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dc.contributor.authorReis, Lindomar A.-
dc.contributor.authorLigiéro, Carolina Bastos Pereira-
dc.contributor.authorAndrade, Acácio Aparecido de Castro-
dc.contributor.authorTaylor, Jason Guy-
dc.contributor.authorMiranda, Paulo Cesar Muniz de Lacerda-
dc.date.accessioned2015-04-09T10:56:19Z-
dc.date.available2015-04-09T10:56:19Z-
dc.date.issued2012-
dc.identifier.citationREIS, L. A. et al. Preparation of polyaminopyridines using a CuI/L-Proline-Catalyzed C-N polycoupling reaction. Materials, Basel, v. 5, p. 2176-2189, 2012. Disponível em: <http://www.mdpi.com/1996-1944/5/11/2176>. Acesso em: 02 fev. 2015.pt_BR
dc.identifier.issn1996-1944-
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/4965-
dc.description.abstractPolyaminopyridines (PAPy) were chemically prepared from amino-bromopyridines by a CuI/L-proline-catalyzed C-N polycondensation reaction. The formation of the polymer was confirmed by GPC, XRD, XRF, FTIR, UV-vis (λmax = 400 nm), 1H and 13C NMR. The number-average molecular weights (Mn) were estimated by end-group analysis using X-ray fluorescence (up to 6000 Da). TGA analysis of PAPy with higher Mn showed greater thermal stability up to 170 oC. Viscosity measurements of polymer in formic acid at 30 oC indicated a polyelectrolyte nature of PAPy solutions. Furthermore, the amorphicity of the material was observed by X-ray diffraction analysis.pt_BR
dc.language.isoen_USpt_BR
dc.subjectPolyaminopyridinespt_BR
dc.subjectUllmann coupling reactionpt_BR
dc.subjectEnd-group analysis by XRFpt_BR
dc.titlePreparation of polyaminopyridines using a CuI/L-Proline-Catalyzed C-N polycoupling reaction.pt_BR
dc.typeArtigo publicado em periodicopt_BR
dc.rights.licenseO periódico Materials Science Journal permite o arquivamento da versão PDF do editor. Fonte: Sherpa/Romeo <http://www.sherpa.ac.uk/romeo/search.php?issn=1996-1944>. Acesso em: 03 jan. 2017.pt_BR
dc.identifier.doihttps://doi.org/10.3390/ma5112176-
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