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

High Resolution Image Download MS PowerPoint Slide The synergistic use of (organo)photoredox catalysts with hydrogen-atom transfer (HAT) cocatalysts has emerged as a powerful strategy for innate C(sp 3 )–H bond functionalization, particularly for C–H bonds α- to nitrogen. Azide ion (N 3 – ) 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 N 3 – to photoexcited 4CzIPN reveals the participation of the S 1 excited electronic state of the organic photocatalyst as an electron acceptor, but the N 3 • radical product of this reaction is not observed. Instead, both time-resolved infrared and UV–visible spectroscopic measurements implicate rapid association of N 3 • with N 3 – (a favorable process in acetonitrile) to form the N 6 •– radical anion. Electronic structure calculations indicate that N 3 • is the active participant in the HAT reaction, suggesting a role for N 6 •– as a reservoir that regulates the concentration of N 3 • .