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dc.contributor.authorLi, Chenfei
dc.contributor.authorDickson, Robert
dc.contributor.authorRockstroh, Nils
dc.contributor.authorRabeah, Jabor
dc.contributor.authorCordes, David B.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorHünemörder, Paul
dc.contributor.authorSpannenberg, Anke
dc.contributor.authorBuehl, Michael
dc.contributor.authorMejía, Esteban
dc.contributor.authorZysman-Colman, Eli
dc.contributor.authorKamer, Paul C J
dc.date.accessioned2020-10-07T11:30:09Z
dc.date.available2020-10-07T11:30:09Z
dc.date.issued2020-09-18
dc.identifier.citationLi , C , Dickson , R , Rockstroh , N , Rabeah , J , Cordes , D B , Slawin , A M Z , Hünemörder , P , Spannenberg , A , Buehl , M , Mejía , E , Zysman-Colman , E & Kamer , P C J 2020 , ' Ligand electronic fine-tuning and its repercussion on the photocatalytic activity and mechanistic pathways of the copper-photocatalysed aza-Henry Reaction ' , Catalysis Science & Technology , vol. Advance Article . https://doi.org/10.1039/D0CY01221Aen
dc.identifier.issn2044-4753
dc.identifier.otherPURE: 270209165
dc.identifier.otherPURE UUID: 9fd6f867-8f4f-4dc6-877e-768f5f38d1be
dc.identifier.otherORCID: /0000-0002-1095-7143/work/80620055
dc.identifier.otherORCID: /0000-0002-9527-6418/work/80620063
dc.identifier.otherORCID: /0000-0002-5366-9168/work/80620083
dc.identifier.otherORCID: /0000-0001-7183-6022/work/80620644
dc.identifier.otherScopus: 85096566691
dc.identifier.otherWOS: 000589508300027
dc.identifier.urihttp://hdl.handle.net/10023/20735
dc.descriptionC.Li thanks the Prof. & Mrs Purdie Bequests Scholarship and AstraZeneca PhD Studentship.en
dc.description.abstractA family of six structurally related heteroleptic copper(I) complexes of the form of [Cu(N^N)(P^P)]+ bearing a 2,9-dimethyl-1,10-phenanthroline diimine (N^N) ligand and a series of electronically tunable xantphos (P^P) ligands have been synthesized and their optoelectronic properties characterized. The reactivity of these complexes in the copper-photocatalyzed Aza-Henry reaction of N-Phenyltetrahydroisoquinoline was evaluated, while the related excited state kinetics were comprehensively studied. By subtlety changing the electron-donating properties of the P^P ligands with neglegible structural differences, we could tailor the photoredox properties and relate it to their reactivity. Moreover, depending on the exited-state redox potential of the catalysts, the preferred mechanism can shift between reductive quenching, energy transfer and oxidative quenching pathways. A combined study of structural modulation of copper(I) photocatalysts, optoelectronic properties and photocatalytic reactivity resulted in a clearer understanding of both the rational design of the photocatalyst and the complexity of competing photoinduced electron and energy transfer mechanisms.
dc.format.extent12
dc.language.isoeng
dc.relation.ispartofCatalysis Science & Technologyen
dc.rightsCopyright © 2020 the Author(s). This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.en
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleLigand electronic fine-tuning and its repercussion on the photocatalytic activity and mechanistic pathways of the copper-photocatalysed aza-Henry Reactionen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1039/D0CY01221A
dc.description.statusPeer revieweden


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