Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling

Detalhes bibliográficos
Autor(a) principal: Raposo, M. Manuela M.
Data de Publicação: 2004
Outros Autores: Fonseca, A. Maurício C., Kirsch, G.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/2019
Resumo: A synthesis of donor-acceptor-substituted oligothiophenes by Stille coupling is described. The 5´-estanyl derivatives, readily prepared from 5-alkoxy- and 5-amino-2,2´-bithiophenes 7 were coupled with the appropriate aryl or heteroaryl bromides to give the title compounds.
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spelling Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling5-alkoxy- and 5-amino-2,2´-bithiophenesStille couplingDonor-acceptor oligothiophenesUV-visible spectroscopyChromophoresSolvatochromismNon-linear optical (NLO) materialNLO applicationsScience & TechnologyA synthesis of donor-acceptor-substituted oligothiophenes by Stille coupling is described. The 5´-estanyl derivatives, readily prepared from 5-alkoxy- and 5-amino-2,2´-bithiophenes 7 were coupled with the appropriate aryl or heteroaryl bromides to give the title compounds.Fundação para a Ciência e Tecnologia. FEDER - POCTI/QUI/37816/2001.ElsevierUniversidade do MinhoRaposo, M. Manuela M.Fonseca, A. Maurício C.Kirsch, G.20042004-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/2019eng"Tetrahedron". 60:18 (2004) 4071-4078.0040-402010.1016/j.tet.2004.03.022info: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:RCAAP2023-07-21T12:19:37Zoai:repositorium.sdum.uminho.pt:1822/2019Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:12:35.652025Repositório 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 donor-acceptor substituted oligothiophenes by Stille coupling
title Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling
spellingShingle Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling
Raposo, M. Manuela M.
5-alkoxy- and 5-amino-2,2´-bithiophenes
Stille coupling
Donor-acceptor oligothiophenes
UV-visible spectroscopy
Chromophores
Solvatochromism
Non-linear optical (NLO) material
NLO applications
Science & Technology
title_short Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling
title_full Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling
title_fullStr Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling
title_full_unstemmed Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling
title_sort Synthesis of donor-acceptor substituted oligothiophenes by Stille coupling
author Raposo, M. Manuela M.
author_facet Raposo, M. Manuela M.
Fonseca, A. Maurício C.
Kirsch, G.
author_role author
author2 Fonseca, A. Maurício C.
Kirsch, G.
author2_role author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Raposo, M. Manuela M.
Fonseca, A. Maurício C.
Kirsch, G.
dc.subject.por.fl_str_mv 5-alkoxy- and 5-amino-2,2´-bithiophenes
Stille coupling
Donor-acceptor oligothiophenes
UV-visible spectroscopy
Chromophores
Solvatochromism
Non-linear optical (NLO) material
NLO applications
Science & Technology
topic 5-alkoxy- and 5-amino-2,2´-bithiophenes
Stille coupling
Donor-acceptor oligothiophenes
UV-visible spectroscopy
Chromophores
Solvatochromism
Non-linear optical (NLO) material
NLO applications
Science & Technology
description A synthesis of donor-acceptor-substituted oligothiophenes by Stille coupling is described. The 5´-estanyl derivatives, readily prepared from 5-alkoxy- and 5-amino-2,2´-bithiophenes 7 were coupled with the appropriate aryl or heteroaryl bromides to give the title compounds.
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/1822/2019
url http://hdl.handle.net/1822/2019
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv "Tetrahedron". 60:18 (2004) 4071-4078.
0040-4020
10.1016/j.tet.2004.03.022
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
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
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
repository.mail.fl_str_mv
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