dc.creatorQuites F.J.
dc.creatorDomingues R.A.
dc.creatorFerbonink G.F.
dc.creatorNome R.A.
dc.creatorAtvars T.D.Z.
dc.date2013
dc.date2015-06-25T19:16:21Z
dc.date2015-11-26T15:14:24Z
dc.date2015-06-25T19:16:21Z
dc.date2015-11-26T15:14:24Z
dc.date.accessioned2018-03-28T22:24:26Z
dc.date.available2018-03-28T22:24:26Z
dc.identifier
dc.identifierEuropean Polymer Journal. , v. 49, n. 3, p. 693 - 705, 2013.
dc.identifier143057
dc.identifier10.1016/j.eurpolymj.2012.12.014
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84874714305&partnerID=40&md5=55d56452fe70190bf66fe2c2616cb0cb
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/89465
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/89465
dc.identifier2-s2.0-84874714305
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1258851
dc.descriptionIn this paper poly[(9,9-dioctylfluorenyl-2,7-diyl)-alt-co-(9,9-di- {5′-pentanyl}-fluorenyl-2,7-diyl)] (PFP) was attached by hydrosilylation reaction to polysiloxanes with lower and higher crosslinking yields. Two types of polysiloxanes were prepared: PDHS-PDVS-l-PFP-X and PDHSS-PDVS-h-PFP-X, with increasing amounts of polyfluorene (X = 4.04 × 10-4 mol (1), 4.04 × 10-5 mol (2) and 4.04 × 10-6 mol (3)), where l and h represent elastomeric and brittle matrices (l = lower crosslinking and h = higher crosslinking yields). Their photophysical properties were studied and compared with the polymer in films, in THF and in two different polysiloxane (poly[(dimethylsiloxane-co-methylvinylsiloxane) dimethylvinylsilyloxyl]-terminated-PDVS and poly[(dimethylsiloxane-co- methylhydrogensiloxane) dimethylhydrogensilyloxy] terminated-PDHS) solutions before the hydrosilylation reactions. Based on the steady-state and dynamical photoluminescence data, the polyfluorene chains are, independent of the polyfluorene amount, disordered in solutions, in films and in PDHS-PDVS-l-PFP-X. Nevertheless, in both PDHSS solutions and in the PDHSS-PDVS-h-PFP-X hybrid, crystalline phases of the polyfluorene were formed. Moreover, aggregates with green emission are also observed with increasing contents of conjugated polymer. Aggregates emitting in longer wavelengths are only formed when other crystalline phases are present in PDHSS-PDVS-h-PFP-X (X = 2 and 3) silicones. The driving force for this formation is probably a combination of π-π interaction between the planar backbone and the hydrophobic interactions of the lateral groups in the poor solvent PDHSS in a more confined environment such as brittle PDHSS-PDVS-h-PFP. © 2013 Elsevier Ltd. All rights reserved.
dc.description49
dc.description3
dc.description693
dc.description705
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dc.languageen
dc.publisher
dc.relationEuropean Polymer Journal
dc.rightsfechado
dc.sourceScopus
dc.titleFacile Control Of System-bath Interactions And The Formation Of Crystalline Phases Of Poly[(9,9-dioctylfluorenyl-2,7-diyl)-alt-co-(9,9-di-{5′- Pentanyl}-fluorenyl-2,7-diyl)] In Silicone-based Polymer Hosts
dc.typeArtículos de revistas


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