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用于可见光驱动不对称催化的可调谐手性金属有机框架

Tunable chiral metal organic frameworks toward visible light-driven asymmetric catalysis.

作者信息

Zhang Yin, Guo Jun, Shi Lin, Zhu Yanfei, Hou Ke, Zheng Yonglong, Tang Zhiyong

机构信息

Chinese Academy of Science (CAS) Key Laboratory of Nanosystem and Hierarchy Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology and University of Chinese Academy of Sciences, Beijing 100190, P. R. China.

Center for Nanochemistry, Peking University, Beijing 100871, P. R. China.

出版信息

Sci Adv. 2017 Aug 18;3(8):e1701162. doi: 10.1126/sciadv.1701162. eCollection 2017 Aug.

Abstract

A simple and effective strategy is developed to realize visible light-driven heterogeneous asymmetric catalysis. A chiral organic molecule, which only has very weak catalytic activity in asymmetric α-alkylation of aldehydes under visible light, is utilized as the ligand to coordinate with different types of metal ions, including Zn, Zr, and Ti, for construction of crystalline metal organic frameworks (MOFs). Impressively, when used as heterogeneous catalysts, all of the synthesized MOFs exhibit markedly enhanced activity. Furthermore, the asymmetric catalytic performance of these MOFs could be easily altered by selecting different metal ions, owing to the tunable electron transfer property between metal ions and chiral ligands. This work will provide a new approach for fabrication of heterogeneous catalysts and trigger more enthusiasm to conduct the asymmetric catalysis driven by visible light.

摘要

开发了一种简单有效的策略来实现可见光驱动的多相不对称催化。一种在手性有机分子在可见光下醛的不对称α-烷基化反应中仅具有非常弱的催化活性,被用作配体与不同类型的金属离子(包括Zn、Zr和Ti)配位,以构建结晶金属有机框架(MOF)。令人印象深刻的是,当用作多相催化剂时,所有合成的MOF都表现出显著增强的活性。此外,由于金属离子和手性配体之间的电子转移性质可调,通过选择不同的金属离子可以很容易地改变这些MOF的不对称催化性能。这项工作将为制备多相催化剂提供一种新方法,并激发更多人开展可见光驱动的不对称催化研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2325/5562422/7d4678f29361/1701162-S1.jpg

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