A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations

Detalhes bibliográficos
Autor(a) principal: Chen,Jingwen
Data de Publicação: 2009
Outros Autores: Cao,Shuhong, Wang,Dandan, Wu,Shengde, Wang,Xiaoyong
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=S0103-50532009000100004
Resumo: An "end-off"-type compartmental Lewis base, 2,6-bis(2-hydroxybenzyl-2-hydroxyethylamino)methyl-4-methylphenol (L), was synthesized as a potential chemosensor for Zn2+ ions. L coordinates two Zn2+ cations in methanol-water solution, forming a dinuclear complex whose formulation was confirmed by ESI-MS spectroscopy and Job's plot. The fluorescence of L is remarkably enhanced by Zn2+ as compared with K+, Ca2+, Mg2+, Cu2+, Pb2+, Mn2+, Fe3+, Fe2+, Co2+, Cd2+ and Ni2+ ions. The fluorescence enhancement is attributed to the complexation of Zn2+ with L, which interrupts the photoinduced electron transfer process and rigidifies the molecular skeleton of L. The fluorescence of L is greatly dependent on the acidity and polarity of the solvents. This compound may be used as a probe to sense Zn2+ ion in polar protic solvents after proper modification.
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spelling A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cationschemosensorfluorescence mechanismphenol derivativesolvent effectszinc(II)An "end-off"-type compartmental Lewis base, 2,6-bis(2-hydroxybenzyl-2-hydroxyethylamino)methyl-4-methylphenol (L), was synthesized as a potential chemosensor for Zn2+ ions. L coordinates two Zn2+ cations in methanol-water solution, forming a dinuclear complex whose formulation was confirmed by ESI-MS spectroscopy and Job's plot. The fluorescence of L is remarkably enhanced by Zn2+ as compared with K+, Ca2+, Mg2+, Cu2+, Pb2+, Mn2+, Fe3+, Fe2+, Co2+, Cd2+ and Ni2+ ions. The fluorescence enhancement is attributed to the complexation of Zn2+ with L, which interrupts the photoinduced electron transfer process and rigidifies the molecular skeleton of L. The fluorescence of L is greatly dependent on the acidity and polarity of the solvents. This compound may be used as a probe to sense Zn2+ ion in polar protic solvents after proper modification.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000100004Journal of the Brazilian Chemical Society v.20 n.1 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009000100004info:eu-repo/semantics/openAccessChen,JingwenCao,ShuhongWang,DandanWu,ShengdeWang,Xiaoyongeng2009-01-14T00:00:00Zoai:scielo:S0103-50532009000100004Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2009-01-14T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
title A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
spellingShingle A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
Chen,Jingwen
chemosensor
fluorescence mechanism
phenol derivative
solvent effects
zinc(II)
title_short A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
title_full A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
title_fullStr A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
title_full_unstemmed A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
title_sort A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
author Chen,Jingwen
author_facet Chen,Jingwen
Cao,Shuhong
Wang,Dandan
Wu,Shengde
Wang,Xiaoyong
author_role author
author2 Cao,Shuhong
Wang,Dandan
Wu,Shengde
Wang,Xiaoyong
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Chen,Jingwen
Cao,Shuhong
Wang,Dandan
Wu,Shengde
Wang,Xiaoyong
dc.subject.por.fl_str_mv chemosensor
fluorescence mechanism
phenol derivative
solvent effects
zinc(II)
topic chemosensor
fluorescence mechanism
phenol derivative
solvent effects
zinc(II)
description An "end-off"-type compartmental Lewis base, 2,6-bis(2-hydroxybenzyl-2-hydroxyethylamino)methyl-4-methylphenol (L), was synthesized as a potential chemosensor for Zn2+ ions. L coordinates two Zn2+ cations in methanol-water solution, forming a dinuclear complex whose formulation was confirmed by ESI-MS spectroscopy and Job's plot. The fluorescence of L is remarkably enhanced by Zn2+ as compared with K+, Ca2+, Mg2+, Cu2+, Pb2+, Mn2+, Fe3+, Fe2+, Co2+, Cd2+ and Ni2+ ions. The fluorescence enhancement is attributed to the complexation of Zn2+ with L, which interrupts the photoinduced electron transfer process and rigidifies the molecular skeleton of L. The fluorescence of L is greatly dependent on the acidity and polarity of the solvents. This compound may be used as a probe to sense Zn2+ ion in polar protic solvents after proper modification.
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=S0103-50532009000100004
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000100004
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532009000100004
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.20 n.1 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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