一种用于脱氢交叉偶联的铜(I)索烃修饰金属有机层异相催化剂。

A Copper(I) Catenane Decorated Metal-Organic Layer as a Heterogenous Catalyst for Dehydrogenative Cross-Coupling.

作者信息

Shi Yi-Xiang, Zhu Lihui, Doan Hoai Son, Deng Yulin, Mo Xiaoyong, Wang Yufeng, Tse Edmund C M, Au-Yeung Ho Yu

机构信息

Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, P. R. China.

State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, P. R. China.

出版信息

Chemistry. 2025 Jun 3;31(31):e202500866. doi: 10.1002/chem.202500866. Epub 2025 Apr 26.

Abstract

While earth-abundant metals are green and sustainable alternatives to precious metals for catalytic chemical conversions, the fast ligand exchange involving most of the base metals renders their development into robust, reusable catalysts very challenging. Described in this work is a new type of heterogeneous catalyst derived from a 2D metal-organic layer (MOL) grafted with catenane-coordinated Cu(I) complexes. In addition to the good substrate accessibility, easy functionalization, and other favorable features due to the MOL support, the mechanical bond in the anchored catenane ligands also represents a new mechanism to dynamically confine the coordination environment and kinetically stabilize the coordinated Cu(I) to give a well-defined, active yet stable heterogeneous catalyst. Pilot catalytic studies using a model dehydrogenative C─O cross-coupling reaction showed that the Cu(I) catenane-grafted MOL led to exclusive formation of the C─O coupled product, whereas control catalysis using a similar Cu(I) catalyst supported by non-interlocked macrocyclic ligands was found to also give a C─C coupled by-product, whose formation was found to be mediated by the uncontrolled oxidation of the Cu(I) to Cu(II), highlighting the distinctive roles and untapped potential of the catenane coordination in developing base metal-derived catalysts for challenging catalytic conditions.

摘要

尽管地壳中储量丰富的金属是用于催化化学转化的贵金属的绿色可持续替代品,但大多数贱金属涉及的快速配体交换使其发展成为坚固、可重复使用的催化剂极具挑战性。本文描述了一种新型的非均相催化剂,它由接枝有连环烷配位的Cu(I)配合物的二维金属有机层(MOL)衍生而来。除了由于MOL载体具有良好的底物可及性、易于功能化和其他有利特性外,锚定的连环烷配体中的机械键还代表了一种新机制,可动态限制配位环境并在动力学上稳定配位的Cu(I),从而得到定义明确、活性高且稳定的非均相催化剂。使用模型脱氢C─O交叉偶联反应进行的初步催化研究表明,接枝有Cu(I)连环烷的MOL导致C─O偶联产物的独家形成,而使用由非互锁大环配体支持的类似Cu(I)催化剂进行的对照催化也发现会产生C─C偶联副产物,发现其形成是由Cu(I)不受控制地氧化为Cu(II)介导的,突出了连环烷配位在开发用于具有挑战性催化条件的贱金属衍生催化剂中的独特作用和未开发的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e35e/12133629/f09c1bbfefac/CHEM-31-e202500866-g001.jpg

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