催化作用
选择性
金属
氢化物
纳米颗粒
化学
离解(化学)
组合化学
金属有机化学
氢
光化学
基质(水族馆)
材料科学
纳米技术
有机化学
地质学
海洋学
作者
Maodi Wang,Zhenchao Zhao,Chunzhi Li,He Li,Jiali Liu,Qihua Yang
标识
DOI:10.1038/s41467-022-33312-x
摘要
Abstract Most, if not all, of the hydrogenation reactions are catalyzed by organometallic complexes (M) or heterogeneous metal catalysts, but to improve both the activity and selectivity simultaneously in one reaction via a rational combination of the two types of catalysts remains largely unexplored. In this work, we report a hydrogenation mode though H species relay from supported metal nanoparticles (NPs) to M, where the former is responsible for H 2 dissociation, and M is for further hydride transferring to reactants. The synergy between metal NPs and M yields an efficient NAD(P)H regeneration system with >99% selectivity and a magnitude higher activity than the corresponding metal NPs and M. The modularizing of hydrogenation reaction into hydrogen activation with metal NPs and substrate activation with metal complex paves a new way to rationally address the challenging hydrogenation reactions.
科研通智能强力驱动
Strongly Powered by AbleSci AI