Photochemistry and photophysics of thienocarbazoles

Detalhes bibliográficos
Autor(a) principal: Melo, J. Seixas de
Data de Publicação: 2003
Outros Autores: Rodrigues, L.M., Serpa, C., Arnaut, L.G., Ferreira, Isabel C.F.R., Queiroz, Maria João R.P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10198/816
Resumo: Two methylated thienocarbazoles and two of their synthetic nitro-precursors have been examined by absorption, luminescence, laser flash photolysis and photoacoustic techniques. Their spectroscopic and photophysical characterization involves fluorescence spectra, fluorescence quantum yields and lifetimes, and phosphorescence spectra and phosphorescence lifetimes for all the compounds. Triplet–singlet difference absorption spectra, triplet molar absorption coefficients, triplet lifetimes, intersystem crossing S1 ~~→T1 and singlet molecular oxygen yields were obtained for the thienocarbazoles. In the case of the thienocarbazoles it was found that the lowest-lying singlet and triplet excited states, S1 and T1, are of ╥, ╥* origin, whereas for their precursors S1 is n,╥*, and T1 is ╥, ╥*. In both thienocarbazoles it appears that the thianaphthene ring dictates the S1 ~~→T1 yield, albeit there is less predominance of that ring in the triplet state of the linear thienocarbazole, which leads to a decrease in the observed /T value
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spelling Photochemistry and photophysics of thienocarbazolesTwo methylated thienocarbazoles and two of their synthetic nitro-precursors have been examined by absorption, luminescence, laser flash photolysis and photoacoustic techniques. Their spectroscopic and photophysical characterization involves fluorescence spectra, fluorescence quantum yields and lifetimes, and phosphorescence spectra and phosphorescence lifetimes for all the compounds. Triplet–singlet difference absorption spectra, triplet molar absorption coefficients, triplet lifetimes, intersystem crossing S1 ~~→T1 and singlet molecular oxygen yields were obtained for the thienocarbazoles. In the case of the thienocarbazoles it was found that the lowest-lying singlet and triplet excited states, S1 and T1, are of ╥, ╥* origin, whereas for their precursors S1 is n,╥*, and T1 is ╥, ╥*. In both thienocarbazoles it appears that the thianaphthene ring dictates the S1 ~~→T1 yield, albeit there is less predominance of that ring in the triplet state of the linear thienocarbazole, which leads to a decrease in the observed /T valueWiley IntersicenceBiblioteca Digital do IPBMelo, J. Seixas deRodrigues, L.M.Serpa, C.Arnaut, L.G.Ferreira, Isabel C.F.R.Queiroz, Maria João R.P.2008-09-12T11:11:10Z20032003-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10198/816engMelo, J. Seixas de; Rodrigues, L.M.; Serpa, C.; Arnaut, L.G.; Ferreira, Isabel C.F.R.; Queiroz, Maria João R.P. (2003). Photochemistry and photophysics of thienocarbazoles. Photochemistry and Photobiology. ISSN 1751-1097. p. 121-1281751-109710.1562/0031-8655(2003)0770121PAPOT2.0.CO2info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-06-21T01:18:19ZPortal AgregadorONG
dc.title.none.fl_str_mv Photochemistry and photophysics of thienocarbazoles
title Photochemistry and photophysics of thienocarbazoles
spellingShingle Photochemistry and photophysics of thienocarbazoles
Melo, J. Seixas de
title_short Photochemistry and photophysics of thienocarbazoles
title_full Photochemistry and photophysics of thienocarbazoles
title_fullStr Photochemistry and photophysics of thienocarbazoles
title_full_unstemmed Photochemistry and photophysics of thienocarbazoles
title_sort Photochemistry and photophysics of thienocarbazoles
author Melo, J. Seixas de
author_facet Melo, J. Seixas de
Rodrigues, L.M.
Serpa, C.
Arnaut, L.G.
Ferreira, Isabel C.F.R.
Queiroz, Maria João R.P.
author_role author
author2 Rodrigues, L.M.
Serpa, C.
Arnaut, L.G.
Ferreira, Isabel C.F.R.
Queiroz, Maria João R.P.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Biblioteca Digital do IPB
dc.contributor.author.fl_str_mv Melo, J. Seixas de
Rodrigues, L.M.
Serpa, C.
Arnaut, L.G.
Ferreira, Isabel C.F.R.
Queiroz, Maria João R.P.
description Two methylated thienocarbazoles and two of their synthetic nitro-precursors have been examined by absorption, luminescence, laser flash photolysis and photoacoustic techniques. Their spectroscopic and photophysical characterization involves fluorescence spectra, fluorescence quantum yields and lifetimes, and phosphorescence spectra and phosphorescence lifetimes for all the compounds. Triplet–singlet difference absorption spectra, triplet molar absorption coefficients, triplet lifetimes, intersystem crossing S1 ~~→T1 and singlet molecular oxygen yields were obtained for the thienocarbazoles. In the case of the thienocarbazoles it was found that the lowest-lying singlet and triplet excited states, S1 and T1, are of ╥, ╥* origin, whereas for their precursors S1 is n,╥*, and T1 is ╥, ╥*. In both thienocarbazoles it appears that the thianaphthene ring dictates the S1 ~~→T1 yield, albeit there is less predominance of that ring in the triplet state of the linear thienocarbazole, which leads to a decrease in the observed /T value
publishDate 2003
dc.date.none.fl_str_mv 2003
2003-01-01T00:00:00Z
2008-09-12T11:11:10Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10198/816
url http://hdl.handle.net/10198/816
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Melo, J. Seixas de; Rodrigues, L.M.; Serpa, C.; Arnaut, L.G.; Ferreira, Isabel C.F.R.; Queiroz, Maria João R.P. (2003). Photochemistry and photophysics of thienocarbazoles. Photochemistry and Photobiology. ISSN 1751-1097. p. 121-128
1751-1097
10.1562/0031-8655(2003)0770121PAPOT2.0.CO2
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Wiley Intersicence
publisher.none.fl_str_mv Wiley Intersicence
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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