超分子化学
自组装
催化作用
纳米技术
乙腈
甲醇
化学
产量(工程)
纳米尺度
微流控
连续流动
组合化学
材料科学
有机化学
生化工程
分子
工程类
冶金
作者
Hongyu Lin,Le‐Yong Zhou,Fang Mei,Wei‐Tao Dou,Lianrui Hu,Hai‐Bo Yang,Lin Xu
标识
DOI:10.1002/anie.202301900
摘要
Developing a new strategy to improve the self-assembly efficiency of functional assemblies in a confined space and construct hybrid functional materials is a significant and fascinating endeavor. Herein, we present a highly efficient strategy for achieving the supramolecular self-assembly of well-defined metallacages in microdroplets through continuous-flow microfluidic devices. The high efficiency and versatility of this approach are demonstrated by the generation of five representative metallacages in different solvents containing water, DMF, acetonitrile, and methanol in a few minutes with nearly quantitative yields, in contrast to the yields obtained with the hour-scale reaction time in a batch reactor. A ring-opening catalytic reaction of the metallacages was selected as a model reaction for exploring supramolecular catalysis in microdroplets, whereby the catalytic yield was enhanced by 2.22-fold compared to that of the same reaction in the batch reactor. This work illustrates a new promising approach for the self-assembly of supramolecular systems.
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