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dc.contributor.authordeAzevedo, E. R.-
dc.contributor.authorReichert, D.-
dc.contributor.authorVidoto, ELG-
dc.contributor.authorDahmouche, K.-
dc.contributor.authorJudeinstein, P.-
dc.contributor.authorBonagamba, T. J.-
dc.date.accessioned2014-05-20T15:25:29Z-
dc.date.accessioned2016-10-25T17:59:58Z-
dc.date.available2014-05-20T15:25:29Z-
dc.date.available2016-10-25T17:59:58Z-
dc.date.issued2003-05-20-
dc.identifierhttp://dx.doi.org/10.1021/cm020947v-
dc.identifier.citationChemistry of Materials. Washington: Amer Chemical Soc, v. 15, n. 10, p. 2070-2078, 2003.-
dc.identifier.issn0897-4756-
dc.identifier.urihttp://hdl.handle.net/11449/35899-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/35899-
dc.description.abstractC-13 exchange solid-state NMR methods were used to study two families of siloxane/poly-(ethylene glycol) hybrid materials: Types I and II, where the polymer chains interact with the inorganic phase through physical (hydrogen bonds or van der Waals forces) or chemical (covalent bonds) interactions, respectively. These methods were employed to analyze the effects of the interactions between the organic and inorganic phases on the polymer dynamics in the milliseconds to seconds time scale, which occurs at temperatures below the motional narrowing of the NMR line width and around the polymer glass transition. Motional heterogeneities associated with these interactions and evidence of both small and large amplitude motions were directly observed for both types of hybrids. The results revealed that the hindrance to the slow molecular motions of the polymer chains due to the siloxane structures depends on the chain length and the nature of the interaction between the organic and inorganic phases.en
dc.format.extent2070-2078-
dc.language.isoeng-
dc.publisherAmer Chemical Soc-
dc.sourceWeb of Science-
dc.titleMotional heterogeneities in siloxane/poly(ethylene glycol) ormolyte nanocomposites studied by C-13 solid-state exchange NMRen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniv Halle Wittenberg-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniv Paris 11-
dc.description.affiliationUniv São Paulo, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil-
dc.description.affiliationUniv Halle Wittenberg, FB Phys, D-06108 Halle Saale, Germany-
dc.description.affiliationUNESP, Inst Quim Araraquara, BR-14800900 São Paulo, Brazil-
dc.description.affiliationUniv Paris 11, CNRS 8074, UPRESA, Chim Organ Struct Lab, F-91405 Orsay, France-
dc.description.affiliationUnespUNESP, Inst Quim Araraquara, BR-14800900 São Paulo, Brazil-
dc.identifier.doi10.1021/cm020947v-
dc.identifier.wosWOS:000182956200023-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofChemistry of Materials-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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