NAD+激酶
选择性
催化作用
化学
金属
电催化剂
区域选择性
氢化物
组合化学
无机化学
氢
光化学
电极
酶
电化学
有机化学
物理化学
作者
Fengyuan Liu,Wenwen Shi,Shujie Tian,Yiyang Zhou,Chengcheng Feng,Chunmei Ding,Can Li
标识
DOI:10.1021/acs.jpcc.4c00832
摘要
(Photo)electrocatalytic NAD+ reduction provides a promising approach for 1,4-NADH regeneration, but it remains challenging to achieve both high activity and selectivity. Here, we found prominent synergetic effects between various metals (Cu, Fe, Co, and Ni) and Rh-based complexes (M and M') for electrocatalytic NAD+ reduction, promoting the activity and selectivity simultaneously. Typically, the normalized activity of the Cu and M coupled system is 15.6 times that of M, while Cu alone shows negligible activity at the same potential. Meanwhile, the selectivity of 1,4-NADH is enhanced from 63.3% for Cu alone to as high as 95.3% for the coupled system. We found that the transfer of hydrogen atoms from the metal electrode to the M complex accelerates the formation of metal-hydride active species, which catalyzes the regioselective production of 1,4-NADH. This work provides a universal strategy of coupling proton-reduction electrocatalysts and regioselective molecular catalysts for efficient (photo)electrocatalytic 1,4-NAD(P)H regeneration.
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