<?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>S1870-249X2007000100003</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Catalytic Activity of Rhodium (I) Complexes with Bidentate Phosphinic Ligands in the Hydrogenation of Unsaturated Alycyclic Substrates]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Montalvo]]></surname>
<given-names><![CDATA[Liliana]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bolaños]]></surname>
<given-names><![CDATA[Alberto]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cabrera]]></surname>
<given-names><![CDATA[Armando]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad del Cauca Facultad de Ciencias Naturales, Exactas y de la Educación Departamento de Química]]></institution>
<addr-line><![CDATA[Popayán Cauca]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad del Valle Facultad de Ciencias Departamento de Química]]></institution>
<addr-line><![CDATA[Cali Valle del Cauca]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Universidad Nacional Autónoma de México, Instituto de Química ]]></institution>
<addr-line><![CDATA[México Distrito Federal]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2007</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2007</year>
</pub-date>
<volume>51</volume>
<numero>1</numero>
<fpage>08</fpage>
<lpage>14</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2007000100003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2007000100003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2007000100003&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[RhCl(dppe)2, RhCl(dppp)2 and RhCl(dppb)2 where dppe = diphenylphosphinoethane; dppp = diphenylphosphinopropane; dppb = diphenylphosphinobutane complexes were prepared by treating RhCl3.3H2O with the appropriate di(tertiaryphosphine). These complexes were used as catalytic precursors in the hydrogenation of limonene, camphene and 1,5- cyclooctadiene at different concentrations and temperatures. It was found that the Rhodium complex having dppp as ligand was the best catalytic precursor.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Los complejos RhCl(dppe)2, RhCl(dppp)2 y RhCl(dppb)2 donde dppe = difenilfosfino etano; dppp = difenilfosfinopropano; dppb = difenilfosfinobutano fueron preparados por el tratamiento del RhCl3.3H2O con las fosfinas diterciarias apropiadas. Estos complejos fueron usados como precursores catalíticos en las reacciones de hidrogenación de limoneno, canfeno y 1,5-ciclooctadieno a diferentes concentraciones y temperaturas. Se encontró que el mejor precursor catalítico es el complejo de Rodio con el ligante dppp.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Rhodium]]></kwd>
<kwd lng="en"><![CDATA[bidentate phosphinic ligands]]></kwd>
<kwd lng="en"><![CDATA[homogeneous catalysis]]></kwd>
<kwd lng="en"><![CDATA[catalytic hydrogenation]]></kwd>
<kwd lng="en"><![CDATA[unsaturated alycyclic compounds]]></kwd>
<kwd lng="es"><![CDATA[Rodio]]></kwd>
<kwd lng="es"><![CDATA[ligantes fosfínicos bidentados]]></kwd>
<kwd lng="es"><![CDATA[catálisis homogénea]]></kwd>
<kwd lng="es"><![CDATA[hidrogenación catalítica]]></kwd>
<kwd lng="es"><![CDATA[alicíclicos insaturados]]></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="2">&nbsp;</font></p>  	    <p align="center"><font face="verdana" size="4"><b>Catalytic Activity of Rhodium (I) Complexes with Bidentate Phosphinic Ligands in the Hydrogenation of Unsaturated Alycyclic Substrates</b></font></p>  	    <p align="center"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="center"><font face="verdana" size="2"><b>Liliana Montalvo,<sup>1</sup> Alberto Bola&ntilde;os,<sup>2</sup> Armando Cabrera<sup>3</sup></b></font></p>  	    <p align="center"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><sup>1</sup> <i>Departamento de Qu&iacute;mica, Facultad de Ciencias Naturales, Exactas y de la Educaci&oacute;n, Universidad del Cauca, Popay&aacute;n&#45;Cauca&#45;Colombia, Tel: 0057&#45;2&#45;8209800 ext. 2320,</i> <a href="mailto:lmontalvo@unicauca.edu.co">lmontalvo@unicauca.edu.co</a>.</font></p>  	    <p align="justify"><font face="verdana" size="2"><sup>2</sup><i>&nbsp;Departamento de Qu&iacute;mica, Facultad de Ciencias, Universidad del Valle, Cali&#45;Valle&#45;Colombia, Apartado 25360, Tel: 0057&#45;2&#45;3334921,</i> <a href="mailto:albolan@univalle.edu.co">albolan@univalle.edu.co</a>.</font></p>  	    <p align="justify"><font face="verdana" size="2"><sup>3</sup><i>&nbsp;Instituto de Qu&iacute;mica, Universidad Nacional Aut&oacute;noma de M&eacute;xico,</i> <i>Ciudad Universitaria, Coyoac&aacute;n 04510, M&eacute;xico D. F., M&eacute;xico.</i> <a href="mailto:arcaor1@servidor.unam.mx">arcaor1@servidor.unam.mx</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">Recibido el 6 de marzo del 2006;    <br> 	Aceptado el 12 de septiembre del 2006.</font></p>  	    <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">RhCl(dppe)<sub>2</sub>, RhCl(dppp)<sub>2</sub> and RhCl(dppb)<sub>2</sub> where dppe = diphenylphosphinoethane; dppp = diphenylphosphinopropane; dppb = diphenylphosphinobutane complexes were prepared by treating RhCl<sub>3</sub>.3H<sub>2</sub>O with the appropriate di(tertiaryphosphine). These complexes were used as catalytic precursors in the hydrogenation of limonene, camphene and 1,5&#45; cyclooctadiene at different concentrations and temperatures. It was found that the Rhodium complex having dppp as ligand was the best catalytic precursor.</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Key words:</b> Rhodium; bidentate phosphinic ligands; homogeneous catalysis; catalytic hydrogenation, unsaturated alycyclic compounds.</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">Los complejos RhCl(dppe)<sub>2</sub>, RhCl(dppp)<sub>2</sub> y RhCl(dppb)<sub>2</sub> donde dppe = difenilfosfino etano; dppp = difenilfosfinopropano; dppb = difenilfosfinobutano fueron preparados por el tratamiento del RhCl<sub>3</sub>.3H<sub>2</sub>O con las fosfinas diterciarias apropiadas. Estos complejos fueron usados como precursores catal&iacute;ticos en las reacciones de hidrogenaci&oacute;n de limoneno, canfeno y 1,5&#45;ciclooctadieno a diferentes concentraciones y temperaturas. Se encontr&oacute; que el mejor precursor catal&iacute;tico es el complejo de Rodio con el ligante dppp.</font></p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><b>Palabras clave:</b> Rodio, ligantes fosf&iacute;nicos bidentados, cat&aacute;lisis homog&eacute;nea; hidrogenaci&oacute;n catal&iacute;tica, alic&iacute;clicos insaturados.</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><a href="/pdf/jmcs/v51n1/v51n1a3.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></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. Chaloner, P. A.; Esteruelas, M. A.; Jo&oacute;, F.; Gold, L. A. <i>Homogeneous Hydrogenation,</i> Kluwer Academic, Dordrecht, <b>1994.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4921846&pid=S1870-249X200700010000300001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></b></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">2. Brieger G.; Nestrick, T. <i>Chem. Rev.</i> <b>1974,</b> <i>74,</i> 567&#45;580.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4921848&pid=S1870-249X200700010000300002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">3. Johnstone, R. A.W.; Wilby, A. H.; Entwistle, I. D. <i>Chem. Rev.</i> <b>1985,</b> <i>85,</i> 129&#45;167.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4921850&pid=S1870-249X200700010000300003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">4. Zassinovich, G.; Mestroni, G. <i>Chem. Rev.</i> <b>1992,</b> <i>92,</i> 1051&#45;1068.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4921852&pid=S1870-249X200700010000300004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">5. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. <i>J. Chem. Soc. A.</i> <b>1966,</b> 1711&#45;1732.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4921854&pid=S1870-249X200700010000300005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">6. James, B. R.; Mahajan, D. <i>Can. J. Chem.</i> <b>1979,</b> <i>57</i>, 180&#45;187.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4921856&pid=S1870-249X200700010000300006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>      ]]></body><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chaloner]]></surname>
<given-names><![CDATA[P. A.]]></given-names>
</name>
<name>
<surname><![CDATA[Esteruelas]]></surname>
<given-names><![CDATA[M. A.]]></given-names>
</name>
<name>
<surname><![CDATA[Joó]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Gold]]></surname>
<given-names><![CDATA[L. A.]]></given-names>
</name>
</person-group>
<source><![CDATA[Homogeneous Hydrogenation]]></source>
<year>1994</year>
<publisher-loc><![CDATA[Dordrecht ]]></publisher-loc>
<publisher-name><![CDATA[Kluwer Academic]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Brieger]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<name>
<surname><![CDATA[Nestrick]]></surname>
<given-names><![CDATA[T.]]></given-names>
</name>
</person-group>
<source><![CDATA[Chem. Rev.]]></source>
<year>1974</year>
<volume>74</volume>
<page-range>567-580</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Johnstone]]></surname>
<given-names><![CDATA[R. A.W.]]></given-names>
</name>
<name>
<surname><![CDATA[Wilby]]></surname>
<given-names><![CDATA[A. H.]]></given-names>
</name>
<name>
<surname><![CDATA[Entwistle]]></surname>
<given-names><![CDATA[I. D.]]></given-names>
</name>
</person-group>
<source><![CDATA[Chem. Rev.]]></source>
<year>1985</year>
<volume>85</volume>
<page-range>129-167</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zassinovich]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<name>
<surname><![CDATA[Mestroni]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
</person-group>
<source><![CDATA[Chem. Rev.]]></source>
<year>1992</year>
<volume>92</volume>
<page-range>1051-1068</page-range></nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Osborn]]></surname>
<given-names><![CDATA[J. A.]]></given-names>
</name>
<name>
<surname><![CDATA[Jardine]]></surname>
<given-names><![CDATA[F. H.]]></given-names>
</name>
<name>
<surname><![CDATA[Young]]></surname>
<given-names><![CDATA[J. F.]]></given-names>
</name>
<name>
<surname><![CDATA[Wilkinson]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Chem. Soc. A.]]></source>
<year>1966</year>
<page-range>1711-1732</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[James]]></surname>
<given-names><![CDATA[B. R.]]></given-names>
</name>
<name>
<surname><![CDATA[Mahajan]]></surname>
<given-names><![CDATA[D.]]></given-names>
</name>
</person-group>
<source><![CDATA[Can. J. Chem.]]></source>
<year>1979</year>
<volume>57</volume>
<page-range>180-187</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
