Photoinduced Catalytic Organic-Hydride Transfer to CO₂ Mediated with Ruthenium Complexes as NAD⁺/NADH Redox Couple Models

Abstract

The catalytic organic-hydride transfer to CO2 was first achieved through the photoinduced two-electron reduction of the [Ru(bpy)2(pbn)]²⁺/[Ru(bpy)2(pbnHH)]²⁺ (bpy=2, 2'-bipyridine, pbn=2-(pyridin-2-yl)benzo[b]-1, 5-naphthyridine, and pbnHH=2-(pyridin-2-yl)-5, 10-dihydrobenzo[b]-1, 5-naphthyridine) redox couple in the presence of 1, 3-dimethyl-2-phenyl-2, 3-dihydro-1H-benzo[d]imidazole (BIH). The active species for the catalytic hydride transfer to carbon dioxide giving formate is [Ru(bpy)(bpy⋅−)(pbnHH)]+ formed by one-electron reduction of [Ru(bpy)2(pbnHH)]²⁺ with BI⋅.