Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene

Detalhes bibliográficos
Autor(a) principal: Ghorbanloo,Massomeh
Data de Publicação: 2014
Outros Autores: Ghamari,Somayeh, Shahbakhsh,Nahid, Ng,Seik Weng
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=S0103-50532014001100019
Resumo: L-Phenylalanine reacts with nickel-exchanged zeolite Y to form diaquabis(L-phenylalaninato)nickel(II), which is encapsulated in the pores of the zeolite. In this zeolite-encapsulated form, the nickel derivative functions as an efficient catalyst when cyclohexene, toluene and ethyl benzene are oxidized by hydrogen peroxide in the presence of sodium bicarbonate (as co-catalyst). The catalyst was readily recovered from the reaction mixture, and it could be re-used for other three runs without noticeable loss of activity. The heterogeneous catalyst exhibited significantly higher activity and selectivity compared with diaquabis(L-phenylalaninato)nickel(II) itself.
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spelling Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzeneencapsulated catalystzeoliteheterogeneoushydrogen peroxideco-catalystL-Phenylalanine reacts with nickel-exchanged zeolite Y to form diaquabis(L-phenylalaninato)nickel(II), which is encapsulated in the pores of the zeolite. In this zeolite-encapsulated form, the nickel derivative functions as an efficient catalyst when cyclohexene, toluene and ethyl benzene are oxidized by hydrogen peroxide in the presence of sodium bicarbonate (as co-catalyst). The catalyst was readily recovered from the reaction mixture, and it could be re-used for other three runs without noticeable loss of activity. The heterogeneous catalyst exhibited significantly higher activity and selectivity compared with diaquabis(L-phenylalaninato)nickel(II) itself.Sociedade Brasileira de Química2014-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014001100019Journal of the Brazilian Chemical Society v.25 n.11 2014reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20140194info:eu-repo/semantics/openAccessGhorbanloo,MassomehGhamari,SomayehShahbakhsh,NahidNg,Seik Wengeng2014-11-13T00:00:00Zoai:scielo:S0103-50532014001100019Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2014-11-13T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene
title Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene
spellingShingle Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene
Ghorbanloo,Massomeh
encapsulated catalyst
zeolite
heterogeneous
hydrogen peroxide
co-catalyst
title_short Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene
title_full Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene
title_fullStr Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene
title_full_unstemmed Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene
title_sort Diaquabis(L-phenylalaninato)nickel(II) encapsulated in zeolite: an efficient heterogeneous catalyst system for the oxidation of cyclohexene, toluene and ethyl benzene
author Ghorbanloo,Massomeh
author_facet Ghorbanloo,Massomeh
Ghamari,Somayeh
Shahbakhsh,Nahid
Ng,Seik Weng
author_role author
author2 Ghamari,Somayeh
Shahbakhsh,Nahid
Ng,Seik Weng
author2_role author
author
author
dc.contributor.author.fl_str_mv Ghorbanloo,Massomeh
Ghamari,Somayeh
Shahbakhsh,Nahid
Ng,Seik Weng
dc.subject.por.fl_str_mv encapsulated catalyst
zeolite
heterogeneous
hydrogen peroxide
co-catalyst
topic encapsulated catalyst
zeolite
heterogeneous
hydrogen peroxide
co-catalyst
description L-Phenylalanine reacts with nickel-exchanged zeolite Y to form diaquabis(L-phenylalaninato)nickel(II), which is encapsulated in the pores of the zeolite. In this zeolite-encapsulated form, the nickel derivative functions as an efficient catalyst when cyclohexene, toluene and ethyl benzene are oxidized by hydrogen peroxide in the presence of sodium bicarbonate (as co-catalyst). The catalyst was readily recovered from the reaction mixture, and it could be re-used for other three runs without noticeable loss of activity. The heterogeneous catalyst exhibited significantly higher activity and selectivity compared with diaquabis(L-phenylalaninato)nickel(II) itself.
publishDate 2014
dc.date.none.fl_str_mv 2014-11-01
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=S0103-50532014001100019
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014001100019
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20140194
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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.25 n.11 2014
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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