<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1870-249X</journal-id>
<journal-title><![CDATA[Journal of the Mexican Chemical Society]]></journal-title>
<abbrev-journal-title><![CDATA[J. Mex. Chem. Soc]]></abbrev-journal-title>
<issn>1870-249X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Química de México A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-249X2011000100006</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Controlled Synthesis of Block Copolymers containing N-isopropylacrylamide by Reversible Addition-Fragmentation Chain-Transfer (RAFT) Polymerization]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vega-Rios]]></surname>
<given-names><![CDATA[Alejandro]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Licea-Claveríe]]></surname>
<given-names><![CDATA[Angel]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Instituto Tecnológico de Tijuana Centro de Graduados e Investigación ]]></institution>
<addr-line><![CDATA[Tijuana B.C.]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2011</year>
</pub-date>
<volume>55</volume>
<numero>1</numero>
<fpage>21</fpage>
<lpage>32</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2011000100006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2011000100006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2011000100006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Synthesis of diblock copolymers of N-isopropylacrylamide with n-hexyl acrylate, styrene, methyl methacrylate and 2-hydroxyethyl methacrylate, were carried out by using a sequential "living" polymerization method in the presence of chain transfer agent (CTA) 4-Cyano-4-(phenylcarbonothioylthio)pentanoic acid. The block copo-lymer composition and molecular weight could be well controlled while maintaining a narrow molecular weight distribution. The block copolymers were characterized by ¹H NMR, GPC with MALLS detection and DSC. The molar ratio CTA/Initiator rather than the sequence of monomer addition is the key parameter for achieving the desired materials. We report the first synthesis of poly(HEMA)-b-poly(NIPAAm) with a polydispersity index (IPD) of 1.20 by RAFT.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[La síntesis de copolímeros en dibloques de N-isopropila-crilamida con acrilato de n-hexilo, estireno metacrilato de metilo y metacrilato de 2-hidroxietilo, se llevó a cabo mediante polimerización viviente secuencial en presencia del agente de transferencia de cadena (CTA) ácido 4-ciano-4-[fenilcarbonotioiltio] pentanoico. La composición y peso molecular de los copolímeros en bloques se pudo controlar manteniendo un índice de polidispersidad bajo. Los copolímeros en bloque se caracterizaron por ¹H RMN, GPC con MALLS y por DSC. La relación CTA/Iniciador resultó ser más relevante que la secuencia de adición de monómeros para lograr los materiales deseados. Se reporta por primera vez la síntesis de poli(HEMA)-b-poli(NIPAAm) con un índice de polidispersidad de 1.20 por RAFT.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Block Copolymer]]></kwd>
<kwd lng="en"><![CDATA[RAFT]]></kwd>
<kwd lng="en"><![CDATA[poly(NIPAAm)]]></kwd>
<kwd lng="en"><![CDATA[poly(MMA)]]></kwd>
<kwd lng="en"><![CDATA[poly(HEMA)]]></kwd>
<kwd lng="en"><![CDATA[poly(St)]]></kwd>
<kwd lng="es"><![CDATA[Copolímeros en bloques]]></kwd>
<kwd lng="es"><![CDATA[RAFT]]></kwd>
<kwd lng="es"><![CDATA[poli(NIPAAm)]]></kwd>
<kwd lng="es"><![CDATA[poli(MMA)]]></kwd>
<kwd lng="es"><![CDATA[poli(HEMA)]]></kwd>
<kwd lng="es"><![CDATA[poli(St)]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Article</font></p>     <p align="justify"><font face="verdana" size="4">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b>Controlled Synthesis of Block Copolymers containing <i>N</i>&#150;isopropylacrylamide by Reversible Addition&#150;Fragmentation Chain&#150;Transfer (RAFT) Polymerization</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>Alejandro Vega&#150;Rios and Angel Licea&#150;Claver&iacute;e<sup>*</sup></b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i>Centro de Graduados e Investigaci&oacute;n, Instituto Tecnol&oacute;gico de Tijuana, A.P. 1166, 22414 Tijuana, B.C., M&eacute;xico. *e&#150;mail:</i> <a href="mailto:aliceac@tectijuana.mx">aliceac@tectijuana.mx</a>.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Received June 14, 2010.    <br> Accepted November 8, 2010.</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>     <p align="justify"><font face="verdana" size="2">Synthesis of diblock copolymers of <i>N</i>&#150;isopropylacrylamide with n&#150;hexyl acrylate, styrene, methyl methacrylate and 2&#150;hydroxyethyl methacrylate, were carried out by using a sequential "living" polymerization method in the presence of chain transfer agent (CTA) 4&#150;Cyano&#150;4&#150;(phenylcarbonothioylthio)pentanoic acid. The block copo&#150;lymer composition and molecular weight could be well controlled while maintaining a narrow molecular weight distribution. The block copolymers were characterized by <sup>1</sup>H NMR, GPC with MALLS detection and DSC. The molar ratio CTA/Initiator rather than the sequence of monomer addition is the key parameter for achieving the desired materials. We report the first synthesis of poly(HEMA)&#150;<i>b</i>&#150;poly(NIPAAm) with a polydispersity index (IPD) of 1.20 by RAFT. </font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords</b>: Block Copolymer, RAFT, poly(NIPAAm), poly(MMA), poly(HEMA), poly(St).</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2">La s&iacute;ntesis de copol&iacute;meros en dibloques de <i>N</i>&#150;isopropila&#150;crilamida con acrilato de n&#150;hexilo, estireno metacrilato de metilo y metacrilato de 2&#150;hidroxietilo, se llev&oacute; a cabo mediante polimerizaci&oacute;n viviente secuencial en presencia del agente de transferencia de cadena (CTA) &aacute;cido 4&#150;ciano&#150;4&#150;&#91;fenilcarbonotioiltio&#93; pentanoico. La composici&oacute;n y peso molecular de los copol&iacute;meros en bloques se pudo controlar manteniendo un &iacute;ndice de polidispersidad bajo. Los copol&iacute;meros en bloque se caracterizaron por <sup>1</sup>H RMN, GPC con MALLS y por DSC. La relaci&oacute;n CTA/Iniciador result&oacute; ser m&aacute;s relevante que la secuencia de adici&oacute;n de mon&oacute;meros para lograr los materiales deseados. Se reporta por primera vez la s&iacute;ntesis de poli(HEMA)&#150;<i>b</i>&#150;poli(NIPAAm) con un &iacute;ndice de polidispersidad de 1.20 por RAFT. </font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave: </b>Copol&iacute;meros en bloques, RAFT, poli(NIPAAm), poli(MMA), poli(HEMA), poli(St).</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font size="2" face="verdana"><a href="/pdf/jmcs/v55n1/v55n1a6.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Acknowledgements</b></font></p>     <p align="justify"><font face="verdana" size="2">This investigation was supported by a grants of CONACYT No SEP2006&#150;60792 and DGEST No. 947&#150;08&#150;P. We thank A. Ochoa and I. Rivero for performing NMR analysis and U. P&eacute;rez and F. Soto for some synthetic work.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>References</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">1. Sebenik, A. <i>Prog. Polym. 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