Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)

Detalhes bibliográficos
Autor(a) principal: Pina, J.
Data de Publicação: 2006
Outros Autores: Burrows, H. D., Becker, R. S., Dias, F. B., Maçanita, A. L., Melo, J. Seixas de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10392
https://doi.org/10.1021/jp055455v
Resumo: The photophysics of six oligothiophenes end-capped with cyano groups (CNαn) was investigated in solution at room and low temperature. The study comprises singlet−singlet and triplet−triplet absorption and emission spectra together with lifetimes and quantum yields for all the radiative and nonradiative processes. From the lifetimes and quantum yields, it was possible to extract the rate constants for all the processes. Singlet oxygen yields were also determined, revealing an efficient sensitization (SΔ ≈ 1) of its formation by the triplet state of the CNαn. The introduction of the cyano groups is found to decrease the energetic separation between the highest occupied molecular orbital and the lowest unoccupied molecular orbital, leading to a red shift of the absorption and the emission when compared with the unsubstituted counterparts, the α-oligothiophenes. Phosphorescence is only observed for the first member of the series, CNα1.
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spelling Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)The photophysics of six oligothiophenes end-capped with cyano groups (CNαn) was investigated in solution at room and low temperature. The study comprises singlet−singlet and triplet−triplet absorption and emission spectra together with lifetimes and quantum yields for all the radiative and nonradiative processes. From the lifetimes and quantum yields, it was possible to extract the rate constants for all the processes. Singlet oxygen yields were also determined, revealing an efficient sensitization (SΔ ≈ 1) of its formation by the triplet state of the CNαn. The introduction of the cyano groups is found to decrease the energetic separation between the highest occupied molecular orbital and the lowest unoccupied molecular orbital, leading to a red shift of the absorption and the emission when compared with the unsubstituted counterparts, the α-oligothiophenes. Phosphorescence is only observed for the first member of the series, CNα1.American Chemical Society2006-03-06info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10392http://hdl.handle.net/10316/10392https://doi.org/10.1021/jp055455vengThe Journal of Physical Chemistry B. 110:13 (2006) 6499-65051520-6106Pina, J.Burrows, H. D.Becker, R. S.Dias, F. B.Maçanita, A. L.Melo, J. Seixas deinfo: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:RCAAP2021-09-22T11:00:52Zoai:estudogeral.uc.pt:10316/10392Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:15.681808Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)
title Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)
spellingShingle Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)
Pina, J.
title_short Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)
title_full Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)
title_fullStr Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)
title_full_unstemmed Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)
title_sort Photophysical Studies of α,ω-Dicyano-oligothiophenes NC(C4H2S)nCN (n = 1−6)
author Pina, J.
author_facet Pina, J.
Burrows, H. D.
Becker, R. S.
Dias, F. B.
Maçanita, A. L.
Melo, J. Seixas de
author_role author
author2 Burrows, H. D.
Becker, R. S.
Dias, F. B.
Maçanita, A. L.
Melo, J. Seixas de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Pina, J.
Burrows, H. D.
Becker, R. S.
Dias, F. B.
Maçanita, A. L.
Melo, J. Seixas de
description The photophysics of six oligothiophenes end-capped with cyano groups (CNαn) was investigated in solution at room and low temperature. The study comprises singlet−singlet and triplet−triplet absorption and emission spectra together with lifetimes and quantum yields for all the radiative and nonradiative processes. From the lifetimes and quantum yields, it was possible to extract the rate constants for all the processes. Singlet oxygen yields were also determined, revealing an efficient sensitization (SΔ ≈ 1) of its formation by the triplet state of the CNαn. The introduction of the cyano groups is found to decrease the energetic separation between the highest occupied molecular orbital and the lowest unoccupied molecular orbital, leading to a red shift of the absorption and the emission when compared with the unsubstituted counterparts, the α-oligothiophenes. Phosphorescence is only observed for the first member of the series, CNα1.
publishDate 2006
dc.date.none.fl_str_mv 2006-03-06
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/10392
http://hdl.handle.net/10316/10392
https://doi.org/10.1021/jp055455v
url http://hdl.handle.net/10316/10392
https://doi.org/10.1021/jp055455v
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv The Journal of Physical Chemistry B. 110:13 (2006) 6499-6505
1520-6106
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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