K10-montmorillonite as support for a cationic manganese(III)-salen complex

Detalhes bibliográficos
Autor(a) principal: Kuźniarska-Biernacka,Iwona
Data de Publicação: 2009
Outros Autores: Pereira,Clara, Carvalho,Ana P., Pires,João, Freire,Cristina
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000700017
Resumo: A commercial K10-montmorillonite was used as support for the immobilization of a cationic manganese(III)-salen complex. The catalytic behavior of the resulting material was tested in the enantioselective epoxidation of three different alkenes, viz.: styrene, α-methylstyrene and 6-cyano-2,2-dimethylchromene, at 0 ºC, using three different oxidant systems: m-chloroperoxybenzoic acid (m-CPBA) and N-methylmorpholine (NMO) as co-oxidant, iodosylbenzene (PhIO) and sodium hypochlorite. All samples, before and after the catalytic studies, were characterised by nitrogen adsorption at -196 ºC, DRX, FTIR and chemical analysis, in order to evaluate the influence of the substrate/oxidant system on catalyst integrity. The catalytic results demonstrated a strong influence of the substrate and oxidant system on the enantiomeric excess (%ee) values. In some cases, these values were comparable to those in the corresponding homogeneous phase reactions. The results also highlighted the importance of optimizing the oxidant systems, since they may lead to the disruption of the complex from the support, and the consequent catalyst deactivation.
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spelling K10-montmorillonite as support for a cationic manganese(III)-salen complexK10-montmorillonitealkene epoxidationcatalyst supportmanganese(III)-salenA commercial K10-montmorillonite was used as support for the immobilization of a cationic manganese(III)-salen complex. The catalytic behavior of the resulting material was tested in the enantioselective epoxidation of three different alkenes, viz.: styrene, α-methylstyrene and 6-cyano-2,2-dimethylchromene, at 0 ºC, using three different oxidant systems: m-chloroperoxybenzoic acid (m-CPBA) and N-methylmorpholine (NMO) as co-oxidant, iodosylbenzene (PhIO) and sodium hypochlorite. All samples, before and after the catalytic studies, were characterised by nitrogen adsorption at -196 ºC, DRX, FTIR and chemical analysis, in order to evaluate the influence of the substrate/oxidant system on catalyst integrity. The catalytic results demonstrated a strong influence of the substrate and oxidant system on the enantiomeric excess (%ee) values. In some cases, these values were comparable to those in the corresponding homogeneous phase reactions. The results also highlighted the importance of optimizing the oxidant systems, since they may lead to the disruption of the complex from the support, and the consequent catalyst deactivation.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000700017Journal of the Brazilian Chemical Society v.20 n.7 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009000700017info:eu-repo/semantics/openAccessKuźniarska-Biernacka,IwonaPereira,ClaraCarvalho,Ana P.Pires,JoãoFreire,Cristinaeng2009-08-27T00:00:00Zoai:scielo:S0103-50532009000700017Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2009-08-27T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv K10-montmorillonite as support for a cationic manganese(III)-salen complex
title K10-montmorillonite as support for a cationic manganese(III)-salen complex
spellingShingle K10-montmorillonite as support for a cationic manganese(III)-salen complex
Kuźniarska-Biernacka,Iwona
K10-montmorillonite
alkene epoxidation
catalyst support
manganese(III)-salen
title_short K10-montmorillonite as support for a cationic manganese(III)-salen complex
title_full K10-montmorillonite as support for a cationic manganese(III)-salen complex
title_fullStr K10-montmorillonite as support for a cationic manganese(III)-salen complex
title_full_unstemmed K10-montmorillonite as support for a cationic manganese(III)-salen complex
title_sort K10-montmorillonite as support for a cationic manganese(III)-salen complex
author Kuźniarska-Biernacka,Iwona
author_facet Kuźniarska-Biernacka,Iwona
Pereira,Clara
Carvalho,Ana P.
Pires,João
Freire,Cristina
author_role author
author2 Pereira,Clara
Carvalho,Ana P.
Pires,João
Freire,Cristina
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Kuźniarska-Biernacka,Iwona
Pereira,Clara
Carvalho,Ana P.
Pires,João
Freire,Cristina
dc.subject.por.fl_str_mv K10-montmorillonite
alkene epoxidation
catalyst support
manganese(III)-salen
topic K10-montmorillonite
alkene epoxidation
catalyst support
manganese(III)-salen
description A commercial K10-montmorillonite was used as support for the immobilization of a cationic manganese(III)-salen complex. The catalytic behavior of the resulting material was tested in the enantioselective epoxidation of three different alkenes, viz.: styrene, α-methylstyrene and 6-cyano-2,2-dimethylchromene, at 0 ºC, using three different oxidant systems: m-chloroperoxybenzoic acid (m-CPBA) and N-methylmorpholine (NMO) as co-oxidant, iodosylbenzene (PhIO) and sodium hypochlorite. All samples, before and after the catalytic studies, were characterised by nitrogen adsorption at -196 ºC, DRX, FTIR and chemical analysis, in order to evaluate the influence of the substrate/oxidant system on catalyst integrity. The catalytic results demonstrated a strong influence of the substrate and oxidant system on the enantiomeric excess (%ee) values. In some cases, these values were comparable to those in the corresponding homogeneous phase reactions. The results also highlighted the importance of optimizing the oxidant systems, since they may lead to the disruption of the complex from the support, and the consequent catalyst deactivation.
publishDate 2009
dc.date.none.fl_str_mv 2009-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000700017
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000700017
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532009000700017
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.20 n.7 2009
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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