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<dc:date>2013-01-29T00:00:00+01:00</dc:date>
<dc:publisher>Wiley-VCH</dc:publisher>
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<title>Rational Heme Protein Design: All Roads Lead to Rome</title>
<link>http://dx.doi.org/10.1002/asia.201300291</link>
<dc:creator>Ying-Wu Lin, Elizabeth B. Sawyer, Jiangyun Wang</dc:creator>
<dc:date>2013-05-23T13:05+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300291.gif" width="216" height="197" alt="Rational Heme Protein Design: All Roads Lead to Rome" title="Rational Heme Protein Design: All Roads Lead to Rome" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>All roads lead to Rome:</B> During the last few decades, various approaches for rational heme protein design have emerged. These techniques not only enhance our understanding of the structure and function of heme proteins in nature but also facilitate the creation of novel biocatalysts and biosensors beyond nature.</P><p> [Focus Review]<br />Ying-Wu Lin, Elizabeth B. Sawyer, Jiangyun Wang<br /><i>Chem. Asian J.</i>, May 23, 2013, DOI: 10.1002/asia.201300291. <a href="http://dx.doi.org/10.1002/asia.201300291">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300153">
<title>Measurement of the Quantum Conductance of Germanium by an Electrochemical Scanning Tunneling Microscope Break Junction Based on a Jump-To-Contact Mechanism</title>
<link>http://dx.doi.org/10.1002/asia.201300153</link>
<dc:creator>Xufen Xie, Jiawei Yan, Jinghong Liang, Jijun Li, Meng Zhang, Bingwei Mao</dc:creator>
<dc:date>2013-05-23T13:02+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300153.gif" width="214" height="162" alt="Measurement of the Quantum Conductance of Germanium by an Electrochemical Scanning Tunneling Microscope Break Junction Based on a Jump-To-Contact Mechanism" title="Measurement of the Quantum Conductance of Germanium by an Electrochemical Scanning Tunneling Microscope Break Junction Based on a Jump-To-Contact Mechanism" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Gimme a break!</B> Quantum conductance of germanium was measured by electrochemical STM break junction based on a jump-to-contact mechanism. The conductance histogram indicated that the conductance of germanium nanowires was located between 0.02 and 0.15 <I>G</I><sub>0</sub> (see picture).</P><p> [Full Paper]<br />Xufen Xie, Jiawei Yan, Jinghong Liang, Jijun Li, Meng Zhang, Bingwei Mao<br /><i>Chem. Asian J.</i>, May 23, 2013, DOI: 10.1002/asia.201300153. <a href="http://dx.doi.org/10.1002/asia.201300153">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19203.en.html">
<title>Full Paper: Double Functionalization of Carbon Nanotubes with Purine and Pyrimidine Derivatives</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19203.en.html</link>
<dc:date>2013-05-23T00:30:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/asia_2013_201300116.png" alt="Full Paper: Double Functionalization of Carbon Nanotubes with Purine and Pyrimidine Derivatives" align="left" hspace="5" vspace="5" border="0" /></p><i>Prabhpreet Singh, C&#xE9;cilia M&#xE9;nard-Moyon, Alessia Battigelli, Francesca Maria Toma, Jesus Raya, Jitendra Kumar, Nagapradeep Nidamanuri, Sandeep Verma, Alberto Bianco</i></p><p>doi: 10.1002/asia.201300116</p><P>Herein, we have developed a synthetic strategy for the covalent double functionalization of single-walled carbon nanotubes (SWCNTs) with a combination of purine&#x2013;pyrimidine and purine&#x2013;purine nucleobase systems. The nucleobases were introduced on the sidewall of oxidized SWCNTs through 1,3-dipolar cycloaddition and by amidation of the carboxylic acids located at the tips and defect sites of the nanotubes. The new nanohybrids were characterized by transmission electron microscopy, thermogravimetric analysis, FTIR and Raman spectroscopy, magic-angle spinning NMR spectroscopy, and Kaiser test. The nucleobase/SWCNT conjugates can be envisaged for the modulation of the interactions with nucleic acids by means of base pairing, thereby opening new possibilities in the development of DNA/CNT nanobioconjugates.</P><p align="right"><a href="http://dx.doi.org/10.1002/asia.201300116">Read Full Text</a></p>]]>
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</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19204.en.html">
<title>Full Paper: Measurement of the Quantum Conductance of Germanium by an Electrochemical Scanning Tunneling Microscope Break Junction Based on a Jump-To-Contact Mechanism</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19204.en.html</link>
<dc:date>2013-05-23T00:20:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/asia_2013_201300153.png" alt="Full Paper: Measurement of the Quantum Conductance of Germanium by an Electrochemical Scanning Tunneling Microscope Break Junction Based on a Jump-To-Contact Mechanism" align="left" hspace="5" vspace="5" border="0" /></p><i>Xufen Xie, Jiawei Yan, Jinghong Liang, Jijun Li, Meng Zhang, Bingwei Mao</i></p><p>doi: 10.1002/asia.201300153</p><P>We present quantum conductance measurements of germanium by means of an electrochemical scanning tunneling microscope (STM) break junction based on a jump-to-contact mechanism. Germanium nanowires between a platinum/iridium tip and different substrates were constructed to measure the quantum conductance. By applying appropriate potentials to the substrate and the tip, the process of heterogeneous contact and homogeneous breakage was realized. Typical conductance traces exhibit steps at 0.025 and 0.05 <I>G</I><sub>0</sub>. The conductance histogram indicates that the conductance of germanium nanowires is located between 0.02 and 0.15 <I>G</I><sub>0</sub> in the low-conductance region and is free from the influence of substrate materials. However, the distribution of conductance plateaus is too discrete to display distinct peaks in the conductance histogram of the high-conductance region.</P><p align="right"><a href="http://dx.doi.org/10.1002/asia.201300153">Read Full Text</a></p>]]>
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</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19205.en.html">
<title>Focus Review: Rational Heme Protein Design: All Roads Lead to Rome</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19205.en.html</link>
<dc:date>2013-05-23T00:10:00+02:00</dc:date>
<taxo:topics>
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<content:encoded>
<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/asia_2013_201300291.png" alt="Focus Review: Rational Heme Protein Design: All Roads Lead to Rome" align="left" hspace="5" vspace="5" border="0" /></p><i>Ying-Wu Lin, Elizabeth B. Sawyer, Jiangyun Wang</i></p><p>doi: 10.1002/asia.201300291</p><P>Heme proteins are among the most abundant and important metalloproteins, exerting diverse biological functions including oxygen transport, small molecule sensing, selective C-H bond activation, nitrite reduction, and electron transfer. Rational heme protein designs focus on the modification of the heme-binding active site and the heme group, protein hybridization and domain swapping, and de novo design. These strategies not only provide us with unique advantages for illustrating the structure&#x2013;property&#x2013;reactivity&#x2013;function (SPRF) relationship of heme proteins in nature but also endow us with the ability to create novel biocatalysts and biosensors.</P><p align="right"><a href="http://dx.doi.org/10.1002/asia.201300291">Read Full Text</a></p>]]>
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</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19206.en.html">
<title>Focus Review: Artificial Metalloenzymes Constructed From Hierarchically-Assembled Proteins</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19206.en.html</link>
<dc:date>2013-05-23T00:00:00+02:00</dc:date>
<taxo:topics>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/asia_2013_201300347.png" alt="Focus Review: Artificial Metalloenzymes Constructed From Hierarchically-Assembled Proteins" align="left" hspace="5" vspace="5" border="0" /></p><i>Takafumi Ueno, Hiroyasu Tabe, Yuya Tanaka</i></p><p>doi: 10.1002/asia.201300347</p><P>The design of artificial metalloenzymes has become an important topic in biological chemistry and inorganic chemistry due to the potential applications of artificial metalloenzymes in nanoscience and biotechnology. One of the general methods used to produce artificially metalloenzymes involves the encapsulation of non-natural metal cofactors within protein scaffolds. This method has been used in the construction of small artificial metalloproteins with high activity and selectivity. However, the important roles of protein assemblies have not yet been systematically investigated in this field, even though natural enzymatic systems employ protein assemblies as molecular scaffolds for elaborate enzymatic reactions. In recent years, the above-mentioned general strategy has been applied to functionalize protein assemblies such as protein cages and protein crystals. These assembled structures form confined interior environments, which can be used to accommodate metal complex catalysts and to prepare metal nanoparticles. The development of artificial metalloenzymes with hierarchically-assembled proteins would enable us to provide powerful tools for industrial and biological applications. In this Focus Review, we discuss the most significant recent research in this field as well as future directions.</P><p align="right"><a href="http://dx.doi.org/10.1002/asia.201300347">Read Full Text</a></p>]]>
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</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201300347">
<title>Artificial Metalloenzymes Constructed From Hierarchically-Assembled Proteins</title>
<link>http://dx.doi.org/10.1002/asia.201300347</link>
<dc:creator>Takafumi Ueno, Hiroyasu Tabe, Yuya Tanaka</dc:creator>
<dc:date>2013-05-22T14:38+05:00</dc:date>
<taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300347.gif" width="216" height="82" alt="Artificial Metalloenzymes Constructed From Hierarchically-Assembled Proteins" title="Artificial Metalloenzymes Constructed From Hierarchically-Assembled Proteins" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>I am still just a cat. in the cage</B>: The most significant recent research in the field of artificial metalloenzymes is reviewed with a commentary on future directions. In particular, the review is focused on the potential of protein assemblies such as protein cages and crystals composed of assemblies of protein monomers in efforts to design unique catalytic metal complex systems or metal nanoparticles beyond finely tuned small artificial metalloproteins.</P><p> [Focus Review]<br />Takafumi Ueno, Hiroyasu Tabe, Yuya Tanaka<br /><i>Chem. Asian J.</i>, May 22, 2013, DOI: 10.1002/asia.201300347. <a href="http://dx.doi.org/10.1002/asia.201300347">Read article.</a></p> ]]>
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</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201300116">
<title>Double Functionalization of Carbon Nanotubes with Purine and Pyrimidine Derivatives</title>
<link>http://dx.doi.org/10.1002/asia.201300116</link>
<dc:creator>Prabhpreet Singh, Cécilia Ménard-Moyon, Alessia Battigelli, Francesca Maria Toma, Jesus Raya, Jitendra Kumar, Nagapradeep Nidamanuri, Sandeep Verma, Alberto Bianco</dc:creator>
<dc:date>2013-05-22T14:37+05:00</dc:date>
<taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300116.gif" width="215" height="176" alt="Double Functionalization of Carbon Nanotubes with Purine and Pyrimidine Derivatives" title="Double Functionalization of Carbon Nanotubes with Purine and Pyrimidine Derivatives" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>On the double</B>: The covalent double functionalization of single-walled carbon nanotubes (SWCNTs) with a combination of purine&ndash;pyrimidine and purine&ndash;purine nucleobase systems was achieved through 1,3-dipolar cycloaddition and by amidation of the carboxylic acids at the tips and defect sites of the nanotubes, which could find application in the development of DNA/CNT nanobioconjugates.</P><p> [Full Paper]<br />Prabhpreet Singh, C&#xE9;cilia M&#xE9;nard-Moyon, Alessia Battigelli, Francesca Maria Toma, Jesus Raya, Jitendra Kumar, Nagapradeep Nidamanuri, Sandeep Verma, Alberto Bianco<br /><i>Chem. Asian J.</i>, May 22, 2013, DOI: 10.1002/asia.201300116. <a href="http://dx.doi.org/10.1002/asia.201300116">Read article.</a></p> ]]>
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</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201300380">
<title>Asymmetric Transfer Hydrogenation of 3-Nitroquinolines: Facile Access to Cyclic Nitro Compounds with Two Contiguous Stereocenters</title>
<link>http://dx.doi.org/10.1002/asia.201300380</link>
<dc:creator>Xian-Feng Cai, Mu-Wang Chen, Zhi-Shi Ye, Ran-Ning Guo, Lei Shi, Yan-Qin Li, Yong-Gui Zhou</dc:creator>
<dc:date>2013-05-17T11:40+05:00</dc:date>
<taxo:topics>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300380.gif" width="369" height="92" alt="Asymmetric Transfer Hydrogenation of 3-Nitroquinolines: Facile Access to Cyclic Nitro Compounds with Two Contiguous Stereocenters" title="Asymmetric Transfer Hydrogenation of 3-Nitroquinolines: Facile Access to Cyclic Nitro Compounds with Two Contiguous Stereocenters" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Hi, neighbor!</B> The first organocatalyzed asymmetric transfer hydrogenation of aromatic nitro compounds was successfully developed with up to 99&nbsp;% <I>ee</I>. The new methodology provides a direct and facile access to enantiopure cyclic nitro compounds with two contiguous stereocenters.</P><p> [Communication]<br />Xian-Feng Cai, Mu-Wang Chen, Zhi-Shi Ye, Ran-Ning Guo, Lei Shi, Yan-Qin Li, Yong-Gui Zhou<br /><i>Chem. Asian J.</i>, May 17, 2013, DOI: 10.1002/asia.201300380. <a href="http://dx.doi.org/10.1002/asia.201300380">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300131">
<title>Site-Selective Functionalization of Periodic Mesoporous Organosilica (PMO) with Macrocyclic Host for Specific and Reversible Recognition of Heavy Metal</title>
<link>http://dx.doi.org/10.1002/asia.201300131</link>
<dc:creator>Gang Ye, Yuxiao Leng, Feifei Bai, Jichao Wei, Jianchen Wang, Jing Chen</dc:creator>
<dc:date>2013-05-17T11:39+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300131.gif" width="215" height="150" alt="Site-Selective Functionalization of Periodic Mesoporous Organosilica (PMO) with Macrocyclic Host for Specific and Reversible Recognition of Heavy Metal" title="Site-Selective Functionalization of Periodic Mesoporous Organosilica (PMO) with Macrocyclic Host for Specific and Reversible Recognition of Heavy Metal" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Playing the host</B>: A novel class of macrocyclic-host-functionalized periodic mesoporous organosilica (PMO) materials with excellent and reversible recognition of Pb<SUP>II</SUP> was developed and upgraded by a site-selective post-modification method (see figure).</P><p> [Full Paper]<br />Gang Ye, Yuxiao Leng, Feifei Bai, Jichao Wei, Jianchen Wang, Jing Chen<br /><i>Chem. Asian J.</i>, May 17, 2013, DOI: 10.1002/asia.201300131. <a href="http://dx.doi.org/10.1002/asia.201300131">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19180.en.html">
<title>Full Paper: Site-Selective Functionalization of Periodic Mesoporous Organosilica (PMO) with Macrocyclic Host for Specific and Reversible Recognition of Heavy Metal</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19180.en.html</link>
<dc:date>2013-05-17T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/asia_2013_201300131.png" alt="Full Paper: Site-Selective Functionalization of Periodic Mesoporous Organosilica (PMO) with Macrocyclic Host for Specific and Reversible Recognition of Heavy Metal" align="left" hspace="5" vspace="5" border="0" /></p><i>Gang Ye, Yuxiao Leng, Feifei Bai, Jichao Wei, Jianchen Wang, Jing Chen</i></p><p>doi: 10.1002/asia.201300131</p><P>A novel kind of macrocyclic-host-functionalized periodic mesoporous organosilica (PMO) with excellent and reversible recognition of Pb<SUP>II</SUP> was developed. The macrocyclic host molecule <I>cis</I>-dicyclohexano[18]crown-6, with strong affinity to Pb<SUP>II</SUP>, was carefully modified as a bridged precursor to build the PMO material. To break down the limit of the functionalization degree for PMOs incorporated with large-sized moieties, a site-selective post-functionalization method was proposed to further decorate the external surface of the PMO material. The selective recognition ability of the upgraded PMO material towards Pb<SUP>II</SUP> was remarkably enhanced without destroying the mesoporous ordering. Solid-state <SUP>13</SUP>C and <SUP>29</SUP>Si&#xA0;NMR spectroscopy, X-ray photoelectron spectroscopy (XPS), XRD, TEM, and nitrogen adsorption&#x2013;desorption isotherm measurements were utilized for a full characterization of the structure, micromorphology, and surface properties. Reversible binding of Pb<SUP>II</SUP> was realized in the binding&#x2013;elution cycle experiments. The mechanism of the supramolecular interaction between the macrocyclic host and metal ion was discussed. The synthetic strategy can be considered a general way to optimize the properties of PMOs as binding materials for practical use while preserving the mesostructure.</P><p align="right"><a href="http://dx.doi.org/10.1002/asia.201300131">Read Full Text</a></p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300047">
<title>Low-Background, Highly Sensitive DNA Biosensor by Using an Electrically Neutral Cobalt(II) Complex as the Redox Hybridization Indicator</title>
<link>http://dx.doi.org/10.1002/asia.201300047</link>
<dc:creator>Qingxiang Wang, Yingtao Ding, Liheng Wang, Jiancong Ni, Zhanglong Yu, Haibin Lin, Feng Gao</dc:creator>
<dc:date>2013-05-16T14:38+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300047.gif" width="389" height="83" alt="Low-Background, Highly Sensitive DNA Biosensor by Using an Electrically Neutral Cobalt(II) Complex as the Redox Hybridization Indicator" title="Low-Background, Highly Sensitive DNA Biosensor by Using an Electrically Neutral Cobalt(II) Complex as the Redox Hybridization Indicator" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Die another DNA</B>: An electrically neutral cobalt complex, [Co(GA)<sub>2</sub>(phen)] (GA=glycollic acid, phen=1,10-phenathroline), could intercalate into the DNA duplex through the planar phen ligand with a binding constant of 6.2(&plusmn;0.2)&times;10<SUP>5</SUP>&nbsp;<span style="font-variant:small-caps">M</span><SUP>&minus;1</SUP>.</P><p> [Full Paper]<br />Qingxiang Wang, Yingtao Ding, Liheng Wang, Jiancong Ni, Zhanglong Yu, Haibin Lin, Feng Gao<br /><i>Chem. Asian J.</i>, May 16, 2013, DOI: 10.1002/asia.201300047. <a href="http://dx.doi.org/10.1002/asia.201300047">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300352">
<title>One-Pot, Template-Free Synthesis of Pd-Pt Single-Crystalline Hollow Cubes with Enhanced Catalytic Activity</title>
<link>http://dx.doi.org/10.1002/asia.201300352</link>
<dc:creator>Long Sun, Zhicheng Zhang, Biao Xu, Xun Wang</dc:creator>
<dc:date>2013-05-15T17:19+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300352.gif" width="188" height="194" alt="One-Pot, Template-Free Synthesis of Pd-Pt Single-Crystalline Hollow Cubes with Enhanced Catalytic Activity" title="One-Pot, Template-Free Synthesis of Pd-Pt Single-Crystalline Hollow Cubes with Enhanced Catalytic Activity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Crystal clear</B>: Pd-Pt single-crystalline hollow cubes with enhanced catalytic activities have been obtained by using a one-pot template-free method with inorganic salts, such as PdCl<sub>2</sub> and H<sub>2</sub>PtCl<sub>6</sub><B>&middot;</B>6&nbsp;H<sub>2</sub>O, as precursors.</P><p> [Full Paper]<br />Long Sun, Zhicheng Zhang, Biao Xu, Xun Wang<br /><i>Chem. Asian J.</i>, May 15, 2013, DOI: 10.1002/asia.201300352. <a href="http://dx.doi.org/10.1002/asia.201300352">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300267">
<title>DDQ-Induced Dehydrogenation of Heterocycles for C-C Double Bond Formation: Synthesis of 2-Thiazoles and 2-Oxazoles</title>
<link>http://dx.doi.org/10.1002/asia.201300267</link>
<dc:creator>Xiangnan Li, Cheng Li, Bing Yin, Cong Li, Ping Liu, Jianli Li, Zhen Shi</dc:creator>
<dc:date>2013-05-15T17:03+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300267.gif" width="214" height="115" alt="DDQ-Induced Dehydrogenation of Heterocycles for C-C Double Bond Formation: Synthesis of 2-Thiazoles and 2-Oxazoles" title="DDQ-Induced Dehydrogenation of Heterocycles for C-C Double Bond Formation: Synthesis of 2-Thiazoles and 2-Oxazoles" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Strong as an Ox:</B> 2-Thiazoles and 2-oxazoles are formed by oxidation of 2-thiazolines and 2-oxazolines without requiring substituents at the C4 and C5 positions. DDQ plays an important role as the oxidant in this transformation and metal is unnecessary. This general procedure shows good functional group tolerance and provides a wide variety of 2-thiazoles and 2-oxazoles in moderate to excellent yields.</P><p> [Communication]<br />Xiangnan Li, Cheng Li, Bing Yin, Cong Li, Ping Liu, Jianli Li, Zhen Shi<br /><i>Chem. Asian J.</i>, May 15, 2013, DOI: 10.1002/asia.201300267. <a href="http://dx.doi.org/10.1002/asia.201300267">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300311">
<title>Widely Applicable Synthesis of Enantiomerically Pure Tertiary Alkyl-Containing 1-Alkanols by Zirconium-Catalyzed Asymmetric Carboalumination of Alkenes and Palladium- or Copper-Catalyzed Cross-Coupling</title>
<link>http://dx.doi.org/10.1002/asia.201300311</link>
<dc:creator>Shiqing Xu, Ching-Tien Lee, Guangwei Wang, Ei-ichi Negishi</dc:creator>
<dc:date>2013-05-13T16:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300311.gif" width="350" height="100" alt="Widely Applicable Synthesis of Enantiomerically Pure Tertiary Alkyl-Containing 1-Alkanols by Zirconium-Catalyzed Asymmetric Carboalumination of Alkenes and Palladium- or Copper-Catalyzed Cross-Coupling" title="Widely Applicable Synthesis of Enantiomerically Pure Tertiary Alkyl-Containing 1-Alkanols by Zirconium-Catalyzed Asymmetric Carboalumination of Alkenes and Palladium- or Copper-Catalyzed Cross-Coupling" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Look, mom, one hand!</B> 2-Alkyl-1-alkanols of feeble chirality have been synthesized by a sequence of zirconium-catalyzed asymmetric carboalumination of alkenes (ZACA), lipase-catalyzed acetylation, and Pd- or Cu-catalyzed cross-coupling in high enantiomeric purity of &ge;99&nbsp;% <I>ee</I>. The synthetic utility of this method has been demonstrated in highly enantioselective and efficient syntheses of (<I>R</I>)-2-methyl-1-butanol, (<I>R</I>)- and (<I>S</I>)-arundic acids.</P><p> [Full Paper]<br />Shiqing Xu, Ching-Tien Lee, Guangwei Wang, Ei-ichi Negishi<br /><i>Chem. Asian J.</i>, May 13, 2013, DOI: 10.1002/asia.201300311. <a href="http://dx.doi.org/10.1002/asia.201300311">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300365">
<title>Seed-Assisted, One-Pot Synthesis of Hollow Zeolite Beta without Using Organic Structure-Directing Agents</title>
<link>http://dx.doi.org/10.1002/asia.201300365</link>
<dc:creator>Kenta Iyoki, Keiji Itabashi, Tatsuya Okubo</dc:creator>
<dc:date>2013-05-13T16:29+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300365.gif" width="214" height="170" alt="Seed-Assisted, One-Pot Synthesis of Hollow Zeolite Beta without Using Organic Structure-Directing Agents" title="Seed-Assisted, One-Pot Synthesis of Hollow Zeolite Beta without Using Organic Structure-Directing Agents" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Nobody does it beta</B>: Hollow aluminosilicate zeolite beta was successfully synthesized by adding CIT-6, that is, zincosilicate zeolite, which has the same topology as beta, as seeds to the Na-aluminosilicate gel without any organic structure-directing agents. It was estimated that the intra-crystalline voids were formed by the dissolution of the seed crystals just after the crystal growth of new beta on the outer surface of the seeds.</P><p> [Full Paper]<br />Kenta Iyoki, Keiji Itabashi, Tatsuya Okubo<br /><i>Chem. Asian J.</i>, May 13, 2013, DOI: 10.1002/asia.201300365. <a href="http://dx.doi.org/10.1002/asia.201300365">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300362">
<title>Stereocontrolled Total Synthesis of Polygalolide&#160;A</title>
<link>http://dx.doi.org/10.1002/asia.201300362</link>
<dc:creator>Hitomi Yamada, Masaatsu Adachi, Minoru Isobe, Toshio Nishikawa</dc:creator>
<dc:date>2013-05-13T16:29+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300362.gif" width="444" height="118" alt="Stereocontrolled Total Synthesis of Polygalolide&nbsp;A" title="Stereocontrolled Total Synthesis of Polygalolide&nbsp;A" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Grade A synthesis</B>: The total synthesis of polygalolide A was accomplished through an intramolecular Ferrier-type C-glycosylation of a glucal modified with siloxyfuran as a key step, leading to the desired oxabicyclo[3.2.1]octene with the correct quaternary stereogenic centers. The siloxy group at the C-3 position played a crucial role in the stereocontrol.</P><p> [Full Paper]<br />Hitomi Yamada, Masaatsu Adachi, Minoru Isobe, Toshio Nishikawa<br /><i>Chem. Asian J.</i>, May 13, 2013, DOI: 10.1002/asia.201300362. <a href="http://dx.doi.org/10.1002/asia.201300362">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300222">
<title>Oligonorbornenes with Hammock-Like Crown Ether Pendants as Artificial Transmembrane Ion Channel</title>
<link>http://dx.doi.org/10.1002/asia.201300222</link>
<dc:creator>Nai-Ti Lin, Chen-Yu Xie, Shou-Ling Huang, Chung-Hsuan Chen, Tien-Yau Luh</dc:creator>
<dc:date>2013-05-13T16:29+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300222.gif" width="151" height="204" alt="Oligonorbornenes with Hammock-Like Crown Ether Pendants as Artificial Transmembrane Ion Channel" title="Oligonorbornenes with Hammock-Like Crown Ether Pendants as Artificial Transmembrane Ion Channel" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Let&#x27;s change the channel</B>: Trimeric oligonorbornenes with hammock-like crown ether pendants are impregnated in egg yolk phosphatidylcholine (EYPC) liposome as artificial sodium ion channels. The presence of a polar hydroxy end group results in a high ion channel efficiency. The orientation of the crown ether moieties in these oligomers may be critical for the ion channel properties.</P><p> [Full Paper]<br />Nai-Ti Lin, Chen-Yu Xie, Shou-Ling Huang, Chung-Hsuan Chen, Tien-Yau Luh<br /><i>Chem. Asian J.</i>, May 13, 2013, DOI: 10.1002/asia.201300222. <a href="http://dx.doi.org/10.1002/asia.201300222">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300089">
<title>Electric Double-Layer Capacitor Based on an Ionic Clathrate Hydrate</title>
<link>http://dx.doi.org/10.1002/asia.201300089</link>
<dc:creator>Wonhee Lee, Minchul Kwon, Seongmin Park, Dongwook Lim, Jong-Ho Cha, Huen Lee</dc:creator>
<dc:date>2013-05-13T16:29+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300089.gif" width="184" height="94" alt="Electric Double-Layer Capacitor Based on an Ionic Clathrate Hydrate" title="Electric Double-Layer Capacitor Based on an Ionic Clathrate Hydrate" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Double trouble</B>: A new approach to an electric double-layer capacitor (EDLC) is suggested, which is based on proton-conducting ionic clathrate hydrate (ICH) Me<sub>4</sub>NOH<B>&middot;</B>5&nbsp;H<sub>2</sub>O. The carbon materials in the ICH show high specific capacitance, reversible charge&ndash;discharge behavior, and a long cycle life. These ICHs are expected to find practical applications in versatile energy devices that incorporate electrochemical systems.</P><p> [Full Paper]<br />Wonhee Lee, Minchul Kwon, Seongmin Park, Dongwook Lim, Jong-Ho Cha, Huen Lee<br /><i>Chem. Asian J.</i>, May 13, 2013, DOI: 10.1002/asia.201300089. <a href="http://dx.doi.org/10.1002/asia.201300089">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300341">
<title>Rhodium(III)-Catalyzed Synthesis of Cyclopenta[&lt;I&gt;b&lt;/I&gt;]pyrroles from 1,2-Diketones, 2-Aminopyridine, and Alkynes</title>
<link>http://dx.doi.org/10.1002/asia.201300341</link>
<dc:creator>Juanjuan Du, Bing Zhou, Yaxi Yang, Yuanchao Li</dc:creator>
<dc:date>2013-05-10T16:10+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300341.gif" width="366" height="118" alt="Rhodium(III)-Catalyzed Synthesis of Cyclopenta[b]pyrroles from 1,2-Diketones, 2-Aminopyridine, and Alkynes" title="Rhodium(III)-Catalyzed Synthesis of Cyclopenta[b]pyrroles from 1,2-Diketones, 2-Aminopyridine, and Alkynes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Pyrrole victory</B>: Cyclopenta[<I>b</I>]pyrroles have been synthesized by the rhodium(III)-catalyzed oxidative annulative coupling of 1,2-diketones, 2-aminopyridine, and alkynes. This transformation can also be carried out in a one-pot sequence, thereby providing a quick and straightforward access to synthetically and pharmaceutically important cyclopenta[<I>b</I>]pyrroles.</P><p> [Communication]<br />Juanjuan Du, Bing Zhou, Yaxi Yang, Yuanchao Li<br /><i>Chem. Asian J.</i>, May 10, 2013, DOI: 10.1002/asia.201300341. <a href="http://dx.doi.org/10.1002/asia.201300341">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300250">
<title>Two Lanthanide(III)-Copper(II) Organic Frameworks Based on {OLn&lt;sub&gt;6&lt;/sub&gt;} Clusters that Exhibited a Large Magnetocaloric Effect and Slow Relaxation of the Magnetization</title>
<link>http://dx.doi.org/10.1002/asia.201300250</link>
<dc:creator>Yanmin Bing, Na Xu, Wei Shi, Ke Liu, Peng Cheng</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/asia201300250.gif" width="203" height="224" alt="Two Lanthanide(III)-Copper(II) Organic Frameworks Based on {OLn6} Clusters that Exhibited a Large Magnetocaloric Effect and Slow Relaxation of the Magnetization" title="Two Lanthanide(III)-Copper(II) Organic Frameworks Based on {OLn6} Clusters that Exhibited a Large Magnetocaloric Effect and Slow Relaxation of the Magnetization" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Penny Ln</B>: Two lanthanide(III)-copper(II) organic frameworks based on {OLn<sub>6</sub>} clusters were synthesized. Isotropic <B>Gd-Cu</B> showed a large magnetocaloric effect while anisotropic <B>Dy-Cu</B> exhibited slow relaxation of the magnetization at low temperatures.</P><p> [Full Paper]<br />Yanmin Bing, Na Xu, Wei Shi, Ke Liu, Peng Cheng<br /><i>Chem. Asian J.</i>, May 09, 2013, DOI: 10.1002/asia.201300250. <a href="http://dx.doi.org/10.1002/asia.201300250">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300329">
<title>Osmium(III) and Osmium(V) Complexes Bearing a Macrocyclic Ligand: A Simple and Efficient Catalytic System for &lt;I&gt;cis&lt;/I&gt;-Dihydroxylation of Alkenes with Hydrogen Peroxide</title>
<link>http://dx.doi.org/10.1002/asia.201300329</link>
<dc:creator>Hideki Sugimoto, Kenji Ashikari, Shinobu Itoh</dc:creator>
<dc:date>2013-05-07T19:26+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300329.gif" width="237" height="173" alt="Osmium(III) and Osmium(V) Complexes Bearing a Macrocyclic Ligand: A Simple and Efficient Catalytic System for cis-Dihydroxylation of Alkenes with Hydrogen Peroxide" title="Osmium(III) and Osmium(V) Complexes Bearing a Macrocyclic Ligand: A Simple and Efficient Catalytic System for cis-Dihydroxylation of Alkenes with Hydrogen Peroxide" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>The wizard of Os</B>: A simple protocol that uses [Os<SUP>III</SUP>(OH)(H<sub>2</sub>O)(<span style="font-variant:small-caps">L</span>-N<sub>4</sub>Me<sub>2</sub>)](PF<sub>6</sub>)<sub>2</sub> (<B>1</B>) and H<sub>2</sub>O<sub>2</sub> for efficient <I>cis</I>-1,2-dihydroxylation of alkenes is presented. Unfunctionalized (or aliphatic) alkenes and alkenes/styrenes containing electron-withdrawing groups were converted into the corresponding vicinal diols in good to excellent yields.It has been confirmed that the Os<SUP>V</SUP>(O)(OH) species (<B>2</B>) is the active oxidant, which is formed via the hydroperoxide adduct A.</P><p> [Full Paper]<br />Hideki Sugimoto, Kenji Ashikari, Shinobu Itoh<br /><i>Chem. Asian J.</i>, May 07, 2013, DOI: 10.1002/asia.201300329. <a href="http://dx.doi.org/10.1002/asia.201300329">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300337">
<title>Synergistic Effect of SnO&lt;sub&gt;2&lt;/sub&gt;/ZnWO&lt;sub&gt;4&lt;/sub&gt; Core–Shell Nanorods with High Reversible Lithium Storage Capacity</title>
<link>http://dx.doi.org/10.1002/asia.201300337</link>
<dc:creator>Li-Li Xing, Shuang Yuan, Bin He, Ya-Yu Zhao, Xiao-Ling Wu, Xin-Yu Xue</dc:creator>
<dc:date>2013-05-07T19:24+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300337.gif" width="216" height="142" alt="Synergistic Effect of SnO2/ZnWO4 Core&ndash;Shell Nanorods with High Reversible Lithium Storage Capacity" title="Synergistic Effect of SnO2/ZnWO4 Core&ndash;Shell Nanorods with High Reversible Lithium Storage Capacity" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Team work:</B> The synergistic effect in novel SnO<sub>2</sub>/ZnWO<sub>4</sub> core&ndash;shell nanorods leads to their high reversible lithium storage capacity. At C/20 (20&nbsp;h per half cycle) rate, the reversible capacity of SnO<sub>2</sub>/ZnWO<sub>4</sub> core&ndash;shell nanorods is up to ~1000&nbsp;mAh&nbsp;g<SUP>&minus;1</SUP>.</P><p> [Full Paper]<br />Li-Li Xing, Shuang Yuan, Bin He, Ya-Yu Zhao, Xiao-Ling Wu, Xin-Yu Xue<br /><i>Chem. Asian J.</i>, May 07, 2013, DOI: 10.1002/asia.201300337. <a href="http://dx.doi.org/10.1002/asia.201300337">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300279">
<title>Rational Design of Anode Materials Based on Group&#160;IVA Elements (Si, Ge, and Sn) for Lithium-Ion Batteries</title>
<link>http://dx.doi.org/10.1002/asia.201300279</link>
<dc:creator>Xing-Long Wu, Yu-Guo Guo, Li-Jun Wan</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/asia201300279.gif" width="214" height="137" alt="Rational Design of Anode Materials Based on Group&nbsp;IVA Elements (Si, Ge, and Sn) for Lithium-Ion Batteries" title="Rational Design of Anode Materials Based on Group&nbsp;IVA Elements (Si, Ge, and Sn) for Lithium-Ion Batteries" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Group therapy</B>: This Focus Review summarizes the rational designs that have been proposed for effectively addressing the challenges of anode materials based on Group&nbsp;IVA (Si, Ge, and Sn) elements for high-energy lithium-ion batteries (LIBs), which include nanostructures with a sufficient number of voids, &ldquo;plum-pudding&rdquo; nanohybrids, and nanohybrids with efficient and permanent transport pathways for electrons and stable surface coatings.</P><p> [Focus Review]<br />Xing-Long Wu, Yu-Guo Guo, Li-Jun Wan<br /><i>Chem. Asian J.</i>, May 06, 2013, DOI: 10.1002/asia.201300279. <a href="http://dx.doi.org/10.1002/asia.201300279">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300132">
<title>Chain Folding Controlled by an Isomeric Repeat Unit: Helix Formation versus Random Aggregation in Acetylene-Bridged Carbazole–Bipyridine Co-Oligomers</title>
<link>http://dx.doi.org/10.1002/asia.201300132</link>
<dc:creator>Kizhmuri P. Divya, Sivaramapanicker Sreejith, Cherumuttathu H. Suresh, Divya S. Philips, Ayyappanpillai Ajayaghosh</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/asia201300132.gif" width="215" height="100" alt="Chain Folding Controlled by an Isomeric Repeat Unit: Helix Formation versus Random Aggregation in Acetylene-Bridged Carbazole&ndash;Bipyridine Co-Oligomers" title="Chain Folding Controlled by an Isomeric Repeat Unit: Helix Formation versus Random Aggregation in Acetylene-Bridged Carbazole&ndash;Bipyridine Co-Oligomers" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Stick, twist, or fold?</B> The acetylinic linkage in two isomeric oligomers controls the conformation of the bipyridyl moiety. Although both oligomers have potentially foldable structures, only oligomer <B>1</B> adopts a folded conformation in polar solvents.</P><p> [Full Paper]<br />Kizhmuri P. Divya, Sivaramapanicker Sreejith, Cherumuttathu H. Suresh, Divya S. Philips, Ayyappanpillai Ajayaghosh<br /><i>Chem. Asian J.</i>, May 06, 2013, DOI: 10.1002/asia.201300132. <a href="http://dx.doi.org/10.1002/asia.201300132">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300244">
<title>Oligothiophene-Bridged Bis(arylene ethynylene) Small Molecules for Solution-Processible Organic Solar Cells with High Open-Circuit Voltage</title>
<link>http://dx.doi.org/10.1002/asia.201300244</link>
<dc:creator>Qian Liu, Hongmei Zhan, Cheuk-Lam Ho, Feng-Rong Dai, Yingying Fu, Zhiyuan Xie, Lixiang Wang, Jin-Hua Li, Feng Yan, Shu-Ping Huang, Wai-Yeung Wong</dc:creator>
<dc:date>2013-05-06T12:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300244.gif" width="331" height="149" alt="Oligothiophene-Bridged Bis(arylene ethynylene) Small Molecules for Solution-Processible Organic Solar Cells with High Open-Circuit Voltage" title="Oligothiophene-Bridged Bis(arylene ethynylene) Small Molecules for Solution-Processible Organic Solar Cells with High Open-Circuit Voltage" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Building bridges</B>: New oligothiophene-bridged bis(arylene ethynylene) small molecules (see picture) are developed and applied in solution-processed organic solar cells. All of these photovoltaic devices showed very high open-circuit voltage of over 0.90&nbsp;V, and the best power conversion efficiency achieved was 3.68&nbsp;%.</P><p> [Full Paper]<br />Qian Liu, Hongmei Zhan, Cheuk-Lam Ho, Feng-Rong Dai, Yingying Fu, Zhiyuan Xie, Lixiang Wang, Jin-Hua Li, Feng Yan, Shu-Ping Huang, Wai-Yeung Wong<br /><i>Chem. Asian J.</i>, May 06, 2013, DOI: 10.1002/asia.201300244. <a href="http://dx.doi.org/10.1002/asia.201300244">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19140.en.html">
<title>Focus Review: Rational Design of Anode Materials Based on Group&#160;IVA Elements (Si, Ge, and Sn) for Lithium-Ion Batteries</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19140.en.html</link>
<dc:date>2013-05-06T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/asia_2013_201300279.png" alt="Focus Review: Rational Design of Anode Materials Based on Group&#xA0;IVA Elements (Si, Ge, and Sn) for Lithium-Ion Batteries" align="left" hspace="5" vspace="5" border="0" /></p><i>Xing-Long Wu, Yu-Guo Guo, Li-Jun Wan</i></p><p>doi: 10.1002/asia.201300279</p><P>Lithium-ion batteries (LIBs) represent the state-of-the-art technology in rechargeable energy-storage devices and they currently occupy the prime position in the marketplace for powering an increasingly diverse range of applications. However, the fast development of these applications has led to increasing demands being placed on advanced LIBs in terms of higher energy/power densities and longer life cycles. For LIBs to meet these requirements, researchers have focused on active electrode materials, owing to their crucial roles in the electrochemical performance of batteries. For anode materials, compounds based on Group&#xA0;IVA (Si, Ge, and Sn) elements represent one of the directions in the development of high-capacity anodes. Although these compounds have many significant advantages when used as anode materials for LIBs, there are still some critical problems to be solved before they can meet the high requirements for practical applications. In this Focus Review, we summarize a series of rational designs for Group&#xA0;IVA-based anode materials, in terms of their chemical compositions and structures, that could address these problems, that is, huge volume variations during cycling, unstable surfaces/interfaces, and invalidation of transport pathways for electrons upon cycling. These designs should at least include one of the following structural benefits: 1)&#xA0;Contain a sufficient number of voids to accommodate the volume variations during cycling; 2)&#xA0;adopt a &#x201C;plum-pudding&#x201D;-like structure to limit the volume variations during cycling; 3)&#xA0;facilitate an efficient and permanent transport pathway for electrons and lithium ions; or 4)&#xA0;show stable surfaces/interfaces to stabilize the in&#xA0;situ formed SEI layers.</P><p align="right"><a href="http://dx.doi.org/10.1002/asia.201300279">Read Full Text</a></p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300332">
<title>Concise Enantioselective Synthesis of Cephalosporolide&#160;B, (4&lt;I&gt;R&lt;/I&gt;)-4-OMe-Cephalosporolide&#160;C, and (4&lt;I&gt;S&lt;/I&gt;)-4-OMe-Cephalosporolide&#160;C</title>
<link>http://dx.doi.org/10.1002/asia.201300332</link>
<dc:creator>Bin Ma, Zhuliang Zhong, Haitao Hu, Huilin Li, Changgui Zhao, Xingang Xie, Xuegong She</dc:creator>
<dc:date>2013-05-03T16:02+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300332.gif" width="264" height="124" alt="Concise Enantioselective Synthesis of Cephalosporolide&nbsp;B, (4R)-4-OMe-Cephalosporolide&nbsp;C, and (4S)-4-OMe-Cephalosporolide&nbsp;C" title="Concise Enantioselective Synthesis of Cephalosporolide&nbsp;B, (4R)-4-OMe-Cephalosporolide&nbsp;C, and (4S)-4-OMe-Cephalosporolide&nbsp;C" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Ring around the rosie</B>: The effective enantioselective synthesis of the antimalarial nonenolide title compounds was achieved in a convergent strategy. Oxy-Michael addition reaction was used to introduce the chiral methoxy group at C-4, and ring-closing metathesis (RCM) reaction (53&nbsp;% yield) facilitated the key construction of the 10-membered ring.</P><p> [Communication]<br />Bin Ma, Zhuliang Zhong, Haitao Hu, Huilin Li, Changgui Zhao, Xingang Xie, Xuegong She<br /><i>Chem. Asian J.</i>, May 03, 2013, DOI: 10.1002/asia.201300332. <a href="http://dx.doi.org/10.1002/asia.201300332">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300327">
<title>2,3-Di(2-pyridyl)-5-phenylpyrazine: A NN-CNN-Type Bridging Ligand for Dinuclear Transition-Metal Complexes</title>
<link>http://dx.doi.org/10.1002/asia.201300327</link>
<dc:creator>Si-Hai Wu, Yu-Wu Zhong, Jiannian Yao</dc:creator>
<dc:date>2013-05-02T18:27+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300327.gif" width="181" height="205" alt="2,3-Di(2-pyridyl)-5-phenylpyrazine: A NN-CNN-Type Bridging Ligand for Dinuclear Transition-Metal Complexes" title="2,3-Di(2-pyridyl)-5-phenylpyrazine: A NN-CNN-Type Bridging Ligand for Dinuclear Transition-Metal Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>NN-CNN breaking news</B>: 2,3-Di(2-pyridyl)-5-phenylpyrazine, which is able to bind two metals through a NN-CNN-type coordination mode, has been designed and synthesized. A RuPt heterobimetallic complex with this bridging ligand shows near-infrared emission at 750&nbsp;nm, with a quantum yield of 0.41&nbsp;% and an excited-state lifetime of 170&nbsp;ns.</P><p> [Full Paper]<br />Si-Hai Wu, Yu-Wu Zhong, Jiannian Yao<br /><i>Chem. Asian J.</i>, May 02, 2013, DOI: 10.1002/asia.201300327. <a href="http://dx.doi.org/10.1002/asia.201300327">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300149">
<title>Polymer Brushes: Promises and Challenges</title>
<link>http://dx.doi.org/10.1002/asia.201300149</link>
<dc:creator>Basit Yameen, Aleeza Farrukh</dc:creator>
<dc:date>2013-05-02T18:26+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300149.gif" width="215" height="168" alt="Polymer Brushes: Promises and Challenges" title="Polymer Brushes: Promises and Challenges" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Bedknobs and broomsticks</B>: This Focus Review discusses the current status in the development of synthetic procedures, recently explored substrates, innovative applications, and the accompanying challenges of surface-grafted macromolecular assemblies.</P><p> [Focus Review]<br />Basit Yameen, Aleeza Farrukh<br /><i>Chem. Asian J.</i>, May 02, 2013, DOI: 10.1002/asia.201300149. <a href="http://dx.doi.org/10.1002/asia.201300149">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201201204">
<title>Synthesis and Characterization of Sulfated Gal-&lt;I&gt;β&lt;/I&gt;-1,3/4-GlcNAc Disaccharides through Consecutive Protection/Glycosylation Steps</title>
<link>http://dx.doi.org/10.1002/asia.201201204</link>
<dc:creator>Zhijay Tu, Hsiao-Wu Hsieh, Chih-Ming Tsai, Chia-Wei Hsu, Shy-Guey Wang, Kuan-Jung Wu, Kuo-I Lin, Chun-Hung Lin</dc:creator>
<dc:date>2013-05-02T18:26+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201201204.gif" width="423" height="83" alt="Synthesis and Characterization of Sulfated Gal-&beta;-1,3/4-GlcNAc Disaccharides through Consecutive Protection/Glycosylation Steps" title="Synthesis and Characterization of Sulfated Gal-&beta;-1,3/4-GlcNAc Disaccharides through Consecutive Protection/Glycosylation Steps" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>A spoonful of sugars</B>: An efficient and practical consecutive protection/glycosylation strategy afforded orthogonally protected disaccharides. Further deprotection and/or sulfation steps led to the formation of non- and mono-sulfated glycans.</P><p> [Full Paper]<br />Zhijay Tu, Hsiao-Wu Hsieh, Chih-Ming Tsai, Chia-Wei Hsu, Shy-Guey Wang, Kuan-Jung Wu, Kuo-I Lin, Chun-Hung Lin<br /><i>Chem. Asian J.</i>, May 02, 2013, DOI: 10.1002/asia.201201204. <a href="http://dx.doi.org/10.1002/asia.201201204">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300183">
<title>Differential Detection of Zn&lt;SUP&gt;2+&lt;/SUP&gt; and Cd&lt;SUP&gt;2+&lt;/SUP&gt; Ions by BODIPY-Based Fluorescent Sensors</title>
<link>http://dx.doi.org/10.1002/asia.201300183</link>
<dc:creator>Hui He, Dennis K. P. Ng</dc:creator>
<dc:date>2013-05-02T18:25+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300183.gif" width="362" height="123" alt="Differential Detection of Zn2+ and Cd2+ Ions by BODIPY-Based Fluorescent Sensors" title="Differential Detection of Zn2+ and Cd2+ Ions by BODIPY-Based Fluorescent Sensors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Plenty of ions in the fire</B>: Two monostyryl BODIPY derivatives have been prepared that can selectively detect Zn<SUP>2+</SUP> and Cd<SUP>2+</SUP> ions in MeCN or in aqueous medium.</P><p> [Full Paper]<br />Hui He, Dennis K. P. Ng<br /><i>Chem. Asian J.</i>, May 02, 2013, DOI: 10.1002/asia.201300183. <a href="http://dx.doi.org/10.1002/asia.201300183">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19126.en.html">
<title>Focus Review: Polymer Brushes: Promises and Challenges</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19126.en.html</link>
<dc:date>2013-05-02T00:00:00+02:00</dc:date>
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<![CDATA[<p><img src="http://www.wiley-vch.de/img/news/asia_2013_201300149.png" alt="Focus Review: Polymer Brushes: Promises and Challenges" align="left" hspace="5" vspace="5" border="0" /></p><i>Basit Yameen, Aleeza Farrukh</i></p><p>doi: 10.1002/asia.201300149</p><P>Surface-tethered polymers, or &#x201C;polymer brushes&#x201D;, are emerging as key elements in the context of regulating the surface characteristics of materials. Their properties, such as biocompatibility, antifouling, colloidal stability, wettability, and corrosion resistance, play a vital role in ascertaining their potential applications. The availability of straightforward procedures for polymer brush synthesis, which are applicable to a wide range of monomers and are adaptable to a range of substrates, is a clear advantage over other surface-modification strategies. Herein, the important advancements that are pertinent to the fabrication of polymer brushes are outlined. Furthermore, an exhaustive up-to-date overview of the developments in different application domains, including smart drug-delivery systems, biosensing, antifouling, stimuli-responsive surfaces, and ion-conducting membranes, that benefit from the developments in the field of polymer brushes, is presented.</P><p align="right"><a href="http://dx.doi.org/10.1002/asia.201300149">Read Full Text</a></p>]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300176">
<title>Colorless to Purple–Red Switching Electrochromic Anthraquinone Imides with Broad Visible/Near-IR Absorptions in the Radical Anion State: Simulation-Aided Molecular Design</title>
<link>http://dx.doi.org/10.1002/asia.201300176</link>
<dc:creator>Fengkun Chen, Jie Zhang, Hong Jiang, Xinhua Wan</dc:creator>
<dc:date>2013-04-29T16:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300176.gif" width="217" height="187" alt="Colorless to Purple&ndash;Red Switching Electrochromic Anthraquinone Imides with Broad Visible/Near-IR Absorptions in the Radical Anion State: Simulation-Aided Molecular Design" title="Colorless to Purple&ndash;Red Switching Electrochromic Anthraquinone Imides with Broad Visible/Near-IR Absorptions in the Radical Anion State: Simulation-Aided Molecular Design" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>All change!</B> The delocalization effect of electron-withdrawing substituents on anthraquinone imide (AQI) derivatives is enhanced in the radical anion state, which leads to the design and synthesis of a new AQI molecule (di-CN-AQI) substituted with a strongly electron-withdrawing dicyanovinyl substituent. Upon one-electron reduction, this compound reveals broad absorptions in the ranges of <I>&lambda;</I>=700&ndash;1000 and 1100&ndash;1800&nbsp;nm together with a colorless to purple&ndash;red transition.</P><p> [Full Paper]<br />Fengkun Chen, Jie Zhang, Hong Jiang, Xinhua Wan<br /><i>Chem. Asian J.</i>, Apr 29, 2013, DOI: 10.1002/asia.201300176. <a href="http://dx.doi.org/10.1002/asia.201300176">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300063">
<title>Synthesis and Characterization of 5-(1,2,4-Triazol-3-yl)tetrazoles with various energetic functionalities</title>
<link>http://dx.doi.org/10.1002/asia.201300063</link>
<dc:creator>Alexander A. Dippold, Thomas M. Klapötke</dc:creator>
<dc:date>2013-04-29T16:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300063.gif" width="289" height="78" alt="Synthesis and Characterization of 5-(1,2,4-Triazol-3-yl)tetrazoles with various energetic functionalities" title="Synthesis and Characterization of 5-(1,2,4-Triazol-3-yl)tetrazoles with various energetic functionalities" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Going full blast</B>: The synthesis and full structural as well as spectroscopic characterization of three 5-(triazol-3-yl) tetrazoles in combination with selected energetic moieties like nitro, nitrimino, and azido groups is presented. As expected, the properties strongly depend on the energetic moiety at the triazole ring. The connection via the C-C bond of a triazole ring with its opportunity to introduce a large variety of energetic moieties and a tetrazole ring leads to the selective synthesis of primary and secondary explosives.</P><p> [Full Paper]<br />Alexander A. Dippold, Thomas M. Klap&#xF6;tke<br /><i>Chem. Asian J.</i>, Apr 29, 2013, DOI: 10.1002/asia.201300063. <a href="http://dx.doi.org/10.1002/asia.201300063">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300143">
<title>Heterometallic Mixed-Valence Copper(I,II) Cyanides that were Tuned by Using the Chelate Effect: Discovery of Famous Cairo Pentagonal Tiling and Unprecedented (3,4)-Connected {8&lt;SUP&gt;3&lt;/SUP&gt;}&lt;sub&gt;2&lt;/sub&gt;{8&lt;SUP&gt;6&lt;/SUP&gt;} Topological 3D Net</title>
<link>http://dx.doi.org/10.1002/asia.201300143</link>
<dc:creator>Ying-Lian Qin, Ru-Xin Yao, Guo-Xing Wu, Min-Min Liu, Xian-Ming Zhang</dc:creator>
<dc:date>2013-04-26T14:58+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300143.gif" width="213" height="177" alt="Heterometallic Mixed-Valence Copper(I,II) Cyanides that were Tuned by Using the Chelate Effect: Discovery of Famous Cairo Pentagonal Tiling and Unprecedented (3,4)-Connected {83}2{86} Topological 3D Net" title="Heterometallic Mixed-Valence Copper(I,II) Cyanides that were Tuned by Using the Chelate Effect: Discovery of Famous Cairo Pentagonal Tiling and Unprecedented (3,4)-Connected {83}2{86} Topological 3D Net" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Back of the net</B>: Three heterometallic cyano-bridged mixed-valence Cu<SUP>I</SUP>/Cu<SUP>II</SUP> coordination networks show Macmahon-type (5,<SUP>3</SUP><sub>4</sub>) 2D Cairo tiling sheets or a two-fold-interpenetrated (3,4)-connected {8<SUP>3</SUP>}<sub>2</sub>{8<SUP>6</SUP>} 3D topological framework. Their structural difference is due to water molecules on the octahedrally coordinated Cu<SUP>II</SUP> atom, which are gradually replaced by 1,2-propane diamine chelate groups.</P><p> [Full Paper]<br />Ying-Lian Qin, Ru-Xin Yao, Guo-Xing Wu, Min-Min Liu, Xian-Ming Zhang<br /><i>Chem. Asian J.</i>, Apr 26, 2013, DOI: 10.1002/asia.201300143. <a href="http://dx.doi.org/10.1002/asia.201300143">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201201162">
<title>Solid-State Form Screen of Cardiosulfa and Its Analogues</title>
<link>http://dx.doi.org/10.1002/asia.201201162</link>
<dc:creator>S. Sudalai Kumar, Soumendra Rana, Ashwini Nangia</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/asia201201162.gif" width="215" height="180" alt="Solid-State Form Screen of Cardiosulfa and Its Analogues" title="Solid-State Form Screen of Cardiosulfa and Its Analogues" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>A twist to solubility</B>: A solid form screen of aryl hydrocarbon receptor (AhR) modulator molecule cardiosulfa <B>1</B> and its analogues <B>2</B>&ndash;<B>6</B> showed that cardiosulfa exists in only one crystalline form, whereas <B>2</B>&ndash;<B>5</B> are polymorphic. The more soluble compounds <B>2</B> and <B>5</B> adopt twisted conformations in the crystal structure (see figure), unlike a near-planar conformation of the less soluble <B>1</B>.</P><p> [Full Paper]<br />S. Sudalai Kumar, Soumendra Rana, Ashwini Nangia<br /><i>Chem. Asian J.</i>, Apr 24, 2013, DOI: 10.1002/asia.201201162. <a href="http://dx.doi.org/10.1002/asia.201201162">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300320">
<title>Gold&lt;SUP&gt;III&lt;/SUP&gt;–Iridium&lt;SUP&gt;III&lt;/SUP&gt; Hybrid Complexes of Hexaphyrin(1.1.1.1.1.1)</title>
<link>http://dx.doi.org/10.1002/asia.201300320</link>
<dc:creator>Koji Naoda, Hirotaka Mori, Atsuhiro Osuka</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/asia201300320.gif" width="161" height="190" alt="GoldIII&ndash;IridiumIII Hybrid Complexes of Hexaphyrin(1.1.1.1.1.1)" title="GoldIII&ndash;IridiumIII Hybrid Complexes of Hexaphyrin(1.1.1.1.1.1)" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Au revoIR</B>: Hexaphyrin Au<SUP>III</SUP>&ndash;Ir<SUP>III</SUP> complexes were prepared from the reaction of a mono-Au<SUP>III</SUP> [26]hexaphyrin complex with [IrCl(cod)]<sub>2</sub> followed by treatment with pyridine. <I>N</I>-Fusion reaction of this complex gave a syn-doubly <I>N</I>-fused hexaphyrin as the major product, which displayed antiaromatic properties such as strong paratropic ring current, a small HOMO&ndash;LUMO gap and a low-energy forbidden absorption. The oxidation of this fused product with MnO<sub>2</sub> afforded an oxidatively cleaved product.</P><p> [Communication]<br />Koji Naoda, Hirotaka Mori, Atsuhiro Osuka<br /><i>Chem. Asian J.</i>, Apr 24, 2013, DOI: 10.1002/asia.201300320. <a href="http://dx.doi.org/10.1002/asia.201300320">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300340">
<title>Synthesis of Allyl Allenes through Three-Component Cross-Coupling Reaction of &lt;I&gt;N-&lt;/I&gt;Tosylhydrazones, Terminal Alkynes, and Allyl Halides</title>
<link>http://dx.doi.org/10.1002/asia.201300340</link>
<dc:creator>Fei Ye, Mohammad Lokman Hossain, Yan Xu, Xiaoshen Ma, Qing Xiao, Yan Zhang, Jianbo Wang</dc:creator>
<dc:date>2013-04-24T08:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300340.gif" width="282" height="54" alt="Synthesis of Allyl Allenes through Three-Component Cross-Coupling Reaction of N-Tosylhydrazones, Terminal Alkynes, and Allyl Halides" title="Synthesis of Allyl Allenes through Three-Component Cross-Coupling Reaction of N-Tosylhydrazones, Terminal Alkynes, and Allyl Halides" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Three&rsquo;s a crowd</B>: Tri- and tetrasubstituted allyl allenes can be easily accessed by this Cu<SUP>I</SUP>-catalyzed three-component coupling reaction of <I>N</I>-tosylhydrazones, terminal alkynes, and allyl halides. The reaction proceeds through a mechanism involving copper carbene migratory insertion.</P><p> [Communication]<br />Fei Ye, Mohammad Lokman Hossain, Yan Xu, Xiaoshen Ma, Qing Xiao, Yan Zhang, Jianbo Wang<br /><i>Chem. Asian J.</i>, Apr 24, 2013, DOI: 10.1002/asia.201300340. <a href="http://dx.doi.org/10.1002/asia.201300340">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300026">
<title>One-Pot Solvothermal Synthesis of Highly Water-Dispersible Size-Tunable Functionalized Magnetite Nanocrystal Clusters for Lipase Immobilization</title>
<link>http://dx.doi.org/10.1002/asia.201300026</link>
<dc:creator>Hao Zhu, Chen Hou, Yijing Li, Guanghui Zhao, Xiao Liu, Ke Hou, Yanfeng Li</dc:creator>
<dc:date>2013-04-24T08:34+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300026.gif" width="206" height="197" alt="One-Pot Solvothermal Synthesis of Highly Water-Dispersible Size-Tunable Functionalized Magnetite Nanocrystal Clusters for Lipase Immobilization" title="One-Pot Solvothermal Synthesis of Highly Water-Dispersible Size-Tunable Functionalized Magnetite Nanocrystal Clusters for Lipase Immobilization" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>MNC Hammer:</B> A simple and facile one-pot synthesis of highly water-dispersible size-tunable Fe<sub>3</sub>O<sub>4</sub> nanocrystal clusters end-functionalized with amino or carboxyl groups by a modified solvothermal reduction process has been presented. The particle size could be tuned over a wide range from 175 to 500&nbsp;nm by varying the concentration of dopamine (DA) and 3,4-dihydroxyhydroxycinnamic acid (DHCA).</P><p> [Full Paper]<br />Hao Zhu, Chen Hou, Yijing Li, Guanghui Zhao, Xiao Liu, Ke Hou, Yanfeng Li<br /><i>Chem. Asian J.</i>, Apr 24, 2013, DOI: 10.1002/asia.201300026. <a href="http://dx.doi.org/10.1002/asia.201300026">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300260">
<title>Click To Bind: Metal Sensors</title>
<link>http://dx.doi.org/10.1002/asia.201300260</link>
<dc:creator>Jonathan J. Bryant, Uwe H. F. Bunz</dc:creator>
<dc:date>2013-04-24T08:33+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300260.gif" width="410" height="101" alt="Click To Bind: Metal Sensors" title="Click To Bind: Metal Sensors" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Ties that bind</B>: Triazole rings function as a metal-ion ligand or as part of a conjugated system. These properties, as well as the utility of the click reaction that is used to form them, have led to their inclusion in optical metal-ion sensors.</P><p> [Focus Review]<br />Jonathan J. Bryant, Uwe H. F. Bunz<br /><i>Chem. Asian J.</i>, Apr 24, 2013, DOI: 10.1002/asia.201300260. <a href="http://dx.doi.org/10.1002/asia.201300260">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19095.en.html">
<title>VIP: 2,3,17,18-Tetrahalohexaphyrins and the First Phlorin-Type Hexaphyrins</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19095.en.html</link>
<dc:date>2013-04-24T00:00:00+02:00</dc:date>
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<![CDATA[<p>Tomohiro Higashino and Atsuhiro Osuka*</p><p>Convenient preparations of 3,4-dichloropyrrole and 3,4-difluoropyrrole are reported. 2,3,17,18-Tetrahalohexaphyrins were synthesized and <i>meso</i>-reduced hexaphyrins were obtained by reduction of tetrabromo- and tetrachloro[28]hexaphyrin with NaBH<sub>4</sub> as the first example of phlorin-type hexaphyrin.<p>Coming soon.</p><!-- DOI: 10.1002/asia.201300474 -->]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19075.en.html">
<title>VIP: Synthesis, Characterization, and Properties of Few-Layer MoO3</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/19075.en.html</link>
<dc:date>2013-04-22T00:00:00+02:00</dc:date>
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<![CDATA[<p>M.B. Sreedhara, H.S.S. Ramakrishna Matte, A. Govindaraj, and C.N.R. Rao*</p><p>This study shows that graphene-like nanosheets of MoO<sub>3</sub> can be prepared by a variety of chemical methods besides ultrasonication. The prepared few-layer materials exhibit good photocatalytic activity for the degradation of dyes. Composites of MoO<sub>3</sub> nanosheets with a conducting borocarbonitride show excellent performance as supercapacitor electrodes.<p>Coming soon.</p><!-- DOI: 10.1002/asia.201300470 -->]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300208">
<title>Synthesis, Physical Properties, and Anion Recognition of Two Novel Larger Azaacenes: Benzannelated Hexazaheptacene and Benzannelated &lt;I&gt;N&lt;/I&gt;,&lt;I&gt;N&lt;/I&gt;'-Dihydrohexazaheptacene</title>
<link>http://dx.doi.org/10.1002/asia.201300208</link>
<dc:creator>Gang Li, Yuechao Wu, Junkuo Gao, Junbo Li, Yang Zhao, Qichun Zhang</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/asia201300208.gif" width="444" height="78" alt="Synthesis, Physical Properties, and Anion Recognition of Two Novel Larger Azaacenes: Benzannelated Hexazaheptacene and Benzannelated N,N&#x27;-Dihydrohexazaheptacene" title="Synthesis, Physical Properties, and Anion Recognition of Two Novel Larger Azaacenes: Benzannelated Hexazaheptacene and Benzannelated N,N&#x27;-Dihydrohexazaheptacene" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>At the drop of a HAT</B>: Two novel azaacenes with six or ten N atoms in their backbones, <B>HATBH (1)</B> and <B>DHATPH (2)</B>, have been successfully synthesized in two steps. Interestingly, <B>HATBH (1)</B> can act as efficient anion sensor for F<SUP>&minus;</SUP> and H<sub>2</sub>PO<sub>4</sub><SUP>&minus;</SUP>, while <B>DHATPH (2)</B> selectively responds to F<SUP>&minus;</SUP> (see figure).</P><p> [Full Paper]<br />Gang Li, Yuechao Wu, Junkuo Gao, Junbo Li, Yang Zhao, Qichun Zhang<br /><i>Chem. Asian J.</i>, Apr 19, 2013, DOI: 10.1002/asia.201300208. <a href="http://dx.doi.org/10.1002/asia.201300208">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300138">
<title>Combining Oxidative N-Heterocyclic Carbene Catalysis with Click Chemistry: A Facile One-Pot Approach to 1,2,3-Triazole Derivatives</title>
<link>http://dx.doi.org/10.1002/asia.201300138</link>
<dc:creator>B. T. Ramanjaneyulu, Virsinha Reddy, Panjab Arde, Sriram Mahesh, R. Vijaya Anand</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/asia201300138.gif" width="390" height="89" alt="Combining Oxidative N-Heterocyclic Carbene Catalysis with Click Chemistry: A Facile One-Pot Approach to 1,2,3-Triazole Derivatives" title="Combining Oxidative N-Heterocyclic Carbene Catalysis with Click Chemistry: A Facile One-Pot Approach to 1,2,3-Triazole Derivatives" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>NHCs click into place</B>: A one-pot synthesis of 1,2,3-triazoles has been developed by combining oxidative N-heterocyclic carbene catalysis with click chemistry. A range of 1,2,3-triazoles were prepared in moderate-to-good yields under mild conditions.</P><p> [Full Paper]<br />B. T. Ramanjaneyulu, Virsinha Reddy, Panjab Arde, Sriram Mahesh, R. Vijaya Anand<br /><i>Chem. Asian J.</i>, Apr 19, 2013, DOI: 10.1002/asia.201300138. <a href="http://dx.doi.org/10.1002/asia.201300138">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300262">
<title>RAFT Polymerization and Some of its Applications</title>
<link>http://dx.doi.org/10.1002/asia.201300262</link>
<dc:creator>Graeme Moad, Ezio Rizzardo, San H. Thang</dc:creator>
<dc:date>2013-04-18T16:02+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300262.gif" width="345" height="82" alt="RAFT Polymerization and Some of its Applications" title="RAFT Polymerization and Some of its Applications" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Enjoy the RAFTing tour</B>: Reversible addition&ndash;fragmentation chain transfer (RAFT) is one of the most robust and versatile methods for controlling radical polymerization to produce low dispersity polymers with well-defined architecture and composition. Applications described in this review include polymers for optoelectronics, block copolymer therapeutics, and star polymer rheology control agents.</P><p> [Focus Review]<br />Graeme Moad, Ezio Rizzardo, San H. Thang<br /><i>Chem. Asian J.</i>, Apr 18, 2013, DOI: 10.1002/asia.201300262. <a href="http://dx.doi.org/10.1002/asia.201300262">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300185">
<title>Squaraine Dyes for Dye-Sensitized Solar Cells: Recent Advances and Future Challenges</title>
<link>http://dx.doi.org/10.1002/asia.201300185</link>
<dc:creator>Chuanjiang Qin, Wai-Yeung Wong, Liyuan Han</dc:creator>
<dc:date>2013-04-17T12:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300185.gif" width="216" height="167" alt="Squaraine Dyes for Dye-Sensitized Solar Cells: Recent Advances and Future Challenges" title="Squaraine Dyes for Dye-Sensitized Solar Cells: Recent Advances and Future Challenges" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Toward NIR response</B>: Recent progress in squaraine dyes has led to a rapid increase in the energy conversion efficiency of dye-sensitized solar cells. Squaraine dyes are also a promising candidate as near-infrared (NIR) co-sensitizers in co-sensitized solar cells. In this Focus Review, we highlight some recent advances of squaraine sensitizers and their applications in dye-sensitized solar cells.</P><p> [Focus Review]<br />Chuanjiang Qin, Wai-Yeung Wong, Liyuan Han<br /><i>Chem. Asian J.</i>, Apr 17, 2013, DOI: 10.1002/asia.201300185. <a href="http://dx.doi.org/10.1002/asia.201300185">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300065">
<title>Water-Soluble Tetraphenylethene Derivatives as Fluorescent “Light-Up” Probes for Nucleic Acid Detection and Their Applications in Cell Imaging</title>
<link>http://dx.doi.org/10.1002/asia.201300065</link>
<dc:creator>Yuning Hong, Sijie Chen, Chris Wai Tung Leung, Jacky Wing Yip Lam, Ben Zhong Tang</dc:creator>
<dc:date>2013-04-17T12:28+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300065.gif" width="216" height="178" alt="Water-Soluble Tetraphenylethene Derivatives as Fluorescent &ldquo;Light-Up&rdquo; Probes for Nucleic Acid Detection and Their Applications in Cell Imaging" title="Water-Soluble Tetraphenylethene Derivatives as Fluorescent &ldquo;Light-Up&rdquo; Probes for Nucleic Acid Detection and Their Applications in Cell Imaging" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Nucleic acids stand out</B>: Cationic tetraphenylethenes selectively light up nucleic acids by fluorescence and thus can be applied for DNA/RNA quantitation and visualization, chromosome staining, and differentiation of live/dead cells (see figure).</P><p> [Full Paper]<br />Yuning Hong, Sijie Chen, Chris Wai Tung Leung, Jacky Wing Yip Lam, Ben Zhong Tang<br /><i>Chem. Asian J.</i>, Apr 17, 2013, DOI: 10.1002/asia.201300065. <a href="http://dx.doi.org/10.1002/asia.201300065">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300174">
<title>Charge-Transfer Interaction between Few-Layer MoS&lt;sub&gt;2&lt;/sub&gt; and Tetrathiafulvalene</title>
<link>http://dx.doi.org/10.1002/asia.201300174</link>
<dc:creator>Sunita Dey, H. S. S. Ramakrishna Matte, Sharmila N. Shirodkar, Umesh V. Waghmare, C. N. R. Rao</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/asia201300174.gif" width="189" height="104" alt="Charge-Transfer Interaction between Few-Layer MoS2 and Tetrathiafulvalene" title="Charge-Transfer Interaction between Few-Layer MoS2 and Tetrathiafulvalene" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Graphene look-alike</B>: MoS<sub>2</sub> has a layered structure similar to graphene. Tetrathiafulvalene (TTF) interacts with thin, few-layer MoS<sub>2</sub> material by donating an electron, resulting in the formation of TTF radical cation and n-type doping of MoS<sub>2</sub>. Electron-withdrawing tetracyanoethylene, in contrast, does not cause p-type doping in MoS<sub>2</sub>.</P><p> [Communication]<br />Sunita Dey, H. S. S. Ramakrishna Matte, Sharmila N. Shirodkar, Umesh V. Waghmare, C. N. R. Rao<br /><i>Chem. Asian J.</i>, Apr 16, 2013, DOI: 10.1002/asia.201300174. <a href="http://dx.doi.org/10.1002/asia.201300174">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300251">
<title>Catalytic Asymmetric Synthesis of Spirooxindoles via Addition of Isothiocyanato Oxindoles to Aldehydes Under Dinuclear Nickel Schiff Base Catalysis</title>
<link>http://dx.doi.org/10.1002/asia.201300251</link>
<dc:creator>Shota Kato, Motomu Kanai, Shigeki Matsunaga</dc:creator>
<dc:date>2013-04-15T14:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300251.gif" width="282" height="85" alt="Catalytic Asymmetric Synthesis of Spirooxindoles via Addition of Isothiocyanato Oxindoles to Aldehydes Under Dinuclear Nickel Schiff Base Catalysis" title="Catalytic Asymmetric Synthesis of Spirooxindoles via Addition of Isothiocyanato Oxindoles to Aldehydes Under Dinuclear Nickel Schiff Base Catalysis" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>One-step approach</B>: A homodinuclear nickel Schiff base catalyst was utilized for the title reaction, thus providing easy access to spirocyclic oxindole compounds in one step. High enantioselectivity as well as high catalyst turnover number (TON, up to 850) were achieved at ambient temperature.</P><p> [Communication]<br />Shota Kato, Motomu Kanai, Shigeki Matsunaga<br /><i>Chem. Asian J.</i>, Apr 15, 2013, DOI: 10.1002/asia.201300251. <a href="http://dx.doi.org/10.1002/asia.201300251">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300247">
<title>Fullerene Nanoarchitectonics: From Zero to Higher Dimensions</title>
<link>http://dx.doi.org/10.1002/asia.201300247</link>
<dc:creator>Lok Kumar Shrestha, Qingmin Ji, Taizo Mori, Kun'ichi Miyazawa, Yusuke Yamauchi, Jonathan P. Hill, Katsuhiko Ariga</dc:creator>
<dc:date>2013-04-15T14:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300247.gif" width="207" height="209" alt="Fullerene Nanoarchitectonics: From Zero to Higher Dimensions" title="Fullerene Nanoarchitectonics: From Zero to Higher Dimensions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Zero to hero</B>: Because fullerenes can be regarded as ideal zero-dimensional (0D) functional building units, the construction of higher-dimensional objects from fullerenes, that is, 1D, 2D, and 3D nanomaterials, can facilitate powerful aspects of nanoarchitectonics. This Focus Review summarizes recent developments in the production of nanostructured fullerenes and in techniques to elaborate fullerene nanomaterials into hierarchical structures.</P><p> [Focus Review]<br />Lok Kumar Shrestha, Qingmin Ji, Taizo Mori, Kun&#x27;ichi Miyazawa, Yusuke Yamauchi, Jonathan P. Hill, Katsuhiko Ariga<br /><i>Chem. Asian J.</i>, Apr 15, 2013, DOI: 10.1002/asia.201300247. <a href="http://dx.doi.org/10.1002/asia.201300247">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300151">
<title>Cucurbit[8]uril-Based Supramolecular Polymers</title>
<link>http://dx.doi.org/10.1002/asia.201300151</link>
<dc:creator>Yiliu Liu, Hui Yang, Zhiqiang Wang, Xi Zhang</dc:creator>
<dc:date>2013-04-15T14:08+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300151.gif" width="216" height="157" alt="Cucurbit[8]uril-Based Supramolecular Polymers" title="Cucurbit[8]uril-Based Supramolecular Polymers" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Sk[8]er boi</B>: Cucurbit[8]uril-based host&ndash;guest interactions are described, with a special emphasis on the fabrication of supramolecular polymers, including small-molecule-based supramolecular polymers and polymer-based supramolecular polymers.</P><p> [Focus Review]<br />Yiliu Liu, Hui Yang, Zhiqiang Wang, Xi Zhang<br /><i>Chem. Asian J.</i>, Apr 15, 2013, DOI: 10.1002/asia.201300151. <a href="http://dx.doi.org/10.1002/asia.201300151">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300240">
<title>Reactions of 13-Vertex Carboranes with Strong Bases: Synthesis and Structural Characterization of Carborane Monoanions with &lt;I&gt;exo&lt;/I&gt;-π&#160;Bonding</title>
<link>http://dx.doi.org/10.1002/asia.201300240</link>
<dc:creator>Fangrui Zheng, Jian Zhang, Xiaodu Fu, Zuowei Xie</dc:creator>
<dc:date>2013-04-15T14:07+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300240.gif" width="299" height="91" alt="Reactions of 13-Vertex Carboranes with Strong Bases: Synthesis and Structural Characterization of Carborane Monoanions with exo-&pi;&nbsp;Bonding" title="Reactions of 13-Vertex Carboranes with Strong Bases: Synthesis and Structural Characterization of Carborane Monoanions with exo-&pi;&nbsp;Bonding" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Unlucky for some</B>: 13-Vertex carborane monoanions with <I>exo</I> C=C &pi;&nbsp;bonding to hypercarbon atoms were characterized by deprotonation of their &alpha;-methylene atoms. These monoanions had the same cage geometry as their parent neutral molecules.</P><p> [Full Paper]<br />Fangrui Zheng, Jian Zhang, Xiaodu Fu, Zuowei Xie<br /><i>Chem. Asian J.</i>, Apr 15, 2013, DOI: 10.1002/asia.201300240. <a href="http://dx.doi.org/10.1002/asia.201300240">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300258">
<title>Structural Transformation between Supramolecular Nanofibers with Drastic Change of Conductivity by Heat and Ultrasound</title>
<link>http://dx.doi.org/10.1002/asia.201300258</link>
<dc:creator>Hajime Shigemitsu, Ichiro Hisaki, Hirofumi Senga, Daisuke Yasumiya, Tejender S. Thakur, Akinori Saeki, Shu Seki, Norimitsu Tohnai, Mikiji Miyata</dc:creator>
<dc:date>2013-04-12T08:30+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300258.gif" width="173" height="135" alt="Structural Transformation between Supramolecular Nanofibers with Drastic Change of Conductivity by Heat and Ultrasound" title="Structural Transformation between Supramolecular Nanofibers with Drastic Change of Conductivity by Heat and Ultrasound" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Transformation with every fiber of its being</B>: Dehydrobenzoannulene derivatives with a boomerang shape, dipole moment, and substituents that make diverse interactions enable the contruction of stimuli-responsive nanofibers despite the lack of stimuli-responsive groups in these compounds. Interestingly, the supramolecular nanofibers obtained after ultrasonic treatment displayed an 80% decrease in conductivity as compared to untreated nanofibers. This is the first example of an electronic wire for which the conductivity can be controlled by ultrasound.</P><p> [Communication]<br />Hajime Shigemitsu, Ichiro Hisaki, Hirofumi Senga, Daisuke Yasumiya, Tejender S. Thakur, Akinori Saeki, Shu Seki, Norimitsu Tohnai, Mikiji Miyata<br /><i>Chem. Asian J.</i>, Apr 12, 2013, DOI: 10.1002/asia.201300258. <a href="http://dx.doi.org/10.1002/asia.201300258">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300134">
<title>Interconvertible Self-Assembly and Rheological Properties of Planar Bilayers and Vesicle Gels in Anionic/Nonionic (CF/CH) Surfactant Solutions</title>
<link>http://dx.doi.org/10.1002/asia.201300134</link>
<dc:creator>Renhao Dong, Jing Wu, Shuli Dong, Shasha Song, Feng Tian, Jingcheng Hao</dc:creator>
<dc:date>2013-04-09T16:23+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300134.gif" width="274" height="101" alt="Interconvertible Self-Assembly and Rheological Properties of Planar Bilayers and Vesicle Gels in Anionic/Nonionic (CF/CH) Surfactant Solutions" title="Interconvertible Self-Assembly and Rheological Properties of Planar Bilayers and Vesicle Gels in Anionic/Nonionic (CF/CH) Surfactant Solutions" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Avengers self-assemble</B>: The interconvertible self-assembly of planar bilayers and vesicle gels was achieved in anionic/nonionic (CF/CH) surfactant solutions, which could be of practical use for controlled drug delivery and release.</P><p> [Full Paper]<br />Renhao Dong, Jing Wu, Shuli Dong, Shasha Song, Feng Tian, Jingcheng Hao<br /><i>Chem. Asian J.</i>, Apr 09, 2013, DOI: 10.1002/asia.201300134. <a href="http://dx.doi.org/10.1002/asia.201300134">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300066">
<title>Formation of Ag&lt;sub&gt;2&lt;/sub&gt;S Cages from Polyhedral Ag&lt;sub&gt;2&lt;/sub&gt;O Nanocrystals and their Electrochemical Properties</title>
<link>http://dx.doi.org/10.1002/asia.201300066</link>
<dc:creator>Lian-Ming Lyu, Michael H. Huang</dc:creator>
<dc:date>2013-03-28T13:46+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300066.gif" width="216" height="123" alt="Formation of Ag2S Cages from Polyhedral Ag2O Nanocrystals and their Electrochemical Properties" title="Formation of Ag2S Cages from Polyhedral Ag2O Nanocrystals and their Electrochemical Properties" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Be on etch</B>: Large polyhedral Ag<sub>2</sub>S cages (bottom) with thin shells can be readily obtained by first forming a sulfide layer over various polyhedral Ag<sub>2</sub>O crystal templates (top) such as cubes, octahedra, and hexapods through a rapid sulfidation process, and subsequent treatment with an ammonia solution to remove the Ag<sub>2</sub>O cores; the Ag<sub>2</sub>S cages retain the morphologies of the original templates (scale bar=500&nbsp;nm).</P><p> [Full Paper]<br />Lian-Ming Lyu, Michael H. Huang<br /><i>Chem. Asian J.</i>, Mar 28, 2013, DOI: 10.1002/asia.201300066. <a href="http://dx.doi.org/10.1002/asia.201300066">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300209">
<title>Organic and Organometallic Nanofibers Formed by Supramolecular Assembly of Diamond-Shaped Macrocyclic Ligands and Pd&lt;SUP&gt;II&lt;/SUP&gt; Complexes</title>
<link>http://dx.doi.org/10.1002/asia.201300209</link>
<dc:creator>Masumi Kuritani, Shohei Tashiro, Mitsuhiko Shionoya</dc:creator>
<dc:date>2013-03-28T13:45+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300209.gif" width="214" height="144" alt="Organic and Organometallic Nanofibers Formed by Supramolecular Assembly of Diamond-Shaped Macrocyclic Ligands and PdII Complexes" title="Organic and Organometallic Nanofibers Formed by Supramolecular Assembly of Diamond-Shaped Macrocyclic Ligands and PdII Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Stacked rings</B>: A diamond-shaped macrocycle with two inward phenanthroline ligands and outward long alkyl chains, and its Pd<SUP>II</SUP> complex form organic and organometallic fibrous aggregates, respectively, as revealed by NMR, UV/Vis, AFM, and TEM measurements. The most likely structures are face-to-face stacked macrocycles, generating nanotubes.</P><p> [Communication]<br />Masumi Kuritani, Shohei Tashiro, Mitsuhiko Shionoya<br /><i>Chem. Asian J.</i>, Mar 28, 2013, DOI: 10.1002/asia.201300209. <a href="http://dx.doi.org/10.1002/asia.201300209">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300084">
<title>Recent Advances in Metal–Organic Framework-Based Mixed Matrix Membranes</title>
<link>http://dx.doi.org/10.1002/asia.201300084</link>
<dc:creator>Ilknur Erucar, Gamze Yilmaz, Seda Keskin</dc:creator>
<dc:date>2013-03-25T06:50+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300084.gif" width="213" height="180" alt="Recent Advances in Metal&ndash;Organic Framework-Based Mixed Matrix Membranes" title="Recent Advances in Metal&ndash;Organic Framework-Based Mixed Matrix Membranes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Trapped in the matrix</B>: Metal&ndash;organic frameworks (MOFs) have been recently used as filler particles in mixed matrix membranes (MMMs), and significant improvements have been reported for gas selectivity and gas permeability in these MOF-based membranes (see figure). This review covers the opportunities and challenges of MOF-based MMMs in gas-separation applications.</P><p> [Focus Review]<br />Ilknur Erucar, Gamze Yilmaz, Seda Keskin<br /><i>Chem. Asian J.</i>, Mar 25, 2013, DOI: 10.1002/asia.201300084. <a href="http://dx.doi.org/10.1002/asia.201300084">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300010">
<title>Further Enhancement of the Second-Order Nonlinear Optical (NLO) Coefficient and the Stability of NLO Polymers that Contain Isolation Chromophore Moieties by Using the “Suitable Isolation Group” Concept and the Ar/Ar&lt;SUP&gt;F&lt;/SUP&gt; Self-Assembly Effect</title>
<link>http://dx.doi.org/10.1002/asia.201300010</link>
<dc:creator>Wenbo Wu, Cheng Ye, Jingui Qin, Zhen Li</dc:creator>
<dc:date>2013-03-25T06:49+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300010.gif" width="347" height="115" alt="Further Enhancement of the Second-Order Nonlinear Optical (NLO) Coefficient and the Stability of NLO Polymers that Contain Isolation Chromophore Moieties by Using the &ldquo;Suitable Isolation Group&rdquo; Concept and the Ar/ArF Self-Assembly Effect" title="Further Enhancement of the Second-Order Nonlinear Optical (NLO) Coefficient and the Stability of NLO Polymers that Contain Isolation Chromophore Moieties by Using the &ldquo;Suitable Isolation Group&rdquo; Concept and the Ar/ArF Self-Assembly Effect" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Second the best</B>: Second-order NLO poly(arylene-ethynylene)s that contained an isolation chromophore were obtained, in which the isolation groups were introduced by using the &ldquo;suitable isolation group&rdquo; concept or the Ar-Ar<SUP>F</SUP> self-assembly effect.</P><p> [Full Paper]<br />Wenbo Wu, Cheng Ye, Jingui Qin, Zhen Li<br /><i>Chem. Asian J.</i>, Mar 25, 2013, DOI: 10.1002/asia.201300010. <a href="http://dx.doi.org/10.1002/asia.201300010">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201201249">
<title>New Entry to Polycyclic Fused Indoles via Gold(I)-catalyzed Cascade Reaction</title>
<link>http://dx.doi.org/10.1002/asia.201201249</link>
<dc:creator>Michel Chiarucci, Elia Matteucci, Gianpiero Cera, Giancarlo Fabrizi, Marco Bandini</dc:creator>
<dc:date>2013-03-15T00:59+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201201249.gif" width="295" height="92" alt="New Entry to Polycyclic Fused Indoles via Gold(I)-catalyzed Cascade Reaction" title="New Entry to Polycyclic Fused Indoles via Gold(I)-catalyzed Cascade Reaction" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>The gold standard</B>: A gold-catalyzed cascade reaction sequence for the preparation of polycyclic fused indole cores exploits the ready availability and chemical flexibility of propargylic alcohols. The desired tri- or tetracyclic compounds are obtained in good yields with water as the only stoichiometric by-product.</P><p> [Communication]<br />Michel Chiarucci, Elia Matteucci, Gianpiero Cera, Giancarlo Fabrizi, Marco Bandini<br /><i>Chem. Asian J.</i>, Mar 15, 2013, DOI: 10.1002/asia.201201249. <a href="http://dx.doi.org/10.1002/asia.201201249">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300106">
<title>Synthesis of Benzotrifuran and Benzotripyrrole Derivatives and Molecular Orientations on the Surface and in the Solid State</title>
<link>http://dx.doi.org/10.1002/asia.201300106</link>
<dc:creator>Hayato Tsuji, Guillaume Cantagrel, Yasuyuki Ueda, Ting Chen, Li-Jun Wan, Eiichi Nakamura</dc:creator>
<dc:date>2013-03-14T03:26+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300106.gif" width="165" height="194" alt="Synthesis of Benzotrifuran and Benzotripyrrole Derivatives and Molecular Orientations on the Surface and in the Solid State" title="Synthesis of Benzotrifuran and Benzotripyrrole Derivatives and Molecular Orientations on the Surface and in the Solid State" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Pack like a (benzotri)p(yr)ro(le)</B>: A synthetic method for benzotrifuran and benzotripyrrole derivatives was developed. 2-D and 3-D molecular structures of these compounds were investigated, and diverse molecular orientations of them and correlation between their packing structures and emission properties were revealed.</P><p> [Full Paper]<br />Hayato Tsuji, Guillaume Cantagrel, Yasuyuki Ueda, Ting Chen, Li-Jun Wan, Eiichi Nakamura<br /><i>Chem. Asian J.</i>, Mar 14, 2013, DOI: 10.1002/asia.201300106. <a href="http://dx.doi.org/10.1002/asia.201300106">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201201146">
<title>Highly Efficient Solution-Processable Organic Light-Emitting Devices with Pincer-Type Cyclometalated Platinum(II) Arylacetylide Complexes</title>
<link>http://dx.doi.org/10.1002/asia.201201146</link>
<dc:creator>Gang Cheng, Yong Chen, Chuluo Yang, Wei Lu, Chi-Ming Che</dc:creator>
<dc:date>2013-03-06T12:56+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201201146.gif" width="204" height="152" alt="Highly Efficient Solution-Processable Organic Light-Emitting Devices with Pincer-Type Cyclometalated Platinum(II) Arylacetylide Complexes" title="Highly Efficient Solution-Processable Organic Light-Emitting Devices with Pincer-Type Cyclometalated Platinum(II) Arylacetylide Complexes" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Let your light shine</B>: By using pincer-type cyclometalated Pt<SUP>II</SUP> arylacetylide complexes as dopants, a maximum current efficiency of 26.57&nbsp;cd&nbsp;A<SUP>&minus;1</SUP> (22.12&nbsp;cd&nbsp;A<SUP>&minus;1</SUP> at 1000&nbsp;cd&nbsp;m<SUP>&minus;2</SUP>) has been achieved with solution-processable phosphorescent OLEDs, the highest ever reported for this type of devices based on phosphorescent Pt<SUP>II</SUP> emitters.</P><p> [Communication]<br />Gang Cheng, Yong Chen, Chuluo Yang, Wei Lu, Chi-Ming Che<br /><i>Chem. Asian J.</i>, Mar 06, 2013, DOI: 10.1002/asia.201201146. <a href="http://dx.doi.org/10.1002/asia.201201146">Read article.</a></p> ]]>
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<item rdf:about="http://dx.doi.org/10.1002/asia.201300020">
<title>Rapid Detection of Phenol Using a Membrane Containing Laccase Nanoflowers</title>
<link>http://dx.doi.org/10.1002/asia.201300020</link>
<dc:creator>Lin Zhu, Lu Gong, Yifei Zhang, Rui Wang, Jun Ge, Zheng Liu, Richard N. Zare</dc:creator>
<dc:date>2013-02-19T17:55+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201300020.gif" width="439" height="117" alt="Rapid Detection of Phenol Using a Membrane Containing Laccase Nanoflowers" title="Rapid Detection of Phenol Using a Membrane Containing Laccase Nanoflowers" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Like a red, red rose</B>: Rapid and sensitive detection of phenol in water was achieved using laccase nanoflowers to catalyze the oxidative coupling of phenol to 4-aminopyrine to form an antipyrine dye, which was detected by absorption at 495&nbsp;nm. The analysis was performed using a commercial syringe filter, in which the membrane with a pore size of 0.2&nbsp;&mu;m accommodated the laccase nanoflowers of 4&nbsp;&mu;m in diameter.</P><p> [Communication]<br />Lin Zhu, Lu Gong, Yifei Zhang, Rui Wang, Jun Ge, Zheng Liu, Richard N. Zare<br /><i>Chem. Asian J.</i>, Feb 19, 2013, DOI: 10.1002/asia.201300020. <a href="http://dx.doi.org/10.1002/asia.201300020">Read article.</a></p> ]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/18835.en.html">
<title>VIP: Transition Metal (Mn, Fe, Co, Ni)-Doped Graphene Hybrids for Electrocatalysis</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/18835.en.html</link>
<dc:date>2013-02-14T00:00:00+01:00</dc:date>
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<![CDATA[<p>Rou Jun Toh, Hwee Ling Poh, Zden&#x11B;k Sofer, Martin Pumera*</p><p>Transition metal-doped graphene hybrids were prepared by exfoliation of metal-doped graphite oxide precursors in either H<sub>2</sub> or N<sub>2</sub> atmosphere. Characterizations of the materials suggest that the H<sub>2</sub> exfoliated materials had higher C/O ratios in general. The electrocatalytic activities of the transition metal-doped graphene hybrids were reflected in an enhancement of the kinetics of oxygen reduction under alkaline conditions, which is important for renewable energy applications such as fuel cells. It was found that hybrid materials exfoliated in N<sub>2</sub> atmosphere exhibited greater electrocatalytic activities than those exfoliated in H<sub>2</sub> atmosphere.</p><p>Coming soon.</p><!-- BNR: asia.201300068 -->]]>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/18741.en.html">
<title>VIP: A Facile Phosphine-Free Method for Synthesizing PbSe Nanocrystals with Strong Optical Limiting Effects</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1861-471X/homepage/news/18741.en.html</link>
<dc:date>2013-01-29T00:00:00+01:00</dc:date>
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<![CDATA[<p>Tian-Ming Wang, Bao Gao, Qiang Wang, Min Zhao, Kai-Bin Kang, Zhu-Guo Xu,* and Hao-Li Zhang*</p><p>The current fabrication strategy for colloidal PbSe semiconductor nanocrystals (NCs) frequently involves acutely toxic reagents and tedious reaction procedures, and is plagued by products with poorly controlled size and morphology. Herein, a facile and phosphine-free method for synthesizing PbSe NCs is reported by the reaction of elemental Se and PbCl2 that involves only oleylamine as both ligand and reaction medium. This method results in monodispersed PbSe NCs with well-controlled size and morphology. In addition, the obtained NCs display strong optical limiting effects, and thus hold potential for the development of nonlinear optical devices.</p><!-- DOI: 10.1002/asia.201201154 -->
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<item rdf:about="http://dx.doi.org/10.1002/asia.201200016">
<title>Retracted: Nanoporous PdCu Near-Surface Alloy for Nonenzymatic Glucose Biosensing</title>
<link>http://dx.doi.org/10.1002/asia.201200016</link>
<dc:creator>Qiaolin Lang, Liang Li, Aihua Liu, Huajun Qiu</dc:creator>
<dc:date>2012-11-29T13:32+05:00</dc:date>
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<![CDATA[ <p><img src="http://www.wiley-vch.de/util/hottopics/img/asia201200016.gif" width="259" height="116" alt="Retracted: Nanoporous PdCu Near-Surface Alloy for Nonenzymatic Glucose Biosensing" title="Retracted: Nanoporous PdCu Near-Surface Alloy for Nonenzymatic Glucose Biosensing" style="float:left; padding-right: 10px; padding-bottom: 10px" /></p><P><B>Sugar sugar</B>: Nanoporous PdCu near-surface alloys that were prepared by two-step dealloying exhibited significantly enhanced electrocatalytic activity for glucose oxidation, which could be used for enhanced nonenzymatic glucose biosensing.</P><p> [Full Paper]<br />Qiaolin Lang, Liang Li, Aihua Liu, Huajun Qiu<br /><i>Chem. Asian J.</i>, Nov 29, 2012, DOI: 10.1002/asia.201200016. <a href="http://dx.doi.org/10.1002/asia.201200016">Read article.</a></p> ]]>
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