反应性(心理学)
配体(生物化学)
催化作用
化学
金属
氧化还原
过渡金属
组合化学
无机化学
有机化学
生物化学
医学
病理
受体
替代医学
作者
Alexandre Barrozo,Maylis Orio
标识
DOI:10.1002/cphc.202200056
摘要
The quest to develop and optimize catalysts for H2 production requires a thorough understanding in the possible catalytic mechanisms involved. Transition metals are very often the centers of reactivity in the catalysis, although this can change in the presence of a redox-active ligand. Investigating the differences in catalysis when considering ligand- and metal-centered reactivity is important to find the most optimal mechanisms for hydrogen evolution reaction. Here, we investigated this change of reactivity in two versions of a thiosemicarbazone-based complex, using Co and Ni metal centers. While the Ni version has a ligand-centered reactivity, Co switches it toward a metal-centered one. Comparison between the mechanisms show differences in rate-limiting steps, and shows the importance of identifying those steps in order to optimize the system for hydrogen production.
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