Rogge S M J, Bavykina A, Hajek J, Garcia H, Olivos-Suarez A I, Sepúlveda-Escribano A, Vimont A, Clet G, Bazin P, Kapteijn F, Daturi M, Ramos-Fernandez E V, Llabrés I Xamena F X, Van Speybroeck V, Gascon J
Center for Molecular Modeling, Ghent University, Technologiepark 903, 9052 Zwijnaarde, Belgium.
Chem Soc Rev. 2017 Jun 6;46(11):3134-3184. doi: 10.1039/c7cs00033b.
Heterogeneous single-site catalysts consist of isolated, well-defined, active sites that are spatially separated in a given solid and, ideally, structurally identical. In this review, the potential of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) as platforms for the development of heterogeneous single-site catalysts is reviewed thoroughly. In the first part of this article, synthetic strategies and progress in the implementation of such sites in these two classes of materials are discussed. Because these solids are excellent playgrounds to allow a better understanding of catalytic functions, we highlight the most important recent advances in the modelling and spectroscopic characterization of single-site catalysts based on these materials. Finally, we discuss the potential of MOFs as materials in which several single-site catalytic functions can be combined within one framework along with their potential as powerful enzyme-mimicking materials. The review is wrapped up with our personal vision on future research directions.
多相单中心催化剂由孤立、明确且在给定固体中空间分离且理想情况下结构相同的活性位点组成。在本综述中,对金属有机框架(MOF)和共价有机框架(COF)作为开发多相单中心催化剂平台的潜力进行了全面综述。在本文的第一部分,讨论了在这两类材料中实现此类位点的合成策略和进展。由于这些固体是有助于更好理解催化功能的理想平台,我们重点介绍了基于这些材料的单中心催化剂建模和光谱表征方面最重要的最新进展。最后,我们讨论了MOF作为可在一个框架内结合多种单中心催化功能的材料的潜力以及它们作为强大的模拟酶材料的潜力。综述以我们对未来研究方向的个人见解作为结尾。