A highly efficient strategy for the supramolecular self‐assembly of well‐defined metallacages in microdroplets through continuous‐flow microfluidic devices is described by Lin Xu and co‐workers in their Research Article (e202301900). The strategy adds a highly efficient approach to the toolbox of metallacage self‐assembly.
Developing a new strategy to improve the selfassembly 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.
Microfluidics has received extensive attention due to its ability to rapidly prepare a large number of microdroplets with controlled sizes and defined morphologies. In addition to having large surface areas and controllable confinement environments, these prepared microdroplets can be used as analytical detection devices to screen and optimize various kinetic parameters. This review summarizes recent advances in the microfluidic control of droplet‐based catalytic reactions and discusses the role of these droplets in both homogeneous and heterogeneous catalyzes and in the catalysis of macromolecular biological enzymes in water‐in‐oil and oil‐in‐oil environments. Additionally, the existing problems and future development directions of droplets in catalysis are highlighted to promote the development of catalytic reactions in droplet media and provide guidance for the high‐throughput screening of catalysts and the directed evolution of biological enzymes.
A highly efficient strategy for achieving the supramolecular self‐assembly of well‐defined metallacages in microdroplets through continuous‐flow microfluidic devices is demonstrated by Lin Xu et al. in their Research Article (e202301900). The strategy adds a highly efficient approach to the toolbox of metallacage self‐assembly.
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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