A phenol-based compartmental ligand as a potential chemosensor for zinc(ii) cations
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , |
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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Journal of the Brazilian Chemical Society (Online) |
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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 |
_version_ |
1750318169422036992 |