Abstract
Photoactivation of M-X bonds is a challenge for photochemical HX splitting, particularly with first-row transition metal complexes because of short intrinsic excited state lifetimes. Herein, we report a tandem H(2) photocycle based on combination of a non-basic photoredox phosphine mediator and nickel metal catalyst. Synthetic studies and time-resolved photochemical studies have revealed that phosphines serve as photochemical H-atom donors to Ni(ii) trihalide complexes to deliver a Ni(i) centre. The H(2) evolution catalytic cycle is closed by sequential disproportionation of Ni(i) to afford Ni(0) and Ni(ii) and protolytic H(2) evolution from the Ni(0) intermediate. The results of these investigations suggest that H(2) photogeneration proceeds by two sequential catalytic cycles: a photoredox cycle catalyzed by phosphines and an H(2)-evolution cycle catalyzed by Ni complexes to circumvent challenges of photochemistry with first-row transition metal complexes.