Atomically precise copper clusters with dual sites for highly chemoselective and efficient hydroboration
Year: 2024
Type: article
Abstract: The hydroboration of alkynes into vinylboronate esters is a vital transformation, but achieving high chemoselectivity of targeted functional groups and an appreciable turnover number is a considerable challenge. Herein, we develop two dynamically regulating dual-catalytic-site copper clusters (Cu 4 NC and Cu 8 NC) bearing N-heterocyclic thione ligands that endow Cu 4 NC and Cu 8 NC catalysts with performance. In particular, the performance of microcrystalline Cu 4 NC in hydroboration is characterized by a high turnover number (77786), a high chemoselectivity, high recovery and reusability under mild conditions. Mechanistic studies and density functional theory calculations reveal that, compared with the Cu 8 NC catalyst, the Cu 4 NC catalyst has a lower activation energy for hydroboration, accounting for its high catalytic activity. This work reveals that precisely constructed cluster catalysts with dual catalytic sites may provide a way to substantially improve catalytic properties by fully leveraging synergistic interactions and dynamic ligand effects, thus promoting the development of cluster catalysts.
Source: Nature Communications
Authors: Teng Jia, Jie Ai, Xiaoguang Li, Miao-Miao Zhang, Yue Hua, Yi-Xin Li, Cai-Fang Sun, Feng Liu, Ren-Wu Huang, Zheng Wang, Shuang-Quan Zang
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $6,790
OpenAlex ID: W4404067700
