催化作用
化学
氧化还原
电位滴定法
硝酸盐
硝酸还原酶
水溶液
滴定法
活动站点
钼
组合化学
无机化学
有机化学
离子
作者
Yamei Li,Yoo Kyung Go,Hideshi Ooka,Daoping He,Fangming Jin,Sun Hee Kim,Ryuhei Nakamura
标识
DOI:10.1002/ange.202002647
摘要
Abstract Nitrate is a pervasive aquatic contaminant of global environmental concern. In nature, the most effective nitrate reduction reaction (NRR) is catalyzed by nitrate reductase enzymes at neutral pH, using a highly‐conserved Mo center ligated mainly by oxo and thiolate groups. Mo‐based NRR catalysts mostly function in organic solvents with a low water stability. Recently, an oxo‐containing molybdenum sulfide nanoparticle that serves as an NRR catalyst at neutral pH was first reported. Herein, in a nanoparticle‐catalyzed NRR system a pentavalent Mo V (=O)S 4 species, an enzyme mimetic, served as an active intermediate for the NRR. Potentiometric titration analysis revealed that a redox synergy among Mo V −S, S radicals, and Mo V (=O)S 4 likely play a key role in stabilizing Mo V (=O)S 4 , showing the importance of secondary interactions in facilitating NRR. The first identification and characterization of an oxo‐ and thiolate‐ligated Mo intermediates pave the way to the molecular design of efficient enzyme mimetic NRR catalysts in aqueous solution.
科研通智能强力驱动
Strongly Powered by AbleSci AI