Clark, Ian P.

Cresswell, Alexander

Espley, Samuel

Grayson, Matthew

Lewis-Borrell, Luke J

Orr-Ewing, Andrew J

Ryder, Alison

Sneha, Mahima

Thornton, Georgia L

The synergistic use of (organo)photoredox catalysts with hydrogen atom transfer (HAT) co-catalysts has emerged as a powerful strategy for innate C(sp3)–H bond functionalization, and particularly for C–H bonds α- to nitrogen. Azide ion (N3–) was recently identified as an effective HAT catalyst for the challenging α-C–H alkylation of unprotected, primary alkylamines, in combination with dicyanoarene photocatalysts such as 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN). Here, time-resolved transient absorption spectroscopy over sub-picosecond to microsecond timescales provides kinetic and mechanistic details of the photoredox catalytic cycle in acetonitrile solution. Direct observation of the electron transfer from N3– to photoexcited 4CzIPN reveals the participation of the S1 excited electronic state of the organic photocatalyst as an electron acceptor, but the N3• radical product of this reaction is not observed. Instead, both time-resolved infra-red and UV-visible spectroscopic measurements implicate rapid association of N3• with N3– (a favourable process in acetonitrile) to form the N6•– radical anion. Electronic structure calculations indicate that N3• is the active participant in the HAT reaction, suggesting a role for N6•– as a reservoir which regulates the concentration of N3•

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Photoredox-HAT Catalysis for Primary Amine α-C–H Alkylation: Mechanistic Insight with Transient Absorption Spectroscopy

Photoredox-HAT Catalysis for Primary Amine α-C–H Alkylation: Mechanistic Insight with Transient Absorption Spectroscopy

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