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dc.contributor.authorAvellanal-Zaballa, E.-
dc.contributor.authorPrieto-Castañeda, A.-
dc.contributor.authorGarcía-Garrido, F.-
dc.contributor.authorAgarrabeitia, A.R.-
dc.contributor.authorRebollar, Esther-
dc.contributor.authorBañuelos, J.-
dc.contributor.authorGarcia-Moreno, I.-
dc.contributor.authorOrtiz, M.J.-
dc.date.accessioned2021-02-11T13:40:18Z-
dc.date.available2021-02-11T13:40:18Z-
dc.date.issued2020-10-29-
dc.identifierdoi: 10.1002/chem.202002916-
dc.identifierissn: 1521-3765-
dc.identifier.citationChemistry - A European Journal 26: 16080-16088 (2020)-
dc.identifier.urihttp://hdl.handle.net/10261/229344-
dc.description9 pags., 5 figs., 2 tabs.-
dc.description.abstractThe search for long-lived red and NIR fluorescent dyes is challenging and hitherto scarcely reported. Herein, the viability of aza-BODIPY skeleton as a promising system for achieving thermal activated delayed fluorescent (TADF) probes emitting in this target region is demonstrated for the first time. The synthetic versatility of this scaffold allows the design of energy and charge transfer cassettes modulating the stereoelectronic properties of the energy donors, the spacer moieties and the linkage positions. Delayed emission from these architectures is recorded in the red spectral region (695–735 nm) with lifetimes longer than 100 μs in aerated solutions at room temperature. The computational-aided photophysical study under mild and hard irradiation regimes disclose the interplay between molecular structure and photonic performance to develop long-lived fluorescence red emitters through thermally activated reverse intersystem crossing. The efficient and long-lasting NIR emission of the newly synthesized aza-BODIPY systems provides a basis to develop advanced optical materials with exciting and appealing photonic response.-
dc.description.sponsorshipWe gratefully acknowledge the Spanish Ministerio de Economia y Competitividad for financial support (projects MAT2017-83856-C3-1-P,2-P and3-P). We also thank the Gobierno Vasco for financial support (project IT912-16) and for apredoctoralfellowship to E.A.-Z. The authors thank SGIker of UPV/EHUfortechnical support with the computational calculations, whichwere carriedout in the “ARIN A” informatic cluster.-
dc.languageeng-
dc.publisherJohn Wiley & Sons-
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/MAT2017-83856-C3-1-P-
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/MAT2017-83856-C3-3-P-
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/MAT2017-83856-C3-2-P-
dc.relation.isversionofPostprint-
dc.rightsopenAccessen_EN
dc.subjectCharge transfer-
dc.subjectDelayed fluorescence-
dc.subjectDyechemistry-
dc.subjectEnergy transfer-
dc.subjectNIR emission-
dc.titleRed/NIR Thermally Activated Delayed Fluorescence from Aza-BODIPYs-
dc.typeartículo-
dc.identifier.doi10.1002/chem.202002916-
dc.relation.publisherversionhttp://dx.doi.org/10.1002/chem.202002916-
dc.date.updated2021-02-11T13:40:18Z-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderEusko Jaurlaritza-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003086es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
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