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dc.contributor.authorBryden, Megan
dc.contributor.authorVilla, Marco
dc.contributor.authorFermi, Andrea
dc.contributor.authorCeroni, Paola
dc.contributor.authorZysman-Colman, Eli
dc.date.accessioned2023-08-31T09:30:03Z
dc.date.available2023-08-31T09:30:03Z
dc.date.issued2023-10-24
dc.identifier292588315
dc.identifiera400c0af-614a-4fae-ac66-ee3612a1d62e
dc.identifier85169335595
dc.identifier.citationBryden , M , Villa , M , Fermi , A , Ceroni , P & Zysman-Colman , E 2023 , ' Dual photosensitizer cycles working synergistically in a C(sp)-C(sp 3 ) cross-coupling reaction ' , Asian Journal of Organic Chemistry , vol. 12 , no. 10 , e202300347 . https://doi.org/10.1002/ajoc.202300347en
dc.identifier.issn2193-5807
dc.identifier.otherRIS: urn:D811A6D123DB53F5C8AC8ACDC3AE4456
dc.identifier.otherORCID: /0000-0001-7183-6022/work/141644170
dc.identifier.urihttps://hdl.handle.net/10023/28273
dc.descriptionFunding: Authors thank the University of St Andrews, Syngenta and the EPSRC Centre for Doctoral Training in Critical Resource Catalysis (CRITICAT) for financial support [Ph.D. studentship to “M.B.”; Grant code: EP/L016419/1]. We thank Umicore AG for the gift of materials. E.Z.-C. and P.C. acknowledge the European Union H2020 research and innovation program under the Marie Skłodowska Curie Grant Agreement (PhotoReAct, No 956324).en
dc.description.abstractTo assess the value and reactivity of new photocatalysts (PCs), their performance should be evaluated in one or more established reactions and benchmarked against the performance using known PCs. Here, we evaluated our recently developed PC, pDTCz- DPmS, in a C(sp)-C(sp3) cross-coupling reaction that had been documented in the literature. Previous findings indicated this reaction could not proceed in the absence of PC; however, under our conditions this was not the case. Without PC, a moderate product yield was obtained, while this yield increased significantly upon addition of pDTCz-DPmS. UV-Vis absorption studies indicated that the Hantzsch ester (HE) additive was acting as a competitive absorber of the light from the excitation source, and quenching studies confirmed that the HE was quenched by the radical precursor, N-(acyloxy)phthalimide. Mechanistic investigations established that two parallel photosensitization pathways were in operation; a reductive quenching photocatalytic pathway (using pDTCz-DPmS) and a sacrificial photoreductant pathway (employing HE). These pathways work synergistically to enhance the yield of target product.
dc.format.extent8
dc.format.extent1820568
dc.language.isoeng
dc.relation.ispartofAsian Journal of Organic Chemistryen
dc.subjectThermally activated delayed fluorescence (TADF)en
dc.subjectPhotoredox catalysisen
dc.subjectHantzsch esteren
dc.subjectPhotocatalysten
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleDual photosensitizer cycles working synergistically in a C(sp)-C(sp3) cross-coupling reactionen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEuropean Commissionen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Centre for Energy Ethicsen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1002/ajoc.202300347
dc.description.statusPeer revieweden
dc.identifier.urlhttps://doi.org/10.26434/chemrxiv-2023-bjmh1en
dc.identifier.grantnumberEP/L016419/1en
dc.identifier.grantnumber956324en


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