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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 approach

dc.contributor.authorMartins, Lucas Michelão [UNESP]
dc.contributor.authorde Faria Vieira, Samuel [UNESP]
dc.contributor.authorBaldacim, Gabriel Baldo [UNESP]
dc.contributor.authorBregadiolli, Bruna Andressa [UNESP]
dc.contributor.authorCaraschi, José Cláudio [UNESP]
dc.contributor.authorBatagin-Neto, Augusto [UNESP]
dc.contributor.authorda Silva-Filho, Luiz Carlos [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:14:35Z
dc.date.available2018-12-11T17:14:35Z
dc.date.issued2018-01-01
dc.description.abstractPyrrolo-[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.en
dc.description.affiliationLaboratory of Organic Synthesis and Processes Department of Chemistry São Paulo State University (UNESP) – School of Sciences, Av. Eng. Luiz Edmundo Carrijo Coube, 14-01
dc.description.affiliationSão Paulo State University (UNESP) Campus Itapeva, Rua Geraldo Alckmin, 519
dc.description.affiliationUnespLaboratory of Organic Synthesis and Processes Department of Chemistry São Paulo State University (UNESP) – School of Sciences, Av. Eng. Luiz Edmundo Carrijo Coube, 14-01
dc.description.affiliationUnespSão Paulo State University (UNESP) Campus Itapeva, Rua Geraldo Alckmin, 519
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 16/01599-1
dc.description.sponsorshipIdCNPq: 302753/2015-0
dc.description.sponsorshipIdCNPq: 448310/2014-7
dc.format.extent81-90
dc.identifierhttp://dx.doi.org/10.1016/j.dyepig.2017.08.056
dc.identifier.citationDyes and Pigments, v. 148, p. 81-90.
dc.identifier.doi10.1016/j.dyepig.2017.08.056
dc.identifier.file2-s2.0-85029088418.pdf
dc.identifier.issn1873-3743
dc.identifier.issn0143-7208
dc.identifier.scopus2-s2.0-85029088418
dc.identifier.urihttp://hdl.handle.net/11449/175150
dc.language.isoeng
dc.relation.ispartofDyes and Pigments
dc.relation.ispartofsjr0,819
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectDensity functional calculations
dc.subjectFluorescence
dc.subjectHeterocycles
dc.subjectMulticomponent reactions
dc.subjectNiobium pentachloride
dc.titleImproved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approachen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes2813393825580000[6]
unesp.author.orcid000-0003-4609-9002[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciências e Engenharia, Itapevapt
unesp.departmentEngenharia Industrial Madeireira - ICEpt

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