<?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>0120-6230</journal-id>
<journal-title><![CDATA[Revista Facultad de Ingeniería Universidad de Antioquia]]></journal-title>
<abbrev-journal-title><![CDATA[Rev.fac.ing.univ. Antioquia]]></abbrev-journal-title>
<issn>0120-6230</issn>
<publisher>
<publisher-name><![CDATA[Facultad de Ingeniería, Universidad de Antioquia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-62302021000100083</article-id>
<article-id pub-id-type="doi">10.17533/udea.redin.20200477</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[A kinetic study of the photoinduced oxo-transfer using a Mo complex anchored to TiO2]]></article-title>
<article-title xml:lang="es"><![CDATA[Un estudio cinético de la oxo-transferencia fotoinducida usando un complejo de Mo anclado a TiO2]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez-Velandia]]></surname>
<given-names><![CDATA[Julián E.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Páez-Mozo]]></surname>
<given-names><![CDATA[Edgar A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martínez-Ortega]]></surname>
<given-names><![CDATA[Fernando]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Industrial de Santander Facultad de Ciencias Escuela de Química]]></institution>
<addr-line><![CDATA[Piedecuesta ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad de Antioquia Facultad de Ingeniería Departamento de Ingeniería Química]]></institution>
<addr-line><![CDATA[Medellín ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2021</year>
</pub-date>
<numero>98</numero>
<fpage>83</fpage>
<lpage>93</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-62302021000100083&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-62302021000100083&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-62302021000100083&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Kinetic study of the photo-assisted oxygen atom transfer reaction (OAT) using a dioxo-Mo complex anchored on TiO2, stimulated by light, was performed at ambient conditions using triphenylphosphine (PPh3) as a model molecule. The kinetic of the OAT reaction was studied with three catalytic systems: 4,4&#8217;-dicarboxylate-2,2&#8217;-bipyridine-dioxochloromolybdenum (MoO2L/TiO2), H2MoO4 (H2MoO4/TiO2) and molybdenum oxide (MoO3/ TiO2) anchored to TiO2. The MoO2L/TiO2 gives conversion higher than 90% and selectivity (to phosphine oxide) close to 100%. MoO3/TiO2 did not allow the oxo-transference, suggesting the importance of the bipyridine ligand as an electronic connector between MoO2L unit and TiO2. With the MoO2L/TiO2 system was observed that when the photonic flux increases, the quantum yield, and the OAT reaction rate increases.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN El estudio cinético de la reacción de transferencia de átomos de oxígeno (TAO) foto asistida se estudió usando un complejo de dioxo-Mo anclado al TiO2, estimulada por la luz en condiciones ambientales usando trifenilfosfina como molécula modelo. La cinética de la reacción TAO fue estudiada con tres sistemas catalíticos anclados al TiO2: 4,4&#8217;-dicarboxilato-2,2&#8217;-bipiridina-dioxocloromolibdeno (MoO2L/TiO2), H2MoO4 (H2MoO4/TiO2) y óxido de molibdeno (MoO3/ TiO2).. El catalizador MoO2L/TiO2 permitió la conversión más alta del 90% y una selectividad (al óxido de fosfina) cercana al 100%. MoO3/TiO2 no permitió la oxo-transferencia sugiriendo la importancia del ligando bipiridinico como una conexión electrónica entre la unidad MoO2L y el TiO2. Adicionalmente, se observó que cuando se incrementa el flujo fotónico, el rendimiento cuántico y la concentración inicial de la PPh3, aumenta la velocidad de reacción de la TAO para el sistema MoO2L/TiO2.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Photonic flux]]></kwd>
<kwd lng="en"><![CDATA[selective photooxidation]]></kwd>
<kwd lng="en"><![CDATA[dioxomolybdenum complex]]></kwd>
<kwd lng="en"><![CDATA[quantum yield]]></kwd>
<kwd lng="es"><![CDATA[Flujo fotónico]]></kwd>
<kwd lng="es"><![CDATA[fotooxidación selectiva]]></kwd>
<kwd lng="es"><![CDATA[complejo dioxo-Molibdeno]]></kwd>
<kwd lng="es"><![CDATA[rendimiento cuántico]]></kwd>
</kwd-group>
</article-meta>
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