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Despite the recent emergence of photocatalytic strategies for incorporating heavier hydrogen isotopes─deuterium and tritium─in therapeutic molecules, most established methods focus on the cleavage and labeling of relatively weak C(sp 3 )–H bonds adjacent to heteroatoms or conjugated systems. Herein, we report a mild, transition metal-free photocatalytic method for selective C(sp 2 )–H/D exchange via D-atom transfer to an in situ generated arene radical cation intermediate. This protocol enables efficient hydrogen isotope exchange (HIE) across a diverse range of aniline, pyrrole, and indole substrates. Mechanistic studies reveal that the electron donor–acceptor (EDA) complex formed between the electron-deficient photocatalyst and the arene substrate plays a critical role in promoting photoinduced electron transfer (PET) and the selective deuteration of C(sp 2 )–H bonds. This work highlights the potential of EDA catalysis to enable radical-based functionalization of strong C(sp 2 )–H bonds mediated by noncovalent photocatalyst–substrate interactions, in contrast to the more precedented cleavage and functionalization of weaker C(sp 3 )–H bonds.
Way et al. (Mon,) studied this question.