Photocatalytic hydrogen evolution using a Ru(ii)-bound heteroaromatic ligand as a reactive site

Takuya Sawaki, Tomoya Ishizuka, Nanase Namura, Dachao Hong, Mayuko Miyanishi, Yoshihito Shiota, Hiroaki Kotani, Kazunari Yoshizawa, Jieun Jung, Shunichi Fukuzumi, Takahiko Kojima

研究成果: ジャーナルへの寄稿学術誌査読

11 被引用数 (Scopus)


A RuII complex, [RuII(tpphz)(bpy)2]2+ (1) (tpphz = tetrapyridophenazine, bpy = 2,2′-bipyridine), whose tpphz ligand has a pyrazine moiety, is converted efficiently to [RuII(tpphz-HH)(bpy)2]2+ (2) having a dihydropyrazine moiety upon photoirradiation of a water-methanol mixed solvent solution of 1 in the presence of an electron donor. In this reaction, the triplet metal-to-ligand charge-transfer excited state (3MLCT∗) of 1 is firstly formed upon photoirradiation and the 3MLCT∗ state is reductively quenched with an electron donor to afford [RuII(tpphz-)(bpy)2]+, which is converted to 2 without the observation of detectable reduced intermediates by nano-second laser flash photolysis. The inverse kinetic isotope effect (KIE) was observed to be 0.63 in the N-H bond formation of 2 at the dihydropyrazine moiety. White-light (380-670 nm) irradiation of a solution of 1 in a protic solvent, in the presence of an electron donor under an inert atmosphere, led to photocatalytic H2 evolution and the hydrogenation of organic substrates. In the reactions, complex 2 is required to be excited to form its 3MLCT∗ state to react with a proton and aldehydes. In photocatalytic H2 evolution, the H-H bond formation between photoexcited 2 and a proton is involved in the rate-determining step with normal KIE being 5.2 on H2 evolving rates. Density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations on the reaction mechanism of H2 evolution from the ground and photo-excited states of 2 were performed to have a better understanding of the photocatalytic processes.

ジャーナルDalton Transactions
出版ステータス出版済み - 12月 21 2020

!!!All Science Journal Classification (ASJC) codes

  • 無機化学


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