Spectroscopic and photochemical properties of some annulated boldine derivatives

Detalhes bibliográficos
Autor(a) principal: Hidalgo,María E
Data de Publicação: 2010
Outros Autores: Alarcón,Myriam G., Ojeda,Juan R., Fernández,Ernesto C., Sobarzo-Sánchez,Eduardo M., De la Fuent,Julio R.
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=S0103-50532010001200006
Resumo: The aim of this study was to determine the influence of the substituent groups on the photostability of eight boldine derivatives, including some oxazole and oxazinone derivatives, in order to increase the sunscreen protection properties previously demonstrated for boldine. Such derivatives showed bands similar to those of boldine in the absorption and emission spectrum. The spectroscopic properties are pH dependent. The photostability of the derivative compounds was higher than that of boldine, in accordance with the low value of the photoconsumption quantum yield determined. The low fluorescence quantum yield values observed for boldine 1 and 4 as both base and hydrochloride derivative compounds led us to postulate that these compounds are deactivated by a mechanism different to the fluorescence pathway, probably due to the electron-withdrawing inductive effect of NO for boldine 1, and to the increase of the aromatic framework for boldine 4.
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spelling Spectroscopic and photochemical properties of some annulated boldine derivativesboldineoxazol-oxazinone derivativesphotostabilityThe aim of this study was to determine the influence of the substituent groups on the photostability of eight boldine derivatives, including some oxazole and oxazinone derivatives, in order to increase the sunscreen protection properties previously demonstrated for boldine. Such derivatives showed bands similar to those of boldine in the absorption and emission spectrum. The spectroscopic properties are pH dependent. The photostability of the derivative compounds was higher than that of boldine, in accordance with the low value of the photoconsumption quantum yield determined. The low fluorescence quantum yield values observed for boldine 1 and 4 as both base and hydrochloride derivative compounds led us to postulate that these compounds are deactivated by a mechanism different to the fluorescence pathway, probably due to the electron-withdrawing inductive effect of NO for boldine 1, and to the increase of the aromatic framework for boldine 4.Sociedade Brasileira de Química2010-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010001200006Journal of the Brazilian Chemical Society v.21 n.12 2010reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532010001200006info:eu-repo/semantics/openAccessHidalgo,María EAlarcón,Myriam G.Ojeda,Juan R.Fernández,Ernesto C.Sobarzo-Sánchez,Eduardo M.De la Fuent,Julio R.eng2010-12-16T00:00:00Zoai:scielo:S0103-50532010001200006Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2010-12-16T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Spectroscopic and photochemical properties of some annulated boldine derivatives
title Spectroscopic and photochemical properties of some annulated boldine derivatives
spellingShingle Spectroscopic and photochemical properties of some annulated boldine derivatives
Hidalgo,María E
boldine
oxazol-oxazinone derivatives
photostability
title_short Spectroscopic and photochemical properties of some annulated boldine derivatives
title_full Spectroscopic and photochemical properties of some annulated boldine derivatives
title_fullStr Spectroscopic and photochemical properties of some annulated boldine derivatives
title_full_unstemmed Spectroscopic and photochemical properties of some annulated boldine derivatives
title_sort Spectroscopic and photochemical properties of some annulated boldine derivatives
author Hidalgo,María E
author_facet Hidalgo,María E
Alarcón,Myriam G.
Ojeda,Juan R.
Fernández,Ernesto C.
Sobarzo-Sánchez,Eduardo M.
De la Fuent,Julio R.
author_role author
author2 Alarcón,Myriam G.
Ojeda,Juan R.
Fernández,Ernesto C.
Sobarzo-Sánchez,Eduardo M.
De la Fuent,Julio R.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Hidalgo,María E
Alarcón,Myriam G.
Ojeda,Juan R.
Fernández,Ernesto C.
Sobarzo-Sánchez,Eduardo M.
De la Fuent,Julio R.
dc.subject.por.fl_str_mv boldine
oxazol-oxazinone derivatives
photostability
topic boldine
oxazol-oxazinone derivatives
photostability
description The aim of this study was to determine the influence of the substituent groups on the photostability of eight boldine derivatives, including some oxazole and oxazinone derivatives, in order to increase the sunscreen protection properties previously demonstrated for boldine. Such derivatives showed bands similar to those of boldine in the absorption and emission spectrum. The spectroscopic properties are pH dependent. The photostability of the derivative compounds was higher than that of boldine, in accordance with the low value of the photoconsumption quantum yield determined. The low fluorescence quantum yield values observed for boldine 1 and 4 as both base and hydrochloride derivative compounds led us to postulate that these compounds are deactivated by a mechanism different to the fluorescence pathway, probably due to the electron-withdrawing inductive effect of NO for boldine 1, and to the increase of the aromatic framework for boldine 4.
publishDate 2010
dc.date.none.fl_str_mv 2010-12-01
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=S0103-50532010001200006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010001200006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532010001200006
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.21 n.12 2010
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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