Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide
The activity of complex heteropolytungstates of general formula B-α-[M<sup>II</sup><sub>4</sub>(H<sub>2</sub>O)<sub>2</sub>(PW<sub>9</sub>O<sub>34</sub>)<sub>2</sub>]<sup>10-</sup> with M= Co(II), Zn(II),...
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Autores principales: | , , , , , , |
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Formato: | Articulo |
Lenguaje: | Inglés |
Publicado: |
2009
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Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/104497 http://hdl.handle.net/11336/56016 https://www.aqa.org.ar/images/anales/pdf9701/9701art15.pdf |
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I19-R120-10915-104497 |
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institution |
Universidad Nacional de La Plata |
institution_str |
I-19 |
repository_str |
R-120 |
collection |
SEDICI (UNLP) |
language |
Inglés |
topic |
Química Ciencias Exactas Heteropolytungstates Diphenylsulfoxides Selective oxidation Tert-butyl-hydroperoxide Heteropolitungstatos Difenilsulfóxidos Oxidación selectiva Tert-butilhidroperóxido |
spellingShingle |
Química Ciencias Exactas Heteropolytungstates Diphenylsulfoxides Selective oxidation Tert-butyl-hydroperoxide Heteropolitungstatos Difenilsulfóxidos Oxidación selectiva Tert-butilhidroperóxido Egusquiza, María Gabriela Ben Tayeb, Karima Muñoz, Mercedes Romanelli, Gustavo Pablo Cabello, Carmen Inés Botto, Irma Lía Thomas, Horacio Jorge Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
topic_facet |
Química Ciencias Exactas Heteropolytungstates Diphenylsulfoxides Selective oxidation Tert-butyl-hydroperoxide Heteropolitungstatos Difenilsulfóxidos Oxidación selectiva Tert-butilhidroperóxido |
description |
The activity of complex heteropolytungstates of general formula B-α-[M<sup>II</sup><sub>4</sub>(H<sub>2</sub>O)<sub>2</sub>(PW<sub>9</sub>O<sub>34</sub>)<sub>2</sub>]<sup>10-</sup> with M= Co(II), Zn(II), Mn(II) and Cu(II) (PWM) was investigated in the selective oxidation reaction of diphenylsulfide to diphenylsulfoxide in presence of <i>tert</i>-butylhydroperoxide as oxidant. The characterization of phases was performed by X Ray Powder Diffraction, XRD. All phases resulted isomorphous although PWCu is obtained as a mixture of two structural isomers [Cu<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>PW<sub>10</sub>O<sub>38</sub>]<sup>7-</sup>.
The oxidation reaction was carried out in batch at 80°C using toluene as solvent and tbutylhydroperoxide 5-6 M in decane as oxidant for 6 h. The catalytic evaluation made by gas chromatography revealed a similar behavior with conversions of diphenylsulfide around 60% and high selectivity to diphenylsulfoxide near to 95% for most of phases studied while PWCu resulted the most active catalyst presenting a conversion of 84%. The activity rise was correlated with the increase of the oxidant character of the cluster metal(II). |
format |
Articulo Articulo |
author |
Egusquiza, María Gabriela Ben Tayeb, Karima Muñoz, Mercedes Romanelli, Gustavo Pablo Cabello, Carmen Inés Botto, Irma Lía Thomas, Horacio Jorge |
author_facet |
Egusquiza, María Gabriela Ben Tayeb, Karima Muñoz, Mercedes Romanelli, Gustavo Pablo Cabello, Carmen Inés Botto, Irma Lía Thomas, Horacio Jorge |
author_sort |
Egusquiza, María Gabriela |
title |
Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
title_short |
Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
title_full |
Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
title_fullStr |
Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
title_full_unstemmed |
Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
title_sort |
potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
publishDate |
2009 |
url |
http://sedici.unlp.edu.ar/handle/10915/104497 http://hdl.handle.net/11336/56016 https://www.aqa.org.ar/images/anales/pdf9701/9701art15.pdf |
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Repositorios |
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1764820442349043714 |