Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
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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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 |
|
_version_ |
1808129431759224832 |