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dc.contributor.authorCamerel, Franck-
dc.contributor.authorBarberá, Joaquín-
dc.date.accessioned2017-04-03T08:55:42Z-
dc.date.available2017-04-03T08:55:42Z-
dc.date.issued2015-
dc.identifierdoi: 10.1002/chem.201502780-
dc.identifiere-issn: 1521-3765-
dc.identifierissn: 0947-6539-
dc.identifier.citationChemistry - A European Journal 21(52): 19149-19158 (2015)-
dc.identifier.urihttp://hdl.handle.net/10261/147759-
dc.description.abstractA series of ionic associates based on the platinum(II) chelate of 5-sulfo-8-quinolinol, [Pt(qS)], and ammonium-based amphiphiles is described. At variance with the prototypical neutral complex Pt(q) (q=8-quinolinol), these dianionic fluorophores, functionalized at the periphery with sulfonate groups, can be associated by the ionic self-assembly approach with various ammonium cations, such as (HC)MeN (n=12, 16, 18) or complex ammonium cations carrying three C carbon chains (n=12, 14, 16) and an additional amide group. Investigations of their luminescence properties in solution, in the solid state, and, when possible, in thin films revealed that the phosphorescence properties in condensed phases are directly correlated to intermolecular interactions between the luminescent [Pt(qS)] centers. Of particular interest is also the formation of a columnar liquid-crystalline phase around room temperature (between -25 and +180 C), as well as the very good film-forming ability of some of these fluorophores from organic solvents.-
dc.description.sponsorshipThe CNRS and the University of Rennes 1 are gratefully acknowledgedfor financial support. J.B. thanks financial support by the MINECO, Spain, under the projectCTQ2012-35692, which included FEDER funding.-
dc.publisherWiley-VCH-
dc.rightsclosedAccess-
dc.subjectLiquid crystals-
dc.subjectN,O ligands-
dc.subjectSelf-assembly-
dc.subjectPlatinum-
dc.subjectLuminescence-
dc.titleIonic self-assembly and red-phosphorescence properties of a charged platinum(II) 8-quinolinol complex associated with ammonium-based amphiphiles-
dc.typeartículo-
dc.identifier.doi10.1002/chem.201502780-
dc.date.updated2017-04-03T08:55:43Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderUniversité de Rennes 1-
dc.contributor.funderCentre National de la Recherche Scientifique (France)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004794es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100007525es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
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