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Turning on Asymmetric Catalysis of Achiral Metal-Organic Frameworks by Imparting Chiral Microenvironment
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2023-08-08 , DOI: 10.1002/anie.202308089 Ge Yang 1 , Wenwen Shi 2 , Yunyang Qian 1 , Xiao Zheng 2, 3 , Zheng Meng 1 , Hai-Long Jiang 1
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2023-08-08 , DOI: 10.1002/anie.202308089 Ge Yang 1 , Wenwen Shi 2 , Yunyang Qian 1 , Xiao Zheng 2, 3 , Zheng Meng 1 , Hai-Long Jiang 1
Affiliation
The chiral microenvironment around catalytically active metal clusters in a MOF, PCN-222(Cu), is created by simply grafting chiral molecules (R)−Cn−COOH (n=1, 2, 3). Owing to multi-level modulation such as hydrogen interaction, steric hindrance, and confinement effect caused by the microenvironment, the resulting (R)−Cn@PCN-222(Cu) exhibits high activity and enantioselectivity in the asymmetric ring-opening of cyclohexene oxide with aniline.
中文翻译:
通过赋予手性微环境开启非手性金属有机框架的不对称催化
MOF PCN-222(Cu) 中催化活性金属簇周围的手性微环境是通过简单地接枝手性分子 ( R )−C n −COOH ( n =1, 2, 3) 来创建的。由于微环境引起的氢相互作用、空间位阻和限域效应等多级调节,所得的( R )−C n @PCN-222(Cu)在环己烯的不对称开环中表现出高活性和对映选择性与苯胺氧化。
更新日期:2023-08-08
中文翻译:
通过赋予手性微环境开启非手性金属有机框架的不对称催化
MOF PCN-222(Cu) 中催化活性金属簇周围的手性微环境是通过简单地接枝手性分子 ( R )−C n −COOH ( n =1, 2, 3) 来创建的。由于微环境引起的氢相互作用、空间位阻和限域效应等多级调节,所得的( R )−C n @PCN-222(Cu)在环己烯的不对称开环中表现出高活性和对映选择性与苯胺氧化。