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dc.contributor.authorVallan, Lorenzo
dc.contributor.authorBui, Anh Thy
dc.contributor.authorJonusauskas, Gediminas
dc.contributor.authorMcClenaghan, Nathan D.
dc.contributor.authorIstif, Emin
dc.contributor.authorMantione, Daniele
dc.contributor.authorPavlopoulou, Eleni
dc.date.accessioned2023-10-19T15:11:32Z
dc.date.available2023-10-19T15:11:32Z
dc.date.issued2023
dc.identifier.issn0024-9297
dc.identifier.issn1520-5835
dc.identifier.urihttps://doi.org/10.1021/acs.macromol.3c00463
dc.identifier.urihttps://hdl.handle.net/20.500.12469/5069
dc.description.abstractIn recent years, nonconjugated organic luminophores arereceivingconsiderable interest from the scientific community, offering a newconceptual basis for the development of alternative photoluminescence-basedtechnologies. In this work, the polymerization of 3,4-dihydropyranwas exploited for the preparation of nonconjugated photoluminescentpolymer nanoparticles. Remarkably, excitation-dependent multicoloremission ranging from blue to yellow was observed in both solid andsolution. In contrast with similar materials, this behavior was notattributed to aggregation-induced emission, but rather to the presenceof independent, noninteracting chromophores located on the polymerstructure. Structural and optical characterizations along with furtherchemical modifications suggest that the emission is related to thepresence of acetal groups formed by ring-opening polymerization. Inaddition, it was shown that the removal of unsaturated structurescould enhance the photoluminescence quantum yield of the polymer (QY)up to 0.20 (lambda(ex) = 355 nm). This work provides a newtype of nonconjugated organic luminophore with both high QY and multicoloremission.en_US
dc.description.sponsorshipEuropean Union; Ministerio de Ciencia e Innovacion (MCIN/AEI, Spain); Agencia Estatal de Investigacion [RYC2021-031668-I]; European Union (NextGenerationEU/PRTR); [800926]en_US
dc.description.sponsorshipThe European Union is acknowledged for funding this research through Horizon 2020 research and innovation program under the grant agreement No. 800926 (HyPhOE). Ministerio de Ciencia e Innovacion and Agencia Estatal de Investigacion (MCIN/AEI/10.13039/501100011033, Spain) and the European Union (NextGenerationEU/PRTR) are acknowledged for funding: Ayuda RYC2021-031668-I. Dr. Andrea Turcati is acknowledged for his kind help. This work has benefited from the facilities and expertise of the CESAMO platform (Bordeaux University) and in particular Christelle Absalon and Yann Rayssac.en_US
dc.language.isoengen_US
dc.publisherAmer Chemical Socen_US
dc.relation.ispartofMacromoleculesen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectClustering-Triggered EmissionEn_Us
dc.subjectCationic-PolymerizationEn_Us
dc.subjectFluorescenceEn_Us
dc.subjectDotsEn_Us
dc.subjectLuminescenceEn_Us
dc.subjectDendrimersEn_Us
dc.subjectMechanismEn_Us
dc.titleMulticolor Photoluminescence from Nonconjugated Poly(3,4-dihydropyran) Nanoparticlesen_US
dc.typearticleen_US
dc.authoridIstif, Emin/0000-0003-4700-7050
dc.authoridMcClenaghan, Nathan/0000-0003-0285-1741
dc.authoridCloutet, Eric/0000-0002-5616-2979
dc.departmentN/Aen_US
dc.identifier.wosWOS:001006223000001en_US
dc.identifier.doi10.1021/acs.macromol.3c00463en_US
dc.institutionauthorN/A
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorwosidIstif, Emin/JGM-0202-2023
dc.authorwosidMcClenaghan, Nathan/I-2597-2015
dc.authorwosidCloutet, Eric/B-3487-2014
dc.khas20231019-WoSen_US


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