Jing Xuemeng, Fu Fangyu, Wang Ruijie, Xin Xing, Qin Lin, Lv Hongjin, Yang Guo-Yu
MOE Key Laboratory of Cluster Science, Beijing Key Laboratory of Photoelectric/Electrophotonic Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 102488, People's Republic of China.
ACS Nano. 2022 Sep 27;16(9):15188-15196. doi: 10.1021/acsnano.2c06492. Epub 2022 Sep 2.
The facile syntheses of enantiomeric atomically precise silver clusters starting from achiral ligands remain a substantial challenge to explore. In this work, a pair of atomically precise enantiomers of /-[AgCl(PrS)S(CHCOO)HO] (, PrS = isopropanethiolate) clusters have been synthesized using a viable solvothermal approach. The chirality of the resulting enantiomeric clusters is attributed to the asymmetric arrangement of surface achiral ligands. Both enantiomers could form the two-dimensional (2D) assemblies via intercluster interactions of basic building blocks containing AgS moieties, PrS-Ag motifs, and S linkers. Such a small ligand-induced 2D assembly greatly contributes to the enhancement of thermal stability and photocatalytic activity of clusters, providing possibilities for exploring robust coinage cluster-based assembly with attractive catalytic properties.
从非手性配体出发简便合成对映体原子精确的银簇仍然是一个有待探索的重大挑战。在这项工作中,使用可行的溶剂热方法合成了一对/ - [AgCl(PrS)S(CHCOO)HO](,PrS =异丙硫醇盐)簇的原子精确对映体。所得对映体簇的手性归因于表面非手性配体的不对称排列。两种对映体都可以通过包含AgS部分、PrS-Ag基序和S连接体的基本结构单元的簇间相互作用形成二维(2D)组装体。这种小配体诱导的2D组装极大地有助于提高簇的热稳定性和光催化活性,为探索具有吸引人的催化性能的稳健的硬币金属簇基组装体提供了可能性。