Ren Xiaomin, Guo Miao, Li He, Li Chengbin, Yu Liang, Liu Jian, Yang Qihua
State Key Laboratory of Catalysis,iChEM, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Angew Chem Int Ed Engl. 2019 Oct 7;58(41):14483-14488. doi: 10.1002/anie.201908602. Epub 2019 Aug 19.
It is a challenging task to promote the activity and selectivity of a catalyst via precisely engineering the microenvironment, an important factor related with the catalytic performance of natural catalysts. Motivated by the water effect in promoting the catalytic activity explored in this work, a nanoreactor modified with phosphine ligand enabled the efficient hydrogenation of benzoic acid (BA) over Ru nanoparticles (NPs) in organic solvent under mild conditions, which cannot be achieved in unmodified nanoreactors. Both density functional theory (DFT) calculations and catalytic performance tests showed that the phosphine ligands can manipulate the adsorption strength of BA on Ru NPs by tuning the surface properties as well as preferentially interacting with the carboxyl of BA. The insights obtained in the present study provide a novel concept of nanoreactor design by anchoring ligands near catalytically active centers.
通过精确设计微环境来提高催化剂的活性和选择性是一项具有挑战性的任务,微环境是与天然催化剂催化性能相关的一个重要因素。受本工作中探索的促进催化活性的水效应的启发,一种用膦配体修饰的纳米反应器能够在温和条件下使苯甲酸(BA)在有机溶剂中于钌纳米颗粒(NPs)上高效氢化,而在未修饰的纳米反应器中无法实现这一过程。密度泛函理论(DFT)计算和催化性能测试均表明,膦配体可通过调节表面性质以及优先与BA的羧基相互作用来控制BA在Ru NPs上的吸附强度。本研究中获得的见解为通过在催化活性中心附近锚定配体来设计纳米反应器提供了一个新的概念。