Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach

Detalhes bibliográficos
Autor(a) principal: Martins, Lucas Michelão [UNESP]
Data de Publicação: 2018
Outros Autores: de Faria Vieira, Samuel [UNESP], Baldacim, Gabriel Baldo [UNESP], Bregadiolli, Bruna Andressa [UNESP], Caraschi, José Cláudio [UNESP], Batagin-Neto, Augusto [UNESP], da Silva-Filho, Luiz Carlos [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.dyepig.2017.08.056
http://hdl.handle.net/11449/175150
Resumo: Pyrrolo-[3,2-b]pyrroles represent a class of promising materials for application in organic electronics with interesting optoelectronic properties and great synthesis versatility, but yields obtained from varied synthetic routes are still very low, hindering their effective application for industrial purposes. In this report, we present a method for the synthesis of tetraaryl-1,4-dihydropyrrolo-[3,2-b]pyrrole derivatives by multicomponent reactions employing niobium pentachloride as a catalyst. The optical characterization of the products is also presented. Electronic structure calculations were performed to help the interpretation of the synthesis process, as well as the optical properties of the systems. Excellent yields and low reaction times were obtained, indicating that NbCl5 is an efficient catalyst for such systems. The products show promising properties for optoelectronic applications that can be adjusted by the choice of benzaldehyde derivatives used in the synthesis.
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spelling Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approachDensity functional calculationsFluorescenceHeterocyclesMulticomponent reactionsNiobium pentachloridePyrrolo-[3,2-b]pyrroles represent a class of promising materials for application in organic electronics with interesting optoelectronic properties and great synthesis versatility, but yields obtained from varied synthetic routes are still very low, hindering their effective application for industrial purposes. In this report, we present a method for the synthesis of tetraaryl-1,4-dihydropyrrolo-[3,2-b]pyrrole derivatives by multicomponent reactions employing niobium pentachloride as a catalyst. The optical characterization of the products is also presented. Electronic structure calculations were performed to help the interpretation of the synthesis process, as well as the optical properties of the systems. Excellent yields and low reaction times were obtained, indicating that NbCl5 is an efficient catalyst for such systems. The products show promising properties for optoelectronic applications that can be adjusted by the choice of benzaldehyde derivatives used in the synthesis.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Laboratory of Organic Synthesis and Processes Department of Chemistry São Paulo State University (UNESP) – School of Sciences, Av. Eng. Luiz Edmundo Carrijo Coube, 14-01São Paulo State University (UNESP) Campus Itapeva, Rua Geraldo Alckmin, 519Laboratory of Organic Synthesis and Processes Department of Chemistry São Paulo State University (UNESP) – School of Sciences, Av. Eng. Luiz Edmundo Carrijo Coube, 14-01São Paulo State University (UNESP) Campus Itapeva, Rua Geraldo Alckmin, 519FAPESP: 16/01599-1CNPq: 302753/2015-0CNPq: 448310/2014-7Universidade Estadual Paulista (Unesp)Martins, Lucas Michelão [UNESP]de Faria Vieira, Samuel [UNESP]Baldacim, Gabriel Baldo [UNESP]Bregadiolli, Bruna Andressa [UNESP]Caraschi, José Cláudio [UNESP]Batagin-Neto, Augusto [UNESP]da Silva-Filho, Luiz Carlos [UNESP]2018-12-11T17:14:35Z2018-12-11T17:14:35Z2018-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article81-90application/pdfhttp://dx.doi.org/10.1016/j.dyepig.2017.08.056Dyes and Pigments, v. 148, p. 81-90.1873-37430143-7208http://hdl.handle.net/11449/17515010.1016/j.dyepig.2017.08.0562-s2.0-850290884182-s2.0-85029088418.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDyes and Pigments0,819info:eu-repo/semantics/openAccess2024-01-09T06:25:03Zoai:repositorio.unesp.br:11449/175150Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:29:55.301045Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
title Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
spellingShingle Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
Martins, Lucas Michelão [UNESP]
Density functional calculations
Fluorescence
Heterocycles
Multicomponent reactions
Niobium pentachloride
title_short Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
title_full Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
title_fullStr Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
title_full_unstemmed Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
title_sort Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
author Martins, Lucas Michelão [UNESP]
author_facet Martins, Lucas Michelão [UNESP]
de Faria Vieira, Samuel [UNESP]
Baldacim, Gabriel Baldo [UNESP]
Bregadiolli, Bruna Andressa [UNESP]
Caraschi, José Cláudio [UNESP]
Batagin-Neto, Augusto [UNESP]
da Silva-Filho, Luiz Carlos [UNESP]
author_role author
author2 de Faria Vieira, Samuel [UNESP]
Baldacim, Gabriel Baldo [UNESP]
Bregadiolli, Bruna Andressa [UNESP]
Caraschi, José Cláudio [UNESP]
Batagin-Neto, Augusto [UNESP]
da Silva-Filho, Luiz Carlos [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Martins, Lucas Michelão [UNESP]
de Faria Vieira, Samuel [UNESP]
Baldacim, Gabriel Baldo [UNESP]
Bregadiolli, Bruna Andressa [UNESP]
Caraschi, José Cláudio [UNESP]
Batagin-Neto, Augusto [UNESP]
da Silva-Filho, Luiz Carlos [UNESP]
dc.subject.por.fl_str_mv Density functional calculations
Fluorescence
Heterocycles
Multicomponent reactions
Niobium pentachloride
topic Density functional calculations
Fluorescence
Heterocycles
Multicomponent reactions
Niobium pentachloride
description Pyrrolo-[3,2-b]pyrroles represent a class of promising materials for application in organic electronics with interesting optoelectronic properties and great synthesis versatility, but yields obtained from varied synthetic routes are still very low, hindering their effective application for industrial purposes. In this report, we present a method for the synthesis of tetraaryl-1,4-dihydropyrrolo-[3,2-b]pyrrole derivatives by multicomponent reactions employing niobium pentachloride as a catalyst. The optical characterization of the products is also presented. Electronic structure calculations were performed to help the interpretation of the synthesis process, as well as the optical properties of the systems. Excellent yields and low reaction times were obtained, indicating that NbCl5 is an efficient catalyst for such systems. The products show promising properties for optoelectronic applications that can be adjusted by the choice of benzaldehyde derivatives used in the synthesis.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:14:35Z
2018-12-11T17:14:35Z
2018-01-01
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://dx.doi.org/10.1016/j.dyepig.2017.08.056
Dyes and Pigments, v. 148, p. 81-90.
1873-3743
0143-7208
http://hdl.handle.net/11449/175150
10.1016/j.dyepig.2017.08.056
2-s2.0-85029088418
2-s2.0-85029088418.pdf
url http://dx.doi.org/10.1016/j.dyepig.2017.08.056
http://hdl.handle.net/11449/175150
identifier_str_mv Dyes and Pigments, v. 148, p. 81-90.
1873-3743
0143-7208
10.1016/j.dyepig.2017.08.056
2-s2.0-85029088418
2-s2.0-85029088418.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Dyes and Pigments
0,819
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 81-90
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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