Model studies demonstrate electron transfer catalysis in substrates using a dinuclear ni(0) complex, suggesting new catalytic pathways.
Model studies have been conducted to mimic the function of enzymes called [NiFe] and [FeFe] hydrogenases, which generate electrons via a hydride ion through the heterolytic activation of H2. Although several syntheses of hydride species or low-valent species of Ni or Fe complexes from H2 have been reported, the synthesis of dinuclear Ni(0) complexes from H2 has not been reported. Here, we report on such a dinuclear Ni(0) complex, synthesized from a mononuclear Ni(II) complex and H2. The structures of the mononuclear and dinuclear complexes were determined by X-ray analysis. Catalytic reduction of ethyl viologen or decamethylferrocenium ions as substrates using the Ni complexes and H2 was demonstrated. DFT calculations revealed that the acetate ion, added as a Lewis base, efficiently promotes the heterolytic cleavage of H2, thereby facilitating the formation of the Ni(0) complex.
No takes yet. Share an insight, caveat, or question.
Takahashi et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: