Zhang Yujun, Ye Shenghua, Gao Min, Li Yong, Huang Xuan, Song Jun, Cai Hong, Zhang Qianling, Zhang Junmin
International Joint Research Center for Molecular Science, College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, P. R. China.
College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, P. R. China.
ACS Nano. 2022 Jan 25;16(1):1142-1149. doi: 10.1021/acsnano.1c08898. Epub 2022 Jan 4.
Heterogenization of homogeneous catalysis through supported single-atom catalysts (SACs) provided a feasible solution to recycling catalysts while keeping its efficiency in chemical synthesis. In this work, Cu SACs anchored on N-doped graphene (Cu SACs/NG) were prepared and first used for C-N coupling reactions. During the preparation, Cu-N-C structures, including Cu-N moieties, were formed in a one-step pyrolysis method. As-prepared Cu SACs/NG exhibited excellent catalytic activity toward C-N coupling reactions with a broad scope of substrates and showed outstanding performance of recycling. Compared with Cu nanoparticles (Cu NPs/NG), the advantages of single-atom catalysts were validated via experimental and theoretical calculations. The enhanced performances were attributed to increasing the number of active sites and increasing the intrinsic activity of each active site. This work provides an alternative synthetic strategy for fabricating atomically dispersed SACs and represents a significant advance for coupling reactions.
通过负载型单原子催化剂(SACs)实现均相催化的多相化,为在保持化学合成效率的同时回收催化剂提供了一种可行的解决方案。在这项工作中,制备了锚定在氮掺杂石墨烯上的铜单原子催化剂(Cu SACs/NG),并首次将其用于C-N偶联反应。在制备过程中,通过一步热解方法形成了包括Cu-N部分在内的Cu-N-C结构。所制备的Cu SACs/NG对C-N偶联反应表现出优异的催化活性,底物范围广泛,并且显示出出色的循环性能。与铜纳米颗粒(Cu NPs/NG)相比,通过实验和理论计算验证了单原子催化剂的优势。性能的提高归因于活性位点数量的增加以及每个活性位点固有活性的增加。这项工作为制备原子分散的SACs提供了一种替代合成策略,并代表了偶联反应的一项重大进展。