Photoresponsive Covalent Organic Frameworks: Visible‐Light Controlled Conversion of Porous Structures and Its Impacts

Author:

Feng Yu12,Wang Guangtong13,Liu Ruoyang1,Ye Xingyao14,Tao Shanshan1,Addicoat Matthew A.5,Li Zhongping1,Jiang Qiuhong1,Jiang Donglin14ORCID

Affiliation:

1. Department of Chemistry, Faculty of Science National University of Singapore, 3 Science Drive 3 Singapore 117543 Singapore

2. School of Materials Science and Engineering Changzhou University Changzhou 213164 China

3. Key Laboratory of Micro-systems and Micro-structures Manufacturing, Ministry of Education Harbin Institute of Technology Harbin 150080 China

4. Joint School of National University of Singapore and Tianjin University International Campus of Tianjin University Binhai New City, Fuzhou 350207 China

5. School of Science and Technology Nottingham Trent University Clifton Lane Nottingham NG11 8NS UK

Abstract

AbstractCovalent 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.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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