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Multicomponent reactions mediated by NbCl5 for the synthesis of phthalonitrile-quinoline dyads: Methodology, scope, mechanistic insights and applications in phthalocyanine synthesis

dc.contributor.authorBartolomeu, Aloisio de A.
dc.contributor.authorBrocksom, Timothy J.
dc.contributor.authorda Silva Filho, Luiz C. [UNESP]
dc.contributor.authorde Oliveira, Kleber T.
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T16:51:42Z
dc.date.available2018-12-11T16:51:42Z
dc.date.issued2018-04-01
dc.description.abstractHerein, we demonstrate the efficiency of NbCl5 to promote a multicomponent reaction (MCR) for the synthesis of a library of phthalonitrile-quinoline dyads, which are very useful and new functionalized building blocks for phthalocyanine (PC) synthesis. Experimental mechanistic insights on the key MCR process are described, using a deuterated reagent, clearly showing the pericyclic nature of a hetero-Diels-Alder reaction. Examples of phthalocyanine (PC) syntheses were performed in order to demonstrate the versatility of the phthalonitrile-quinoline dyads. Preliminary photophysical measurements show that our phthalonitrile library is very promising for the production of new molecular scaffolds of PC derivatives with potential applications.en
dc.description.affiliationDepartment of Chemistry Federal University of São Carlos (UFSCar)
dc.description.affiliationDepartment of Chemistry São Paulo State University (UNESP) School of Sciences
dc.description.affiliationUnespDepartment of Chemistry São Paulo State University (UNESP) School of Sciences
dc.description.sponsorshipCompanhia Brasileira de Metalurgia e Mineração
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2011/13993-2
dc.description.sponsorshipIdFAPESP: 2013/07276-1
dc.description.sponsorshipIdFAPESP: 2014/24506-3
dc.description.sponsorshipIdFAPESP: 2015/21110-4
dc.format.extent391-402
dc.identifierhttp://dx.doi.org/10.1016/j.dyepig.2017.12.065
dc.identifier.citationDyes and Pigments, v. 151, p. 391-402.
dc.identifier.doi10.1016/j.dyepig.2017.12.065
dc.identifier.file2-s2.0-85041472046.pdf
dc.identifier.issn1873-3743
dc.identifier.issn0143-7208
dc.identifier.scopus2-s2.0-85041472046
dc.identifier.urihttp://hdl.handle.net/11449/170617
dc.language.isoeng
dc.relation.ispartofDyes and Pigments
dc.relation.ispartofsjr0,819
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectMulticomponent reactions
dc.subjectNbCl5
dc.subjectPhthalocyanines
dc.subjectPhthalonitrile-quinoline dyads
dc.titleMulticomponent reactions mediated by NbCl5 for the synthesis of phthalonitrile-quinoline dyads: Methodology, scope, mechanistic insights and applications in phthalocyanine synthesisen
dc.typeArtigo
dspace.entity.typePublication

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