<?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>S1870-249X2017000200128</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Aqueous-biphasic hydroformylation of 1-hexene catalyzed by the complex HCo(CO)[P(o-C6H4SO3Na)]3]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Modroño-Alonso]]></surname>
<given-names><![CDATA[María]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Castro]]></surname>
<given-names><![CDATA[William]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lopez-Linares]]></surname>
<given-names><![CDATA[Francisco]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rosales]]></surname>
<given-names><![CDATA[Merlín]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Baricelli]]></surname>
<given-names><![CDATA[Pablo Jose]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Carabobo Facultad de Ingeniería Centro de Investigaciones Químicas]]></institution>
<addr-line><![CDATA[Valencia ]]></addr-line>
<country>Venezuela</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto Venezolano de Investigaciones Científicas Centro de Química ]]></institution>
<addr-line><![CDATA[Caracas ]]></addr-line>
<country>Venezuela</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Chevron Energy Technology Company  ]]></institution>
<addr-line><![CDATA[ California]]></addr-line>
<country>United States of America</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Universidad del Zulia Facultad Experimental de Ciencia Departamento de Química]]></institution>
<addr-line><![CDATA[Maracaibo ]]></addr-line>
<country>Venezuela</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2017</year>
</pub-date>
<volume>61</volume>
<numero>2</numero>
<fpage>128</fpage>
<lpage>137</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2017000200128&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2017000200128&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2017000200128&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract. The water soluble cobalt complex HCo(CO)[P(o-C6H4SO3Na)]3 was used as catalyst precursor for the biphasic aqueous hydroformylation of 1-hexene. The complex was synthesized by reductive carbonylation of CoCl2.6H2O in the presence of o-TPPTS ([P(o-C6H4SO3Na)]3) under nitrogen atmosphere and characterized by FTIR, 1H NMR and 31P {1H} NMR, 13C NMR, DEPT - 135, COSY, HSQC, MS (ESI). The catalytic activity of the complex in the biphasic hydroformylation reaction of 1-hexene was evaluated under moderate reaction conditions. The pressure and temperature were varied from 4137 - 7584 kPa (600-1100 psi) of syngas and from 353 - 383 K (80 - 110 oC), respectively. The 1-hexene concentration was varied from 0.021-0,11M and the catalyst from 4x10-4 - 1.1x10-3 M. The best conversion at 363 K and 7584 kPa and 7.5 h was 62% with selectivity towards aldehydes (heptanal and 2-methyl-hexanal) of 66% to with l/b ratio of 2.6. The recycling of the catalytic precursor after four successive times, did not show any loss on the activity, having selectivity towards aldehyde up to 60%.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen. El complejo soluble en agua HCo(CO)[P(o-C6H4SO3Na)]3 fue usado como precursor catalítico para la hidroformilación de 1-hexeno. El complejo fue sintetizado por carbonilación reductiva de CoCl2.6H2O en presencia de o-TFFTS,([P(o-C6H4SO3Na)]3) en atmosfera de nitrógeno y caracterizado por IRFT 1H RMN y 31P {1H} RMN, 13C RMN, DEPT - 135, COSY, HSQC, MS (ESI). La actividad catalítica del complejo en la hidroformilación bifásica acuosa de1-hexeno fue evaluada bajo condiciones moderadas de reacción. La presión y la temperatura se variaron desde 4137 - 7584 kPa (600-1100 psi) de gas de síntesis y de 353 - 383 K (80 - 110 oC), respectivamente. La concentración de 1-hexeno se varió desde 0.021-0.11M y la del catalizador desde 4x10-4 - 1.1x10-3 M. La mejor conversión fue 62% a 363 K y 7584 kPa en 7.5 h con una selectividad de 66% hacia los aldehídos (heptanal y 2-metil-hexanal), obteniéndose y una relación n/i de 2.6. El precursor catalítico fue reciclado durante cuatro veces sucesivas sin mostrar perdida en la actividad catalítica y con una selectividad hacia aldehídos de 60 %.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Biphasic hydroformylation]]></kwd>
<kwd lng="en"><![CDATA[Cobalt complexes]]></kwd>
<kwd lng="en"><![CDATA[1-hexene]]></kwd>
<kwd lng="en"><![CDATA[recycling]]></kwd>
<kwd lng="en"><![CDATA[o-TPPTS]]></kwd>
<kwd lng="es"><![CDATA[Hidroformilación bifásica]]></kwd>
<kwd lng="es"><![CDATA[complejos de cobalto]]></kwd>
<kwd lng="es"><![CDATA[1-hexeno]]></kwd>
<kwd lng="es"><![CDATA[reciclo]]></kwd>
<kwd lng="es"><![CDATA[o-TFFTS]]></kwd>
</kwd-group>
</article-meta>
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