt="A Chemical Lift-off Process: Removing Non-Specific Adsorption in an Electrochemical Epstein&ndash;Barr Virus Immunoassay" title="A Chemical Lift-off Process: Removing Non-Specific Adsorption in an Electrochemical Epstein&ndash;Barr Virus Immunoassay" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The anti-protein lift-off</B>: An ester group containing a self-assembled monolayer is used in an electrochemical Epstein&ndash;Barr virus immunoassay with native recombinant antigens and electrochemical readout. The electrode interface is adapted to microstructuring using scanning electrochemical microscopy. A chemical lift-off process based on the hydrolysis of the ester groups is proposed to remove non-specifically adsorbed molecules.</P>
<p> [Article]<br />Lutz Stratmann, Magdalena Gebala, Wolfgang Schuhmann<br /><i>ChemPhysChem</i>, May 16, 2013, DOI: 10.1002/cphc.201300029. <a href="http://dx.doi.org/10.1002/cphc.201300029">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300173">
<title>AFM Study of Gibbs Films of Semifluorinated Alkanes at Liquid Crystal/Air Interfaces</title>
<link>http://dx.doi.org/10.1002/cphc.201300173</link>
<dc:creator>Xunda Feng, Ahmed Mourran, Martin Möller, Christian Bahr</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/cphc201300173.gif" width="198" height="123" alt="AFM Study of Gibbs Films of Semifluorinated Alkanes at Liquid Crystal/Air Interfaces" title="AFM Study of Gibbs Films of Semifluorinated Alkanes at Liquid Crystal/Air Interfaces" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Forming micelles:</B> The first in&nbsp;situ AFM study of Gibbs films of semifluorinated alkanes at liquid crystal/air interfaces is presented. The Gibbs films self-organize in a hexagonal close packing of surface micelles with shapes and lateral dimensions that are similar to micelles forming on aqueous and solid surfaces. It is concluded that he formation of surfaces micelles and their self-organization in large-area dense hexagonal arrays are intrinsic properties of semifluorinated alkane molecules.</P>
<p> [Communication]<br />Xunda Feng, Ahmed Mourran, Martin M&#xF6;ller, Christian Bahr<br /><i>ChemPhysChem</i>, May 14, 2013, DOI: 10.1002/cphc.201300173. <a href="http://dx.doi.org/10.1002/cphc.201300173">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300169">
<title>Chitosan-Cross-linked Osmium Polymer Composites as an Efficient Platform for Electrochemical Biosensors</title>
<link>http://dx.doi.org/10.1002/cphc.201300169</link>
<dc:creator>Harishchandra Digambar Jirimali, Rajaram Krishna Nagarale, Jong Myung Lee, Durai Saravanakumar, Woonsup Shin</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/cphc201300169.gif" width="195" height="166" alt="Chitosan-Cross-linked Osmium Polymer Composites as an Efficient Platform for Electrochemical Biosensors" title="Chitosan-Cross-linked Osmium Polymer Composites as an Efficient Platform for Electrochemical Biosensors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Coated with pores:</B> Dropcoating of randomly cross-linked poly(4-vinylpyridine) osmium bipyridyl and chitosan composites creates a hydrophilic porous (see picture) film on the electrode surface and shows reversible electron-transfer behavior up to 200&nbsp;mV&nbsp;s<SUP>&minus;1</SUP> owing to the fast mass- and electron-transfer capabilities of the film. Oxidation of glucose by immobilization of glucose oxidase also shows enhanced electrocatalytic performance.</P>
<p> [Article]<br />Harishchandra Digambar Jirimali, Rajaram Krishna Nagarale, Jong Myung Lee, Durai Saravanakumar, Woonsup Shin<br /><i>ChemPhysChem</i>, May 14, 2013, DOI: 10.1002/cphc.201300169. <a href="http://dx.doi.org/10.1002/cphc.201300169">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300045">
<title>Kinetic and Thermodynamic Hysteresis Imposed by Intercalation of Proflavine in Ferrocene-Modified Double-Stranded DNA</title>
<link>http://dx.doi.org/10.1002/cphc.201300045</link>
<dc:creator>Magdalena Gebala, Fabio La Mantia, Wolfgang Schuhmann</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/cphc201300045.gif" width="310" height="139" alt="Kinetic and Thermodynamic Hysteresis Imposed by Intercalation of Proflavine in Ferrocene-Modified Double-Stranded DNA" title="Kinetic and Thermodynamic Hysteresis Imposed by Intercalation of Proflavine in Ferrocene-Modified Double-Stranded DNA" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>DNA-bound ferrocene</B> (Fc) undergoes rapid electron transfer with the electrode surface, which is sensitive to the ion transport along the DNA strands&mdash;a phenomenon that is modulated upon specific intercalation of proflavine into double-stranded DNA (dsDNA). The electron-transfer rate of the Fc/Fc<SUP>+</SUP> redox process is influenced by the cationic permselectivity of the DNA monolayer.</P>
<p> [Article]<br />Magdalena Gebala, Fabio La&#xA0;Mantia, Wolfgang Schuhmann<br /><i>ChemPhysChem</i>, May 14, 2013, DOI: 10.1002/cphc.201300045. <a href="http://dx.doi.org/10.1002/cphc.201300045">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300167">
<title>Water and Protein Dynamics in Sedimented Systems: A Relaxometric Investigation</title>
<link>http://dx.doi.org/10.1002/cphc.201300167</link>
<dc:creator>Claudio Luchinat, Giacomo Parigi, Enrico Ravera</dc:creator>
<dc:date>2013-05-13T16:35+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300167.gif" width="181" height="192" alt="Water and Protein Dynamics in Sedimented Systems: A Relaxometric Investigation" title="Water and Protein Dynamics in Sedimented Systems: A Relaxometric Investigation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Crowding out:</B> Sedimented proteins provide solid-state NMR spectra of high quality, suitable for structural investigation. The relaxation profile of sedimented bovine serum albumin (see figure) indicates that reorientation is largely abolished as a consequence of the self-crowding effect related to the extremely high protein concentration.</P>
<p> [Article]<br />Claudio Luchinat, Giacomo Parigi, Enrico Ravera<br /><i>ChemPhysChem</i>, May 13, 2013, DOI: 10.1002/cphc.201300167. <a href="http://dx.doi.org/10.1002/cphc.201300167">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300114">
<title>Series Circuit of Organic Thin-Film Solar Cells for Conversion of Water into Hydrogen</title>
<link>http://dx.doi.org/10.1002/cphc.201300114</link>
<dc:creator>Atsushi Aoki, Mitsuru Naruse, Takayuki Abe</dc:creator>
<dc:date>2013-05-13T16:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300114.gif" width="191" height="94" alt="Series Circuit of Organic Thin-Film Solar Cells for Conversion of Water into Hydrogen" title="Series Circuit of Organic Thin-Film Solar Cells for Conversion of Water into Hydrogen" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>It takes six:</B> A series circuit of organic thin-film solar cells (OSCs) is investigated for electrolyzing water to gaseous hydrogen and oxygen. The combination of a series circuit composed of six OSCs, based on poly(3-hexylthiophene) as a donor and [6,6]-phenyl C61 butyric acid methyl ester as an acceptor, with an electrolysis cell produces hydrogen and oxygen gases under light irradiation.</P>
<p> [Article]<br />Atsushi Aoki, Mitsuru Naruse, Takayuki Abe<br /><i>ChemPhysChem</i>, May 13, 2013, DOI: 10.1002/cphc.201300114. <a href="http://dx.doi.org/10.1002/cphc.201300114">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300200">
<title>From Molecular Complexes to Complex Metallic Nanostructures—&lt;SUP&gt;2&lt;/SUP&gt;H Solid-State NMR Studies of Ruthenium-Containing Hydrogenation Catalysts</title>
<link>http://dx.doi.org/10.1002/cphc.201300200</link>
<dc:creator>Torsten Gutmann, Iker del Rosal, Bruno Chaudret, Romuald Poteau, Hans-Heinrich Limbach, Gerd Buntkowsky</dc:creator>
<dc:date>2013-05-09T07:54+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300200.gif" width="196" height="149" alt="From Molecular Complexes to Complex Metallic Nanostructures&mdash;2H Solid-State NMR Studies of Ruthenium-Containing Hydrogenation Catalysts" title="From Molecular Complexes to Complex Metallic Nanostructures&mdash;2H Solid-State NMR Studies of Ruthenium-Containing Hydrogenation Catalysts" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>D will do what H can&rsquo;t:</B> An overview on advanced <SUP>2</SUP>H solid-state NMR investigations combined with quantum-chemical calculations aimed at the study of structure and dynamics of deuterium/hydrogen in molecular complexes and clusters. This approach contributes to the understanding of the interaction of hydrogen with the surface of metal nanoparticles at the molecular level, as well as the mechanistic implications in catalytic reactions such as hydrogenation.</P>
<p> [Minireview]<br />Torsten Gutmann, Iker del&#xA0;Rosal, Bruno Chaudret, Romuald Poteau, Hans-Heinrich Limbach, Gerd Buntkowsky<br /><i>ChemPhysChem</i>, May 09, 2013, DOI: 10.1002/cphc.201300200. <a href="http://dx.doi.org/10.1002/cphc.201300200">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300161">
<title>Experimental and First-Principles Characterization of Functionalized Magnetic Nanoparticles</title>
<link>http://dx.doi.org/10.1002/cphc.201300161</link>
<dc:creator>Georgios S. E. Antipas, Eleftherios Statharas, Philippos Tserotas, Nikolaos Papadopoulos, E. Hristoforou</dc:creator>
<dc:date>2013-05-06T12:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300161.gif" width="196" height="98" alt="Experimental and First-Principles Characterization of Functionalized Magnetic Nanoparticles" title="Experimental and First-Principles Characterization of Functionalized Magnetic Nanoparticles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>An iron constitution:</B> Magnetic iron oxide nanoparticles (NPs) synthesized by coprecipitation and thermal decomposition methods are magnetite-rich and maghemite-rich, respectively (see images). IR spectroscopy reveals that the NPs are coated with layers of oleic acid (OA) surfactant. The inner layer is chemically adsorbed on the NP surface whereas the rest of the OA is physically adsorbed.</P>
<p> [Article]<br />Georgios S. E. Antipas, Eleftherios Statharas, Philippos Tserotas, Nikolaos Papadopoulos, E. Hristoforou<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201300161. <a href="http://dx.doi.org/10.1002/cphc.201300161">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300250">
<title>Probing the γ-Turn in a Short Proline Dipeptide Chain</title>
<link>http://dx.doi.org/10.1002/cphc.201300250</link>
<dc:creator>Carlos Cabezas, Marcelino Varela, José L. Alonso</dc:creator>
<dc:date>2013-05-06T12:33+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300250.gif" width="191" height="164" alt="Probing the &gamma;-Turn in a Short Proline Dipeptide Chain" title="Probing the &gamma;-Turn in a Short Proline Dipeptide Chain" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Taking turns:</B> The small peptide derived from proline, <I>N</I>-acetyl-prolinamide (Ac-Pro-NH<sub>2</sub>), is investigated using a combination of Fourier transform microwave spectroscopy with laser ablation. Spectral signatures belonging to only one conformer are detected in the supersonic expansion. Rotational constants and nuclear quadrupole coupling constants of the two <SUP>14</SUP>N nuclei are used in the characterization of a &gamma;-turn structure in the gas phase.</P>
<p> [Article]<br />Carlos Cabezas, Marcelino Varela, Jos&#xE9; L. Alonso<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201300250. <a href="http://dx.doi.org/10.1002/cphc.201300250">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300172">
<title>Continuous Glucose Monitoring: 40&#160;Years, What We've Learned and What’s Next</title>
<link>http://dx.doi.org/10.1002/cphc.201300172</link>
<dc:creator>Raeann Gifford</dc:creator>
<dc:date>2013-05-06T12:33+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300172.gif" width="184" height="170" alt="Continuous Glucose Monitoring: 40&nbsp;Years, What We&#x27;ve Learned and What&rsquo;s Next" title="Continuous Glucose Monitoring: 40&nbsp;Years, What We&#x27;ve Learned and What&rsquo;s Next" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>How sweet it is:</B> Continuous glucose monitoring (CGM) is demonstrating the benefit it provides for millions with diabetes, and the information obtained from these systems reveals the impact of glucose variation on patient health. The various methods available for CGM are discussed, as is their impact on the quality of life of patients using these devices. Future possibilities and developments in this area are also surveyed.</P>
<p> [Review]<br />Raeann Gifford<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201300172. <a href="http://dx.doi.org/10.1002/cphc.201300172">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300098">
<title>Recombination of Lophyl Radicals in Pyrrolidinium-Based Ionic Liquids</title>
<link>http://dx.doi.org/10.1002/cphc.201300098</link>
<dc:creator>Stefan Berdzinski, Joachim Horst, Petra Straßburg, Veronika Strehmel</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/cphc201300098.gif" width="216" height="159" alt="Recombination of Lophyl Radicals in Pyrrolidinium-Based Ionic Liquids" title="Recombination of Lophyl Radicals in Pyrrolidinium-Based Ionic Liquids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Rate increases:</B> Long alkyl chains bound at the cation of 1-alkyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide ionic liquids change the steric requirements on the transition state of the bimolecular lophyl radical recombination reaction (see picture). Recombination of the photolytically generated radicals is faster in the ionic liquids than in traditional organic solvents.</P>
<p> [Article]<br />Stefan Berdzinski, Joachim Horst, Petra Stra&#xDF;burg, Veronika Strehmel<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201300098. <a href="http://dx.doi.org/10.1002/cphc.201300098">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300086">
<title>Viscosity Mixing Rules for Binary Systems Containing One Ionic Liquid</title>
<link>http://dx.doi.org/10.1002/cphc.201300086</link>
<dc:creator>Mohammed Tariq, Tausif Altamash, Daniel Salavera, Alberto Coronas, Luis P. N. Rebelo, Jose N. Canongia Lopes</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/cphc201300086.gif" width="364" height="103" alt="Viscosity Mixing Rules for Binary Systems Containing One Ionic Liquid" title="Viscosity Mixing Rules for Binary Systems Containing One Ionic Liquid" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A good mix:</B> The applicability to [ionic liquid (IL)+molecular solvent (MS)] systems of four of the most commonly used viscosity mixing rules is assessed. More than 100&nbsp;systems subdivided into different IL of MS series are analyzed and the corresponding trends discussed in terms of the average deviations produced by the use of each type of mixing rule.</P>
<p> [Article]<br />Mohammed Tariq, Tausif Altamash, Daniel Salavera, Alberto Coronas, Luis P. N. Rebelo, Jose N. Canongia Lopes<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201300086. <a href="http://dx.doi.org/10.1002/cphc.201300086">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300040">
<title>Protein Resistance of Surfaces Modified with Oligo(Ethylene Glycol) Aryl Diazonium Derivatives</title>
<link>http://dx.doi.org/10.1002/cphc.201300040</link>
<dc:creator>Callie Fairman, Joshua Z. Ginges, Stuart B. Lowe, J. Justin Gooding</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/cphc201300040.gif" width="186" height="174" alt="Protein Resistance of Surfaces Modified with Oligo(Ethylene Glycol) Aryl Diazonium Derivatives" title="Protein Resistance of Surfaces Modified with Oligo(Ethylene Glycol) Aryl Diazonium Derivatives" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Surface modification for protein resistance:</B> Oligo(ethylene glycol) aryl diazonium derivatives electrochemically deposited on carbon and gold surfaces reduce non-specific protein adsorption (see picture). The influence of ligand length, distal end group, and ligand packing density on protein resistance is investigated. This approach could be used to produce stable antifouling layers for electrochemical biosensors.</P>
<p> [Article]<br />Callie Fairman, Joshua Z. Ginges, Stuart B. Lowe, J. Justin Gooding<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201300040. <a href="http://dx.doi.org/10.1002/cphc.201300040">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201003">
<title>New Deposition Technique for Metal Films Containing Inorganic Fullerene-Like (IF) Nanoparticles</title>
<link>http://dx.doi.org/10.1002/cphc.201201003</link>
<dc:creator>Ohad Goldbart, Alexander Yoffe, Sidney R. Cohen, Rita Rosentsveig, Yishay Feldman, Lev Rapoport, Reshef Tenne</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/cphc201201003.gif" width="186" height="194" alt="New Deposition Technique for Metal Films Containing Inorganic Fullerene-Like (IF) Nanoparticles" title="New Deposition Technique for Metal Films Containing Inorganic Fullerene-Like (IF) Nanoparticles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A new method for fabrication of thin composite films</B> using physical vapor deposition (PVD) is described. Titanium (Ti) and hybrid films of titanium containing tungsten disulphide nanoparticles with inorganic fullerene-like structure (Ti/IF-WS<sub>2</sub>) are fabricated (see picture). The Ti/IF-WS<sub>2</sub> shows better wear resistance and a lower friction coefficient when compared to the Ti layer or Ti substrate.</P>
<p> [Article]<br />Ohad Goldbart, Alexander Yoffe, Sidney R. Cohen, Rita Rosentsveig, Yishay Feldman, Lev Rapoport, Reshef Tenne<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201201003. <a href="http://dx.doi.org/10.1002/cphc.201201003">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300091">
<title>Coherent Anti-Stokes Emission from Gold Nanorods and Its Potential for Imaging Applications</title>
<link>http://dx.doi.org/10.1002/cphc.201300091</link>
<dc:creator>Li Jiang, Iwan W. Schie, Jun Qian, Sailing He, Thomas Huser</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/cphc201300091.gif" width="213" height="158" alt="Coherent Anti-Stokes Emission from Gold Nanorods and Its Potential for Imaging Applications" title="Coherent Anti-Stokes Emission from Gold Nanorods and Its Potential for Imaging Applications" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Scattered in all directions:</B> Coherent anti-Stokes scattering (CAS) is used to characterize individual gold nanorods (GNRs) and GNR aggregates. The CAS signal is also examined as a function of the excitation polarization. Irregularly oriented GNRs exhibit a different scattering pattern to that observed for regularly oriented GNRs. The polarization-dependent scattering from oriented GNRs shows cos<SUP>6</SUP>&nbsp;(<I>&thgr;</I>) behavior (see picture).</P>
<p> [Article]<br />Li Jiang, Iwan W. Schie, Jun Qian, Sailing He, Thomas Huser<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201300091. <a href="http://dx.doi.org/10.1002/cphc.201300091">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300054">
<title>Large-Area Plasmonic Substrate of Silver-Coated Iron Oxide Nanorod Arrays for Plasmon-Enhanced Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cphc.201300054</link>
<dc:creator>Waldemir Moura Carvalho, Jr. Diogo Volpati, Vitor A. Nunes Carvalho, Ricardo F. Aroca, Carlos J. L. Constantino, Flavio L. Souza</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/cphc201300054.gif" width="215" height="216" alt="Large-Area Plasmonic Substrate of Silver-Coated Iron Oxide Nanorod Arrays for Plasmon-Enhanced Spectroscopy" title="Large-Area Plasmonic Substrate of Silver-Coated Iron Oxide Nanorod Arrays for Plasmon-Enhanced Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Stand up straight!</B> Vertically oriented &alpha;-Fe<sub>2</sub>O<sub>3</sub> nanorod arrays are synthesized under hydrothermal conditions over a large area, as an active platform for surface-enhanced resonance Raman scattering (SERRS) and surface-enhanced fluorescence (SEF, see picture; LB=Langmuir&ndash;Blodgett layer of probe molecule). The morphology of the arrays is preserved after the surface is covered with a 6&nbsp;nm Ag layer deposited by physical vapor deposition (PVD).</P>
<p> [Article]<br />Waldemir Moura Carvalho, Jr. Diogo Volpati, Vitor A. Nunes&#xA0;Carvalho, Ricardo F. Aroca, Carlos J. L. Constantino, Flavio L. Souza<br /><i>ChemPhysChem</i>, May 06, 2013, DOI: 10.1002/cphc.201300054. <a href="http://dx.doi.org/10.1002/cphc.201300054">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300352">
<title>Dissolution Kinetics of Nanocrystals</title>
<link>http://dx.doi.org/10.1002/cphc.201300352</link>
<dc:creator>Marek Petrik, Bernd Harbrecht</dc:creator>
<dc:date>2013-05-03T15:50+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300352.gif" width="194" height="185" alt="Dissolution Kinetics of Nanocrystals" title="Dissolution Kinetics of Nanocrystals" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A simple series of test-tube experiments</B> is all it takes to quantify a largely neglected nano-effect responsible for a dramatic increase&mdash;by orders of magnitude&mdash;in the surface-area-normalized rate of dissolution of nanocrystals. Though the observed variation in this specific rate as a function of size is unprecedented, the effect may be rationalized in terms of the classic atomistic theory of crystal growth and dissolution.</P>
<p> [Communication]<br />Marek Petrik, Bernd Harbrecht<br /><i>ChemPhysChem</i>, May 03, 2013, DOI: 10.1002/cphc.201300352. <a href="http://dx.doi.org/10.1002/cphc.201300352">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300201">
<title>Fast Ion Transport and Phase Separation in a Mechanically Driven Flow of Electrolytes through Tortuous Sub-Nanometer Nanochannels</title>
<link>http://dx.doi.org/10.1002/cphc.201300201</link>
<dc:creator>Ling Liu, Xi Chen</dc:creator>
<dc:date>2013-05-03T15:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300201.gif" width="150" height="192" alt="Fast Ion Transport and Phase Separation in a Mechanically Driven Flow of Electrolytes through Tortuous Sub-Nanometer Nanochannels" title="Fast Ion Transport and Phase Separation in a Mechanically Driven Flow of Electrolytes through Tortuous Sub-Nanometer Nanochannels" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Check my flow:</B> The coupled structural and flow characteristics of electrolytes in torturous sub-nanometer confinement are illustrated by simulating the mechanically driven flow of a NaCl solution in a zeolite-type nanochannel system. Ion transport is faster than the transport of water molecules, thus leading to phase separation. However, neither of these phenomena are observed in a straight silica nanotube.</P>
<p> [Article]<br />Ling Liu, Xi Chen<br /><i>ChemPhysChem</i>, May 03, 2013, DOI: 10.1002/cphc.201300201. <a href="http://dx.doi.org/10.1002/cphc.201300201">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300151">
<title>Deposition and Characterization of Luminescent Eu(tta)&lt;sub&gt;3&lt;/sub&gt;phen-Doped Parylene-Based Thin-Film Materials</title>
<link>http://dx.doi.org/10.1002/cphc.201300151</link>
<dc:creator>Gianluigi Maggioni, Antonio Campagnaro, Michele Tonezzer, Sara Carturan, Alberto Quaranta</dc:creator>
<dc:date>2013-05-03T15:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300151.gif" width="188" height="129" alt="Deposition and Characterization of Luminescent Eu(tta)3phen-Doped Parylene-Based Thin-Film Materials" title="Deposition and Characterization of Luminescent Eu(tta)3phen-Doped Parylene-Based Thin-Film Materials" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Let there be light!</B> Luminescent host&ndash;guest films are produced by finely dispersing Eu(tta)<sub>3</sub>phen [tta = tris(2-thenoyl trifluoroacetone), phen = 1,10-phenantroline] in a parylene matrix by using a new coarse vacuum cosublimation technique. Fine dispersion of the Eu complex molecules and energy transfer between parylene and the Eu complex afford emitted light that is five times more intense than the light emitted by films of the Eu complex alone.</P>
<p> [Article]<br />Gianluigi Maggioni, Antonio Campagnaro, Michele Tonezzer, Sara Carturan, Alberto Quaranta<br /><i>ChemPhysChem</i>, May 03, 2013, DOI: 10.1002/cphc.201300151. <a href="http://dx.doi.org/10.1002/cphc.201300151">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300089">
<title>Impact of the Chirality and Curvature of Carbon Nanostructures on Their Interaction with Aromatics and Amino Acids</title>
<link>http://dx.doi.org/10.1002/cphc.201300089</link>
<dc:creator>Deivasigamani Umadevi, G. Narahari Sastry</dc:creator>
<dc:date>2013-05-03T15:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300089.gif" width="195" height="89" alt="Impact of the Chirality and Curvature of Carbon Nanostructures on Their Interaction with Aromatics and Amino Acids" title="Impact of the Chirality and Curvature of Carbon Nanostructures on Their Interaction with Aromatics and Amino Acids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>All wrapped up:</B> Planar graphene exhibits stronger binding with aromatic molecules than curved carbon nanotubes, whereas zigzag carbon nanotubes appear to show stronger binding affinity than armchair carbon nanotubes. The polarizability and HOMO energy of the carbon nanotubes are found to be the key factors that determine the binding energies.</P>
<p> [Article]<br />Deivasigamani Umadevi, G. Narahari Sastry<br /><i>ChemPhysChem</i>, May 03, 2013, DOI: 10.1002/cphc.201300089. <a href="http://dx.doi.org/10.1002/cphc.201300089">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300199">
<title>The Distorted Tropane of Scopoline</title>
<link>http://dx.doi.org/10.1002/cphc.201300199</link>
<dc:creator>Patricia Ecija, Emilio J. Cocinero, Alberto Lesarri, Francisco J. Basterretxea, José A. Fernández, Fernando Castaño</dc:creator>
<dc:date>2013-05-02T18:20+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300199.gif" width="378" height="106" alt="The Distorted Tropane of Scopoline" title="The Distorted Tropane of Scopoline" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Live isomerization</B>: The uncommon three-ring structure of scopoline (oscine), an alkaloid, is revealed from gas-phase isomerization of scopine using rotational spectroscopy.</P>
<p> [Article]<br />Patricia Ecija, Emilio J. Cocinero, Alberto Lesarri, Francisco J. Basterretxea, Jos&#xE9; A. Fern&#xE1;ndez, Fernando Casta&#xF1;o<br /><i>ChemPhysChem</i>, May 02, 2013, DOI: 10.1002/cphc.201300199. <a href="http://dx.doi.org/10.1002/cphc.201300199">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300186">
<title>Evaluating the COSMO-RS Method for Modeling Hydrogen Bonding in Solution</title>
<link>http://dx.doi.org/10.1002/cphc.201300186</link>
<dc:creator>Sofja Tshepelevitsh, Merit Oss, Astrid Pung, Ivo Leito</dc:creator>
<dc:date>2013-04-29T16:02+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300186.gif" width="197" height="130" alt="Evaluating the COSMO-RS Method for Modeling Hydrogen Bonding in Solution" title="Evaluating the COSMO-RS Method for Modeling Hydrogen Bonding in Solution" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Bond, hydrogen bond:</B> The hydrogen bond modeling ability of the COSMO-RS method is evaluated using a range of acceptors and donors in different solvents.</P>
<p> [Article]<br />Sofja Tshepelevitsh, Merit Oss, Astrid Pung, Ivo Leito<br /><i>ChemPhysChem</i>, Apr 29, 2013, DOI: 10.1002/cphc.201300186. <a href="http://dx.doi.org/10.1002/cphc.201300186">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300210">
<title>Recent Methodological Advances in the Analysis of Protein Tyrosine Nitration</title>
<link>http://dx.doi.org/10.1002/cphc.201300210</link>
<dc:creator>Irene Díaz-Moreno, José M. García-Heredia, Katiuska González-Arzola, Antonio Díaz-Quintana, Miguel A. De la Rosa</dc:creator>
<dc:date>2013-04-29T16:01+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300210.gif" width="192" height="200" alt="Recent Methodological Advances in the Analysis of Protein Tyrosine Nitration" title="Recent Methodological Advances in the Analysis of Protein Tyrosine Nitration" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>To stress a protein:</B> Understanding how tyrosine nitration (see picture) affects the structure and functionality of proteins is of considerable interest, as this reaction is associated with pathogenesis in diseases related to (nitro)oxidative stress. The advantages and limitations of the chemical and biological methods to incorporate nitrotyrosines in native proteins are discussed, and a fast and non-damaging NMR-based method for the detection of nitrotyrosines with a broad applicability is revisited.</P>
<p> [Minireview]<br />Irene D&#xED;az-Moreno, Jos&#xE9; M. Garc&#xED;a-Heredia, Katiuska Gonz&#xE1;lez-Arzola, Antonio D&#xED;az-Quintana, Miguel A. De&#xA0;la&#xA0;Rosa<br /><i>ChemPhysChem</i>, Apr 29, 2013, DOI: 10.1002/cphc.201300210. <a href="http://dx.doi.org/10.1002/cphc.201300210">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300117">
<title>Extracellular Electron Transfer across Bacterial Cell Membranes via a Cytocompatible Redox-Active Polymer</title>
<link>http://dx.doi.org/10.1002/cphc.201300117</link>
<dc:creator>Koichi Nishio, Ryuhei Nakamura, Xiaojie Lin, Tomohiro Konno, Kazuhiko Ishihara, Shuji Nakanishi, Kazuhito Hashimoto</dc:creator>
<dc:date>2013-04-29T16:01+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300117.gif" width="384" height="131" alt="Extracellular Electron Transfer across Bacterial Cell Membranes via a Cytocompatible Redox-Active Polymer" title="Extracellular Electron Transfer across Bacterial Cell Membranes via a Cytocompatible Redox-Active Polymer" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Biocompatible electron shuttle:</B> A redox-active phospholipid polymer with a phospholipid-mimicking structure is synthesized to construct a biocompatible electron mediator between bacteria and an electrode.</P>
<p> [Article]<br />Koichi Nishio, Ryuhei Nakamura, Xiaojie Lin, Tomohiro Konno, Kazuhiko Ishihara, Shuji Nakanishi, Kazuhito Hashimoto<br /><i>ChemPhysChem</i>, Apr 29, 2013, DOI: 10.1002/cphc.201300117. <a href="http://dx.doi.org/10.1002/cphc.201300117">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300077">
<title>Adsorption of Water on an MgSO&lt;sub&gt;4&lt;/sub&gt;(100) Surface: A First-Principles Investigation</title>
<link>http://dx.doi.org/10.1002/cphc.201300077</link>
<dc:creator>Jin-Hua Luo, Yun-Hong Zhang, Ze-Sheng Li</dc:creator>
<dc:date>2013-04-29T16:01+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300077.gif" width="184" height="156" alt="Adsorption of Water on an MgSO4(100) Surface: A First-Principles Investigation" title="Adsorption of Water on an MgSO4(100) Surface: A First-Principles Investigation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Surface factors:</B> The adsorption properties of water molecules on an MgSO<sub>4</sub>(100) surface are studied by using density functional theory (see picture). The configurations of water molecules adsorbed on atoms of the second and third atomic layers of MgSO<sub>4</sub>(100) are quite stable. In addition, water molecules preferentially adsorb onto a defective surface.</P>
<p> [Article]<br />Jin-Hua Luo, Yun-Hong Zhang, Ze-Sheng Li<br /><i>ChemPhysChem</i>, Apr 29, 2013, DOI: 10.1002/cphc.201300077. <a href="http://dx.doi.org/10.1002/cphc.201300077">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300242">
<title>Controlling the π-Stacking Behavior of Pyrene Derivatives: Influence of H-Bonding and Steric Effects in Different States of Aggregation</title>
<link>http://dx.doi.org/10.1002/cphc.201300242</link>
<dc:creator>Andreas T. Haedler, Holger Misslitz, Christian Buehlmeyer, Rodrigo Q. Albuquerque, Anna Köhler, Hans-Werner Schmidt</dc:creator>
<dc:date>2013-04-25T15:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300242.gif" width="385" height="85" alt="Controlling the &pi;-Stacking Behavior of Pyrene Derivatives: Influence of H-Bonding and Steric Effects in Different States of Aggregation" title="Controlling the &pi;-Stacking Behavior of Pyrene Derivatives: Influence of H-Bonding and Steric Effects in Different States of Aggregation" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The Influence of H-bonding</B> and steric hindrance on the optical properties and the &pi;-stacking of pyrene derivatives is investigated and described in dilute solution, as supramolecular aggregates and in the crystalline state.</P>
<p> [Article]<br />Andreas T. Haedler, Holger Misslitz, Christian Buehlmeyer, Rodrigo Q. Albuquerque, Anna K&#xF6;hler, Hans-Werner Schmidt<br /><i>ChemPhysChem</i>, Apr 25, 2013, DOI: 10.1002/cphc.201300242. <a href="http://dx.doi.org/10.1002/cphc.201300242">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300061">
<title>The Factors Influencing Nonlinear Characteristics of the Short-Circuit Current in Dye-Sensitized Solar Cells Investigated by a Numerical Model</title>
<link>http://dx.doi.org/10.1002/cphc.201300061</link>
<dc:creator>Yushuai Shi , Xiandui Dong</dc:creator>
<dc:date>2013-04-25T15:31+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300061.gif" width="193" height="157" alt="The Factors Influencing Nonlinear Characteristics of the Short-Circuit Current in Dye-Sensitized Solar Cells Investigated by a Numerical Model" title="The Factors Influencing Nonlinear Characteristics of the Short-Circuit Current in Dye-Sensitized Solar Cells Investigated by a Numerical Model" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Super- and sublinear character</B> of the short-circuit current <I>j</I><sub>sc</sub> in dye-sensitized solar cells (see picture) should be attributed to low electron-collection efficiency and low dye-regeneration efficiency, respectively, according to a numerical model developed on the basis of the continuity equation.</P>
<p> [Article]<br />Yushuai Shi&#xA0;, Xiandui Dong<br /><i>ChemPhysChem</i>, Apr 25, 2013, DOI: 10.1002/cphc.201300061. <a href="http://dx.doi.org/10.1002/cphc.201300061">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300188">
<title>Elucidating Inorganic Nanoscale Species in Solution: Complementary and Corroborative Approaches</title>
<link>http://dx.doi.org/10.1002/cphc.201300188</link>
<dc:creator>Anna F. Oliveri, Edward W. Elliott, III Matthew E. Carnes, James E. Hutchison, Darren W. Johnson</dc:creator>
<dc:date>2013-04-24T08:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300188.gif" width="186" height="205" alt="Elucidating Inorganic Nanoscale Species in Solution: Complementary and Corroborative Approaches" title="Elucidating Inorganic Nanoscale Species in Solution: Complementary and Corroborative Approaches" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>SAXS sells:</B> Defining the dimensions of a nanoscale material in solution is non-trivial. Complementary size measurements may describe a number of different material dimensions such as that of the core, shell, or solvation sphere. The determination of the full range of material properties requires multiple techniques in order to corroborate solution and solid-state structures.</P>
<p> [Concept]<br />Anna F. Oliveri, Edward W. Elliott, III Matthew E. Carnes, James E. Hutchison, Darren W. Johnson<br /><i>ChemPhysChem</i>, Apr 24, 2013, DOI: 10.1002/cphc.201300188. <a href="http://dx.doi.org/10.1002/cphc.201300188">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300155">
<title>Computational Studies on Non-covalent Interactions of Carbon and Boron Fullerenes with Graphene</title>
<link>http://dx.doi.org/10.1002/cphc.201300155</link>
<dc:creator>Arun K. Manna, Swapan K. Pati</dc:creator>
<dc:date>2013-04-24T08:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300155.gif" width="189" height="145" alt="Computational Studies on Non-covalent Interactions of Carbon and Boron Fullerenes with Graphene" title="Computational Studies on Non-covalent Interactions of Carbon and Boron Fullerenes with Graphene" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Bound by choice:</B> Energetic and optoelectronic properties of various graphene&ndash;fullerene composites are investigated by DFT calculations (see picture). Both van der Waals and charge-transfer interactions need to be considered to assess the correct stability order of these weakly bound complexes. The composites show diverse electronic and optical properties, which suggest their potential in optoelectronic and photovoltaic devices applications.</P>
<p> [Article]<br />Arun K. Manna, Swapan K. Pati<br /><i>ChemPhysChem</i>, Apr 24, 2013, DOI: 10.1002/cphc.201300155. <a href="http://dx.doi.org/10.1002/cphc.201300155">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300126">
<title>A New Approach for the Simulation of Electrochemiluminescence (ECL)</title>
<link>http://dx.doi.org/10.1002/cphc.201300126</link>
<dc:creator>Oleksiy V. Klymenko, Irina Svir, Christian Amatore</dc:creator>
<dc:date>2013-04-24T08:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300126.gif" width="202" height="130" alt="A New Approach for the Simulation of Electrochemiluminescence (ECL)" title="A New Approach for the Simulation of Electrochemiluminescence (ECL)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Now you can predict even ECL:</B> Fast and accurate prediction and treatment of electrochemiluminescence (ECL) reactions for any complex system is now possible owing to a new numerical approach implemented in KISSA software.</P>
<p> [Article]<br />Oleksiy V. Klymenko, Irina Svir, Christian Amatore<br /><i>ChemPhysChem</i>, Apr 24, 2013, DOI: 10.1002/cphc.201300126. <a href="http://dx.doi.org/10.1002/cphc.201300126">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201200995">
<title>Silica/Silicone Nanofilament Hybrid Coatings with Almost Perfect Superhydrophobicity</title>
<link>http://dx.doi.org/10.1002/cphc.201200995</link>
<dc:creator>Junping Zhang, Stefan Seeger</dc:creator>
<dc:date>2013-04-24T08:35+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201200995.gif" width="374" height="139" alt="Silica/Silicone Nanofilament Hybrid Coatings with Almost Perfect Superhydrophobicity" title="Silica/Silicone Nanofilament Hybrid Coatings with Almost Perfect Superhydrophobicity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Staying dry:</B> Coatings with almost perfect superhydrophobicity are obtained by selective growth of silicone nanofilaments on aggregated silica particles, which generates two-tier structures resembling a field of grassland with thickets.</P>
<p> [Article]<br />Junping Zhang, Stefan Seeger<br /><i>ChemPhysChem</i>, Apr 24, 2013, DOI: 10.1002/cphc.201200995. <a href="http://dx.doi.org/10.1002/cphc.201200995">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300007">
<title>One-Pot in Situ Mixed Film Formation by Azo Coupling and Diazonium Salt Electrografting</title>
<link>http://dx.doi.org/10.1002/cphc.201300007</link>
<dc:creator>Charles Esnault, Nicolas Delorme, Guy Louarn, Jean-François Pilard</dc:creator>
<dc:date>2013-04-23T15:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300007.gif" width="214" height="176" alt="One-Pot in Situ Mixed Film Formation by Azo Coupling and Diazonium Salt Electrografting" title="One-Pot in Situ Mixed Film Formation by Azo Coupling and Diazonium Salt Electrografting" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>So simple:</B> The in situ synthesis of an aryldiazonium salt and an azo-aryldiazonium salt by azo coupling from sulfanilic acid and aniline is reported. Formation of a mixed organic layer is monitored by cyclic voltammetry and atomic force microscopy. A compact mixed layer is obtained with a global roughness of 0.4&nbsp;nm and 10&ndash;15&nbsp;% vertical extension in the range 1.5&ndash;6&nbsp;nm.</P>
<p> [Communication]<br />Charles Esnault, Nicolas Delorme, Guy Louarn, Jean-Fran&#xE7;ois Pilard<br /><i>ChemPhysChem</i>, Apr 23, 2013, DOI: 10.1002/cphc.201300007. <a href="http://dx.doi.org/10.1002/cphc.201300007">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300174">
<title>Nanoparticle Size and Concentration Dependence of the Electroactive Phase Content and Electrical and Optical Properties of Ag/Poly(vinylidene fluoride) Composites</title>
<link>http://dx.doi.org/10.1002/cphc.201300174</link>
<dc:creator>Ana Catarina Lopes, Sonia A. C. Carabineiro, Manuel Fernando R. Pereira, Gabriela Botelho, Senentxu Lanceros-Mendez</dc:creator>
<dc:date>2013-04-22T16:18+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300174.gif" width="185" height="124" alt="Nanoparticle Size and Concentration Dependence of the Electroactive Phase Content and Electrical and Optical Properties of Ag/Poly(vinylidene fluoride) Composites" title="Nanoparticle Size and Concentration Dependence of the Electroactive Phase Content and Electrical and Optical Properties of Ag/Poly(vinylidene fluoride) Composites" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>In phase:</B> Silver nanoparticles incorporated into poly(vinylidene fluoride) induce the nucleation of the electroactive &gamma; phase of the polymer. Surface plasmon resonance absorption in the composites increases with the concentration and size of the nanoparticles. This behavior is correlated to an electrical response and is related to the extra bands and electrons provided by the nanoparticles in the large energy band gap of the polymer.</P>
<p> [Article]<br />Ana Catarina Lopes, Sonia A. C. Carabineiro, Manuel Fernando R. Pereira, Gabriela Botelho, Senentxu Lanceros-Mendez<br /><i>ChemPhysChem</i>, Apr 22, 2013, DOI: 10.1002/cphc.201300174. <a href="http://dx.doi.org/10.1002/cphc.201300174">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300133">
<title>Structural Principles and Thermoelectric Properties of Polytypic Group&#160;14 Clathrate-II Frameworks</title>
<link>http://dx.doi.org/10.1002/cphc.201300133</link>
<dc:creator>Antti J. Karttunen, Thomas F. Fässler</dc:creator>
<dc:date>2013-04-22T16:18+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300133.gif" width="196" height="184" alt="Structural Principles and Thermoelectric Properties of Polytypic Group&nbsp;14 Clathrate-II Frameworks" title="Structural Principles and Thermoelectric Properties of Polytypic Group&nbsp;14 Clathrate-II Frameworks" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Anisotropic clathrates:</B> Quantum chemical investigation shows the highly anisotropic hexagonal clathrate polytypes to be practically as stable as the experimentally known cubic member of the same structural family. The semiconducting group&nbsp;14 clathrates are known to be efficient thermoelectric materials and the structural anisotropy of the novel hexagonal clathrate polytypes significantly affects their thermoelectric properties.</P>
<p> [Article]<br />Antti J. Karttunen, Thomas F. F&#xE4;ssler<br /><i>ChemPhysChem</i>, Apr 22, 2013, DOI: 10.1002/cphc.201300133. <a href="http://dx.doi.org/10.1002/cphc.201300133">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300182">
<title>In Situ Direct Measurement of Vapor Pressures and Thermodynamic Parameters of Volatile Organic Materials in the Vapor Phase: Benzoic Acid, Ferrocene, and Naphthalene</title>
<link>http://dx.doi.org/10.1002/cphc.201300182</link>
<dc:creator>Walid M. Hikal, Brandon L. Weeks</dc:creator>
<dc:date>2013-04-19T09:50+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300182.gif" width="196" height="174" alt="In Situ Direct Measurement of Vapor Pressures and Thermodynamic Parameters of Volatile Organic Materials in the Vapor Phase: Benzoic Acid, Ferrocene, and Naphthalene" title="In Situ Direct Measurement of Vapor Pressures and Thermodynamic Parameters of Volatile Organic Materials in the Vapor Phase: Benzoic Acid, Ferrocene, and Naphthalene" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Reflections on vapor:</B> A commercially available UV-spectrometer is used to determine absorption cross-sections, vapor densities, vapor pressures, and sublimation enthalpies of three reference materials in the vapor phase. The optical and thermodynamic properties are in agreement with the ICTAC recommended values with uncertainties of ~5 and ~1&nbsp;% for vapor pressures and sublimation enthalpies.</P>
<p> [Article]<br />Walid M. Hikal, Brandon L. Weeks<br /><i>ChemPhysChem</i>, Apr 19, 2013, DOI: 10.1002/cphc.201300182. <a href="http://dx.doi.org/10.1002/cphc.201300182">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300141">
<title>Band Gap Engineering of BN Sheets by Interlayer Dihydrogen Bonding and Electric Field Control</title>
<link>http://dx.doi.org/10.1002/cphc.201300141</link>
<dc:creator>Qing Tang, Zhen Zhou, Panwen Shen, Zhongfang Chen</dc:creator>
<dc:date>2013-04-19T09:50+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300141.gif" width="211" height="100" alt="Band Gap Engineering of BN Sheets by Interlayer Dihydrogen Bonding and Electric Field Control" title="Band Gap Engineering of BN Sheets by Interlayer Dihydrogen Bonding and Electric Field Control" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>An unconventional bonding:</B> The presence of interlayer B-H&middot;&middot;&middot;H-N dihydrogen bonds in hydrogenated bilayer BN nanosheets reduces the intrinsic large band gap of the chair-type BN conformation owing to interlayer charge transfer. In contrast, the insulating properties of the thermodynamically more stable stirrup-type bilayer BN can be engineered by applying an electric field. These results illuminate a new pathway for band gap engineering of 2D BN nanomaterials.</P>
<p> [Communication]<br />Qing Tang, Zhen Zhou, Panwen Shen, Zhongfang Chen<br /><i>ChemPhysChem</i>, Apr 19, 2013, DOI: 10.1002/cphc.201300141. <a href="http://dx.doi.org/10.1002/cphc.201300141">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300121">
<title>Fluorine Substitution Effects on Flexibility and Tunneling Pathways: The Rotational Spectrum of 2-Fluorobenzylamine</title>
<link>http://dx.doi.org/10.1002/cphc.201300121</link>
<dc:creator>Camilla Calabrese, Assimo Maris, Luca Evangelisti, Walther Caminati, Sonia Melandri</dc:creator>
<dc:date>2013-04-18T16:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300121.gif" width="314" height="123" alt="Fluorine Substitution Effects on Flexibility and Tunneling Pathways: The Rotational Spectrum of 2-Fluorobenzylamine" title="Fluorine Substitution Effects on Flexibility and Tunneling Pathways: The Rotational Spectrum of 2-Fluorobenzylamine" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Bringing on a substitute:</B> High-resolution spectral data in the gas phase coupled to theoretical calculations for 2-fluorobenzylamine (see picture) show that substitution of a single hydrogen atom with fluorine produces a change of structural and dynamical properties of the fluorine-substituted molecule relative to the unsubstituted form.</P>
<p> [Article]<br />Camilla Calabrese, Assimo Maris, Luca Evangelisti, Walther Caminati, Sonia Melandri<br /><i>ChemPhysChem</i>, Apr 18, 2013, DOI: 10.1002/cphc.201300121. <a href="http://dx.doi.org/10.1002/cphc.201300121">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300066">
<title>Characterizing the Role of Iodine Doping in Improving Photovoltaic Performance of Dye-Sensitized Hierarchically Structured ZnO Solar Cells</title>
<link>http://dx.doi.org/10.1002/cphc.201300066</link>
<dc:creator>Jia-Xing Zhao, Yan-Zhen Zheng, Xin-Hong Lu, Jian-Feng Chen, Xia Tao, Weilie Zhou</dc:creator>
<dc:date>2013-04-18T16:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300066.gif" width="392" height="83" alt="Characterizing the Role of Iodine Doping in Improving Photovoltaic Performance of Dye-Sensitized Hierarchically Structured ZnO Solar Cells" title="Characterizing the Role of Iodine Doping in Improving Photovoltaic Performance of Dye-Sensitized Hierarchically Structured ZnO Solar Cells" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>I for increasing efficency:</B> Inherent drawbacks of ZnO solar cells related to a poor light-harvesting capability and easy recombination of photogenerated electron-hole pairs are progressively circumvented by doping iodine into the hierarchically structured ZnO lattice. This is demonstrated by microscopic characterization, spectroscopic analysis, and electrochemical/photoelectrochemical measurement results.</P>
<p> [Article]<br />Jia-Xing Zhao, Yan-Zhen Zheng, Xin-Hong Lu, Jian-Feng Chen, Xia Tao, Weilie Zhou<br /><i>ChemPhysChem</i>, Apr 18, 2013, DOI: 10.1002/cphc.201300066. <a href="http://dx.doi.org/10.1002/cphc.201300066">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300035">
<title>A Monolayer Assay Tailored to Investigate Lipid–Protein Systems</title>
<link>http://dx.doi.org/10.1002/cphc.201300035</link>
<dc:creator>Grzegorz Chwastek, Petra Schwille</dc:creator>
<dc:date>2013-04-18T16:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300035.gif" width="192" height="194" alt="A Monolayer Assay Tailored to Investigate Lipid&ndash;Protein Systems" title="A Monolayer Assay Tailored to Investigate Lipid&ndash;Protein Systems" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Small and handy:</B> A new simple miniaturized monolayer assay (see picture, monolayer in miniaturized chamber) is proposed to investigate specific features of cellular membranes. The method can be easily combined with standard analytical techniques such as confocal fluorescence microscopy and fluorescence correlation spectroscopy (FCS).</P>
<p> [Article]<br />Grzegorz Chwastek, Petra Schwille<br /><i>ChemPhysChem</i>, Apr 18, 2013, DOI: 10.1002/cphc.201300035. <a href="http://dx.doi.org/10.1002/cphc.201300035">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201023">
<title>Unraveling the Reaction Mechanisms Governing Methanol-to-Olefins Catalysis by Theory and Experiment</title>
<link>http://dx.doi.org/10.1002/cphc.201201023</link>
<dc:creator>Karen Hemelsoet, Jeroen Van der Mynsbrugge, Kristof De Wispelaere, Michel Waroquier, Veronique Van Speybroeck</dc:creator>
<dc:date>2013-04-17T12:32+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201201023.gif" width="196" height="178" alt="Unraveling the Reaction Mechanisms Governing Methanol-to-Olefins Catalysis by Theory and Experiment" title="Unraveling the Reaction Mechanisms Governing Methanol-to-Olefins Catalysis by Theory and Experiment" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Converting methanol:</B> The methanol-to-olefins (MTO) process is one of the most prominent technologies to bypass crude oil in the production of light olefins. The conversion of methanol occurs over an acidic heterogeneous porous material and many parameters influence the MTO activity and selectivity. This review summarizes proposed reaction routes of both olefin production and catalyst deactivation and points out new developments such as emerging MTO materials and the use of molecular dynamics.</P>
<p> [Review]<br />Karen Hemelsoet, Jeroen Van&#xA0;der&#xA0;Mynsbrugge, Kristof De&#xA0;Wispelaere, Michel Waroquier, Veronique Van&#xA0;Speybroeck<br /><i>ChemPhysChem</i>, Apr 17, 2013, DOI: 10.1002/cphc.201201023. <a href="http://dx.doi.org/10.1002/cphc.201201023">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201200843">
<title>Intermolecular Interactions in Li&lt;SUP&gt;+&lt;/SUP&gt;-glyme and Li&lt;SUP&gt;+&lt;/SUP&gt;-glyme–TFSA&lt;SUP&gt;−&lt;/SUP&gt; complexes: Relationship with Physicochemical Properties of [Li(glyme)][TFSA] Ionic Liquids</title>
<link>http://dx.doi.org/10.1002/cphc.201200843</link>
<dc:creator>Seiji Tsuzuki, Wataru Shinoda, Shiro Seki, Yasuhiro Umebayashi, Kazuki Yoshida, Kaoru Dokko, Masayoshi Watanabe</dc:creator>
<dc:date>2013-04-17T12:25+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201200843.gif" width="181" height="91" alt="Intermolecular Interactions in Li+-glyme and Li+-glyme&ndash;TFSA&minus; complexes: Relationship with Physicochemical Properties of [Li(glyme)][TFSA] Ionic Liquids" title="Intermolecular Interactions in Li+-glyme and Li+-glyme&ndash;TFSA&minus; complexes: Relationship with Physicochemical Properties of [Li(glyme)][TFSA] Ionic Liquids" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The interactions in Li<SUP>+</SUP>-glymes-TFSA<SUP>&minus;</SUP></B> <B>complexes:</B> The interactions of Li<SUP>+</SUP> with glymes (tri- and tetra-glyme) are strong (&minus;96 and &minus;108&nbsp;kcal&nbsp;mol<SUP>&minus;1</SUP>), while the interactions of the [Li(glyme)]<SUP>+</SUP> complexes with TFSA<SUP>&minus;</SUP> (&minus;82 and &minus;70&nbsp;kcal&nbsp;mol<SUP>&minus;1</SUP>) are weaker than that between Li<SUP>+</SUP> and TFSA<SUP>&minus;</SUP> (&minus;137&nbsp;kcal&nbsp;mol<SUP>&minus;1</SUP>).</P>
<p> [Article]<br />Seiji Tsuzuki, Wataru Shinoda, Shiro Seki, Yasuhiro Umebayashi, Kazuki Yoshida, Kaoru Dokko, Masayoshi Watanabe<br /><i>ChemPhysChem</i>, Apr 17, 2013, DOI: 10.1002/cphc.201200843. <a href="http://dx.doi.org/10.1002/cphc.201200843">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300291">
<title>Direct &lt;SUP&gt;2&lt;/SUP&gt;H&#160;NMR Observation of the Proton Mobility of the Acidic Sites of Anhydrous 12-Tungstophosphoric Acid</title>
<link>http://dx.doi.org/10.1002/cphc.201300291</link>
<dc:creator>Daniil I. Kolokolov, Maxim S. Kazantsev, Mikhail V. Luzgin, Hervé Jobic, Alexander G. Stepanov</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/cphc201300291.gif" width="312" height="94" alt="Direct 2H&nbsp;NMR Observation of the Proton Mobility of the Acidic Sites of Anhydrous 12-Tungstophosphoric Acid" title="Direct 2H&nbsp;NMR Observation of the Proton Mobility of the Acidic Sites of Anhydrous 12-Tungstophosphoric Acid" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Flip and hop before you&#x27;re caught!</B> The proton dynamics of solid 12-tungstophosphoric acid (TPA) is probed by solid-state <SUP>2</SUP>H&nbsp;NMR in a temperature range from 293&ndash;503&nbsp;K. Protons of TPA are shown to be involved in two types of molecular motion (see picture): the anisotropic local two-site flipping between the two possible orientations of the O-H bond at bridged oxygens of the Keggin anion, and the isotropic diffusion by hopping between neighboring surface oxygens of the anion.</P>
<p> [Communication]<br />Daniil I. Kolokolov, Maxim S. Kazantsev, Mikhail V. Luzgin, Herv&#xE9; Jobic, Alexander G. Stepanov<br /><i>ChemPhysChem</i>, Apr 16, 2013, DOI: 10.1002/cphc.201300291. <a href="http://dx.doi.org/10.1002/cphc.201300291">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300042">
<title>Eletrochemically Actuated Stop–Go Valves for Capillary Force-Operated Diagnostic Microsystems</title>
<link>http://dx.doi.org/10.1002/cphc.201300042</link>
<dc:creator>Alemayehu P. Washe, Pablo Lozano, Diego Bejarano, Ioanis Katakis</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/cphc201300042.gif" width="187" height="147" alt="Eletrochemically Actuated Stop&ndash;Go Valves for Capillary Force-Operated Diagnostic Microsystems" title="Eletrochemically Actuated Stop&ndash;Go Valves for Capillary Force-Operated Diagnostic Microsystems" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Nanoporous graphitic carbon</B> electrodes display a unique electrowetting behavior that depends on specific ion effects. When incorporated into a microfluidic channel, these superhydrophobic electrodes facilitate sequential stop&ndash;go fluidic operations, which are directly applicable to diagnostic microsystems.</P>
<p> [Article]<br />Alemayehu P. Washe, Pablo Lozano, Diego Bejarano, Ioanis Katakis<br /><i>ChemPhysChem</i>, Apr 16, 2013, DOI: 10.1002/cphc.201300042. <a href="http://dx.doi.org/10.1002/cphc.201300042">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201077">
<title>Analyzing the Vibrational Signatures of Thiophenol Adsorbed on Small Gold Clusters by DFT Calculations</title>
<link>http://dx.doi.org/10.1002/cphc.201201077</link>
<dc:creator>Conrard Giresse Tetsassi Feugmo, Vincent Liégeois</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/cphc201201077.gif" width="184" height="135" alt="Analyzing the Vibrational Signatures of Thiophenol Adsorbed on Small Gold Clusters by DFT Calculations" title="Analyzing the Vibrational Signatures of Thiophenol Adsorbed on Small Gold Clusters by DFT Calculations" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Vibrational fingerprint:</B> Using density functional theory, the IR and Raman signatures of thiophenol adsorbed on gold clusters are calculated by mimicking the different types of adsorption sites. The evolution of the vibrational normal modes of isolated TP and TP adsorbed on different clusters is examined, and the IR and Raman signatures are analyzed by using group coupling matrices and atomic contribution patterns.</P>
<p> [Article]<br />Conrard Giresse Tetsassi&#xA0;Feugmo, Vincent Li&#xE9;geois<br /><i>ChemPhysChem</i>, Apr 16, 2013, DOI: 10.1002/cphc.201201077. <a href="http://dx.doi.org/10.1002/cphc.201201077">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201062">
<title>Stacking Interactions of Ni(acac) Chelates with Benzene: Calculated Interaction Energies</title>
<link>http://dx.doi.org/10.1002/cphc.201201062</link>
<dc:creator>Dušan N. Sredojević, Dragan B. Ninković, Goran V. Janjić, Jia Zhou, Michael B. Hall, Snežana D. Zarić</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/cphc201201062.gif" width="189" height="114" alt="Stacking Interactions of Ni(acac) Chelates with Benzene: Calculated Interaction Energies" title="Stacking Interactions of Ni(acac) Chelates with Benzene: Calculated Interaction Energies" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Piling &#x27;em up:</B> The stacking energy of the [Ni(acac)<sub>2</sub>]/benzene system is calculated at local CCSD(T) level and is in good agreement with the values obtained with the SCS-MP2 method. Energies calculated with several DFT-D methods are somewhat overestimated. The calculated stacking energy of the [Ni(acac)<sub>2</sub>]/benzene system is significantly stronger than that of the benzene dimer.</P>
<p> [Communication]<br />Du&#x161;an N. Sredojevi&#x107;, Dragan B. Ninkovi&#x107;, Goran V. Janji&#x107;, Jia Zhou, Michael B. Hall, Sne&#x17E;ana D. Zari&#x107;<br /><i>ChemPhysChem</i>, Apr 16, 2013, DOI: 10.1002/cphc.201201062. <a href="http://dx.doi.org/10.1002/cphc.201201062">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201100">
<title>Bimetallic AuAg Nanoparticles: Enhancing the Catalytic Activity of Au for Reduction Reactions in the Liquid Phase by Addition of Ag</title>
<link>http://dx.doi.org/10.1002/cphc.201201100</link>
<dc:creator>Willian G. Menezes, Björn Neumann, Volkmar Zielasek, Karsten Thiel, Marcus Bäumer</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/cphc201201100.gif" width="418" height="150" alt="Bimetallic AuAg Nanoparticles: Enhancing the Catalytic Activity of Au for Reduction Reactions in the Liquid Phase by Addition of Ag" title="Bimetallic AuAg Nanoparticles: Enhancing the Catalytic Activity of Au for Reduction Reactions in the Liquid Phase by Addition of Ag" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Teamwork of noble partners:</B> The preparation and catalytic properties of small, highly stable, and monodisperse Au-, Ag- and bimetallic AuAg-nanoparticles with well-defined compositions are reported.</P>
<p> [Communication]<br />Willian G. Menezes, Bj&#xF6;rn Neumann, Volkmar Zielasek, Karsten Thiel, Marcus B&#xE4;umer<br /><i>ChemPhysChem</i>, Apr 16, 2013, DOI: 10.1002/cphc.201201100. <a href="http://dx.doi.org/10.1002/cphc.201201100">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201200964">
<title>Interaction Modes and Absolute Affinities of α-Amino Acids for Mn&lt;SUP&gt;2+&lt;/SUP&gt;: A Comprehensive Picture</title>
<link>http://dx.doi.org/10.1002/cphc.201200964</link>
<dc:creator>M. Hassan Khodabandeh, Hamid Reisi, Mehdi D. Davari, Karim Zare, Mansour Zahedi, Gilles Ohanessian</dc:creator>
<dc:date>2013-04-15T14:12+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201200964.gif" width="194" height="138" alt="Interaction Modes and Absolute Affinities of &alpha;-Amino Acids for Mn2+: A Comprehensive Picture" title="Interaction Modes and Absolute Affinities of &alpha;-Amino Acids for Mn2+: A Comprehensive Picture" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The full works:</B> The first complete series of affinities of a divalent metal ion (Mn<SUP>2+</SUP>) for all amino acids calculated at the B3LYP and CCSD(T) levels of theory is presented (see figure). The trends are compared with those for other cations.</P>
<p> [Article]<br />M. Hassan Khodabandeh, Hamid Reisi, Mehdi D. Davari, Karim Zare, Mansour Zahedi, Gilles Ohanessian<br /><i>ChemPhysChem</i>, Apr 15, 2013, DOI: 10.1002/cphc.201200964. <a href="http://dx.doi.org/10.1002/cphc.201200964">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300069">
<title>Direct Bio-electrocatalysis of O&lt;sub&gt;2&lt;/sub&gt; Reduction by &lt;I&gt;Streptomyces coelicolor&lt;/I&gt; Laccase Orientated at Promoter-Modified Graphite Electrodes</title>
<link>http://dx.doi.org/10.1002/cphc.201300069</link>
<dc:creator>Samuel Lörcher, Paula Lopes, Andrey Kartashov, Elena E. Ferapontova</dc:creator>
<dc:date>2013-04-15T14:11+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300069.gif" width="194" height="118" alt="Direct Bio-electrocatalysis of O2 Reduction by Streptomyces coelicolor Laccase Orientated at Promoter-Modified Graphite Electrodes" title="Direct Bio-electrocatalysis of O2 Reduction by Streptomyces coelicolor Laccase Orientated at Promoter-Modified Graphite Electrodes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Taking up the SLAC:</B> Bacterial laccase from <I>Streptomyces coelicolor</I> (SLAC) immobilized at promoter-modified electrodes allows observation of both direct electron-transfer reactions between the T1 and T2/T3 centers of SLAC and the electrodes and direct bio-electrocatalysis of O<sub>2</sub> reduction in basic media, including sea water (see picture). The SLAC-modified electrodes are promising candidates for environmental energy transformation.</P>
<p> [Article]<br />Samuel L&#xF6;rcher, Paula Lopes, Andrey Kartashov, Elena E. Ferapontova<br /><i>ChemPhysChem</i>, Apr 15, 2013, DOI: 10.1002/cphc.201300069. <a href="http://dx.doi.org/10.1002/cphc.201300069">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300043">
<title>Wired Enzyme Electrodes—A Retroperspective Story about an Exciting Time at University of Texas at Austin and Its Impact on My Scientific Career</title>
<link>http://dx.doi.org/10.1002/cphc.201300043</link>
<dc:creator>Sten-Eric Lindquist</dc:creator>
<dc:date>2013-04-15T14:11+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300043.gif" width="207" height="228" alt="Wired Enzyme Electrodes&mdash;A Retroperspective Story about an Exciting Time at University of Texas at Austin and Its Impact on My Scientific Career" title="Wired Enzyme Electrodes&mdash;A Retroperspective Story about an Exciting Time at University of Texas at Austin and Its Impact on My Scientific Career" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Lucky times!</B> This essay features an exciting time in the late 1980s, when the in vivo redox-polymer-wired glucose sensor was developed at Professor Adam Heller&rsquo;s laboratory. Among other things, the author nicely describes this &ldquo;serendipitous&rdquo; early-morning discovery. The picture shows a watercolor portrait of Adam Heller, painted by the author as he remembers him at that time (based on a photo from the University of Texas at Austin Experts Guide).</P>
<p> [Essay]<br />Sten-Eric Lindquist<br /><i>ChemPhysChem</i>, Apr 15, 2013, DOI: 10.1002/cphc.201300043. <a href="http://dx.doi.org/10.1002/cphc.201300043">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300039">
<title>Homogeneous Electrochemical Detection of Hippuric Acid in Urine Based on the Osmium–Antigen Conjugate</title>
<link>http://dx.doi.org/10.1002/cphc.201300039</link>
<dc:creator>Won-Yong Jeon, Young-Bong Choi, Hyug-Han Kim</dc:creator>
<dc:date>2013-04-15T14:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300039.gif" width="195" height="172" alt="Homogeneous Electrochemical Detection of Hippuric Acid in Urine Based on the Osmium&ndash;Antigen Conjugate" title="Homogeneous Electrochemical Detection of Hippuric Acid in Urine Based on the Osmium&ndash;Antigen Conjugate" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Metabolite measurement:</B> Direct conjugation of an osmium complex to a small antigen (hippuric acid, HA) is applied to the quantitative analysis of the antigen and its antibody as the electrical signal of a screen-printed carbon electrode, for homogeneous competitive electrochemical immunoassay (see picture). The proposed immunoassay provides a simple, one-step, separation-free and inexpensive assay without washing steps. The electric signals increase linearly with the concentration of HA.</P>
<p> [Article]<br />Won-Yong Jeon, Young-Bong Choi, Hyug-Han Kim<br /><i>ChemPhysChem</i>, Apr 15, 2013, DOI: 10.1002/cphc.201300039. <a href="http://dx.doi.org/10.1002/cphc.201300039">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201097">
<title>&lt;SUP&gt;13&lt;/SUP&gt;C-Detected Through-Bond Correlation Experiments for Protein Resonance Assignment by Ultra-Fast MAS Solid-State NMR</title>
<link>http://dx.doi.org/10.1002/cphc.201201097</link>
<dc:creator>Emeline Barbet-Massin, Andrew J. Pell, Michael J. Knight, Amy L. Webber, Isabella C. Felli, Roberta Pierattelli, Lyndon Emsley, Anne Lesage, Guido Pintacuda</dc:creator>
<dc:date>2013-04-15T14:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201201097.gif" width="187" height="156" alt="13C-Detected Through-Bond Correlation Experiments for Protein Resonance Assignment by Ultra-Fast MAS Solid-State NMR" title="13C-Detected Through-Bond Correlation Experiments for Protein Resonance Assignment by Ultra-Fast MAS Solid-State NMR" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>MAS-tering sequences:</B> Two pulse sequences aimed at the assignment of protein backbone resonances in the solid state under ultra-fast magic angle spinning (MAS) conditions are presented. Conceived for N&ndash;C correlation experiments, they consist of a combination of (<SUP>1</SUP>H,<SUP>15</SUP>N) and (<SUP>15</SUP>N,<SUP>13</SUP>C) selective cross-polarization steps with a <I>J</I>-based homonuclear transfer scheme, in which a spin-state-selective (S<SUP>3</SUP>E) block is incorporated to improve both resolution and sensitivity in the direct <SUP>13</SUP>C dimension.</P>
<p> [Article]<br />Emeline Barbet-Massin, Andrew J. Pell, Michael J. Knight, Amy L. Webber, Isabella C. Felli, Roberta Pierattelli, Lyndon Emsley, Anne Lesage, Guido Pintacuda<br /><i>ChemPhysChem</i>, Apr 15, 2013, DOI: 10.1002/cphc.201201097. <a href="http://dx.doi.org/10.1002/cphc.201201097">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201074">
<title>Impact of Tube Curvature on the Ground-State Magnetism of Axially Confined Single-Walled Carbon Nanotubes of the Zigzag-Type</title>
<link>http://dx.doi.org/10.1002/cphc.201201074</link>
<dc:creator>Jianhua Wu, Frank Hagelberg</dc:creator>
<dc:date>2013-04-15T14:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201201074.gif" width="197" height="141" alt="Impact of Tube Curvature on the Ground-State Magnetism of Axially Confined Single-Walled Carbon Nanotubes of the Zigzag-Type" title="Impact of Tube Curvature on the Ground-State Magnetism of Axially Confined Single-Walled Carbon Nanotubes of the Zigzag-Type" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Magnetic carbon nanostructures</B> are explored by density functional theory calculations on axially confined, single-walled carbon nanotubes (SWCNTs) of the (<I>n</I>,0)-type with <I>n</I>=5&ndash;24. For SWCNTs with <I>n</I>&ge;7, antiferromagnetic (AFM) order is favored energetically over ferromagnetic (FM) order for all lengths <I>L</I> investigated, whereas for <I>n</I>=5, 6 the magnetic phase varies with tube length (see picture).</P>
<p> [Article]<br />Jianhua Wu, Frank Hagelberg<br /><i>ChemPhysChem</i>, Apr 15, 2013, DOI: 10.1002/cphc.201201074. <a href="http://dx.doi.org/10.1002/cphc.201201074">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201049">
<title>Kinetics of Homolytic Substitutions by Hydrogen Atoms at Thiols and Sulfides</title>
<link>http://dx.doi.org/10.1002/cphc.201201049</link>
<dc:creator>Aäron G. Vandeputte, Marie-Françoise Reyniers, Guy B. Marin</dc:creator>
<dc:date>2013-04-15T14:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201201049.gif" width="161" height="188" alt="Kinetics of Homolytic Substitutions by Hydrogen Atoms at Thiols and Sulfides" title="Kinetics of Homolytic Substitutions by Hydrogen Atoms at Thiols and Sulfides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The group additive coup:</B> This work presents rate rules that allow homolytic substitution reactions of hydrogen radicals on organosulfur compounds to be modeled. The model succeeds in reproducing CBS-QB3//BMK/6-311G(2d,d,p) rate coefficients within a factor of two and experimental data within a factor of five.</P>
<p> [Article]<br />A&#xE4;ron G. Vandeputte, Marie-Fran&#xE7;oise Reyniers, Guy B. Marin<br /><i>ChemPhysChem</i>, Apr 15, 2013, DOI: 10.1002/cphc.201201049. <a href="http://dx.doi.org/10.1002/cphc.201201049">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201036">
<title>Photoelectrochemical Sensor Based on Quantum Dots and Sarcosine Oxidase</title>
<link>http://dx.doi.org/10.1002/cphc.201201036</link>
<dc:creator>Marc Riedel, Gero Göbel, Abuelmagd M. Abdelmonem, Wolfgang J. Parak, Fred Lisdat</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/cphc201201036.gif" width="216" height="72" alt="Photoelectrochemical Sensor Based on Quantum Dots and Sarcosine Oxidase" title="Photoelectrochemical Sensor Based on Quantum Dots and Sarcosine Oxidase" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Sarcosine sensor:</B> A photobioelectrochemical sensor based on the combination of quantum dots (QDs) with an enzyme is developed to allow a light-directed sensor read-out (see picture). The generation of charge carriers in the QDs by illumination is coupled to charge transfer with the electrode and the co-substrate of the enzyme.</P>
<p> [Article]<br />Marc Riedel, Gero G&#xF6;bel, Abuelmagd M. Abdelmonem, Wolfgang J. Parak, Fred Lisdat<br /><i>ChemPhysChem</i>, Apr 15, 2013, DOI: 10.1002/cphc.201201036. <a href="http://dx.doi.org/10.1002/cphc.201201036">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300047">
<title>The Influence of Organic-Film Morphology on the Efficient Electron Transfer at Passivated Polymer-Modified Electrodes to which Nanoparticles are Attached</title>
<link>http://dx.doi.org/10.1002/cphc.201300047</link>
<dc:creator>Abbas Barfidokht, Simone Ciampi, Erwann Luais, Nadim Darwish, J. Justin Gooding</dc:creator>
<dc:date>2013-04-12T08:33+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300047.gif" width="200" height="165" alt="The Influence of Organic-Film Morphology on the Efficient Electron Transfer at Passivated Polymer-Modified Electrodes to which Nanoparticles are Attached" title="The Influence of Organic-Film Morphology on the Efficient Electron Transfer at Passivated Polymer-Modified Electrodes to which Nanoparticles are Attached" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The impact</B> of polymer-film morphology on the electron-transfer process at electrode/organic insulator/nanomaterial architectures is studied. The comparative study of two different organic films, poly(phenylenediamine) and poly(ethylenediamine), reveals that the uniformity of the organic film plays an important role in efficient nanoparticle-mediated electron transfer.</P>
<p> [Article]<br />Abbas Barfidokht, Simone Ciampi, Erwann Luais, Nadim Darwish, J. Justin Gooding<br /><i>ChemPhysChem</i>, Apr 12, 2013, DOI: 10.1002/cphc.201300047. <a href="http://dx.doi.org/10.1002/cphc.201300047">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300179">
<title>Kinetic Evidence for a Non-Langmuir-Hinshelwood Surface Reaction: H/D Exchange over Pd Nanoparticles and Pd(111)</title>
<link>http://dx.doi.org/10.1002/cphc.201300179</link>
<dc:creator>Aditya Savara, Wiebke Ludwig, Swetlana Schauermann</dc:creator>
<dc:date>2013-04-12T08:32+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300179.gif" width="205" height="105" alt="Kinetic Evidence for a Non-Langmuir-Hinshelwood Surface Reaction: H/D Exchange over Pd Nanoparticles and Pd(111)" title="Kinetic Evidence for a Non-Langmuir-Hinshelwood Surface Reaction: H/D Exchange over Pd Nanoparticles and Pd(111)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Tell me how:</B> The mechanism of hydrogen recombination on a Pd(111) single crystal and well-defined Pd nanoparticles is studied using pulsed multi-molecular beam techniques and the H<sub>2</sub>/D<sub>2</sub> isotope exchange reaction. It is found that various kinetic models are required to account for the observed phenomena.</P>
<p> [Article]<br />Aditya Savara, Wiebke Ludwig, Swetlana Schauermann<br /><i>ChemPhysChem</i>, Apr 12, 2013, DOI: 10.1002/cphc.201300179. <a href="http://dx.doi.org/10.1002/cphc.201300179">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300157">
<title>Single-Step Sulfo-Selenization Method to Synthesize Cu&lt;sub&gt;2&lt;/sub&gt;ZnSn(S&lt;sub&gt;&lt;I&gt;y&lt;/I&gt;&lt;/sub&gt;Se&lt;sub&gt;1−&lt;I&gt;y&lt;/I&gt;&lt;/sub&gt;)&lt;sub&gt;4&lt;/sub&gt; Absorbers from Metallic Stack Precursors</title>
<link>http://dx.doi.org/10.1002/cphc.201300157</link>
<dc:creator>Andrew Fairbrother, Xavier Fontané, Victor Izquierdo-Roca, Moises Espindola-Rodriguez, Simon López-Marino, Marcel Placidi, Juan López-García, Alejandro Pérez-Rodríguez, Edgardo Saucedo</dc:creator>
<dc:date>2013-04-10T15:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300157.gif" width="185" height="184" alt="Single-Step Sulfo-Selenization Method to Synthesize Cu2ZnSn(SySe1&minus;y)4 Absorbers from Metallic Stack Precursors" title="Single-Step Sulfo-Selenization Method to Synthesize Cu2ZnSn(SySe1&minus;y)4 Absorbers from Metallic Stack Precursors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Not an ordinary pentenary!</B> A straightforward sulfo-selenization process for the formation of pentenary Cu<sub>2</sub>ZnSn(S<sub><I>y</I></sub>Se<sub>1&minus;<I>y</I></sub>) solar-cell absorber films permits the tuning of the absorber composition from sulfur-rich to selenium-rich in a single annealing process. The resulting films, with compositions in the whole range of S/(S+Se) ratios, aim at pentenary-based solar cells of superior efficiency, which to date have been mostly limited to chalcogen-containing precursors.</P>
<p> [Article]<br />Andrew Fairbrother, Xavier Fontan&#xE9;, Victor Izquierdo-Roca, Moises Espindola-Rodriguez, Simon L&#xF3;pez-Marino, Marcel Placidi, Juan L&#xF3;pez-Garc&#xED;a, Alejandro P&#xE9;rez-Rodr&#xED;guez, Edgardo Saucedo<br /><i>ChemPhysChem</i>, Apr 10, 2013, DOI: 10.1002/cphc.201300157. <a href="http://dx.doi.org/10.1002/cphc.201300157">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300134">
<title>Theoretical Investigation of Generator–Collector Microwell Arrays for Improving Electroanalytical Selectivity: Application to Selective Dopamine Detection in the Presence of Ascorbic Acid</title>
<link>http://dx.doi.org/10.1002/cphc.201300134</link>
<dc:creator>Alexander Oleinick, Feng Zhu, Jiawei Yan, Bingwei Mao, Irina Svir , Christian Amatore</dc:creator>
<dc:date>2013-04-10T15:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300134.gif" width="215" height="104" alt="Theoretical Investigation of Generator&ndash;Collector Microwell Arrays for Improving Electroanalytical Selectivity: Application to Selective Dopamine Detection in the Presence of Ascorbic Acid" title="Theoretical Investigation of Generator&ndash;Collector Microwell Arrays for Improving Electroanalytical Selectivity: Application to Selective Dopamine Detection in the Presence of Ascorbic Acid" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Well separated:</B> A microwell array integrating collector&ndash;generator amplification into a diffusional faradaic cage virtually eliminates irreversible redox interferences, for example, in dopamine (DA) detection in the presence of ascorbic acid (AA). Thus, AA is scavenged but DA enters the nanocavities for oxidation at the disk electrodes, and its signal is further amplified by redox cycling (see picture).</P>
<p> [Article]<br />Alexander Oleinick, Feng Zhu, Jiawei Yan, Bingwei Mao, Irina Svir&#xA0;, Christian Amatore<br /><i>ChemPhysChem</i>, Apr 10, 2013, DOI: 10.1002/cphc.201300134. <a href="http://dx.doi.org/10.1002/cphc.201300134">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201200914">
<title>Strong Light-Molecule Coupling on Plasmonic Arrays of Different Symmetry</title>
<link>http://dx.doi.org/10.1002/cphc.201200914</link>
<dc:creator>Adi Salomon, Shaojun Wang, James A. Hutchison, Cyriaque Genet, Thomas W. Ebbesen</dc:creator>
<dc:date>2013-04-10T15:36+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201200914.gif" width="198" height="132" alt="Strong Light-Molecule Coupling on Plasmonic Arrays of Different Symmetry" title="Strong Light-Molecule Coupling on Plasmonic Arrays of Different Symmetry" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The strong coupling</B> of porphyrin J-aggregates to plasmonic nanostructures of different symmetry is investigated. The nanostructures of higher symmetry show the strongest interaction with the molecular layer. At high coupling strengths a new, weakly dispersive mode appears. These findings point to new ways for optimizing strong coupling and thereby realize its full potential for molecular and material science.</P>
<p> [Article]<br />Adi Salomon, Shaojun Wang, James A. Hutchison, Cyriaque Genet, Thomas W. Ebbesen<br /><i>ChemPhysChem</i>, Apr 10, 2013, DOI: 10.1002/cphc.201200914. <a href="http://dx.doi.org/10.1002/cphc.201200914">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300049">
<title>Mechanism and Nature of the Different Viscosity Sensitivities of Hemicyanine Dyes with Various Heterocycles</title>
<link>http://dx.doi.org/10.1002/cphc.201300049</link>
<dc:creator>Jianfang Cao, Chong Hu, Fei Liu, Wen Sun, Jiangli Fan, Fengling Song, Shiguo Sun, Xiaojun Peng</dc:creator>
<dc:date>2013-04-09T14:40+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300049.gif" width="216" height="100" alt="Mechanism and Nature of the Different Viscosity Sensitivities of Hemicyanine Dyes with Various Heterocycles" title="Mechanism and Nature of the Different Viscosity Sensitivities of Hemicyanine Dyes with Various Heterocycles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Through thick and thin</B>: Two excited-state deactivation pathways exist for carbazole-based hemicyanine molecular rotors: nonradiative by twisted intramolecular charge transfer (TICT) in nonviscous media and fluorescent emission (fluo) in viscous media due to suppression of intramolecular rotation (see picture). They thus have applications as viscosity-sensitive fluorescent probes.</P>
<p> [Article]<br />Jianfang Cao, Chong Hu, Fei Liu, Wen Sun, Jiangli Fan, Fengling Song, Shiguo Sun, Xiaojun Peng<br /><i>ChemPhysChem</i>, Apr 09, 2013, DOI: 10.1002/cphc.201300049. <a href="http://dx.doi.org/10.1002/cphc.201300049">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201200975">
<title>Conformational Sensitivity in Photoelectron Circular Dichroism of 3-Methylcyclopentanone</title>
<link>http://dx.doi.org/10.1002/cphc.201200975</link>
<dc:creator>Stefano Turchini, Daniele Catone, Nicola Zema, Giorgio Contini, Tommaso Prosperi, Piero Decleva, Mauro Stener, Flaminia Rondino, Susanna Piccirillo, Kevin C. Prince , Maurizio Speranza</dc:creator>
<dc:date>2013-04-09T14:38+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201200975.gif" width="213" height="214" alt="Conformational Sensitivity in Photoelectron Circular Dichroism of 3-Methylcyclopentanone" title="Conformational Sensitivity in Photoelectron Circular Dichroism of 3-Methylcyclopentanone" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Dichroism and conformers:</B> Temperature-dependent photoelectron circular dichroism (PECD) studies of the HOMO state and the carbonyl carbon 1s core level of <I>R</I>-3-methylcyclopentanone (<I>R</I>-3-MCP) allowed to separate the contributions of each conformer, showing how the PECD methodology can be sensitive to the conformational and structural changes of unoriented chiral molecules.</P>
<p> [Article]<br />Stefano Turchini, Daniele Catone, Nicola Zema, Giorgio Contini, Tommaso Prosperi, Piero Decleva, Mauro Stener, Flaminia Rondino, Susanna Piccirillo, Kevin C. Prince&#xA0;, Maurizio Speranza<br /><i>ChemPhysChem</i>, Apr 09, 2013, DOI: 10.1002/cphc.201200975. <a href="http://dx.doi.org/10.1002/cphc.201200975">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300046">
<title>Optimization of a Membraneless Glucose/Oxygen Enzymatic Fuel Cell Based on a Bioanode with High Coulombic Efficiency and Current Density</title>
<link>http://dx.doi.org/10.1002/cphc.201300046</link>
<dc:creator>Minling Shao, Muhammad Nadeem Zafar, Magnus Falk, Roland Ludwig, Christoph Sygmund, Clemens K. Peterbauer, Dmitrii A. Guschin, Domhnall MacAodha, Peter O Conghaile, Dónal Leech, Miguel D. Toscano, Sergey Shleev, Wolfgang Schuhmann, Lo Gorton</dc:creator>
<dc:date>2013-04-08T15:48+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300046.gif" width="372" height="133" alt="Optimization of a Membraneless Glucose/Oxygen Enzymatic Fuel Cell Based on a Bioanode with High Coulombic Efficiency and Current Density" title="Optimization of a Membraneless Glucose/Oxygen Enzymatic Fuel Cell Based on a Bioanode with High Coulombic Efficiency and Current Density" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Bio is better:</B> After initially testing and optimizing several anode biocatalysts, the authors fabricate and characterize a membraneless glucose/oxygen enzymatic biofuel cell that shows high coulombic efficiency and power output.</P>
<p> [Article]<br />Minling Shao, Muhammad Nadeem Zafar, Magnus Falk, Roland Ludwig, Christoph Sygmund, Clemens K. Peterbauer, Dmitrii A. Guschin, Domhnall MacAodha, Peter O&#xA0;Conghaile, D&#xF3;nal Leech, Miguel D. Toscano, Sergey Shleev, Wolfgang Schuhmann, Lo Gorton<br /><i>ChemPhysChem</i>, Apr 08, 2013, DOI: 10.1002/cphc.201300046. <a href="http://dx.doi.org/10.1002/cphc.201300046">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300162">
<title>Printable Magnetoelectronics</title>
<link>http://dx.doi.org/10.1002/cphc.201300162</link>
<dc:creator>Denys Makarov, Daniil Karnaushenko, Oliver G. Schmidt</dc:creator>
<dc:date>2013-04-08T15:46+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300162.gif" width="161" height="188" alt="Printable Magnetoelectronics" title="Printable Magnetoelectronics" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Man the presses!</B> A large variety of electronic components assembled as printable optoelectronic devices and communication modules are already commercially available. However, an element that responds to a magnetic field has been realized only recently. Here, the printable magnetic sensorics is positioned in a family of printable electronics and possible application directions of this technology are highlighted.</P>
<p> [Concept]<br />Denys Makarov, Daniil Karnaushenko, Oliver G. Schmidt<br /><i>ChemPhysChem</i>, Apr 08, 2013, DOI: 10.1002/cphc.201300162. <a href="http://dx.doi.org/10.1002/cphc.201300162">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300212">
<title>Chiral Induction and Amplification in Supramolecular Systems at the Liquid–Solid Interface</title>
<link>http://dx.doi.org/10.1002/cphc.201300212</link>
<dc:creator>Hong Xu, Elke Ghijsens, Subi J. George, Martin Wolffs, Željko Tomović, Albertus P. H. J. Schenning, Steven De Feyter</dc:creator>
<dc:date>2013-04-05T14:23+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300212.gif" width="183" height="135" alt="Chiral Induction and Amplification in Supramolecular Systems at the Liquid&ndash;Solid Interface" title="Chiral Induction and Amplification in Supramolecular Systems at the Liquid&ndash;Solid Interface" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Sir, yes sir!</B> Chiral induction and amplification in surface-confined supramolecular monolayers are investigated at the liquid&ndash;solid interface. Scanning tunneling microscopy proves that achiral molecules can self-assemble into globally chiral patterns through induction by chiral solvents or by a novel chiral amplification method.</P>
<p> [Article]<br />Hong Xu, Elke Ghijsens, Subi J. George, Martin Wolffs, &#x17D;eljko Tomovi&#x107;, Albertus P. H. J. Schenning, Steven De&#xA0;Feyter<br /><i>ChemPhysChem</i>, Apr 05, 2013, DOI: 10.1002/cphc.201300212. <a href="http://dx.doi.org/10.1002/cphc.201300212">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300032">
<title>Integrated Devices to Realize Energy Conversion and Storage Simultaneously</title>
<link>http://dx.doi.org/10.1002/cphc.201300032</link>
<dc:creator>Tao Chen, Zhibin Yang, Huisheng Peng</dc:creator>
<dc:date>2013-04-05T14:23+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300032.gif" width="371" height="132" alt="Integrated Devices to Realize Energy Conversion and Storage Simultaneously" title="Integrated Devices to Realize Energy Conversion and Storage Simultaneously" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Live wire:</B> Novel integrated devices are described for the simultaneous realization of photoelectric conversion and energy storage with an emphasis on a wire format. The wire structure enables unique and promising applications, for example being woven into clothes or other complex flexible equipment by conventional textile technology.</P>
<p> [Concept]<br />Tao Chen, Zhibin Yang, Huisheng Peng<br /><i>ChemPhysChem</i>, Apr 05, 2013, DOI: 10.1002/cphc.201300032. <a href="http://dx.doi.org/10.1002/cphc.201300032">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300023">
<title>Proton-Coupled Self-Assembly of a Porphyrin-Naphthalenediimide Dyad</title>
<link>http://dx.doi.org/10.1002/cphc.201300023</link>
<dc:creator>Siyu Tu, Se Hye Kim, Jojo Joseph, David A. Modarelli, Jon R. Parquette</dc:creator>
<dc:date>2013-04-05T14:23+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300023.gif" width="176" height="103" alt="Proton-Coupled Self-Assembly of a Porphyrin-Naphthalenediimide Dyad" title="Proton-Coupled Self-Assembly of a Porphyrin-Naphthalenediimide Dyad" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Proton-coupled 1D assembly:</B> The amphiphilic self-assembly of a porphyrin&ndash;NDI dyad into 1D nanorods proceeds with concomitant proton transfer in CHCl<sub>3</sub>. The nanorods engage in &pi;&ndash;&pi; contacts that improve photoinduced charge-transfer rate constants, in contrast to the short-range aggregates in THF that lack these contacts.</P>
<p> [Article]<br />Siyu Tu, Se Hye Kim, Jojo Joseph, David A. Modarelli, Jon R. Parquette<br /><i>ChemPhysChem</i>, Apr 05, 2013, DOI: 10.1002/cphc.201300023. <a href="http://dx.doi.org/10.1002/cphc.201300023">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300130">
<title>Molecule-Induced Peroxide Homolysis</title>
<link>http://dx.doi.org/10.1002/cphc.201300130</link>
<dc:creator>Natascia Turrà, Ulrich Neuenschwander, Ive Hermans</dc:creator>
<dc:date>2013-04-04T15:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300130.gif" width="181" height="169" alt="Molecule-Induced Peroxide Homolysis" title="Molecule-Induced Peroxide Homolysis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A radical is born:</B> Evidence is provided that radicals are easily generated in a bimolecular reaction between alkyl hydroperoxide, the primary chain product during an auto-oxidation, and compounds featuring weak H atoms, such as olefins and dienes. Such compounds are therefore not only more reactive towards radicals; they also greatly assist in their formation.</P>
<p> [Article]<br />Natascia Turr&#xE0;, Ulrich Neuenschwander, Ive Hermans<br /><i>ChemPhysChem</i>, Apr 04, 2013, DOI: 10.1002/cphc.201300130. <a href="http://dx.doi.org/10.1002/cphc.201300130">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/19015.en.html">
<title>VIP: Angle-Resolved Strong-Field Ionization of Polyatomic Molecules: More than the Orbitals Matters</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/19015.en.html</link>
<dc:date>2013-04-04T00:00:00+02:00</dc:date>
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<![CDATA[<p>Oumarou Njoya, Spiridoula Matsika and Thomas Weinacht</p><p>Strong-field ionization plays a critical role in attosecond pulse generation and molecular imaging. It has been shown to be sensitive to the shape of molecular orbitals, and can therefore be used as a tool for studying time-dependent changes to molecular structure. Using a pump-probe scheme to initiate and capture excited-state dynamics, the authors discuss three molecules whose orbital structures are the same but whose angle and time-dependent yields differ significantly. This suggests that the angle dependence of strong-field molecular ionization is sensitive to more than the shape of the molecular orbital from which an electron is removed. <!-- module_2 --></p><!-- BNR: 201045 --><p>Received December 14, 2012, published online March 20, 2013<!-- Pubdate: 2013-3-20 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201201045">10.1002/cphc.201201045 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201084">
<title>Dispersion of Graphene Sheets in Aqueous Solution by Oligodeoxynucleotides</title>
<link>http://dx.doi.org/10.1002/cphc.201201084</link>
<dc:creator>Li-Jun Liang, Tao Wu, Yu Kang, Qi Wang</dc:creator>
<dc:date>2013-04-02T11:58+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201201084.gif" width="194" height="106" alt="Dispersion of Graphene Sheets in Aqueous Solution by Oligodeoxynucleotides" title="Dispersion of Graphene Sheets in Aqueous Solution by Oligodeoxynucleotides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Squeezed out:</B> Dispersions of graphene sheets in water are stabilized by single-stranded oligodeoxynucleotides (ssODNs) of adequate size and number according to molecular dynamics simulations, but layer-to-layer aggregation of graphene sheets is observed on the nanosecond timescale when the size and number of ssODNs are insufficient (see picture).</P>
<p> [Article]<br />Li-Jun Liang, Tao Wu, Yu Kang, Qi Wang<br /><i>ChemPhysChem</i>, Apr 02, 2013, DOI: 10.1002/cphc.201201084. <a href="http://dx.doi.org/10.1002/cphc.201201084">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300217">
<title>In Situ Study of CO Oxidation on HOPG-Supported Pt Nanoparticles</title>
<link>http://dx.doi.org/10.1002/cphc.201300217</link>
<dc:creator>Soeren Porsgaard, Luis K. Ono, Helene Zeuthen, Jan Knudsen, Joachim Schnadt, Lindsay R. Merte, Jacques Chevallier, Stig Helveg, Miquel Salmeron, Stefan Wendt, Flemming Besenbacher</dc:creator>
<dc:date>2013-03-28T13:56+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300217.gif" width="194" height="131" alt="In Situ Study of CO Oxidation on HOPG-Supported Pt Nanoparticles" title="In Situ Study of CO Oxidation on HOPG-Supported Pt Nanoparticles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Catalyzed CO oxidation:</B> A newly designed high-pressure flow cell is utilized to study CO oxidation on Pt nanoparticles in&nbsp;situ by simultaneous quadrupole mass spectrometry and high-pressure X-ray photoelectron spectroscopy. The spectroscopy data show that the active catalyst consists of metallic Pt with both chemisorbed O and patches/shell of surface oxides.</P>
<p> [Communication]<br />Soeren Porsgaard, Luis K. Ono, Helene Zeuthen, Jan Knudsen, Joachim Schnadt, Lindsay R. Merte, Jacques Chevallier, Stig Helveg, Miquel Salmeron, Stefan Wendt, Flemming Besenbacher<br /><i>ChemPhysChem</i>, Mar 28, 2013, DOI: 10.1002/cphc.201300217. <a href="http://dx.doi.org/10.1002/cphc.201300217">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300205">
<title>Magic Numbers in the Solvation of the Propofol Dimer</title>
<link>http://dx.doi.org/10.1002/cphc.201300205</link>
<dc:creator>Iker León, Judith Millán, Emilio J. Cocinero, Alberto Lesarri, José A. Fernández</dc:creator>
<dc:date>2013-03-28T13:56+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300205.gif" width="188" height="144" alt="Magic Numbers in the Solvation of the Propofol Dimer" title="Magic Numbers in the Solvation of the Propofol Dimer" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Five waters make a pentagon:</B> Formation of particularly stable propofol<sub>2</sub>(H<sub>2</sub>O)<sub>5</sub> clusters in propofol/water/He expansions is observed. Their origin seems to be related to the formation of particularly stable pentameric water clusters.</P>
<p> [Communication]<br />Iker Le&#xF3;n, Judith Mill&#xE1;n, Emilio J. Cocinero, Alberto Lesarri, Jos&#xE9; A. Fern&#xE1;ndez<br /><i>ChemPhysChem</i>, Mar 28, 2013, DOI: 10.1002/cphc.201300205. <a href="http://dx.doi.org/10.1002/cphc.201300205">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300145">
<title>Intramolecular Pnicogen Interactions in PHF-(CH&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;&lt;I&gt;n&lt;/I&gt;&lt;/sub&gt;-PHF (&lt;I&gt;n&lt;/I&gt;=2–6) Systems</title>
<link>http://dx.doi.org/10.1002/cphc.201300145</link>
<dc:creator>Goar Sánchez-Sanz, Ibon Alkorta, Cristina Trujillo, José Elguero</dc:creator>
<dc:date>2013-03-28T13:56+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300145.gif" width="189" height="154" alt="Intramolecular Pnicogen Interactions in PHF-(CH2)n-PHF (n=2&ndash;6) Systems" title="Intramolecular Pnicogen Interactions in PHF-(CH2)n-PHF (n=2&ndash;6) Systems" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The way to interact:</B> A computational study of the intramolecular pnicogen bond in PHF-(CH<sub>2</sub>)<sub><I>n</I></sub>-PHF (<I>n</I>=2&ndash;6) systems is carried out. For each compound, two different conformations, (<I>R</I>,<I>R</I>) and (<I>R</I>,<I>S</I>), are considered on the basis of the chirality of the phosphine groups. The characteristics of the closed conformers, in which the pnicogen interaction occurs, are compared with those of the extended conformer.</P>
<p> [Article]<br />Goar S&#xE1;nchez-Sanz, Ibon Alkorta, Cristina Trujillo, Jos&#xE9; Elguero<br /><i>ChemPhysChem</i>, Mar 28, 2013, DOI: 10.1002/cphc.201300145. <a href="http://dx.doi.org/10.1002/cphc.201300145">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300107">
<title>Harnessing Electron Transfer from the Perchlorotriphenylmethide Anion to Y@C&lt;sub&gt;82&lt;/sub&gt;(&lt;I&gt;C&lt;/I&gt;&lt;sub&gt;2&lt;I&gt;v&lt;/I&gt;&lt;/sub&gt;) to Engineer an Endometallofullerene-Based Salt</title>
<link>http://dx.doi.org/10.1002/cphc.201300107</link>
<dc:creator>Ivan E. Kareev, Elena Laukhina, Vyacheslav P. Bubnov, Vyacheslav M. Martynenko, Vega Lloveras, José Vidal-Gancedo, Marta Mas-Torrent, Jaume Veciana, Concepció Rovira</dc:creator>
<dc:date>2013-03-28T13:56+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300107.gif" width="322" height="93" alt="Harnessing Electron Transfer from the Perchlorotriphenylmethide Anion to Y@C82(C2v) to Engineer an Endometallofullerene-Based Salt" title="Harnessing Electron Transfer from the Perchlorotriphenylmethide Anion to Y@C82(C2v) to Engineer an Endometallofullerene-Based Salt" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Add a pinch of salt:</B> A [Y@C<sub>82</sub>(<I>C</I><sub>2<I>v</I></sub>)]<SUP>&minus;</SUP>-based salt with a complex cation is prepared in high yield by reacting Y@C<sub>82</sub>(<I>C</I><sub>2<I>v</I></sub>) with the [K<SUP>+</SUP>([18]crown-6)]PTM<SUP>&minus;</SUP> salt (PTM=perchlorotriphenylmethide anion; see picture); this ionic Y@C<sub>82</sub>-based compound reveals outstanding stability in solution and in the solid state.</P>
<p> [Article]<br />Ivan E. Kareev, Elena Laukhina, Vyacheslav P. Bubnov, Vyacheslav M. Martynenko, Vega Lloveras, Jos&#xE9; Vidal-Gancedo, Marta Mas-Torrent, Jaume Veciana, Concepci&#xF3; Rovira<br /><i>ChemPhysChem</i>, Mar 28, 2013, DOI: 10.1002/cphc.201300107. <a href="http://dx.doi.org/10.1002/cphc.201300107">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300075">
<title>Influence of the Li···π Interaction on the H/X···π Interactions in HOLi···C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;6&lt;/sub&gt;···HOX/XOH (X=F, Cl, Br, I) Complexes</title>
<link>http://dx.doi.org/10.1002/cphc.201300075</link>
<dc:creator>Yanli Zeng, Wenjie Wu, Xiaoyan Li, Shijun Zheng, Lingpeng Meng</dc:creator>
<dc:date>2013-03-28T13:56+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300075.gif" width="198" height="164" alt="Influence of the Li&middot;&middot;&middot;&pi; Interaction on the H/X&middot;&middot;&middot;&pi; Interactions in HOLi&middot;&middot;&middot;C6H6&middot;&middot;&middot;HOX/XOH (X=F, Cl, Br, I) Complexes" title="Influence of the Li&middot;&middot;&middot;&pi; Interaction on the H/X&middot;&middot;&middot;&pi; Interactions in HOLi&middot;&middot;&middot;C6H6&middot;&middot;&middot;HOX/XOH (X=F, Cl, Br, I) Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Under the influence:</B> MP2 calculations and the quantum theory of atoms in molecules are used to study the influence of the Li&middot;&middot;&middot;&pi; interaction on the interactions in HOLi&middot;&middot;&middot;C<sub>6</sub>H<sub>6</sub>&middot;&middot;&middot;HOX/XOH (X=F, Cl, Br, I) complexes (see picture). Results show that the addition of the Li&middot;&middot;&middot;&pi; interaction to benzene weakens the H&middot;&middot;&middot;&pi; and X&middot;&middot;&middot;&pi; interactions, and that the effect of the Li&middot;&middot;&middot;&pi; interaction on the hydrogen bond is greater than that on the halogen bond.</P>
<p> [Article]<br />Yanli Zeng, Wenjie Wu, Xiaoyan Li, Shijun Zheng, Lingpeng Meng<br /><i>ChemPhysChem</i>, Mar 28, 2013, DOI: 10.1002/cphc.201300075. <a href="http://dx.doi.org/10.1002/cphc.201300075">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/19000.en.html">
<title>ChemElectroChem takes off</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/19000.en.html</link>
<dc:date>2013-03-27T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/2701_flyer.jpg" alt="ChemElectroChem takes off" align="left" hspace="5" vspace="5" border="0" /></p><i>ChemElectroChem</i>, the new sister journal of <i>ChemPhysChem</i> and <i>Angewandte Chemie</i>, is ready for takeoff! The journal is now open to submissions in all the areas of electrochemistry.</p><p><i>ChemElectroChem</i> was launched by Wiley-VCH and ChemPubSoc Europe (an organization of 16 European chemical societies) and is aimed to become a top-ranking peer-reviewed electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, including energy applications, electrochemistry at interfaces, nanoelectrochemistry and bioelectrochemistry.</p><p><i>ChemElectroChem</i> will be edited by Dr. Greta Heydenrych, the editor of <i>ChemPhysChem</i>. All contributions will be published online, ensuring rapid publication and a colorful presentation of the results. Authors who wish to make their articles available to non-subscribers may also use the <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2196-0216/homepage/2701_onlineopen.html">OnlineOpen</a> option provided by the journal. For a great start, Professors Bing-Wei Mao (Xiamen University, China), Wolfgang Schuhmann (Ruhr-Universit&#xE4;t Bochum, Germany) and Jean-Marie Tarascon (Universit&#xE9; de Picardie, France) have agreed to act as Co-Chairs of the Editorial Board.</p><p>"I am personally convinced that a journal with these goals is timely and will play an important role in bringing together different aspects of the broad interdisciplinary approaches based on electrochemistry", said Co-Chairman Schuhmann. "I am very curious and excited about this new possibility to publish high-quality electrochemical research papers".</p><p>Professor Mao is also looking forward to the new journal. "<i>ChemElectroChem</i> offers the most focused platform to publish the latest achievements in electrochemistry", she said. In a statement, Mao also pointed out that "electrochemistry is distinct, with charged interfaces that universally exist in nature and artificial devices, and shares a common physical and chemical basis with many other subjects, making it a truly interdisciplinary science and technology".</p><p>Redox reactions play an important role in life sciences, catalysis, corrosion, photovoltaics, and electrochemical storage, says Co-Chairman Tarason. "These various scientific research disciplines are thus strongly related and we could define the field of electrochemistry as a branch of chemistry that has the precision of physics and the in-depth view of materials science. In this context, having a dedicated journal bridging these different disciplines is appealing and this is what our aim has been in creating <i>ChemElectroChem</i>", he said.</p><p>Read the full statements of the Co-Chairs on the journal&#x27;s homepage: <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2196-0216">www.chemelectrochem.org</a>.</p><p>&#x96;<i>Kira Welter</i></p>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300132">
<title>Enhanced Supercapacitor Performance of N-Doped Mesoporous Carbons Prepared from a Gelatin Biomolecule</title>
<link>http://dx.doi.org/10.1002/cphc.201300132</link>
<dc:creator>Dattatray S. Dhawale, Gurudas P. Mane, Stalin Joseph, Chokkalingam Anand, Katsuhiko Ariga, Ajayan Vinu</dc:creator>
<dc:date>2013-03-26T16:37+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300132.gif" width="199" height="200" alt="Enhanced Supercapacitor Performance of N-Doped Mesoporous Carbons Prepared from a Gelatin Biomolecule" title="Enhanced Supercapacitor Performance of N-Doped Mesoporous Carbons Prepared from a Gelatin Biomolecule" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Nitrogen-containing mesoporous carbon</B> electrodes with tunable pore diameters for supercapacitor applications are synthesized by the nanocasting technique using a naturally abundant gelatin polymer as the single precursor for nitrogen and carbon.</P>
<p> [Communication]<br />Dattatray S. Dhawale, Gurudas P. Mane, Stalin Joseph, Chokkalingam Anand, Katsuhiko Ariga, Ajayan Vinu<br /><i>ChemPhysChem</i>, Mar 26, 2013, DOI: 10.1002/cphc.201300132. <a href="http://dx.doi.org/10.1002/cphc.201300132">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300024">
<title>Surface Properties of Anatase TiO&lt;sub&gt;2&lt;/sub&gt; Nanowire Films Grown from a Fluoride-Containing Solution</title>
<link>http://dx.doi.org/10.1002/cphc.201300024</link>
<dc:creator>Thomas Berger, Juan A. Anta, Víctor Morales-Flórez</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/cphc201300024.gif" width="196" height="145" alt="Surface Properties of Anatase TiO2 Nanowire Films Grown from a Fluoride-Containing Solution" title="Surface Properties of Anatase TiO2 Nanowire Films Grown from a Fluoride-Containing Solution" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Annealing hits the nail</B>: Mild thermal annealing of anatase TiO<sub>2</sub> nanowire films obtained by chemical-bath deposition results in nanostructured anatase with enhanced photoelectrocatalytic properties (see picture) compared to as-deposited films. The improved performance is attributed to a temperature-induced decrease of recombination centers and the concomitant increase of adsorption and reaction sites.</P>
<p> [Article]<br />Thomas Berger, Juan A. Anta, V&#xED;ctor Morales-Fl&#xF3;rez<br /><i>ChemPhysChem</i>, Mar 25, 2013, DOI: 10.1002/cphc.201300024. <a href="http://dx.doi.org/10.1002/cphc.201300024">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300020">
<title>Spectroscopic Analysis of Two Distinct Equilibrium States for the Exchange Reaction of Sodium Cholate and Oligo-DNA on Single-Walled Carbon Nanotubes</title>
<link>http://dx.doi.org/10.1002/cphc.201300020</link>
<dc:creator>Yuichi Kato, Yasuro Niidome, Naotoshi Nakashima</dc:creator>
<dc:date>2013-03-25T06:40+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300020.gif" width="185" height="145" alt="Spectroscopic Analysis of Two Distinct Equilibrium States for the Exchange Reaction of Sodium Cholate and Oligo-DNA on Single-Walled Carbon Nanotubes" title="Spectroscopic Analysis of Two Distinct Equilibrium States for the Exchange Reaction of Sodium Cholate and Oligo-DNA on Single-Walled Carbon Nanotubes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>How to equilibrate?</B> Absorption spectroscopy reveals that two different equilibrium states are existent for the exchange reaction (see picture) of sodium cholate (SC) and oligo-DNA on single-walled carbon nanotubes (SWNTs). This is derived from the transitions of the adsorption structures of different chirality-types of SWNTs and SC/DNA at certain SC concentrations below the critical micelle concentration of SC.</P>
<p> [Article]<br />Yuichi Kato, Yasuro Niidome, Naotoshi Nakashima<br /><i>ChemPhysChem</i>, Mar 25, 2013, DOI: 10.1002/cphc.201300020. <a href="http://dx.doi.org/10.1002/cphc.201300020">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18991.en.html">
<title>Recipients of the 2013 ACS National Awards to Meet in New Orleans</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18991.en.html</link>
<dc:date>2013-03-25T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/moerner_cphc.jpg" alt="Recipients of the 2013 ACS National Awards to Meet in New Orleans" align="left" hspace="5" vspace="5" border="0" /></p>The winners of this year&#x27;s American Chemical Society (<a href="http://portal.acs.org">ACS</a>) National Awards will be honored on April 9th, 2013, at the 245th ACS National Meeting, which will take place in New Orleans, USA.</p><p>One of the awardees is <i>ChemPhysChem</i> Editorial Advisory Board Member <b>W. E. Moerner</b> (<a href="http://www.stanford.edu/group/moerner/">Stanford University</a>), who will receive the <i>Peter Debye Award in Physical Chemistry</i> for his outstanding contributions to the fields of single-molecules spectroscopy, superresolution imaging and nanophotonics. This prize is awarded annually by the ACS "to encourage and reward outstanding research in physical chemistry". It is named after the Dutch scientist Peter Debye, who received the Nobel Prize in Chemistry in 1936 for his contributions to the study of molecular structure.</p><p>W. E. Moerner earned three bachelor&#x27;s degrees from Washington University in 1975 and master&#x27;s and doctoral degrees from Cornell University in 1978 and 1982, respectively. From 1981 to 1995, he was a research staff member at IBM, and from 1993 to 1994, he was Guest Professor of Physical Chemistry at the Swiss Federal Institute of Technology. In 1995, he returned to the USA, where he became Professor and Distinguished Chair in Physical Chemistry at the University of California-San Diego until 1998 (the year he joined the Stanford faculty). He was also a Visiting Professor at Harvard University from 1997 to 1998. Moerner has received many prizes and distinctions throughout his career, including the Wolf Prize in Chemistry (with Allen Bard) in 2008 and his election to the National Academy of Sciences in 2007.</p><p>Some of the other 2013 award winners are: <b>Peter J. Stang</b>, University of Utah (<i>Priestley Medal</i>); <b>Steve Granick</b>, University of Illinois, Urbana-Champaign (<i>ACS Award in Colloid and Surface Chemistry</i>), <b>Younan Xia</b>, Georgia Institute of Technology (<i>ACS Award in the Chemistry of Materials</i>); <b>Frank H. Stillinger</b>, Princeton University (<i>ACS Award in Theoretical Chemistry</i>); and <b>Ulrike Diebold</b>, Vienna University of Technology and Tulane University (<i>Arthur W. Adamson Award for Distinguished Service in the Advancement of Surface Chemistry</i>).</p><p>Read Moerner&#x27;s most recent <i>ChemPhysChem</i> papers on <a href="http://dx.doi.org/10.1002/cphc.201100686">3D super-resolution imaging</a> of subcellular features within bacterial cells using astigmatism, <a href="http://dx.doi.org/10.1002/cphc.201100392">sub-diffraction imaging</a> of fluorescent Huntington&#x27;s disease proteins and <a href="http://dx.doi.org/10.1002/cphc.200800581">DCDHF fluorophores</a> for single-molecule imaging in cells.</p><p>Photo: <i>ChemPhysChem</i> Board Member W. E. Moerner (Stanford University) receives 2013 <i>Peter Debye Award in Physical Chemistry</i></p><p>&#x96;<i>Kira Welter</i></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18989.en.html">
<title>ChemPhysChem 5/2013: Identifying hydrogen bonds</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18989.en.html</link>
<dc:date>2013-03-21T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/resizedblurb5.jpg" alt="ChemPhysChem 5/2013: Identifying hydrogen bonds" align="left" hspace="5" vspace="5" border="0" /></p>H.-M. Cheng et al. present the concept of <a href="http://dx.doi.org/10.1002/cphc.201201075">elemental photocatalysts</a> for applications in pollutant degradation and water splitting. How a combination of an electrochemical flow cell and an inductively coupled plasma mass spectrometer can be used to <a href="http://dx.doi.org/10.1002/cphc.201300017">detect lost trace substances</a> in electrolytes is highlighted by W. Schmickler. Y. Matsuda and S. Wategaonkar et al. identify and evaluate in their article SH&#xB7;&#xB7;&#xB7;Y (Y=S,O) hydrogen bonds in the H<sub>2</sub>S dimer and the H<sub>2</sub>S-methanol binary complex by using VUV ionization-detected IR <a href="http://dx.doi.org/10.1002/cphc.201201012">predissociation spectroscopy</a>. Finally, H. Zuilhof et al. calculate the p<em>K</em><sub>a</sub> of the conjugate acids of alkanolamines, neurotransmitters, alkaloid drugs, and nucleotide bases by means of <a href="http://dx.doi.org/10.1002/cphc.201201085">density functional and ab initio methods</a><!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v14.5">Browse issue 5/2013 now</a>.</p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300022">
<title>Specific Transport of Target Molecules by Motor Proteins in Microfluidic Channels</title>
<link>http://dx.doi.org/10.1002/cphc.201300022</link>
<dc:creator>Mehmet C. Tarhan, Ryuji Yokokawa, Fabrice O. Morin, Hiroyuki Fujita</dc:creator>
<dc:date>2013-03-20T16:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300022.gif" width="198" height="106" alt="Specific Transport of Target Molecules by Motor Proteins in Microfluidic Channels" title="Specific Transport of Target Molecules by Motor Proteins in Microfluidic Channels" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>A good sort:</B> The proof of concept of a sorting device employing selective capture of distinct target molecules and transport of the sorted molecules to different predefined directions is presented (see picture). It combines the bottom-up functionality of biological systems with the top-down handling capabilities of micro-electromechanical systems technology.</P>
<p> [Article]<br />Mehmet C. Tarhan, Ryuji Yokokawa, Fabrice O. Morin, Hiroyuki Fujita<br /><i>ChemPhysChem</i>, Mar 20, 2013, DOI: 10.1002/cphc.201300022. <a href="http://dx.doi.org/10.1002/cphc.201300022">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300144">
<title>Enhancement of the Quinoidal Character for Smaller [&lt;I&gt;n&lt;/I&gt;]Cycloparaphenylenes Probed by Raman Spectroscopy</title>
<link>http://dx.doi.org/10.1002/cphc.201300144</link>
<dc:creator>Mamoru Fujitsuka, Takahiro Iwamoto, Eiichi Kayahara, Shigeru Yamago, Tetsuro Majima</dc:creator>
<dc:date>2013-03-20T16:33+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300144.gif" width="194" height="144" alt="Enhancement of the Quinoidal Character for Smaller [n]Cycloparaphenylenes Probed by Raman Spectroscopy" title="Enhancement of the Quinoidal Character for Smaller [n]Cycloparaphenylenes Probed by Raman Spectroscopy" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Quinoidal hoop-shaped macrocycles:</B> Raman spectra of cycloparaphenylenes of different sizes are measured and compared with those of linear oligoparaphenylenes and theoretical calculations. In the cases of cycloparaphenylenes, peak positions of C=C/C-C stretches significantly depend on the size of the oligomer (see picture), indicating an enhancement of the quinoidal character of smaller cycloparaphenylenes.</P>
<p> [Communication]<br />Mamoru Fujitsuka, Takahiro Iwamoto, Eiichi Kayahara, Shigeru Yamago, Tetsuro Majima<br /><i>ChemPhysChem</i>, Mar 20, 2013, DOI: 10.1002/cphc.201300144. <a href="http://dx.doi.org/10.1002/cphc.201300144">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300076">
<title>Electronic Structures and Energies of Fe&lt;sub&gt;2&lt;/sub&gt;(CO)&lt;sub&gt;n&lt;/sub&gt; (&lt;I&gt;n&lt;/I&gt;=0–9)</title>
<link>http://dx.doi.org/10.1002/cphc.201300076</link>
<dc:creator>Qiang Li, Yan-Ni Li, Tao Wang, Sheng-Guang Wang, Chun-Fang Huo, Yong-Wang Li, Jianguo Wang, Haijun Jiao</dc:creator>
<dc:date>2013-03-19T16:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300076.gif" width="204" height="100" alt="Electronic Structures and Energies of Fe2(CO)n (n=0&ndash;9)" title="Electronic Structures and Energies of Fe2(CO)n (n=0&ndash;9)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The most stable</B> unsaturated Fe<sub>2</sub>(CO)<sub><I>n</I></sub> (<I>n</I>=1&ndash;8) complexes have terminal carbonyls. A stepwise CO coordination takes place first on one Fe center [Fe-Fe(CO)<sub>4</sub>] and then on the second one [(CO)<sub>4</sub>Fe-Fe(CO)<sub>4</sub>].</P>
<p> [Communication]<br />Qiang Li, Yan-Ni Li, Tao Wang, Sheng-Guang Wang, Chun-Fang Huo, Yong-Wang Li, Jianguo Wang, Haijun Jiao<br /><i>ChemPhysChem</i>, Mar 19, 2013, DOI: 10.1002/cphc.201300076. <a href="http://dx.doi.org/10.1002/cphc.201300076">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201092">
<title>Improvement of Solar Energy Conversion with Nb-Incorporated TiO&lt;sub&gt;2&lt;/sub&gt; Hierarchical Microspheres</title>
<link>http://dx.doi.org/10.1002/cphc.201201092</link>
<dc:creator>Son Hoang, Thong Q. Ngo, Sean P. Berglund, Raymond R. Fullon, John G. Ekerdt, C. Buddie Mullins</dc:creator>
<dc:date>2013-03-19T16:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201201092.gif" width="197" height="194" alt="Improvement of Solar Energy Conversion with Nb-Incorporated TiO2 Hierarchical Microspheres" title="Improvement of Solar Energy Conversion with Nb-Incorporated TiO2 Hierarchical Microspheres" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Leading light:</B> Niobium-modified TiO<sub>2</sub> hierarchical microspheres are synthesized solvothermally and characterized for water photo-oxidation and dye-sensitized solar cell (DSSC) applications. DSSCs employing TiO<sub>2</sub> and Nb-incorporated TiO<sub>2</sub> hierarchical structures demonstrate improved light-harvesting efficiency, especially in the long-wavelength region (see picture; FTO=F-doped tin oxide).</P>
<p> [Article]<br />Son Hoang, Thong Q. Ngo, Sean P. Berglund, Raymond R. Fullon, John G. Ekerdt, C. Buddie Mullins<br /><i>ChemPhysChem</i>, Mar 19, 2013, DOI: 10.1002/cphc.201201092. <a href="http://dx.doi.org/10.1002/cphc.201201092">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201200917">
<title>Electrochemical Oxygen Reduction Behavior of Selectively Deposited Platinum Atoms on Gold Nanoparticles</title>
<link>http://dx.doi.org/10.1002/cphc.201200917</link>
<dc:creator>A. Sarkar, J. B. Kerr, E. J. Cairns</dc:creator>
<dc:date>2013-03-15T16:02+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201200917.gif" width="215" height="168" alt="Electrochemical Oxygen Reduction Behavior of Selectively Deposited Platinum Atoms on Gold Nanoparticles" title="Electrochemical Oxygen Reduction Behavior of Selectively Deposited Platinum Atoms on Gold Nanoparticles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Two or four at a time?</B> A new redox-mediated synthetic method for the selective deposition of platinum atoms on pre-fabricated gold nanoparticles is presented along with their oxygen reduction activity. The electrochemical data suggest that individual platinum atoms can reduce oxygen but via a two-electron pathway. For successful four-electron reduction to water, clusters of platinum atoms are required.</P>
<p> [Article]<br />A. Sarkar, J. B. Kerr, E. J. Cairns<br /><i>ChemPhysChem</i>, Mar 15, 2013, DOI: 10.1002/cphc.201200917. <a href="http://dx.doi.org/10.1002/cphc.201200917">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18940.en.html">
<title>ChemPhysChem 4/2013: Structural assignments by quantum chemical calculations</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18940.en.html</link>
<dc:date>2013-03-15T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/Blurb4.jpg" alt="ChemPhysChem 4/2013: Structural assignments by quantum chemical calculations" align="left" hspace="5" vspace="5" border="0" /></p>Issue 4 is a special issue on the Aggregation of Small Molecules, and includes contributions by leading scientists in the field. The special issue has been guest edited by Wolfram Sander (Ruhr-Universit&#xE4;t Bochum, Germany), Gautam Desiraju (Indian Institute of Science, Bangalore, India), and Mark Johnson (Yale University, New Haven, USA). The minireview by T. Ebata, T. R. Rizzo et al. discusses the structure of <a href="http://dx.doi.org/10.1002/cphc.201200746">cold inclusion complexes</a> of crown ethers with various neutral and ionic species in the gas phase. K. Kleinermanns, G. Jansen et al. report in their article the <a href="http://dx.doi.org/10.1002/cphc.201200701">structural assignment</a> of larger benzene-acetylene clusters by comparison of isomer- and mass-selective UV and IR-UV double resonance spectra with quantum chemical calculations. The <a href="http://dx.doi.org/10.1002/cphc.201200860">binding enthalpies</a> for Mg<sub>2</sub>+(H<sub>2</sub>O)<sub>x</sub> complexes (x=2-10) are determined in the article by D. R. Carl and P. B. Armentrout. Finally, R. Sedlak, P. Hobza et al. review the <a href="http://dx.doi.org/10.1002/cphc.201200850">performance of the MP2.5 and MP2.X methods</a>, tested on the S22, S66, X40, and other benchmark datasets.<!-- module_2 --></p><p><a href="http://dx.doi.org/10.1002/cphc.v14.4">Browse issue 4/2013 now</a>.</p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300014">
<title>A Pedagogical Perspective on Ambipolar FETs</title>
<link>http://dx.doi.org/10.1002/cphc.201300014</link>
<dc:creator>Moon Sung Kang, C. Daniel Frisbie</dc:creator>
<dc:date>2013-03-15T00:58+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300014.gif" width="197" height="159" alt="A Pedagogical Perspective on Ambipolar FETs" title="A Pedagogical Perspective on Ambipolar FETs" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>What a picture is worth:</B> The operation of an ambipolar field-effect transistor (FET) is described graphically, based on a simple diagram depicting the gate voltage-channel potential profile relative to the injection threshold voltage of charge carriers.</P>
<p> [Concept]<br />Moon Sung Kang, C. Daniel Frisbie<br /><i>ChemPhysChem</i>, Mar 15, 2013, DOI: 10.1002/cphc.201300014. <a href="http://dx.doi.org/10.1002/cphc.201300014">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201201044">
<title>Unbiased Photoelectrochemical Water Splitting in Z-Scheme Device Using W/Mo-Doped BiVO&lt;sub&gt;4&lt;/sub&gt; and Zn&lt;sub&gt;&lt;I&gt;x&lt;/I&gt;&lt;/sub&gt;Cd&lt;sub&gt;1−&lt;I&gt;x&lt;/I&gt;&lt;/sub&gt;Se</title>
<link>http://dx.doi.org/10.1002/cphc.201201044</link>
<dc:creator>Hyun S. Park, Heung Chan Lee, Kevin C. Leonard, Guanjie Liu, Allen J. Bard</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/cphc201201044.gif" width="273" height="143" alt="Unbiased Photoelectrochemical Water Splitting in Z-Scheme Device Using W/Mo-Doped BiVO4 and ZnxCd1&minus;xSe" title="Unbiased Photoelectrochemical Water Splitting in Z-Scheme Device Using W/Mo-Doped BiVO4 and ZnxCd1&minus;xSe" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Water splitting</B> to generate H<sub>2</sub> and O<sub>2</sub> using only photon energy (with no added electrical energy) is demonstrated with dual n-type-semiconductor (or Z-scheme) systems. The authors investigate two different Z-scheme systems; one is comprised of two cells with the same metal-oxide semiconductor, and the other is comprised of the metal oxide and a chalcogenide semiconductor.</P>
<p> [Article]<br />Hyun S. Park, Heung Chan Lee, Kevin C. Leonard, Guanjie Liu, Allen J. Bard<br /><i>ChemPhysChem</i>, Mar 14, 2013, DOI: 10.1002/cphc.201201044. <a href="http://dx.doi.org/10.1002/cphc.201201044">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18939.en.html">
<title>VIP: Electrochemically Actuated Stop-Go Valves for Capillary Force-Operated Diagnostic Microsystems</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18939.en.html</link>
<dc:date>2013-03-13T00:00:00+01:00</dc:date>
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<![CDATA[<p>Ioanis Katakis, Alemayehu P. Washe, Pablo Lozano Sanchez, and Diego Bejarano-Nosas</p><p>Microchannels containing sequential detection sites for the quantification of analytes and the quality control of reagents are the simplest immunosensing devices if they incorporate a flow control for reagent dissolution and incubation. This can be achieved by printing pairs of superhydrophobic electrodes transversal to the capillary flow direction. Low potentials activate the flow allowing stop/go steps. Since the structural elements, the flow-control device, and the sensors can all be produced by screen printing, and all the operations can be actuated by a portable potentiostat, this work could be an important step towards the development of quantitative, low-cost, easy-to-use diagnostic devices. <!-- module_2 --></p><!-- BNR: 300042 --><p>Received January 15, 2013, published online April 16, 2013<!-- Pubdate: 2013-4-16 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201300042">10.1002/cphc.201300042 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18928.en.html">
<title>VIP: Integrated Devices to Simultaneously Realize Energy Conversion and Storage</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18928.en.html</link>
<dc:date>2013-03-11T00:00:00+01:00</dc:date>
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<![CDATA[<p>H.S. Peng, Tao Chen, and Zhibin Yang</p><p>Other forms of energy are generally converted into electric energy and then stored in electrochemical devices through external electric wires. Peng and colleagues describe novel integrated energy devices that simultaneously realize energy conversion and storage. Both planar and wire architectures are carefully illustrated with an emphasis on the &#x93;energy wire&#x94;. The wire structure enables unique and promising applications; for example, such wires can be woven into clothes or other complex flexible equipments by using a conventional textile technology. <!-- module_2 --></p><!-- BNR: 300032 --><p>Received January 13, 2013, published online April 05, 2013<!-- Pubdate: 2013-4-05 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201300032">10.1002/cphc.201300032 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300068">
<title>Chemiluminescence from Asymmetric Inorganic Surface Layers Generated by Bipolar Electrochemistry</title>
<link>http://dx.doi.org/10.1002/cphc.201300068</link>
<dc:creator>Zahra Fattah, Jérome Roche, Patrick Garrigue, Dodzi Zigah, Laurent Bouffier, Alexander Kuhn</dc:creator>
<dc:date>2013-03-07T15:09+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300068.gif" width="185" height="189" alt="Chemiluminescence from Asymmetric Inorganic Surface Layers Generated by Bipolar Electrochemistry" title="Chemiluminescence from Asymmetric Inorganic Surface Layers Generated by Bipolar Electrochemistry" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Blue light on a Janus rod:</B> Prussian Blue (PB) is locally generated in an asymmetric way on a graphite rod by indirect bipolar electrodeposition (IBED). The presence of this inorganic layer efficiently promotes luminol chemiluminescence, which is revealed by an emission of blue light at one end of the Janus object.</P>
<p> [Communication]<br />Zahra Fattah, J&#xE9;rome Roche, Patrick Garrigue, Dodzi Zigah, Laurent Bouffier, Alexander Kuhn<br /><i>ChemPhysChem</i>, Mar 07, 2013, DOI: 10.1002/cphc.201300068. <a href="http://dx.doi.org/10.1002/cphc.201300068">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300044">
<title>Biofuel Cells for Biomedical Applications: Colonizing the Animal Kingdom</title>
<link>http://dx.doi.org/10.1002/cphc.201300044</link>
<dc:creator>Magnus Falk, Claudia W. Narváez Villarrubia, Sofia Babanova, Plamen Atanassov, Sergey Shleev</dc:creator>
<dc:date>2013-03-04T18:00+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300044.gif" width="374" height="122" alt="Biofuel Cells for Biomedical Applications: Colonizing the Animal Kingdom" title="Biofuel Cells for Biomedical Applications: Colonizing the Animal Kingdom" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>The cyborgs are coming!</B> Implantable fuel cells operating inside living organisms have been envisioned for over fifty years. However, the first report on an implanted biofuel cell was published only in 2003 by Heller et&nbsp;al. The last years have seen a multitude of biodevices being implanted and studied in different living organisms, including animals. This is reviewed herein and further perspectives for biomedical applications of biofuel cells are highlighted.</P>
<p> [Minireview]<br />Magnus Falk, Claudia W. Narv&#xE1;ez&#xA0;Villarrubia, Sofia Babanova, Plamen Atanassov, Sergey Shleev<br /><i>ChemPhysChem</i>, Mar 04, 2013, DOI: 10.1002/cphc.201300044. <a href="http://dx.doi.org/10.1002/cphc.201300044">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18832.en.html">
<title>Two European Research Projects Receive Unprecedented Awards</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18832.en.html</link>
<dc:date>2013-02-13T00:00:00+01:00</dc:date>
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<![CDATA[<p>On January 28, the European Commission announced that they will award one billion euros each for research projects on graphene, and the design of a computer model of the human brain. These two initiatives are the winners of a research-proposal competition organized by the <a href="http://cordis.europa.eu/fp7/ict/programme/fet/flagship/home_en.html">Future and Emerging Technologies (FET) flagship initiatives</a> program. The intention of this program is to provide funding for ambitious large-scale, science-driven, research initiatives that aim to achieve a visionary goal. In terms of both duration and financial incentive, this is the largest research excellence award to date. After the initial ten years of funding, further financial support will be provided by the EU&#x27;s research framework programs, primarily by the Horizon 2020 program, which is part of the EU budget proposal 2014&#x97;2020 that is currently under negotiation in the European Parliament and Council.</p><p>The prospective of receiving ten or more years of funding allows for project proposals that researchers could previously only dream of. However, the expectations that accompany such funding are high as well. Greater long-term benefits are expected from the winning projects, such as the development of new technologies and faster innovation.</p><p>Collaboration is key for such ambitious targets: "Graphene" is led by Prof. Jari Kinaret at Sweden&#x27;s Chalmers University in cooperation with more than one hundred research groups, whereas the "Human Brain Project" is under the supervision of Henry Markram, Professor at the &#xC9;cole Polytechnique F&#xE9;d&#xE9;rale de Lausanne (EPFL) in Switzerland, and involves researchers from as many as 87 different institutions.</p><p>"Europe&#x27;s position as a knowledge superpower depends on thinking the unthinkable", said European Commission Vice President Neelie Kroes during the announcement of the award winners. He went on to explain that "This multi-billion competition rewards home-grown scientific breakthroughs and shows that when we are ambitious we can develop the best research in Europe", thereby underlining the importance of an agreement among the EU governments on the ambitious budget for the Horizon 2020 program.</p><p>Among the two "unthinkable" projects, Graphene is aimed at the investigation and exploration of the unique properties of this carbon-based material, for which the Nobel Prize was awarded in 2010. Graphene shows physical, chemical, and optical properties that lead researchers to think it could become the wonder material of the 21st century, eventually even replacing silicon in information and communication technology products.</p><p>The second winning project is focused on the design of a computer simulation of the human brain, thereby paving the way for medical progress. This should allow researchers to gain insight into how our brain works and to finally make the development of personalized treatment for neurological and related diseases possible.</p><p>The battle for sustained funding will go on, but an example has been set by the European Commission. It remains to be seen if the European Parliament and Council will follow.</p><p>Source and further information: <a href="http://europa.eu/rapid/press-release_IP-13-54_en.htm">http://europa.eu/rapid/press-release_IP-13-54_en.htm</a>.</p><p>&#x96;<i>Michelle Fl&#xFC;ckiger</i></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18814.en.html">
<title>VIP: Visible-Light-Active Elemental Photocatalysts</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18814.en.html</link>
<dc:date>2013-02-11T00:10:00+01:00</dc:date>
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<![CDATA[<p>Hui-Ming Cheng,* Gang Liu, Ping Niu</p><p>Elemental semiconductors are emerging as a fascinating class of photocatalysts for solar-energy conversion. The elemental photocatalysts investigated so far (i.e. Si, Se, P and S) have promising applications in photoelectrochemical water splitting and the photodegradation of organic pollutants. Elemental photocatalysts are still in their infancy, which leaves a huge room for developing them. By applying strategies that are widely used for compound-based photocatalysts, and other special strategies, the activity of elemental photocatalysts can be significantly improved.</p><!-- BNR: 201075 --><p>Received December 21, 2012, published online February 18, 2013<!-- Pubdate: 2013-2-18 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201201075">10.1002/cphc.201201075 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18815.en.html">
<title>VIP: Understanding the Photophysics of Cucurbituril Encapsulation: A Model Study with Acridine Orange in the Gas Phase</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18815.en.html</link>
<dc:date>2013-02-11T00:00:00+01:00</dc:date>
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<![CDATA[<p>Rebecca Jockusch,* Martin F. Czar</p><p>A combination of laser-induced fluorescence and mass spectrometry was employed to study the polarizability-sensing dye cationic acridine orange (AOH<sup>+</sup>) and its host-guest complex with the macrocycle cucurbit[7]uril (CB7) in the gas phase. Spectral and time-resolved fluorescence measurements of gaseous AOH<sup>+</sup> and AOH<sup>+</sup>-CB7 are presented and compared with aqueous-phase measurements to gain insight into how CB7 binding modulates the fluorescence properties of AOH<sup>+</sup>. The authors discuss the relative importance of dye desolvation and CB7 encapsulation in terms of their effects on various spectroscopic properties of AOH<sup>+</sup>, including the fluorescence excitation maximum, the magnitude of the Stokes shift, and the fluorescence lifetime of the dye.</p><!-- BNR: 201008 --><p>Received December 03, 2012, published online February 25, 2013<!-- Pubdate: 2013-2-25 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201201008">10.1002/cphc.201201008 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201300027">
<title>Design of a Highly Efficient O&lt;sub&gt;2&lt;/sub&gt; Cathode Based on Bilirubin Oxidase from &lt;I&gt;Magnaporthe oryzae&lt;/I&gt;</title>
<link>http://dx.doi.org/10.1002/cphc.201300027</link>
<dc:creator>Marine Cadet, Xavier Brilland, Sébastien Gounel, Frédéric Louerat, Nicolas Mano</dc:creator>
<dc:date>2013-02-07T13:56+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201300027.gif" width="196" height="179" alt="Design of a Highly Efficient O2 Cathode Based on Bilirubin Oxidase from Magnaporthe oryzae" title="Design of a Highly Efficient O2 Cathode Based on Bilirubin Oxidase from Magnaporthe oryzae" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Fungi for the better:</B> The so far highest known current density (1.37&nbsp;mA&nbsp;cm<SUP>&minus;2</SUP>) for the enzymatic O<sub>2</sub> reduction under physiological conditions is reported. This is achieved by the design of a new redox polymer with an increased catalytic site density and by using a new bilirubin oxidase (BOD) from <I>Magnaporthe oryzae</I>.</P>
<p> [Communication]<br />Marine Cadet, Xavier Brilland, S&#xE9;bastien Gounel, Fr&#xE9;d&#xE9;ric Louerat, Nicolas Mano<br /><i>ChemPhysChem</i>, Feb 07, 2013, DOI: 10.1002/cphc.201300027. <a href="http://dx.doi.org/10.1002/cphc.201300027">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18816.en.html">
<title>ChemPhysChem 2/2013: Interesting interactions</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18816.en.html</link>
<dc:date>2013-02-04T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_02_2013.jpg" alt="ChemPhysChem 2/2013: Interesting interactions" align="left" hspace="5" vspace="5" border="0" /></p>The cover paper of issue 2, by J.-F. Pilard et al., describes carbon and chromium surfaces for imaging <a href="http://dx.doi.org/10.1002/cphc.201200885">DNA-protein interactions</a>. In a Review, P. Politzer and J. S. Murray discuss the factors governing <a href="http://dx.doi.org/10.1002/cphc.201200799">halogen-bonding interactions</a> (see picture). The Concept by S. Seiffert describes <a href="http://dx.doi.org/10.1002/cphc.201200749">microgel capsules</a> tailored by droplet-based microfluidics. In the Articles section, R. Winter and Y. Zhai study the effect of <a href="http://dx.doi.org/10.1002/cphc.201200767">molecular crowding</a> on the temperature-pressure stability diagram of ribonuclease A, while in the Communications section, K. P. Velikov and co-workers present novel <a href="http://dx.doi.org/10.1002/cphc.201200942">gelator-based microcapsules</a> with controllable morphology and temperature responsiveness, and Murtom&#xE4;ki et al. describe electrochemically controlled <a href="http://dx.doi.org/10.1002/cphc.201200953">proton-transfer-catalyzed reactions</a> at liquid-liquid interfaces.<!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v14.2">Browse issue 2/2013 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18563.en.html">
<title>VIP: Trajectory-Based Nonadiabatic Dynamics with Time-Dependent Density Functional Theory</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18563.en.html</link>
<dc:date>2013-01-22T00:10:00+01:00</dc:date>
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<![CDATA[<p>Basile F. E. Curchod, Ursula Rothlisberger, Ivano Tavernelli*</p><p>The description of radiationless photochemical and photophysical processes using first-principles quantum molecular dynamics calculations is a challenging problem because of the breakdown of the Born-Oppenheimer approximation and the difficulty to obtain an accurate description of the required electronic-structure properties.<p>This review describes, in full detail, a selection of trajectory-based nonadiabatic dynamics schemes within a common framework, and shows how to couple them with time-dependent density functional theory to perform on-the-fly excited-state dynamics.</p><!-- BNR: 200941 --><p>Received November 15, 2012, published online April 29, 2013<!-- Pubdate: 2013-4-29 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200941">10.1002/cphc.201200941 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18564.en.html">
<title>ChemPhysChem 1/2013: Starting good!</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18564.en.html</link>
<dc:date>2013-01-22T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_01_2013.jpg" alt="ChemPhysChem 1/2013: Starting good!" align="left" hspace="5" vspace="5" border="0" /></p>2013 starts with a bumper issue of <i>ChemPhysChem</i>. In a Review, U. Pischel, J. Andr&#xE9;asson et al. discuss the future of <a href="http://dx.doi.org/10.1002/cphc.201200157">information processing with molecules</a>. The Minireview by W.-S. Yeo and I. Choi deals with <a href="http://dx.doi.org/10.1002/cphc.201200293">self-assembled monolayers</a> with dynamicity. J. Wang, F. Ding, and L. Ma report on recent progress and challenges in <a href="http://dx.doi.org/10.1002/cphc.201200253">graphene nanoribbon</a> synthesis. The Concept by S. Shaikhutdinov and H. J. Freund demonstrates that metal-supported aluminosilicate ultrathin films can act as a versatile tool for studying the <a href="http://dx.doi.org/10.1002/cphc.201200826">surface chemistry</a> of zeolites (see picture).</p><p>In the Articles section, B. Dietzek et al. study <a href="http://dx.doi.org/10.1002/cphc.201200545">energy transfer</a> in poly(methyl methacrylate) polymers, and J. Limtrakul et al. investigate the transformation of ethanol into ethene on a <a href="http://dx.doi.org/10.1002/cphc.201200786">zeolite</a>. Finally, in the Communications section, L. Echegoyen, M. E. Plonska-Brzezinska et al. carry out conductance measurements for functionalized <a href="http://dx.doi.org/10.1002/cphc.201200624">carbon nano-onions</a> using an STM-based molecular junction approach, and B. A. Korgel and colleagues present new <a href="http://dx.doi.org/10.1002/cphc.201200738">ordered Si-nanocrystal arrays</a>.<!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v14.1">Browse issue 1/2013 now</a>.</p>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201200961">
<title>An Interference-Free Glucose Biosensor Based on an Anionic Redox Polymer-Mediated Enzymatic Oxidation of Glucose</title>
<link>http://dx.doi.org/10.1002/cphc.201200961</link>
<dc:creator>Huimin Deng, Wei Shen, Zhiqiang Gao</dc:creator>
<dc:date>2013-01-16T09:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201200961.gif" width="209" height="179" alt="An Interference-Free Glucose Biosensor Based on an Anionic Redox Polymer-Mediated Enzymatic Oxidation of Glucose" title="An Interference-Free Glucose Biosensor Based on an Anionic Redox Polymer-Mediated Enzymatic Oxidation of Glucose" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Sweet!</B> A highly selective and sensitive glucose biosensor is constructed through the co-immobilization of glucose oxidase and an anionic redox polymer on the surface of a glassy carbon electrode.</P>
<p> [Article]<br />Huimin Deng, Wei Shen, Zhiqiang Gao<br /><i>ChemPhysChem</i>, Jan 16, 2013, DOI: 10.1002/cphc.201200961. <a href="http://dx.doi.org/10.1002/cphc.201200961">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18428.en.html">
<title>VIP: MP2.5 and MP2.X: Approaching CCSD(T) Quality Description of Noncovalent Interaction at the Cost of Single CCSD Iteration</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18428.en.html</link>
<dc:date>2012-12-19T00:00:00+01:00</dc:date>
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<![CDATA[<p>Robert Sedlak,* Kevin E. Riley, Jan &#x158;ez&#xE1;&#x10D;, Michal Pito&#x148;&#xE1;k, and Pavel Hobza*</p><p>The accurate computational description of noncovalent interactions requires a high-order treatment of the electron correlation; it is known that MP2 does not yield reliable results. The next most efficient approach, MP3, is not better, but the results improve dramatically when the third-order contribution is scaled down. In the MP2.5 method, one half of the MP3 correlation energy is taken while in MP2.X, the scaling coefficient is optimized for each basis set used. We show that for a wide range of noncovalent complexes, these methods provide interaction energies and geometries with the same accuracy as higher-level and more computationally demanding methods. <!-- module_2 --></p><!-- BNR: 200850 --><p>Received October 11, 2012, published online January 11, 2013<!-- Pubdate: 2013-1-11 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200850">10.1002/cphc.201200850 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18330.en.html">
<title>ChemPhysChem 18/2012: CO in an iron fist</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18330.en.html</link>
<dc:date>2012-12-13T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/TOC_Blurb18.jpg" alt="ChemPhysChem 18/2012: CO in an iron fist" align="left" hspace="5" vspace="5" border="0" /></p>The Highlight by X. Liu and X. Huang shows recent developments in the <a href="http://dx.doi.org/10.1002/cphc.201200824">detection of single lanthanide ions</a>, which is optically achieved by implementing a two-step upconversion process in YAG:Pr<sup>3+</sup> nanocrystals. Also, Y. Ooyama and Y. Harima present in their Review a new direction in the epoch-making <a href="http://dx.doi.org/10.1002/cphc.201200218">molecular design of organic dyes for high photovoltaic performance</a> and long-term stability of DSSCs. <a href="http://dx.doi.org/10.1002/cphc.201200426">Solvatochromism and nonradiative decay</a> of intramolecular charge-transfer excited states of fluorophores using the bands-of-energy model, thermodynamics, and self-organization are discussed in the Minireview by V. S. Pavlovich. J. C. Fierro Gonzalez et al. demonstrate in an Article how thermal treatment of iron-oxide-supported gold samples influences the catalyst&#x27;s activity in the <a href="http://dx.doi.org/10.1002/cphc.201200665">oxidation of CO</a>. Finally, the Article by N. K. Sarangi and A. Patnaik reports a novel two-dimensional phase-dependent<br /><a href="http://dx.doi.org/10.1002/cphc.201200655">L-tryptophan-induced electron transport</a> with an insulator-semiconductor transition<!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.18">Browse issue 18/2012 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18327.en.html">
<title>VIP: Threshold Collision-Induced Dissociation of Hydrated Magnesium: Experimental and Theoretical Investigation of the Binding Energies for Mg2+(H2O)x complexes (x=2–10)</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18327.en.html</link>
<dc:date>2012-12-03T00:00:00+01:00</dc:date>
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<![CDATA[<p>Damon R. Carl and P. B. Armentrout*</p><p>The sequential hydration energies of Mg<sup>2+</sup>(H<sub>2</sub>O)<sub><i>x</i></sub> complexes, where <i>x</i>=2&#x96;10, including the first experimental values for the inner-shell <i>x</i>=2&#x96;4 complexes, are measured by threshold collision-induced dissociation (TCID) in a guided ion beam tandem mass spectrometer. Additionally, the thermodynamic onsets leading to the charge-separation products, MgOH<sup>+</sup>(H<sub>2</sub>O)<sub><i>x</i>-2</sub>+H<sub>3</sub>O<sup>+</sup>, from Mg<sup>2+</sup>(H<sub>2</sub>O)<sub>3</sub> and Mg<sup>2+</sup>(H<sub>2</sub>O)<sub>4</sub>, are determined for the first time.  The experimental hydration energies are in generally good agreement with quantum chemical calculations performed here and in the literature.</p><!-- BNR: 200860 --><p>Received October 15, 2012, published online December 12, 2012<!-- Pubdate: 2012-12-12 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200860">10.1002/cphc.201200860 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18321.en.html">
<title>Nicholas J. Turro (1938-2012)</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18321.en.html</link>
<dc:date>2012-12-02T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc.2012_turro.jpg" alt="Nicholas J. Turro (1938-2012)" align="left" hspace="5" vspace="5" border="0" /></p>Nicholas J. Turro, Professor of Chemistry at Columbia University, passed away on November 24, 2012, at the age of 74. He was a world-renowned researcher in the field of organic photochemistry and an excellent teacher and advisor. "He was the greatest mentor I know", says Dr. Steffen Jockusch, who worked with Turro for more than 18 years, first as a Postdoctoral Research Fellow and then as an Associate Research Scientist. "Over the many years I worked in his research group, I have seen how he made all newcomers welcome and shaped them to become good, professional scientists when they left, no matter what their level was when they arrived".</p><p>Dr. Jeffrey Lancaster, a young Associate at Turro&#x27;s group agrees with this: "Professor Turro &#x96;&#x27;Boss&#x27; as he was affectionately known to his group&#x96; was a mentor in the truest sense", he says. "He also apparently had a love for words that started with P; anyone who ever learned from him about &#x27;Professionalism&#x27;, &#x27;Paradigms&#x27; and the differences between what is &#x27;Possible&#x27;, &#x27;Plausible&#x27;, and &#x27;Probable&#x27; knows the clarity with which he could see, communicate, and educate others about scientific problems and their solutions. He will truly be missed by an extensive scientific family that he and his wife, Sandy, nurtured together for over 55 years".</p><p>Turro made important contributions to the understanding of the reaction pathways of highly energetic molecules. He studied the structure and dynamics of photochemically generated species, such as carbenes, singlet oxygen, radicals, radical pairs, and biradicals. His group also developed a new area of research called "supramolecular photochemistry" and made outstanding contributions to the field of spin chemistry. Turro&#x27;s "enthusiasm and unquenchable energy for science was truly inspiring", Jockush says. "I was always amazed by how quickly he adopted new ideas, new research projects and new technology".</p><p>Nicholas Turro earned his B.A. degree in chemistry (summa cum laude) at Wesleyan University (USA) in 1960, and his Ph.D. degree in organic photochemistry at Caltech in 1963. After spending a year as a Postdoctoral Fellow at Harvard University, he joined Columbia&#x27;s chemistry faculty as an instructor. He became Professor in 1969. The US scientist co-authored more than 900 research papers and published several influential books, including <i>Molecular Photochemistry</i> (1965) and <i>Modern Molecular Photochemistry</i> (1978). Turro received numerous prizes throughout his career and was recently selected as the recipient of the inaugural George S. Hammond Award from the Inter-American Photochemical Society. More information on the <a href="http://turroserver.chem.columbia.edu/">group&#x27;s website</a></p><p>Photo: Nicholas J. Turro (credit: Columbia University).</p><p>&#x96;<i>Kira Welter</i></p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/cphc.201200845">
<title>Application of Boron-Doped Diamond Microelectrodes for Dental Treatment with Pinpoint Ozone-Water Production</title>
<link>http://dx.doi.org/10.1002/cphc.201200845</link>
<dc:creator>Tsuyoshi Ochiai, Yuya Ishii, Shoko Tago, Masayuki Hara, Takuya Sato, Kazuo Hirota, Kazuya Nakata, Taketoshi Murakami, Yasuaki Einaga, Akira Fujishima</dc:creator>
<dc:date>2012-11-30T14:56+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/cphc201200845.gif" width="204" height="212" alt="Application of Boron-Doped Diamond Microelectrodes for Dental Treatment with Pinpoint Ozone-Water Production" title="Application of Boron-Doped Diamond Microelectrodes for Dental Treatment with Pinpoint Ozone-Water Production" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p>
<P><B>Diamonds for shiny teeth:</B> A novel pinpoint ozone-water production unit for dental treatment using boron-doped diamond (BDD) microelectrodes is developed (see picture). The superiority of such BDD microelectrodes over simple and easy-to-handle units, in terms of the larger activities for ozone production and disinfection, is demonstrated.</P>
<p> [Communication]<br />Tsuyoshi Ochiai, Yuya Ishii, Shoko Tago, Masayuki Hara, Takuya Sato, Kazuo Hirota, Kazuya Nakata, Taketoshi Murakami, Yasuaki Einaga, Akira Fujishima<br /><i>ChemPhysChem</i>, Nov 30, 2012, DOI: 10.1002/cphc.201200845. <a href="http://dx.doi.org/10.1002/cphc.201200845">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18326.en.html">
<title>ChemPhysChem 17/2012: Promising materials</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18326.en.html</link>
<dc:date>2012-11-29T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_17_2012.jpg" alt="ChemPhysChem 17/2012: Promising materials" align="left" hspace="5" vspace="5" border="0" /></p><a href="http://dx.doi.org/10.1002/cphc.201200163">Divalent europium nanocrystals</a> are a promising class of materials with many interesting applications. The Minireview by Q. Lin and co-workers describes the synthesis, properties, and uses of these materials. In an Article, A. Rebane, H. L. Anderson, D. T. Gryko et al. study the enhancement of <a href="http://dx.doi.org/10.1002/cphc.201200507">two-photon absorption</a> in porphyrins containing nitro groups (see figure). In the Communications section, J. Hao and R. Dong describe how <a href="http://dx.doi.org/10.1002/cphc.201200647">reverse solid vesicles</a> of a metallosurfactant can be prepared by removal of shape-selective organic solvents, and A. R. Patel, K. P. Velikov and colleagues present stable and temperature-responsive surfactant-free <a href="http://dx.doi.org/10.1002/cphc.201200564">foamulsions</a> with high oil&#x96;volume fraction<!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.17">Browse issue 17/2012 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18224.en.html">
<title>VIP: Laser Spectroscopic Study of Cold Host-Guest Complexes of Crown Ethers in the Gas Phase</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18224.en.html</link>
<dc:date>2012-11-19T00:00:00+01:00</dc:date>
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<![CDATA[<p>Yoshiya Inokuchi, Ryoji Kusaka, Takayuki Ebata*, Oleg V. Boyarkin, Thomas R. Rizzo*</p><p>The structures of cold, host-guest complexes of crown ethers (CEs) with various neutral and ionic species formed in the gas phase have been investigated. The combination of laser spectroscopy and theoretical analysis provides a microscopic view of the complex structures as well as the interaction energies. This work highlights the particular importance of the CE flexibility for the formation of a unique complex, which leads to molecular recognition. <!-- module_2 --></p><!-- BNR: 200746 --><p>Received September 12, 2012, published online November 30, 2012<!-- Pubdate: 2012-11-30 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200746">10.1002/cphc.201200746 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18203.en.html">
<title>VIP: Silicon Nanocrystal Superlattices</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18203.en.html</link>
<dc:date>2012-11-08T00:00:00+01:00</dc:date>
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<![CDATA[<p>Brian Korgel,* Yixuan Yu, Christian A. Bosoy, Colin M. Hessel, Detlef-M. Smilgies</p><p>Superlattices of colloidal silicon quantum dots have been made for the first time, enabled by new methods to obtain monodisperse organic ligand-stabilized nanocrystals.  Silicon is the most commercially important semiconductor, used in a wide range of applications from solar cells to computer chips. Nonetheless, silicon has shortcomings: it is a weak light absorber and extremely poor light emitter. These properties change when the crystal shrinks to the nanoscale.  Silicon quantum dots, for example, can exhibit very bright visible luminescence with size-tunable color. Ordered superlattices of silicon quantum dots will provide an interesting new platform to study and implement these unique properties. <!-- module_2 --></p><!-- BNR: 200738 --><p>Received September 10, 2012, published online November 22, 2012<!-- Pubdate: 2012-11-22 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200738">10.1002/cphc.201200738 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18320.en.html">
<title>ChemPhysChem 16/2012: Metals and more…</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18320.en.html</link>
<dc:date>2012-11-03T00:00:00+01:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_16_2012.jpg" alt="ChemPhysChem 16/2012: Metals and more&#x85;" align="left" hspace="5" vspace="5" border="0" /></p>The Highlight by R. C. Haddon discusses recent high-pressure experiments on hydrogen and chalcogenide-nitrogen molecules, showing evidence of the <a href="http://dx.doi.org/10.1002/cphc.201200555">metallic character</a> of these species. In an Article, F. Pourpoint, J. P. Amoureux et al. show that aluminum-carbon <a href="http://dx.doi.org/10.1002/cphc.201200490">internuclear distances</a> can be measured in samples with <sup>13</sup>C natural abundance by rapid fitting of experimental NMR data to an analytical expression. T. Asahi, S. Kobatake, and H. Nishi demonstrate that <a href="http://dx.doi.org/10.1002/cphc.201200442">silver nanoparticles</a> can enhance the photocycloreversion reaction of a photochromic diarylethene in the vicinity of the nanoparticle (see picture); while M. M. Vel&#xE1;zquez and colleagues achieve the functionalization of reduced <a href="http://dx.doi.org/10.1002/cphc.201200501">graphite oxide</a> sheets with a zwitterionic surfactant. Finally, in the Communications section, M. Haranczyk and co-workers describe the similarity-driven discovery of <a href="http://dx.doi.org/10.1002/cphc.201200554">zeolite</a> materials for adsorption-based separations.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.16">Browse issue 16/2012 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18154.en.html">
<title>VIP: Towards a Spectroscopic and Theoretical Identification of the Isolated Building Blocks of the Benzene-Acetylene Cocrystal</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18154.en.html</link>
<dc:date>2012-10-31T00:00:00+01:00</dc:date>
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<![CDATA[<p>Markus B&#xF6;ning,* Benjamin Stuhlmann, Gernot Engler, Matthias Busker, Thomas H&#xE4;ber, Adem Tekin, Georg Jansen, Karl Kleinermanns</p><p>The structural assignment of large benzene-acetylene clusters is achieved by comparison of isomer- and mass-selective UV and IR/UV double-resonance spectra with quantum chemical calculations. A stepwise aggregation of the clusters is predicted, and a possible cluster-formation pathway is discussed. <!-- module_2 --></p><!-- BNR: 200701 --><p>Received August 25, 2012, published online November 26, 2012<!-- Pubdate: 2012-11-26 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200701">10.1002/cphc.201200701 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<title>VIP: Polariton Dynamics under Strong Light-Molecule Coupling</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18132.en.html</link>
<dc:date>2012-10-24T00:10:00+02:00</dc:date>
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<![CDATA[<p>Thomas Ebbesen,* Tal Schwartz, James A. Hutchison, J&#xE9;r&#xE9;mie L&#xE9;onard, Cyriaque Genet, Stefan Haacke</p><p>The generation of hybrid light-matter states opens an unusual path to modify and tailor the properties of molecules and materials. Such hybrid states, formed by the resonant interaction between light and molecules, are expected to have a lifetime that is not longer than that of the shortest lived member involved in the interaction (in this case, the cavity photon). In their contribution, T. Ebbesen and co-workers demonstrate that when such hybrid states involve a larger number of molecules in a collective state (resulting in a great energy-level reorganization), the hybrid-state lifetime can be surprisingly long. This is of fundamental importance and has strong impact on the potential applications of strong light-matter interactions. <!-- module_2 --></p><!-- BNR: 200734 --><p>Received September 08, 2012, published online December 11, 2012<!-- Pubdate: 2012-12-11 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200734">10.1002/cphc.201200734 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<title>Researchers Start Worldwide Campaign against EU Budget Cuts</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18133.en.html</link>
<dc:date>2012-10-24T00:00:00+02:00</dc:date>
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<![CDATA[<p><b>Initiative for Science in Europe supports letter signed by Nobel Laureates to the EU heads of state.</b></p><p>The Initiative for Science in Europe (ISE) is asking scientists worldwide to sign a petition in order to secure the EU research budget for the next seven years. An underfunded budget for the year 2012, additional payments for uncovered bills from 2011, and the current financial crisis dominating the European markets have already led to budget problems for the current EU research funding program. In addition, a request to cut the total EU budget represents an even greater danger for research funding in the period 2014-2020, which will be discussed on November 22-23 at the summit of the EU heads of state. With this petition, the ISE, an independent platform of European learned societies and scientific organizations whose intent it is to promote mechanisms to support all fields of science at a European level, aims to make a statement about the importance of funding research in Europe. In addition, it supports an open letter previously signed by 42 European Nobel Laureates and 5 Fields Medalists to the EU heads of state that warns about short-sighted budget cuts that could result in Europe losing generations of talented scientists just when it needs them most.</p><p>"Europe needs to adapt a forward-looking approach that promotes risky though thoughtful and challenging research", Nobel Laureate Konstantin Novoselov says on the petition site. He was the first one to sign.</p><p>100 billion Euros are proposed as a reasonable growth strategy until 2020 by the European parliament to confront the economic and societal challenges for European research in the years to come. The European commission, however, states an 80 billion Euro strategy as the minimum needed to sustain European research at a world-class level. Fears are that with the financial crisis dominating every budget discussion in Europe at the moment, the final result for the next seven years will be even less than these 80 billion Euros.</p><p>Society and politicians have to consider what science means to them and how they evaluate the importance of a healthy and innovative research community for the overall competitiveness of Europe in a global network.</p><p>After the first day of this action, almost 40000 scientists from all over the world had already signed the petition, with Spain being the leading country at that time.</p><p>Source and further information at the petition site <a href="http://www.no-cuts-on-research.eu">www.no-cuts-on-research.eu</a>.</p><p>&#x96;<i>Michelle Fl&#xFC;ckiger</i></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18062.en.html">
<title>VIP: Mechanistic Studies on the Transformation of Ethanol into Ethene over Fe-ZSM-5 Zeolite</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18062.en.html</link>
<dc:date>2012-10-17T00:00:00+02:00</dc:date>
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<![CDATA[<p>Jumras Limtrakul,* Thana Maihom, Pipat Khongpracha, Jakkapan Sirijaraensre</p><p>The transformation of ethanol, a low-cost biomass product, into fine chemicals is an important process for the development of clean technologies for the chemical industry. The reaction mechanisms of ethanol transformation over an iron exchange zeolite are unraveled by means of quantum chemical calculations -and the possible pathways along a reaction coordinate are discussed and analyzed. The important role of the zeolite framework in lowering the activation barriers and stabilizing the adsorption species is also demonstrated. These results are important for understanding the chemistry of ethanol transformation in detail.<!-- module_2 --></p><!-- BNR: 200786 --><p>Received September 24, 2012, published online November 19, 2012<!-- Pubdate: 2012-11-19 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200786">10.1002/cphc.201200786 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<title>ChemPhysChem 15/2012: Models and methods</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18061.en.html</link>
<dc:date>2012-10-12T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_15_2012.jpg" alt="ChemPhysChem 15/2012: Models and methods" align="left" hspace="5" vspace="5" border="0" /></p>In a Review, H. A. Karimi-Varzaneh, P. Carbone et al. try to explain how good coarse-grained <a href="http://dx.doi.org/10.1002/cphc.201200111">polymer</a> models are (see picture). The Article by A. Gro&#xDF; und co-workers describes how <a href="http://dx.doi.org/10.1002/cphc.201200526">energy barriers</a> can be lowered in surface reactions through concerted reaction mechanisms while that by M. Orrit and colleagues deals with spectral diffusion in <a href="http://dx.doi.org/10.1002/cphc.201200463">single-molecule spectroscopy</a>. Finally, in the Communications section, A. A. Sokol et al. present a study of the <a href="http://dx.doi.org/10.1002/cphc.201200517">activation of CO<sub>2</sub></a> over ZnO by localized electrons and R. G. Compton and colleagues explain how new chemical insights can be obtained using weakly supported <a href="http://dx.doi.org/10.1002/cphc.201200480">voltammetry</a><!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.15">Browse issue 15/2012 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18030.en.html">
<title>2012 Nobel Prize in Chemistry for Work on Cell Receptors</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18030.en.html</link>
<dc:date>2012-10-10T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_Nobel_Medal.jpg" alt="2012 Nobel Prize in Chemistry for Work on Cell Receptors" align="left" hspace="5" vspace="5" border="0" /></p>The 2012 Nobel prize in chemistry has been awarded to Robert Lefkowitz of the Howard Hughes Medical Institute and Duke University in Durham, US, and Brian Kobilka of Stanford University, US, for "studies of G-protein coupled receptors" (GPCRs). Such receptors let body cells sense and respond to outside signals such as light, danger, odor or the flavor of food. "GPCRs mediate most of the physiologic responses to hormones and neurotransmitters", Kobilka told <i>ChemPhysChem</i>. "They are also fascinating membrane proteins from a basic science perspective. We hope that our research will translate into safer and more effective therapeutics."</p><p>Each cell in the body has tiny receptors that enable it to sense its environment, so that it can adapt to new situations. However, for many years, it remained unclear how the cells could "communicate" with the outside world. Scientists knew that hormones, such as adrenalin, had powerful effects on the body &#x96;and they suspected that cell surfaces should contain some kind of recipient for these hormones&#x96; but they didn&#x27;t know exactly what they looked like or how they acted. Thanks to the work of Lefkowitz and Kobilka, we now know what these receptors are, how they are built and how they act. "They work as a gateway to the cell," Lefkowitz told a news conference in Stockholm by phone. "As a result they are crucial... to regulate almost every known physiological process with humans."</p><p>There are many known GPCRs in the human body. Some of them allow us to distinguish between different smells and flavors, others regulate important biological processes, and others control our body&#x27;s reaction to hormones and neurotransmitters such as adrenalin, histamine, dopamine or serotonin.</p><p>Using radioactivity, Lefkowitz managed to unveil several receptors in 1968, including the receptor for adrenaline. With these first results, he and his team started to understand how such receptors work. In the 1980s, shortly after Kobilka had joined Lefkowitz&#x27; group, the US researchers made a second important discovery: They found that there is a whole family of receptors that look alike and function in the same manner &#x96;a family that is now called G-protein-coupled receptors.</p><p>In 2011, Kobilka achieved another breakthrough when his team captured an image of the receptor for adrenaline at the moment when it was being activated by a hormone and was sending a signal into the cell. "This image is a molecular masterpiece &#x96;the result of decades of research", said the Royal Swedish Academy of Sciences in a press release.</p><p>The studies carried out by Lefkowitz and Kobilka are key for developing better drugs, and the 2012 Nobel Prize in Chemistry is a well-deserved recognition for the two scientists. "I&#x27;m very happy and honored to be sharing the prize with Professor Lefkowitz", Kobilka said. About 50% of all medications (including beta blockers and antihistamines) act on these receptors so learning about them will be of great help in pharmaceutics and medicinal chemistry.<!-- module_2 --></p><p>Image: Nobel Medal (&#xA9; &#xAE; The Nobel Foundation). Source and further information at <a href="http://www.nobelprize.org">www.nobelprize.org</a>. Read a related article in  <a href="http://www.chemistryviews.org/details/ezine/2725471/Nobel_Prize_in_Chemistry_2012.html">ChemistryViews</a>.</p><p>&#x96;<i>Kira Welter</i></p>]]>
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<title>VIP: Photoionization Study of Yb(NH3)n Complexes</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17993.en.html</link>
<dc:date>2012-10-09T00:10:00+02:00</dc:date>
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<![CDATA[<p>Andrew Ellis,* M. J. Guttridge, S. H. Don</p><p>Complexes of an Yb atom with multiple NH<sub>3</sub> molecules in the gas phase have been investigated for the first time. The ionization energies of the complexes as a function of the number of NH<sub>3</sub> molecules have been measured and show a behavior analogous to that of alkali metals. This is consistent with a metal that can release an electron into the solvent, yielding a solvated electron when sufficient NH<sub>3</sub> molecules are present. The ionization energies also reveal that Yb can accommodate eight NH<sub>3</sub> molecules in its first solvation shell, a finding consistent with supporting ab initio calculations. <!-- module_2 --></p><!-- BNR: 200691 --><p>Received August 23, 2012, published online October 22, 2012<!-- Pubdate: 2012-10-22 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200691">10.1002/cphc.201200691 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18019.en.html">
<title>2012 Nobel Prize in Physics for Research in Quantum Optics</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/18019.en.html</link>
<dc:date>2012-10-09T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_Nobel_Medal.jpg" alt="2012 Nobel Prize in Physics for Research in Quantum Optics" align="left" hspace="5" vspace="5" border="0" /></p>This year&#x27;s Nobel prize in physics has been awarded to Serge Haroche (Coll&#xE8;ge de France and Ecole Normale Sup&#xE9;rieure, Paris, France) and David J. Wineland (National Institute of Standards and Technology, NIST, and University of Colorado Boulder, CO, USA) for their groundbreaking work in the field of quantum optics. The researchers developed two similar experimental techniques for measuring and manipulating individual particles without affecting their quantum-mechanical properties. "The Nobel Laureates have opened the door to a new era of experimentation with quantum physics by demonstrating the direct observation of individual quantum particles without destroying them", said the Royal Swedish Academy of Sciences in a press release today. "For single particles of light or matter the laws of classical physics cease to apply and quantum physics takes over. But single particles are not easily isolated from their surrounding environment and they lose their mysterious quantum properties as soon as they interact with the outside world".  Haroche and Wineland have developed two methods that now allow scientists to examine, control and count very fragile quantum states that were previously thought inaccessible for direct observation. Their work has important implications in the development of quantum computers and light-based clocks far more precise than the atomic clocks.<!-- module_2 --></p><p>Image: Nobel Medal (&#xA9; &#xAE; The Nobel Foundation). Source and further information at <a href="http://www.nobelprize.org">www.nobelprize.org</a>.</p> Read a related article in  <a href="http://www.chemistryviews.org/details/ezine/2722561/Nobel_Prize_in_Physics_2012.html">ChemistryViews</a>.</p><p>&#x96;<i>Kira Welter</i></p>]]>
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<title>VIP: Matrix Isolation Vibrational Circular Dichroism Spectroscopy of 3-Butyn-2-ol and Its Binary Aggregates</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17992.en.html</link>
<dc:date>2012-10-05T00:00:00+02:00</dc:date>
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<![CDATA[<p>Christian Merten, Yunjie Xu*</p><p>While vibrational circular dichroism (VCD) spectroscopy shows unique specificity to chirality and is highly sensitive to the conformational equilibria of chiral molecules, the matrix isolation (MI) technique offers narrow spectral bandwidth and sample manipulation. The combination of the two is, however, challenging due to the much smaller VCD signal intensity compared to that of regular infrared absorption. Using the example of 3-butyn-2-ol, Merten and Xu show that MI-VCD is a powerful tool to study self-aggregation, chirality transfer, and other exotic chiral species that can be prepared in a cold matrix. <!-- module_2 --></p><!-- BNR: 200758 --><p>Received September 14, 2012, published online October 25, 2012<!-- Pubdate: 2012-10-25 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200758">10.1002/cphc.201200758 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<title>ChemPhysChem 14/2012: Materials and more</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17990.en.html</link>
<dc:date>2012-10-04T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_14_2012.jpg" alt="ChemPhysChem 14/2012: Materials and more" align="left" hspace="5" vspace="5" border="0" /></p>In issue 14, Q. Lou and D. A. Shipp examine recent developments in achieving <a href="http://dx.doi.org/10.1002/cphc.201200166">atom transfer radical polymerization</a> (ATRP) with minimal amounts of catalyst. The Article by C. A. Fernandez, P. K. Thallapally et al. gives insights into the temperature-dependent "breathing" of a flexible fluorinated <a href="http://dx.doi.org/10.1002/cphc.201200243">metal-organic framework</a>. In the same section, Y. Tor and colleagues introduce modified 6-aza-uridines as highly emissive pH-sensitive <a href="http://dx.doi.org/10.1002/cphc.201200375">fluorescent nucleosides</a>, and R. J. Behm and co-workers study the growth of PtRu clusters on Ru(0001)-supported monolayer <a href="http://dx.doi.org/10.1002/cphc.201200294">graphene</a> films. In the Communications section, S. Madhavi et al. present a high-performance insertion anode for <a href="http://dx.doi.org/10.1002/cphc.201200398">lithium-ion batteries</a>; O. J. Curnow and R. G. A. R. Maclagan study two chloride monohydrates trapped in a <a href="http://dx.doi.org/10.1002/cphc.201200402">hydrophobic pocket</a>; and M. Tadokoro and colleagues describe the pre-melting structure transformation of <a href="http://dx.doi.org/10.1002/cphc.201200414">water clusters</a> in nanoporous molecular crystals (see picture)<!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.14">Browse issue 14/2012 now</a>.</p>]]>
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<title>ChemPhysChem 13/2012: Molecular studies</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17989.en.html</link>
<dc:date>2012-09-07T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_13_2012.jpg" alt="ChemPhysChem 13/2012: Molecular studies" align="left" hspace="5" vspace="5" border="0" /></p>The Highlight by R. S. Payal and S. Balasubramanian presents a new massless model for use in dynamic <a href="http://dx.doi.org/10.1002/cphc.201200380">atomic force microscopy</a> (AFM) experiments, which aids in the study of solid-liquid interfaces of viscous liquids (see picture). In an Article by H.-C. Siebert and co-workers, the <a href="http://dx.doi.org/10.1002/cphc.201200284">molecular organization</a> of various collagen fragments is described, as revealed by AFM and diffusion-ordered NMR spectroscopy. Finally, in a Communication, R. Ludwig and colleagues show that <a href="http://dx.doi.org/10.1002/cphc.201200436">ionic liquids</a> can be more hydrophobic than chloroform or benzene.</p></p><p><a href="http://dx.doi.org/10.1002/cphc.v13.13">Browse issue 13/2012 now</a>.</p>]]>
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<title>Detlef Schröder: Scientific Community Loses Prominent Mass Spectrometrist</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17831.en.html</link>
<dc:date>2012-08-27T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/Dedli_f4-small.jpg" alt="Detlef Schr&#xF6;der: Scientific Community Loses Prominent Mass Spectrometrist" align="left" hspace="5" vspace="5" border="0" /></p>Dr. Detlef Schr&#xF6;der of the Institute of Organic Chemistry and Biochemistry (IOCB) at the Academy of Sciences of the Czech Republic died unexpectedly on August 22, 2012, at the age of 49. Schr&#xF6;der was a worldwide recognized scientist in the field of mass spectrometry with a broad experience in all areas of gas-phase ion chemistry. His research interests ranged from the investigation of fundamental aspects of diatomic molecules to the elucidation of organic and inorganic reaction mechanisms or the study of problems of astrochemical and biochemical interest. His premature death is a great loss for the scientific community.</p><p>Detlef Schr&#xF6;der was born in Wilster, Germany, and studied chemistry at the Technical University of Berlin (TU Berlin), where he earned his Ph.D. (with honors) in 1989 under the supervision of Professor Helmut Schwarz. He continued working as a scientific researcher in Berlin until 2006 and obtained his Habilitation from the same university in 2007. Schr&#xF6;der was Distinguished Chair of the IOCB in Prague since 2011.</p><p>Helmut Schwarz, who got to know Schr&#xF6;der as a young, talented student in the 1980s and continued working with him later, when he had become an experienced and successful scientist, was deeply touched by the news: &#x93;I have been privileged throughout my academic career to interact with truly outstanding students and postdoctoral fellows, and the late Detlef Schr&#xF6;der was unique among them", Schwarz told <i>ChemPhysChem</i>. "He embraced science with unparalleled enthusiasm, his energy seemed boundless and his dedication to academic affairs exemplary; undergraduate students and faculty alike loved Detlef for the way he interacted with and supported much less gifted fellow colleagues. No surprise that there is a worldwide community of admirers and friends mourning Detlef Schr&#xF6;der&#x27;s untimely death."</p><p>Dr. Christopher Shaffer, a postdoctoral fellow at Schr&#xF6;der&#x27;s institute and co-author of many of his most recent publications, agrees with this: "Detlef&#x27;s catholic mastery of, and passion for chemistry generated such a level of inspiration that it will be hard, neigh impossible, to match within the hearts of those who were familiar with him", he said.</p><p>Schr&#xF6;der&#x27;s contributions to science are documented in more than 360 publications in peer-reviewed journals and have been honored with several awards including the newly created Rudolf Luke&#x161; Prize, which he received recently from the Czech Chemical Society "for his excellent work in the area of organic, bioorganic and medicinal chemistry". Schr&#xF6;der also served as Editor-in-Chief of the <i>International Journal of Mass Spectrometry</i>. He was an outstanding chemist and a great researcher, who will be greatly missed by friends and colleagues.</p><p>Read more at <a href="http://www.chemistryviews.org/details/ezine/2510851/Detlef_Schroder_1963__2012.html">chemistryviews.org</a></p><p>&#x96;<i>Kira Welter</i></p>]]>
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<title>ChemPhysChem now on twitter</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17826.en.html</link>
<dc:date>2012-08-24T00:00:00+02:00</dc:date>
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<![CDATA[<p>Dear <i>ChemPhysChem</i> users, from now on you can follow us on twitter to stay up to date with top research in chemical physics and physical chemistry, take a look at our latest special issues, find out where to meet us at conferences or tell us what you think about our journal. We look forward to meeting you on twitter soon!</p><p><a href="https://twitter.com/ChemPhysChem" class="twitter-follow-button" data-show-count="false" data-size="large">Follow @ChemPhysChem</a>
<br><script>!function(d,s,id){var js,fjs=d.getElementsByTagName(s)[0];if(!d.getElementById(id)){js=d.createElement(s);js.id=id;js.src="//platform.twitter.com/widgets.js";fjs.parentNode.insertBefore(js,fjs);}}(document,"script","twitter-wjs");</script><!-- module_2 --></p><p><a href="https://twitter.com/ChemPhysChem">Follow now</a>.</p>]]>
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<title>Sason Shaik and Martin Quack to be Honored by the German Chemical Society in Prague</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17810.en.html</link>
<dc:date>2012-08-22T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/ShaikQuack.jpg" alt="Sason Shaik and Martin Quack to be Honored by the German Chemical Society in Prague" align="left" hspace="5" vspace="5" border="0" /></p>Sason Shaik (left), Professor at the Lise Meitner-Minverva Center for Computational Quantum Chemistry at the <a href="http://www.huji.ac.il/huji/eng/">Hebrew University in Jerusalem</a>, and Martin Quack (right), Professor at the Laboratory for Physical Chemistry at the Swiss Federal Institute of Technology Zurich (<a href="http://www.ethz.ch/">ETH Zurich</a>, Switzerland) will each receive the August Wilhelm von Hofmann Medal from the German Chemical Society (GDCh: Gesellschaft Deutscher Chemiker) during the 4th Chemistry Congress of the European Association for Chemical and Molecular Sciences (<a href="http://www.euchems-prague2012.cz/">EuCheMS</a>), which will take place from August 26-30, 2012, in Prague (Czech Republic).<p/><p>This prize is awarded every second year and recognizes outstanding achievements in chemistry from scientists working outside Germany.</p><p>"Germany is one of the superpowers of science, so, by all means receiving any prize from the German Chemical Society is a great honour, let alone the August Wilhelm von Hofmann medal, which is an outstanding honour", Shaik told <em>ChemPhysChem</em>. He further explained: "The medal carries the name of one of chemistry&#x27;s greatest figures of the 19th century, and the list of awardees starts in 1903 with Moissan and Ramsay, and continues through other luminaries, like [Albert von] Szent-Gy&#xF6;rgyi, Robert Robinson, Emilio Segr&#xE9;, Lorence Bragg, Vladimir Prelog, Robert Grubbs and Richard Schrock, my two countrymen David Ginsburg and Joshua Jortner, and Francois Diedrich, and so on. Who would not be proud to be listed in this company?"</p><p>Both awardees are attracted by the fundamental problems of chemistry and want to understand "whatever holds molecules together in its inmost folds"<sup>[1]</sup>. While Shaik develops theoretical models to explain bonding behaviour and analyse reactivity problems in chemistry and biochemistry, Quack is known for his work on high-resolution spectroscopy, which has led to a fundamental understanding and description of molecular quantum dynamics. The contributions made by both scientists have laid the foundation for on-going practical or technological achievements and those still to come.</p><p>"Follow your heart", is the advice of Shaik to young and prospective scientists, "if you do what you like to do, you will always be happier".</p><p></p><p>[1] Freely adapted from J. W. v. Goethe, <em>Faust</em></p><p>&#x96;<i>Michelle Fl&#xFC;ckiger</i></p>]]>
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<title>ChemPhysChem 12/2012: Special issue on electrochemistry and energy</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17799.en.html</link>
<dc:date>2012-08-17T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_12_2012.jpg" alt="ChemPhysChem 12/2012: Special issue on electrochemistry and energy" align="left" hspace="5" vspace="5" border="0" /></p>Issue 12 is a special issue on Electrochemistry and Energy and includes invited contributions by leading scientists in the field. The manuscripts featured in this issue are related to the 5th Gerischer Symposium, which took place in Berlin (Germany) last year. The special issue has been guest edited by Hans-Joachim Lewerenz (Helmholtz Zentrum Berlin for Materials and Energy, Germany), and Dieter Kolb, who sadly passed away in October last year, is the Honorary Guest Editor of the edition. An <a href="http://dx.doi.org/10.1002/cphc.201200109">obituary</a> by G. Ertl and H. J. Lewerenz summarizes his merits and accomplishments. In a review by R. G&#xF3;mez et al., the electrochemistry of <a href="http://dx.doi.org/10.1002/cphc.201200073">nanostructured TiO<sub>2</sub> electrodes</a> is presented. The minireview by L. Gundlach and F. Willig summarizes interesting experimental data related to <a href="http://dx.doi.org/10.1002/cphc.201200151">electron-transfer dynamics</a> at electrodes. Finally, in an article by Scragg et al., the authors show how to maximize the thermal stability of <a href="http://dx.doi.org/10.1002/cphc.201200067">solar-cell materials</a><!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.12">Browse issue 12/2012 now</a>.</p>]]>
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<title>ChemPhysChem 11/2012: Improved techniques</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17794.en.html</link>
<dc:date>2012-07-27T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/issue_11_2012_new.jpg" alt="ChemPhysChem 11/2012: Improved techniques" align="left" hspace="5" vspace="5" border="0" /></p>In issue 11, K. B. Crozier and K. Wang review the fundamentals of <a href="http://dx.doi.org/10.1002/cphc.201200121">optical tweezers</a> and describe an optical nanotweezer that exceeds the performance limitations of conventional tweezers while avoiding thermal effects with a heat-sinking approach (see picture). In a Highlight, J. M. Thomas discusses new ways to determine the crystal structure of organic molecules using sophisticated techniques for the analysis of powder <a href="http://dx.doi.org/10.1002/cphc.201200322">X-ray diffraction</a> data and shows how the application of these techniques has recently led to the first crystal-structure determination reported for L-arginine. In the Articles section, K. Gerwert, C. K&#xF6;tting and co-workers present a universal label-free method for the spectroscopic investigation of polyhistidine-tagged <a href="http://dx.doi.org/10.1002/cphc.201200358">proteins</a>; H. Yao and K. Ashiba show how effective color tuning can be achieved in ion-based <a href="http://dx.doi.org/10.1002/cphc.201200191">organic nanoparticles</a>; and A. Lledos, E. S. Shubina and colleagues report a theoretical study of metal involvement in <a href="http://dx.doi.org/10.1002/cphc.201200097">dihydrogen bonding</a>. Finally, in the Communications section, E. Coronado, A. Palii, et al. describe the electric field control of the spin state in mixed-valence <a href="http://dx.doi.org/10.1002/cphc.201200383">magnetic molecules</a><!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.11">Browse issue 11/2012 now</a>.</p>]]>
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<title>ChemPhysChem updated its author guidelines for LaTeX users</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17594.en.html</link>
<dc:date>2012-07-16T00:00:00+02:00</dc:date>
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<![CDATA[<!-- module_2 --><p>For all our LaTeX users and lovers, <i>ChemPhysChem</i> has updated its guidelines on how to prepare and submit LaTeX manuscripts in order to speed up the publication process. From today you can find a template and some useful instructions on our author guidelines site. Please have a look at: <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/2267_latex.html">Instructions for LaTeX users</a>.</p>]]>
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<title>ChemPhysChem 10/2012: Special issue on nanomaterials</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17787.en.html</link>
<dc:date>2012-07-06T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/issue_10_2012.jpg" alt="ChemPhysChem 10/2012: Special issue on nanomaterials" align="left" hspace="5" vspace="5" border="0" /></p>Issue 10 is a special issue on nanomaterials. It has been guest edited by Professors Florian Banhart (University of Strasbourg, France), Harald Fuchs (University of M&#xFC;nster, Germany), Zhiyong Tang (National Center for Nanoscience and Technology, Beijing, China) and Thomas Webster (Brown University, USA) and contains more than 20 invited contributions in the field. The Concept by M. J. Serpe et al. presents <a href="http://dx.doi.org/10.1002/cphc.201200025">polymer-based microgels</a> and their assemblies for organic-molecule removal from water. In a Minireview, K. Fox, N. Tran, and P. A. Tran discuss recent advances in the applications of nanophase <a href="http://dx.doi.org/10.1002/cphc.201200080">hydroxyapatite</a>. The Article by A. Govorov and Z. Fan deals with the theory of <a href="http://dx.doi.org/10.1002/cphc.201100958">chiral plasmonic nanostructures</a> comprising metal nanocrystals and chiral molecular media and that by R. A. Alvarez-Puebla, L. M. Liz-Marz&#xE1;n et al. presents spiked gold beads as substrates for single-particle <a href="http://dx.doi.org/10.1002/cphc.201101014">surface-enhanced Raman spectroscopy</a> (SERS). In the Communications section, R. S. Weatherup and colleagues study the mechanisms of Ni-catalysed graphene <a href="http://dx.doi.org/10.1002/cphc.201101020">chemical vapour deposition</a> and Y. Gan, Y. Yin and co-workers show how hydrogen peroxide is added in a seed-mediated growth process for producing <a href="http://dx.doi.org/10.1002/cphc.201101018">silver nanoplates</a> with not only significantly improved synthetic yield, but also greatly shortened reaction time and enhanced reproducibility.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.10">Browse issue 10/2012 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17477.en.html">
<title>ChemPhysChem 9/2012: Molecules on the move</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17477.en.html</link>
<dc:date>2012-06-21T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_09_2012.jpg" alt="ChemPhysChem 9/2012: Molecules on the move" align="left" hspace="5" vspace="5" border="0" /></p>In issue 9, W. K. Zhang and N. N. Liu review recent advances in <a href="http://dx.doi.org/10.1002/cphc.201200154">single-molecule force spectroscopy</a> studies of macromolecular interactions. In a Minireview, J. C. G. Esteves da Silva and L. Pinto da Silva discuss the fascinating properties of firefly chemiluminescence and <a href="http://dx.doi.org/10.1002/cphc.201200195">bioluminescence</a> (see picture). The Highlight by H. Terrones shows how <a href="http://dx.doi.org/10.1002/cphc.201200321">fullerene peapods</a> have opened the possibility of studying reactions in a confined space and the Concept by K. Okano and T. Yamashita describes chiral environments formed by a <a href="http://dx.doi.org/10.1002/cphc.201200003">vortex flow</a>. Finally, the Article by H.-L. Xu, Z.-M. Su, Z.-R. Li et al. deals with spiral intramolecular <a href="http://dx.doi.org/10.1002/cphc.201200213">charge transfer</a> in M&#xF6;bius cyclacenes and the Communication by R. Boulatov and Y. Tian presents a quantum-chemical validation of the local assumption of <a href="http://dx.doi.org/10.1002/cphc.201200207">chemomechanics</a> for a unimolecular reaction<!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.9">Browse issue 9/2012 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17474.en.html">
<title>ChemPhysChem 8/2012: Topical issue on nanobubbles</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17474.en.html</link>
<dc:date>2012-06-19T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_08_2012.jpg" alt="ChemPhysChem 8/2012: Topical issue on nanobubbles" align="left" hspace="5" vspace="5" border="0" /></p>Issue 8 is a topical issue on Nanobubbles. Apart from a number of interesting papers in other fields, such as the Review by A. Kraegeloh et al. on <a href="http://dx.doi.org/10.1002/cphc.201100986">STED microscopy</a> and its applications, the paper by W. Q. Deng and co-workers, which presents a computational study on acene-modified dyes for <a href="http://dx.doi.org/10.1002/cphc.201200064">dye-sensitized solar cells</a>, or the Article by L. C. Cune on magic pairs and structural transitions in <a href="http://dx.doi.org/10.1002/cphc.201200084">binary metallic clusters</a> (see picture), the topical issue also contains contributions by J. R. T Seddon and colleagues, who discuss <a href="http://dx.doi.org/10.1002/cphc.201100900">nanobubbles</a> at surfaces and in bulk, D. Lohse et al., who show that <a href="http://dx.doi.org/10.1002/cphc.201100807">diffusive shielding</a> stabilizes bulk nanobubble clusters, and several other authors. The Nanobubbles issue was guest edited by Philip Ball.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.8">Browse issue 8/2012 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17415.en.html">
<title>VIP: Self-Assembled Monolayers with Dynamicity Stemming from (Bio)Chemical Conversions: From Construction to Applications</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17415.en.html</link>
<dc:date>2012-06-04T00:00:00+02:00</dc:date>
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<![CDATA[<p>Inseong Choi and Woon-Seok Yeo*</p><p>Surfaces with &#x91;dynamicity&#x92; stemming from (bio)chemical conversions have been actively developed and harnessed in many research areas. The dynamic surfaces are constructed on numerous materials and activated by various external stimuli. Yeo and Choi focus on self-assembled monolayers (SAMs) as a scaffold and dynamicities that are attributed to (bio)chemical conversions on surfaces. The authors also categorize the dynamic SAMs from the perspective of chemical reactions. <!-- module_2 --></p><!-- BNR: 200293 --><p>Received April 03, 2012, published online June 14, 2012<!-- Pubdate: 2012-6-14 -->, DOI: <a href="http://dx.doi.org/10.1002/cphc.201200293">10.1002/cphc.201200293 &#x2013; read now</a>.<!-- issueyear --></p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17294.en.html">
<title>ChemPhysChem 7/2012: Special issue on ionic liquids</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17294.en.html</link>
<dc:date>2012-05-10T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_07_2012.jpg" alt="ChemPhysChem 7/2012: Special issue on ionic liquids" align="left" hspace="5" vspace="5" border="0" /></p>Issue 07 is a special issue on ionic liquids. It includes around 40 invited contributions by leading scientists in the field and has been guest edited by Ralf Ludwig (Rostock University, Germany), Edward Maginn (University of Notre Dame, USA) and Sundaram Balasubramanian (Jawaharlal Nehru Centre for Advanced Scientific Research, India). The Minireview by H. Shirota shows a comparison of the <a href="http://dx.doi.org/10.1002/cphc.201100731">low-frequency spectra</a> of aromatic and nonaromatic cation-based ionic liquids. In the Articles section, E. L. Quitevis, G. A. Voth et al. study <a href="http://dx.doi.org/10.1002/cphc.201200026">nanostructural organization</a> in acetonitrile/ionic liquid mixtures, and F. Maier and colleagues investigate <a href="http://dx.doi.org/10.1002/cphc.201100965">organic reactions</a> in ionic liquids. In the Communications section, T. Yan and co-workers describe the effects of <a href="http://dx.doi.org/10.1002/cphc.201200013">specific adsorption</a> on the differential capacitance of imidazolium-based ionic-liquid electrolytes.<!-- module_2 -->.</p><p><a href="http://dx.doi.org/10.1002/cphc.v13.7">Browse issue 7/2012 now</a>.</p>]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17293.en.html">
<title>ChemPhysChem 6/2012: Knowing nano</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641/homepage/news/17293.en.html</link>
<dc:date>2012-04-23T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/cphc_06_2012.jpg" alt="ChemPhysChem 6/2012: Knowing nano" align="left" hspace="5" vspace="5" border="0" /></p>In the Minireviews section of issue 6, N. Menzel et al. describe important synthetic routes to the fabrication of <a href="http://dx.doi.org/10.1002/cphc.201100984">porous nanostructured electrocatalysts</a> and discuss their applications, showing how the performance benefits from the nanostructure, and J.-S. Noh, W. Lee and colleagues present design rules for nanogap-based <a href="http://dx.doi.org/10.1002/cphc.201200014">hydrogen gas sensors</a>. The Article by X. Xu and I. Y. Zhan shows that gas-phase thermodynamics can be used as a validation of <a href="http://dx.doi.org/10.1002/cphc.201100909">computational catalysis</a> on surfaces while that by S. Irle, K. Morokuma and co-workers gives theoretical insights into chirality-controlled <a href="http://dx.doi.org/10.1002/cphc.201200055">single-walled carbon nanotube</a> (SWCNT) growth.<p><a href="http://dx.doi.org/10.1002/cphc.v13.6">Browse issue 6/2012 now</a>.</p>]]>
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