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<title>News from Macromolecular Symposia</title>
<link>http://doi.wiley.com/10.1002/(ISSN)1521-3900</link>
<description>News from the journal Macromolecular Symposia</description>
<dc:language>en</dc:language>
<dc:rights>Copyright 2011, Wiley-VCH Verlag GmbH &#x26;amp; Co. KGaA</dc:rights>
<dc:date>2013-06-19T00:07:22Z</dc:date>
<dc:publisher>Wiley-VCH</dc:publisher>
<dc:creator>info@wiley-vch.de</dc:creator>
<dc:subject>Chemistry</dc:subject>
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<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19344.en.html">
<title>TALENT: Tailoring Cellulose Surfaces by Controlled Polymerization Methods</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19344.en.html</link>
<dc:date>2013-06-18T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/Talent_214_3_Carlmark.jpg" alt="TALENT: Tailoring Cellulose Surfaces by Controlled Polymerization Methods" align="left" hspace="5" vspace="5" border="0" /></p><i>Anna Carlmark</i><br><br>To expand the utilization of cellulose beyond its traditional uses, it is necessary to modify the surface of the fibers. This paper summarizes the modification of cellulose by controlled polymerization methods such as ATRP, RAFT, ROP, and ROMP. The combination of the excellent properties of cellulose with functional polymers creates new materials of great potential in advanced material applications.<br><br><a href="http://doi.wiley.com/10.1002/macp.201300272" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201300272</a><br><br>More information on the invited Talent, Trend, and Highlight articles in <i>Macromolecular Chemistry and Physics</i> can be found <a href=" http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_highl.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19300.en.html">
<title>TREND: The Solvent in Physical Gelation: Polymers Versus Organogelators</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19300.en.html</link>
<dc:date>2013-06-11T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/Trend_214_6_Guenet.jpg" alt="TREND: The Solvent in Physical Gelation: Polymers Versus Organogelators" align="left" hspace="5" vspace="5" border="0" /></p><i>Debarshi Dasgupta, Jean-Michel Guenet*</i><br><br>A discussion of the gelation mechanisms involved in polymer thermoreversible gels and organogels is presented. The implication of the solvent as an active actor and not only a mere diluent is shown.<br><br><a href="http://doi.wiley.com/10.1002/macp.201300094" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201300094</a><br><br>More information on the invited Talent, Trend, and Highlight articles in <i>Macromolecular Chemistry and Physics</i> can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_highl.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19255.en.html">
<title>Functional Polymers: Benzo[1,2-b:4,5-b&#x27;]dithiophene-alt-terthiophene Copolymers Containing Styryl-Triphenylamine Side Chains: Synthesis and Photovoltaic Performance Optimization with Fullerene Acceptors</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19255.en.html</link>
<dc:date>2013-06-04T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/functpolym_214_8_Zhang.jpg" alt="Functional Polymers: Benzo[1,2-b:4,5-b']dithiophene-alt-terthiophene Copolymers Containing Styryl-Triphenylamine Side Chains: Synthesis and Photovoltaic Performance Optimization with Fullerene Acceptors" align="left" hspace="5" vspace="5" border="0" /></p><i>Xitian Wang, Zhi-Guo Zhang,* Wenli Tang, Suling Shen, Guo Liu, Dan Chi, Yongfang Li, Jizheng Wang</i><br><br>A new copolymer is designed and synthesized, and the photovoltaic performance is optimized with fullerene acceptors. The energy loss and the increase in the observed open-circuit voltages are quantitatively explained by the up-shifted lowest unoccupied molecular level of indene-C<sub>60</sub> bisadduct (ICBA) and the reduced saturation current in the blends.<br><br><a href="http://doi.wiley.com/10.1002/macp.201300041" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201300041</a><br><br>Other contributions to the special series on functional polymers can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_fp.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19066.en.html">
<title>POLYOLEFINS: Controlling Polyolefin Properties by In-Reactor Blending: 3. Mechanical Properties</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19066.en.html</link>
<dc:date>2013-04-18T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/polyolefins_7_5_Ruff.jpg" alt="POLYOLEFINS: Controlling Polyolefin Properties by In-Reactor Blending: 3. Mechanical Properties" align="left" hspace="5" vspace="5" border="0" /></p><i>Martin Ruff,* Reinhold W. Lang, Christian Paulik</i><br><br>The effects of multi-stage (slurry) polymerization on mechanical properties of in-reactor blended UHMW-PE materials is presented, and it is shown that due to a controlled polymerized particle morphology, mechanical properties, such as impact properties can be regulated. <br><br><a href="http://doi.wiley.com/10.1002/mren.201200077" target="_blank"><i>Macromol. React. Eng.</i> DOI: 10.1002/mren.201200077</a><br><br>Other contributions to the article series on "Polyolefins - Catalyst and Process Innovations" can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1862-8338/homepage/2465_olef.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19012.en.html">
<title>Functional Polymers: ZnII Bisterpyridine Metallopolymers: Improved Processability by the Introduction of Polymeric Side Chains</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/19012.en.html</link>
<dc:date>2013-04-03T00:00:00+02:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/functpolym_214_7_Schubert.jpg" alt="Functional Polymers: ZnII Bisterpyridine Metallopolymers: Improved Processability by the Introduction of Polymeric Side Chains" align="left" hspace="5" vspace="5" border="0" /></p><i>Andreas Wild, Anke Teichler, Christian von der Ehe, Andreas Winter, Martin D. Hager, Bing Yao, Baohua Zhang, Zhiyuan Xie, Wai-Yeung Wong,* Ulrich S. Schubert*</i><br><br>Tailoring of the optical and mechanical properties of bisterpyridine coordination polymers is enabled by the introduction of well-defined polymeric side chains. The resulting metallopolymers exhibit improved solubility and processability and can, therefore, easily be inkjet-printed. The photophysical properties of the so-produced homogeneous films are investigated and a proof-of-principle polymer light-emitting device can be constructed.<br><br><a href="http://doi.wiley.com/10.1002/macp.201300003" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201300003</a><br><br>Other contributions to the special series on functional polymers can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_fp.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18968.en.html">
<title>POLYOLEFINS: Analysis of Slurry-Phase Co-Polymerization of Ethylene and 1-Butene by Ziegler&#x96;Natta Catalysts Part 1: Experimental Activity Profiles</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18968.en.html</link>
<dc:date>2013-03-19T00:00:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/polyolefins_7_3_Rawatal.jpg" alt="POLYOLEFINS: Analysis of Slurry-Phase Co-Polymerization of Ethylene and 1-Butene by ZieglerNatta Catalysts Part 1: Experimental Activity Profiles" align="left" hspace="5" vspace="5" border="0" /></p><i>John T. McCoy, Joao B. P. Soares, Randhir Rawatlal*</i><br><br>The activity of ZieglerNatta catalysts for ethylene polymerization is studied, and a method developed to extract meaningful kinetic parameters from experimental data. Four model parameters are required to reproduce polymerization rate profiles for a range of laboratory experimental conditions. <br><br><a href="http://doi.wiley.com/10.1002/mren.201200078" target="_blank"><i>Macromol. React. Eng.</i> DOI: 10.1002/mren.201200078</a><br><br>Other contributions to the article series on "Polyolefins - Catalyst and Process Innovations" can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1862-8338/homepage/2465_olef.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18961.en.html">
<title>TALENT: Non-Natural Amino Acids for Protein Engineering and New Protein Chemistries</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18961.en.html</link>
<dc:date>2013-03-19T00:10:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/Talent_214_6_Kwon.jpg" alt="TALENT: Non-Natural Amino Acids for Protein Engineering and New Protein Chemistries" align="left" hspace="5" vspace="5" border="0" /></p><i>Inchan Kwon,* Sung In Lim</i><br><br>Two distinct strategies, residue-specific and site-specific incorporation, allow biosynthesis of a protein containing non-natural amino acids. Non-natural amino acids introduced into a protein can be used to manipulate spectral and catalytic properties of a protein and provide new protein chemistries for bioconjugation with versatile molecules. <br><br><a href="http://doi.wiley.com/10.1002/macp.201200710" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201200710</a><br><br>More information on the invited Talent, Trend, and Highlight articles in <i>Macromolecular Chemistry and Physics</i> can be found <a href=" http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_highl.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18786.en.html">
<title>TREND: MAPLE Deposition of Macromolecules</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18786.en.html</link>
<dc:date>2013-02-07T00:00:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/Trend_214_5_Priestley.jpg" alt="TREND: MAPLE Deposition of Macromolecules" align="left" hspace="5" vspace="5" border="0" /></p><i>Kimberly B. Shepard, Rodney D. Priestley*</i><br><br>Matrix-assisted pulsed laser evaporation (MAPLE) is used to deposit thin films of a vast range of macromolecules, including polymers, proteins, and composite materials. The numerous advantages of MAPLE are discussed, and recent reports of MAPLE-deposited films for electronic and medical applications are highlighted. <br><br><a href="http://doi.wiley.com/10.1002/macp.201200621" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201200621</a><br><br>More information on the invited Talent, Trend, and Highlight articles in <i>Macromolecular Chemistry and Physics</i> can be found <a href=" http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_highl.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18753.en.html">
<title>Functional Polymers: Morphology and Field-Effect Transistor Characteristics of Electrospun Nanofibers Prepared From Crystalline Poly(3-hexylthiophene) and Polyacrylate Blends</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18753.en.html</link>
<dc:date>2013-01-31T00:00:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/functpolym_214_4_Chen.jpg" alt="Functional Polymers: Morphology and Field-Effect Transistor Characteristics of Electrospun Nanofibers Prepared From Crystalline Poly(3-hexylthiophene) and Polyacrylate Blends" align="left" hspace="5" vspace="5" border="0" /></p><i>Chih-Chieh Chou, Hung-Chin Wu, Chih-Jung Lin, Ebrahim Ghelichkhani, Wen-Chang Chen*</i><br><br>Nanofiber field-effect transistors (FETs) based on crystalline poly(3-hexylthiophene) (P3HT) and poly(stearyl acrylates) (PSA) or poly(n-lauryl acrylate) (PnLA) blends are fabricated via coaxial electrospinning (ES). The maximum FET mobility is obtained for P3HT/PSA (1:0.2) blends. The crystalline PSA promotes the larger crystallinity of P3HT in the ES nanofibers, which subsequently leads to the observation of higher mobility and improves the air stability. <br><br><a href="http://doi.wiley.com/10.1002/macp.201200580" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201200580</a><br><br>Other contributions to the special series on functional polymers can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_fp.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18560.en.html">
<title>Functional Polymers: Accessing New DPP-Based Copolymers by Direct Heteroarylation Polymerization</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18560.en.html</link>
<dc:date>2013-01-21T00:00:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/functpolym_214_4_Leclerc.jpg" alt="Functional Polymers: Accessing New DPP-Based Copolymers by Direct Heteroarylation Polymerization" align="left" hspace="5" vspace="5" border="0" /></p><i>Jean-Rémi Pouliot, Lauren G. Mercier, Samuel Caron, Mario Leclerc*</i><br><br>The direct heteroarylation polymerization methodology was adapted for the diketopyrrolopyrrole moiety, giving rise to copolymers that were difficult to obtain from standard Stille or Suzuki couplings. These new low-bandgap polymers proved to be efficient electron-transporting materials enabling possible applications in all-plastic solar cells. <br><br><a href="http://doi.wiley.com/10.1002/macp.201200573" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201200573</a><br><br>Other contributions to the special series on functional polymers can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_fp.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18553.en.html">
<title>Functional Polymers: Thermochromic and Photovoltaic Properties of an Alternating Copolymer of Dithieno[3,2-b:2&#x27;,3&#x27;-d]thiophene and Thieno[3,4-c]pyrrole-4,6-dione</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18553.en.html</link>
<dc:date>2013-01-21T00:10:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/functpolym_214_4_Ding.jpg" alt="Functional Polymers: Thermochromic and Photovoltaic Properties of an Alternating Copolymer of Dithieno[3,2-b:2',3'-d]thiophene and Thieno[3,4-c]pyrrole-4,6-dione" align="left" hspace="5" vspace="5" border="0" /></p><i>Zhao Li,* Patrick Malenfant, Ye Tao, Jianfu Ding*</i><br><br>A new alternating conjugated polymer, PDTTTPD, based on electron-rich dithieno[3,2-b:2',3'-d]thiophene (DTT) and electron-deficient thieno[3,4-c]pyrrole-4,6-dione (TPD) building block is designed and synthesized. PDTTTPD shows strong thermochromic effect in chlorobenzene solution and modest PCE of 2.1% in organic solar cell devices due to the steric hindrance induced twisting of the conjugated main chain. A general design rule is then suggested to control the main chain conformation of polymer materials for photovoltaic applications. <br><br><a href="http://doi.wiley.com/10.1002/macp.201200468" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201200468</a><br><br>Other contributions to the special series on functional polymers can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_fp.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18537.en.html">
<title>Functional Polymers: Recent Progress in Polymer White Light-Emitting Materials and Devices</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18537.en.html</link>
<dc:date>2013-01-17T00:00:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/functpolym_214_4_Tang.jpg" alt="Functional Polymers: Recent Progress in Polymer White Light-Emitting Materials and Devices" align="left" hspace="5" vspace="5" border="0" /></p><i>Chao Tang*, Xu-Dong Liu, Feng Liu, Xu-Liang Wang, Hui Xu, Wei Huang*</i><br><br>Polymer white light-emitting diodes (PWLEDs) are one of the most intensively researched topics in PLED. At present, there are two main methods to realize white emission in PLED. The one is to dope the host with different guests with different color, and the other is to prepare single white polymer by designing the molecular structure. Improving the performance of PWLED depends on the understanding of materials structure and properties, materials purification, and device engineering. <br><br><a href="http://doi.wiley.com/10.1002/macp.201200305" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201200305</a><br><br>Other contributions to the special series on functional polymers can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_fp.html" target="_blank">here</a>.]]></content:encoded>
</item>
<item rdf:about="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18530.en.html">
<title>Functional Polymers: Screening of Film-Formation Qualities of Various Solvent Systems for &#x3C0;-Conjugated Polymers Via Combinatorial Inkjet Printing</title>
<link>http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3900/homepage/news/18530.en.html</link>
<dc:date>2013-01-17T00:10:00+01:00</dc:date>
<content:encoded><![CDATA[<p><img src="http://www.wiley-vch.de/img/news/functpolym_214_4_Schubert.jpg" alt="Functional Polymers: Screening of Film-Formation Qualities of Various Solvent Systems for π-Conjugated Polymers Via Combinatorial Inkjet Printing" align="left" hspace="5" vspace="5" border="0" /></p><i>Anke Teichler, Jolke Perelaer, Ulrich S. Schubert*</i><br><br>A systematical investigation of the relationships between the choice of solvent system and the film quality of inkjet printed π-conjugated polymer films is presented. A significant influence of the boiling points of the chosen main and co-solvents is observed, leading to the identification of new solvent systems that reveal improved film qualities.<br><br><a href="http://doi.wiley.com/10.1002/macp.201200547" target="_blank"><i>Macromol. Chem. Phys.</i>, DOI: 10.1002/macp.201200547</a><br><br>Other contributions to the special series on functional polymers can be found <a href="http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935/homepage/2261_fp.html" target="_blank">here</a>.]]></content:encoded>
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