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Synthesis, photophysical and electrochemical properties of π-conjugated pyrene based down-shifting molecules with fluorinated aryl groups

dc.contributor.authorBarros, Helio
dc.contributor.authorEsteves, M. Alexandra
dc.contributor.authorBrites, Maria João
dc.date.accessioned2023-06-05T13:17:36Z
dc.date.available2023-06-05T13:17:36Z
dc.date.issued2023-05
dc.description.abstractABSTRACT: Pyrene molecule, with excellent photophysical properties (strong absorption cross section, excellent emission properties and a long-excited state lifetime), excellent thermal and photochemical stability, has been widely used as a building block for the synthesis of pyrene-based fluorophores for optoelectronic applications. In this work, we report the synthesis of two series of pyrene-pi-A compounds, series I (3-6) and II (10-13), in which nitro, cyano, cyanoacrylonitrile and cyanoacrylic acid as electron acceptor groups are connected to the pyrene core via aryl or fluoroaryl pi-conjugating bridges. The incorporation of fluorine atom on the pi-extension bridge cause a slightly red-shift at emission wavelength (lambda em) in solution and polymethylmethacrylate (PMMA) films and in-crease the Stokes shift due to greater stabilization of molecular orbitals in the excited state, especially for series I. Solvatochromic measurements and theoretical computational studies suggest a higher intramolecular charge transfer in the excited state for series II when compared to series I due to their stronger electron acceptor moieties. All pyrene derivatives are stable and exhibited initial mass loss at temperature above 200 degrees C. The good photophysical and thermal properties of the synthesized pyrene derivatives, associated with high molar ab-sorption coefficients in the UV spectrum and good fluorescence emission in the range of 430-480 nm (series I) and 505-567 nm (series II) in PMMA films, make them possible candidates for organic light-emitting diode (OLED) and luminescent down-shifting (LDS) layers for stable perovskite solar cells, respectively.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBarros, Hélio... [et.al.] - Synthesis, photophysical and electrochemical properties of π-conjugated pyrene based down-shifting molecules with fluorinated aryl groups. In: Dyes and Pigments, 2023, vol. 213, article nº 111103pt_PT
dc.identifier.doi10.1016/j.dyepig.2023.111103pt_PT
dc.identifier.eissn1873-3743
dc.identifier.issn0143-7208
dc.identifier.urihttp://hdl.handle.net/10400.9/4058
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.relationNovel building Integration Designs for increased Efficiencies in Advanced Climatically Tunable Renewable Energy Systems
dc.relation.publisherversionhttps://doi.org/10.1016/j.dyepig.2023.111103pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectDyespt_PT
dc.subjectOptical propertiespt_PT
dc.subjectLuminescentpt_PT
dc.subjectFluorescencept_PT
dc.subjectPerovskite solar cellspt_PT
dc.titleSynthesis, photophysical and electrochemical properties of π-conjugated pyrene based down-shifting molecules with fluorinated aryl groupspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleNovel building Integration Designs for increased Efficiencies in Advanced Climatically Tunable Renewable Energy Systems
oaire.awardURIinfo:eu-repo/grantAgreement/EC/H2020/815271/EU
oaire.citation.titleDyes and Pigmentspt_PT
oaire.citation.volume213pt_PT
oaire.fundingStreamH2020
person.familyNameBarros
person.familyNameEsteves
person.familyNameBrites
person.givenNameHelio
person.givenNameM. Alexandra
person.givenNameMaria João de Sousa
person.identifier.ciencia-id8D1A-97AE-F411
person.identifier.ciencia-id6710-13F6-3011
person.identifier.orcid0000-0003-4797-7292
person.identifier.orcid0000-0002-7010-605X
person.identifier.orcid0000-0002-1081-7191
person.identifier.ridH-2971-2017
person.identifier.scopus-author-id35581297200
project.funder.identifierhttp://doi.org/10.13039/501100008530
project.funder.nameEuropean Commission
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
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relation.isAuthorOfPublication341c4414-3fe7-4a05-99d5-8577bfdd05c8
relation.isAuthorOfPublicationafcf1d4c-fc7e-4486-b0f4-58f27acc6834
relation.isAuthorOfPublication.latestForDiscoveryaf1735af-bb6f-4ca6-a34c-39b6d0ea986b
relation.isProjectOfPublication5e18abb9-c7ff-4b7e-b4c2-338f69e1eae1
relation.isProjectOfPublication.latestForDiscovery5e18abb9-c7ff-4b7e-b4c2-338f69e1eae1

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