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- W2794844603 abstract "A key feature of prominent transition-metal-containing photoredox catalysts (PCs) is high quantum yield access to long-lived excited states characterized by a change in spin multiplicity. For organic PCs, challenges emerge for promoting excited-state intersystem crossing (ISC), particularly when potent excited-state reductants are desired. Herein, we report a design exploiting orthogonal π-systems and an intermediate-energy charge-transfer excited state to maximize ISC yields (ΦISC) in a highly reducing ( E0* = -1.7 V vs SCE), visible-light-absorbing phenoxazine-based PC. Simple substitution of N-phenyl for N-naphthyl is shown to dramatically increase ΦISC from 0.11 to 0.91 without altering catalytically important properties, such as E0*." @default.
- W2794844603 created "2018-04-06" @default.
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- W2794844603 date "2018-03-29" @default.
- W2794844603 modified "2023-10-12" @default.
- W2794844603 title "Exploiting Charge-Transfer States for Maximizing Intersystem Crossing Yields in Organic Photoredox Catalysts" @default.
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- W2794844603 doi "https://doi.org/10.1021/jacs.8b01001" @default.
- W2794844603 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5920652" @default.
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