Multivariate Metal-Organic Frameworks as Multifunctional Heterogeneous Asymmetric Catalysts for Sequential Reactions

被引:210
|
作者
Xia, Qingchun [1 ,2 ]
Li, Zijian [1 ,2 ]
Tan, Chunxia [1 ,2 ]
Liu, Yan [1 ,2 ]
Gong, Wei [1 ,2 ]
Cui, Yong [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[3] Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China
基金
美国国家科学基金会;
关键词
HYDROLYTIC KINETIC RESOLUTION; RING-OPENING REACTIONS; COOPERATIVE CATALYSIS; HIGHLY EFFICIENT; MESO-EPOXIDES; FUNCTIONAL-GROUPS; SCHIFF-BASE; TRANSFORMATIONS; ACTIVATION; COMPLEXES;
D O I
10.1021/jacs.7b03113
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The search for versatile heterogeneous catalysts with multiple active sites for broad asymmetric transformations has long been of great interest, but it remains a formidable synthetic challenge. Here we demonstrate that multivariate metal-organic frameworks (MTV-MOFs) can be used as an excellent platform to engineer heterogeneous catalysts featuring multiple and cooperative active sites. An isostructural series of 2-fold interpenetrated MTV-MOFs that contain up to three different chiral metallosalen catalysts was constructed and used as efficient and recyclable heterogeneous catalysts for a variety of asymmetric sequential alkene epoxidation/epoxide ring-opening reactions. Interpenetration of the frameworks brings metallosalen units adjacent to each other, allowing cooperative activation, which results in improved efficiency and enantioselectivity over the sum of the individual parts. The fact that manipulation of molecular catalysts in MTV-MOFs can control the activities and selectivities would facilitate the design of novel multifunctional materials for enantioselective processes.
引用
收藏
页码:8259 / 8266
页数:8
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