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hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorVALLAN, Lorenzo
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorBUI, Anh Thy
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorJONUSAUSKAS, Gediminas
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorMCCLENAGHAN, Nathan
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorISTIF, Emin
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorMANTIONE, Daniele
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorPAVLOPOULOU, Eleni
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorBROCHON, Cyril
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorHADZIIOANNOU, Georges
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorCLOUTET, Eric
dc.date2023
dc.date.issued2023
dc.identifier.issn0024-9297
dc.description.abstractEnIn recent years, non-conjugated organic luminophores are receiving considerable interest from the scientific community, offering new conceptual basis for the development of alternative photoluminescence-based technologies. In this work, the polymerization of 3,4dihydropyran was exploited for the preparation of non-conjugated photoluminescent polymer nanoparticles. Remarkably, excitation-dependent multicolor emission ranging from blue to yellow 2 was observed both in solid and in solution. In contrast with similar materials, this behavior was not attributed to aggregation-induced emission, but rather to the presence of independent, noninteracting chromophores located on the polymer structure. Structural and optical characterization along with further chemical modifications suggest that the emission is related to the presence of acetal groups formed by ring-opening polymerization. In addition, it was shown that the removal of unsaturated structures could enhance the photoluminescence quantum yield of the polymer (QY) up to 0.20 (λex = 355 nm). This work provides a new type of non-conjugated organic luminophore with both high QY and multicolor emission.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enPhotoluminescence
dc.subject.enPolymer particles
dc.title.enMulticolor photoluminescence from non-conjugated poly(3,4-dihydropyran) nanoparticles
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.macromol.3c00463
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecules
bordeaux.peerReviewedoui
hal.identifierhal-04122672
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-04122672v1
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