Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide
- Autores
- Egusquiza, María Gabriela; Ben Tayeb, Karima; Muñoz, Mercedes; Romanelli, Gustavo Pablo; Cabello, Carmen Inés; Botto, Irma Lía; Thomas, Horacio Jorge
- Año de publicación
- 2009
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The activity of complex heteropolytungstates of general formula B-α- [MII4(H2O)2(PW9O34)2]10- (1) 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 tert-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 [Cu2(H2O)2PW10O38]7-.The oxidation reaction was carried out in batch at 80°C using toluene as solvent and t-butylhydroperoxide 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).
Se investigó la actividad de heteropolitungstatos complejos de fórmula general B-α- [MII4(H2O)2(PW9O34)2]10- (PMW) con M= Co(II), Zn(II), Mn(II) y Cu(II) en la reacción de oxidación selectiva de difenilsulfuro a difenilsulfóxido en presencia de peróxido de ter-butilo como oxidante. La caracterización de las fases se realizó por Difracción de Polvos por Rayos X, DRX. El estudio mostró que a excepción del precursor y la fase conteniendo MII4 Cu(II), las fases con M4 = Co(II), Zn(II) y Mn(II) son isomorfas. La fase correspondiente a Cu(II) se obtiene como componente de una mezcla conteniendo además dos isómeros estructurales de fórmula [Cu2(H2O)2PW10O38]7-. La reacción de oxidación se llevó a cabo en batch a 80°C en tolueno como solvente y peróxido de t-butilo como oxidante, durante un período de 6 h. La evaluación catalítica realizada por cromatografía gaseosa reveló un comportamiento similar con conversiones de difenilsulfuro alrededor del 60% y una alta selectividad a difenilsulfóxido no menor al 95% para la mayoría de las fases estudiadas mientras que el sistema que contiene cobre con M(II) = Cu resultó el catalizador más activo presentando una conversión de 84%. El incremento en la actividad se correlaciona con el incremento del carácter oxidante del metal del cluster.
Centro de Investigación y Desarrollo en Ciencias Aplicadas
Centro de Química Inorgánica - Materia
-
Química
heteropolytungstates
diphenylsulfoxides
selective oxidation
tert-butyl-hydroperoxide - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/177404
Ver los metadatos del registro completo
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Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxideEgusquiza, María GabrielaBen Tayeb, KarimaMuñoz, MercedesRomanelli, Gustavo PabloCabello, Carmen InésBotto, Irma LíaThomas, Horacio JorgeQuímicaheteropolytungstatesdiphenylsulfoxidesselective oxidationtert-butyl-hydroperoxideThe activity of complex heteropolytungstates of general formula B-α- [MII4(H2O)2(PW9O34)2]10- (1) 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 tert-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 [Cu2(H2O)2PW10O38]7-.The oxidation reaction was carried out in batch at 80°C using toluene as solvent and t-butylhydroperoxide 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).Se investigó la actividad de heteropolitungstatos complejos de fórmula general B-α- [MII4(H2O)2(PW9O34)2]10- (PMW) con M= Co(II), Zn(II), Mn(II) y Cu(II) en la reacción de oxidación selectiva de difenilsulfuro a difenilsulfóxido en presencia de peróxido de ter-butilo como oxidante. La caracterización de las fases se realizó por Difracción de Polvos por Rayos X, DRX. El estudio mostró que a excepción del precursor y la fase conteniendo MII4 Cu(II), las fases con M4 = Co(II), Zn(II) y Mn(II) son isomorfas. La fase correspondiente a Cu(II) se obtiene como componente de una mezcla conteniendo además dos isómeros estructurales de fórmula [Cu2(H2O)2PW10O38]7-. La reacción de oxidación se llevó a cabo en batch a 80°C en tolueno como solvente y peróxido de t-butilo como oxidante, durante un período de 6 h. La evaluación catalítica realizada por cromatografía gaseosa reveló un comportamiento similar con conversiones de difenilsulfuro alrededor del 60% y una alta selectividad a difenilsulfóxido no menor al 95% para la mayoría de las fases estudiadas mientras que el sistema que contiene cobre con M(II) = Cu resultó el catalizador más activo presentando una conversión de 84%. El incremento en la actividad se correlaciona con el incremento del carácter oxidante del metal del cluster.Centro de Investigación y Desarrollo en Ciencias AplicadasCentro de Química Inorgánica2009info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf166-173http://sedici.unlp.edu.ar/handle/10915/177404enginfo:eu-repo/semantics/altIdentifier/issn/2545-8655info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-11-05T13:27:09Zoai:sedici.unlp.edu.ar:10915/177404Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-11-05 13:27:09.764SEDICI (UNLP) - Universidad Nacional de La Platafalse |
| dc.title.none.fl_str_mv |
Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
| title |
Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide |
| spellingShingle |
Potentiality of heteropolytungstates as catalysts in the selective oxidation of diphenylsulfide to diphenylsulfoxide Egusquiza, María Gabriela Química heteropolytungstates diphenylsulfoxides selective oxidation tert-butyl-hydroperoxide |
| 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 |
| dc.creator.none.fl_str_mv |
Egusquiza, María Gabriela Ben Tayeb, Karima Muñoz, Mercedes Romanelli, Gustavo Pablo Cabello, Carmen Inés Botto, Irma Lía Thomas, Horacio Jorge |
| author |
Egusquiza, María Gabriela |
| author_facet |
Egusquiza, María Gabriela Ben Tayeb, Karima Muñoz, Mercedes Romanelli, Gustavo Pablo Cabello, Carmen Inés Botto, Irma Lía Thomas, Horacio Jorge |
| author_role |
author |
| author2 |
Ben Tayeb, Karima Muñoz, Mercedes Romanelli, Gustavo Pablo Cabello, Carmen Inés Botto, Irma Lía Thomas, Horacio Jorge |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Química heteropolytungstates diphenylsulfoxides selective oxidation tert-butyl-hydroperoxide |
| topic |
Química heteropolytungstates diphenylsulfoxides selective oxidation tert-butyl-hydroperoxide |
| dc.description.none.fl_txt_mv |
The activity of complex heteropolytungstates of general formula B-α- [MII4(H2O)2(PW9O34)2]10- (1) 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 tert-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 [Cu2(H2O)2PW10O38]7-.The oxidation reaction was carried out in batch at 80°C using toluene as solvent and t-butylhydroperoxide 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). Se investigó la actividad de heteropolitungstatos complejos de fórmula general B-α- [MII4(H2O)2(PW9O34)2]10- (PMW) con M= Co(II), Zn(II), Mn(II) y Cu(II) en la reacción de oxidación selectiva de difenilsulfuro a difenilsulfóxido en presencia de peróxido de ter-butilo como oxidante. La caracterización de las fases se realizó por Difracción de Polvos por Rayos X, DRX. El estudio mostró que a excepción del precursor y la fase conteniendo MII4 Cu(II), las fases con M4 = Co(II), Zn(II) y Mn(II) son isomorfas. La fase correspondiente a Cu(II) se obtiene como componente de una mezcla conteniendo además dos isómeros estructurales de fórmula [Cu2(H2O)2PW10O38]7-. La reacción de oxidación se llevó a cabo en batch a 80°C en tolueno como solvente y peróxido de t-butilo como oxidante, durante un período de 6 h. La evaluación catalítica realizada por cromatografía gaseosa reveló un comportamiento similar con conversiones de difenilsulfuro alrededor del 60% y una alta selectividad a difenilsulfóxido no menor al 95% para la mayoría de las fases estudiadas mientras que el sistema que contiene cobre con M(II) = Cu resultó el catalizador más activo presentando una conversión de 84%. El incremento en la actividad se correlaciona con el incremento del carácter oxidante del metal del cluster. Centro de Investigación y Desarrollo en Ciencias Aplicadas Centro de Química Inorgánica |
| description |
The activity of complex heteropolytungstates of general formula B-α- [MII4(H2O)2(PW9O34)2]10- (1) 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 tert-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 [Cu2(H2O)2PW10O38]7-.The oxidation reaction was carried out in batch at 80°C using toluene as solvent and t-butylhydroperoxide 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). |
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2009 |
| dc.date.none.fl_str_mv |
2009 |
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eng |
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eng |
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