Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles

Detalhes bibliográficos
Autor(a) principal: Batista, Rosa Maria Ferreira
Data de Publicação: 2004
Outros Autores: Costa, Susana P. G., Raposo, M. Manuela M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/1953
Resumo: Bithienyl-1,3-benzothiazole derivatives were synthesised by reacting various 5-formyl-5’-alkoxy- or 5-formyl-5’-N,N-dialkylamino-2,2’-bithiophenes with ortho-aminobenzenethiol in good to excellent yields. Evaluation of the fluorescence properties of these compounds was carried out. They show strong fluorescence in the 450-600 nm region, as well as high quantum yields and large Stokes’ shifts.
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spelling Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazolesFluorescenceSolvatochromism5-formyl-5’-alkoxy-2,2’-bithiophenes5-formyl-5’-N,N-dialkylamino-2,2’-bithiophenes1,3-benzothiazoles2-(2’,2’’-bithienyl)-1,3-benzothiazoles5-formyl-5 '-N,N-dialkylamino-2,2 '-bithiophenes 1,3-benzothiazoles2-(2',2?-bithienyl)-,3-benzothiazolesScience & TechnologyBithienyl-1,3-benzothiazole derivatives were synthesised by reacting various 5-formyl-5’-alkoxy- or 5-formyl-5’-N,N-dialkylamino-2,2’-bithiophenes with ortho-aminobenzenethiol in good to excellent yields. Evaluation of the fluorescence properties of these compounds was carried out. They show strong fluorescence in the 450-600 nm region, as well as high quantum yields and large Stokes’ shifts.Fundação para a Ciência e Tecnologia.ElsevierUniversidade do MinhoBatista, Rosa Maria FerreiraCosta, Susana P. G.Raposo, M. Manuela M.20042004-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/1953eng"Tetrahedron Letters". 45:13 (2004) 2825-2828.0040-403910.1016/j.tetlet.2004.02.048info: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:RCAAP2023-07-21T12:48:15Zoai:repositorium.sdum.uminho.pt:1822/1953Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:46:26.611575Repositório 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 Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles
title Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles
spellingShingle Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles
Batista, Rosa Maria Ferreira
Fluorescence
Solvatochromism
5-formyl-5’-alkoxy-2,2’-bithiophenes
5-formyl-5’-N,N-dialkylamino-2,2’-bithiophenes
1,3-benzothiazoles
2-(2’,2’’-bithienyl)-1,3-benzothiazoles
5-formyl-5 '-N,N-dialkylamino-2,2 '-bithiophenes 1,3-benzothiazoles
2-(2',2?-bithienyl)-,3-benzothiazoles
Science & Technology
title_short Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles
title_full Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles
title_fullStr Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles
title_full_unstemmed Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles
title_sort Synthesis of new fluorescent 2-(2’, 2’’-bithienyl)-1,3-benzothiazoles
author Batista, Rosa Maria Ferreira
author_facet Batista, Rosa Maria Ferreira
Costa, Susana P. G.
Raposo, M. Manuela M.
author_role author
author2 Costa, Susana P. G.
Raposo, M. Manuela M.
author2_role author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Batista, Rosa Maria Ferreira
Costa, Susana P. G.
Raposo, M. Manuela M.
dc.subject.por.fl_str_mv Fluorescence
Solvatochromism
5-formyl-5’-alkoxy-2,2’-bithiophenes
5-formyl-5’-N,N-dialkylamino-2,2’-bithiophenes
1,3-benzothiazoles
2-(2’,2’’-bithienyl)-1,3-benzothiazoles
5-formyl-5 '-N,N-dialkylamino-2,2 '-bithiophenes 1,3-benzothiazoles
2-(2',2?-bithienyl)-,3-benzothiazoles
Science & Technology
topic Fluorescence
Solvatochromism
5-formyl-5’-alkoxy-2,2’-bithiophenes
5-formyl-5’-N,N-dialkylamino-2,2’-bithiophenes
1,3-benzothiazoles
2-(2’,2’’-bithienyl)-1,3-benzothiazoles
5-formyl-5 '-N,N-dialkylamino-2,2 '-bithiophenes 1,3-benzothiazoles
2-(2',2?-bithienyl)-,3-benzothiazoles
Science & Technology
description Bithienyl-1,3-benzothiazole derivatives were synthesised by reacting various 5-formyl-5’-alkoxy- or 5-formyl-5’-N,N-dialkylamino-2,2’-bithiophenes with ortho-aminobenzenethiol in good to excellent yields. Evaluation of the fluorescence properties of these compounds was carried out. They show strong fluorescence in the 450-600 nm region, as well as high quantum yields and large Stokes’ shifts.
publishDate 2004
dc.date.none.fl_str_mv 2004
2004-01-01T00:00:00Z
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/1822/1953
url http://hdl.handle.net/1822/1953
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv "Tetrahedron Letters". 45:13 (2004) 2825-2828.
0040-4039
10.1016/j.tetlet.2004.02.048
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 Elsevier
publisher.none.fl_str_mv Elsevier
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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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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