Photocatalytic Hydrogenation of an N₂‑Derived Re^V Imido Complex

Direct hydrogenation of N₂ at ambient conditions lags behind the recent advances in molecular N₂ (electro-)-fixation. In fact, molecular platforms that couple N₂ and H₂ activation remain rare. Inspired by recent photocatalytic approaches, we report here the photochemical hydrogenation of an N₂-derived rhenium-(V) benzoylimido complex. Self-sensitized photolysis with sacrificial 1,4-cyclohexadiene gave benzamide in a high yield. In turn, a new iridium-(III) porphyrinato hydrido photocatalyst allowed for quantitative photohydrogenation via light-driven net hydride transfer. Transient absorption spectroscopy and computations support a light-driven, stepwise hydride transfer mechanism that is enabled by relativistic effects. This approach provides a new strategy for the reductive transformation of N₂ into nitrogenous products beyond ammonia.