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Mechanistic basis for tuning iridium hydride photochemistry from H₂ evolution to hydride transfer hydrodechlorination.

ABSTRACT: The photochemistry of metal hydride complexes is dominated by H₂ evolution, limiting access to reductive transformations based on photochemical hydride transfer. In this article, the innate H₂ evolution photochemistry of the iridium hydride complexes [Cp*Ir(bpy-OMe)H]⁺ (1, bpy-OMe = 4,4'-dimethoxy-2,2'-bipyridine) and [Cp*Ir(bpy)H]⁺ (2, bpy = 2,2'-bipyridine) is diverted towards photochemical hydrodechlorination. Net hydride transfer from 1 and 2 to dichloromethane produces chloromethane with high selectivity and exceptional photochemical quantum yield (Φ ≤ 1.3). Thermodynamic and kinetic mechanistic studies are consistent with a non-radical-chain reaction sequence initiated by "self-quenching" electron transfer between excited state and ground state hydride complexes, followed by proton-coupled electron transfer (PCET) hydrodechlorination that outcompetes H-H coupling. This unique photochemical mechanism provides a new hope for the development of light-driven hydride transfer reactions.

SUBMITTER: Barrett SM

PROVIDER: S-EPMC8152724 | biostudies-literature |

REPOSITORIES: biostudies-literature

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