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dc.contributor.authorColl, Deysma [Univ Mayor, Fac Ciencias, Nucleo Quim & Bioquim, Santiago, Chile]es_CL
dc.contributor.authorOrtíz, Pablo A. [Univ Mayor, Nucleo Quim & Bioquim, Fac Estudios Interdisciplinarios, Santiago, Chile]es_CL
dc.contributor.authorTerraza, C. A.es_CL
dc.contributor.authorTagle, L. H.es_CL
dc.contributor.authorSantiago-García, J. L.es_CL
dc.contributor.authorCanto-Acosta, R. J.es_CL
dc.contributor.authorAguilar-Vega, M.es_CL
dc.contributor.authorHauyon, R. A.es_CL
dc.contributor.authorPérez, G.es_CL
dc.contributor.authorHerran, L.es_CL
dc.contributor.authorComesana-Gandara, B.es_CL
dc.contributor.authorMcKeown, N. B.es_CL
dc.contributor.authorTundidor-Camba, A.es_CL
dc.date.accessioned2020-04-08T14:11:55Z
dc.date.accessioned2020-04-13T18:12:35Z
dc.date.available2020-04-08T14:11:55Z
dc.date.available2020-04-13T18:12:35Z
dc.date.issued2018es_CL
dc.identifier.citationTerraza, C. A., Tagle, L. H., Santiago-García, J. L., Canto-Acosta, R. J., Aguilar-Vega, M., Hauyon, R. A., ... & Comesaña-Gándara, B. (2018). Synthesis and properties of new aromatic polyimides containing spirocyclic structures. Polymer, 137, 283-292.es_CL
dc.identifier.issn0032-3861es_CL
dc.identifier.issn1873-2291es_CL
dc.identifier.urihttps://doi.org/10.1016/j.polymer.2018.01.013es_CL
dc.identifier.urihttp://repositorio.umayor.cl/xmlui/handle/sibum/6110
dc.description.abstractThe synthesis of three novel aromatic polyimides (PIs) containing spiro units is described. These PIs are soluble at room temperature in most common organic solvents, facilitating their processability. Additionally, they are highly thermally stable, with thermal decomposition temperatures (T-d10%) over 500 degrees C, and had moderately high T-g values between 230 and 265 degrees C. Robust self-standing thin films were prepared from these polyimides, via the solution casting method, which were suitable for gas transport measurements. The relatively low permeability and selectivity of these PIs, as compared to Polymers of Intrinsic Microporosity (PIMs) that also contain spirocyclic structures, demonstrate the importance of restricting rotation within the polymer chain, which is a key structural feature of the PIMs. (C) 2018 Elsevier Ltd. All rights reserved.es_CL
dc.description.sponsorshipFondo Nacional de Investigacion Cientifica y Tecnologica, FONDECYTComision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)CONICYT FONDECYT [11140133]; FONDEQUIP [EQM120021]es_CL
dc.description.sponsorshipA. Tundidor-Camba, acknowledges the financial assistance by Fondo Nacional de Investigacion Cientifica y Tecnologica, FONDECYT, through Project 11140133 and FONDEQUIP through Project EQM120021.es_CL
dc.language.isoenes_CL
dc.publisherELSEVIER SCI LTDes_CL
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourcePolymer, FEB 2018. 137: p. 283-292
dc.subjectPolymer Sciencees_CL
dc.titleSynthesis and properties of new aromatic polyimides containing spirocyclic structureses_CL
dc.typeArtículoes_CL
umayor.facultadCIENCIASes_CL
umayor.politicas.sherpa/romeoRoMEO green journal (Se puede archivar el pre-print y el post-print o versión de editor/PDF). Disponible en: http://sherpa.ac.uk/romeo/index.phpes_CL
umayor.indexadoWOS:000425603800030es_CL
umayor.indexadoSIN PMIDes_CL
dc.identifier.doiDOI: 10.1016/j.polymer.2018.01.013es_CL]
umayor.indicadores.wos-(cuartil)Q1es_CL
umayor.indicadores.scopus-(scimago-sjr)SCIMAGO/ INDICE H: 236 Hes_CL


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