多孔性
共价键
光化学
可见光谱
纳米技术
材料科学
共价有机骨架
金属有机骨架
化学工程
化学
光电子学
有机化学
工程类
吸附
作者
Feng Yu,Guangtong Wang,Ruoyang Liu,Xingyao Ye,Shanshan Tao,Matthew A. Addicoat,Zhongping Li,Qiuhong Jiang,Donglin Jiang
标识
DOI:10.1002/anie.202400009
摘要
Abstract Covalent organic frameworks are a novel class of crystalline porous polymers that enable molecular design of extended polygonal skeletons to attain well‐defined porous structures. However, construction of a framework that allows remote control of pores remains a challenge. Here we report a strategy that merges covalent, noncovalent, and photo chemistries to design photoresponsive frameworks with reversibly and remotely controllable pores. We developed a topology‐guided multicomponent polycondensation system that integrates protruded tetrafluoroazobenzene units as photoresponsive sites on pore walls at predesigned densities, so that a series of crystalline porous frameworks with the same backbone can be constructed to develop a broad spectrum of pores ranging from mesopores to micropores. Distinct from conventional azobenzene‐based systems, the tetrafluoroazobenzene frameworks are highly sensitive to visible lights to undergo high‐rate isomerization. The photoisomerization exerts profound effects on pore size, shape, number, and environment, as well as molecular uptake and release, rendering the system able to convert and switch pores reversibly and remotely with visible lights. Our results open a way to a novel class of smart porous materials with pore structures and functions that are convertible and manageable with visible lights.
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