Metal‐free Semiconductor Photocatalysis for sp2 C−H Functionalization with Molecular Oxygen

Abstract Designing metal‐free catalysts for solar energy conversion is a long‐standing challenge in semiconductor photoredox catalysis (SPC). With visible‐light‐responsive hexagonal boron carbon nitride ( h ‐BCN) as a non‐metal photocatalyst, this system affords C−H/N−H coupling products with broad substitution tolerance and high efficiency with molecular oxygen as the terminal oxidant. The catalyst exhibits remarkable performance for the selective C−H functionalization of electron‐rich arenes to C−N products (yields up to 95 %) and good stability (6 recycles). Both nitrogen heteroarenes and amine salts are competent coupling nucleophiles. Mechanically, the reactive oxygen species are superoxide anion radical (O 2 −. ) and H 2 O 2 , which are proved by electron spin resonance (ESR) data, KI‐starch, and control experiments. In addition, kinetic isotope effect (KIE) experiments indicate that C−H bond cleavage is not involved in the rate limiting step. This semiconductor‐based photoredox system allows for C−H amination free of any metals, ligands, strong oxidants, and additives. It provides a complementary avenue to C−H functionalizations and enables synthetic applications efficiently in a sustainable manner.