New Insights into the Exploitation of BODIPY Derivatives as Organic Photocatalysts

UDC.coleccionInvestigaciónes_ES
UDC.departamentoQuímicaes_ES
UDC.grupoInvQuímica Molecular e de Materiais (QUIMOLMAT)es_ES
UDC.institutoCentroCICA - Centro Interdisciplinar de Química e Bioloxíaes_ES
UDC.issue39es_ES
UDC.journalTitleEuropean Journal of Organic Chemistryes_ES
UDC.startPagee202200622es_ES
UDC.volume22es_ES
dc.contributor.authorDa Lama, Ana
dc.contributor.authorBartolomei, Beatrice
dc.contributor.authorRosso, Cristian
dc.contributor.authorFilippini, Giacomo
dc.contributor.authorMartínez, M. Montserrat
dc.contributor.authorSarandeses, Luis A.
dc.contributor.authorPrato, Maurizio
dc.date.accessioned2025-04-28T07:52:31Z
dc.date.available2025-04-28T07:52:31Z
dc.date.issued2022-10-20
dc.description.abstract[Abstract] Boron-dipyrromethene complexes (BODIPYs) are attracting a growing interest for their notable photophysical properties. Specifically, their application in organic photocatalysis is receiving particular attention thanks to their ability to undergo both electron and energy transfer processes, thus acting as promising photoredox catalysts and photosensitizers. Although the number of examples employing these organic dyes is constantly increasing, there are not so many studies that correlate their chemical composition to their photocatalytic activity. In this work, a rationally designed structure-activity relationship study was performed by selecting a synthetically relevant atom transfer radical addition (ATRA) reaction as a benchmark. We demonstrated how the presence of heavy atoms in the chromophore's core turned out to be essential for achieving high reactivity levels. On the contrary, electron-withdrawing groups in position 8 (meso) undermined the catalytic performances, in agreement with the proposed reaction mechanism.es_ES
dc.description.sponsorshipM.P. is the AXA Chair for Bionanotechnology (2016–2023). This work was supported by the University of Trieste, INSTM, and the Italian Ministry of Education MIUR (cofin Prot. 2017PBXPN4). Part of this work was performed under the Maria de Maeztu Units of Excellence Program from the Spanish State Research Agency Grant No. MDM-2017-0720. M.M.M. and L.A.S. kindly acknowledge Spanish State Research Agency-Ministry of Science, Innovation and Universities (Grant No. PGC2018-097792-B-I00). A.D.L. kindly acknowledges Xunta de Galicia for a predoctoral fellowship (EDA 481A-2020/017). G.F. kindly acknowledges FRA2022 funded by the University of Trieste and Microgrants2021 founded by Region FVG (LR 2/2011, ART. 4). Open Access funding provided by Università degli Studi di Trieste within the CRUI-CARE Agreementes_ES
dc.description.sponsorshipItalia. Ministero dell'Istruzione e del Merito; 2017PBXPN4es_ES
dc.description.sponsorshipXunta de Galicia; EDA 481A-2020/017es_ES
dc.identifier.citationLAMA, Ana Da, et al. New Insights into the Exploitation of BODIPY Derivatives as Organic Photocatalysts. European Journal of Organic Chemistry, 2022, vol. 2022, no 39, p. e202200622.es_ES
dc.identifier.issn1099-0690
dc.identifier.urihttp://hdl.handle.net/2183/41886
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/MDM-2017-0720/ES/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-097792-B-I00/ES/EL INDIO COMO HERRAMIENTA SINTETICA EN REACCIONES DE ACOPLAMIENTO Y EN CATALISISes_ES
dc.relation.urihttps://doi.org/10.1002/ejoc.202200622es_ES
dc.rightsAtribución 3.0 Españaes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectPhotocatalysises_ES
dc.subjectPhotochemistryes_ES
dc.subjectReactiones_ES
dc.subjectMechanismses_ES
dc.subjectRedox chemistryes_ES
dc.subjectSynthetic methodses_ES
dc.titleNew Insights into the Exploitation of BODIPY Derivatives as Organic Photocatalystses_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication6aeff1ad-a46b-4558-8ee4-08311985a32a
relation.isAuthorOfPublication.latestForDiscovery6aeff1ad-a46b-4558-8ee4-08311985a32a

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