Modulating β‐Keto‐enamine‐Based Covalent Organic Frameworks for Photocatalytic Atom‐Transfer Radical Addition Reaction

Author:

Zhao Yuting1,Li Lei1,Zang Jiyuan1,Young David J.2,Ren Zhi‐Gang1,Li Hai‐Yan1,Yu Lei1,Bian Guo‐Qing1,Li Hong‐Xi1ORCID

Affiliation:

1. College of Chemistry, Chemical Engineering and Materials Science Soochow University Suzhou 215123 P. R. China

2. Glasgow College, UESTC University of Electronic Science and Technology of China Chengdu 611731 P. R. China

Abstract

AbstractThe atom‐transfer radical addition (ATRA) reaction simultaneously forges carbon‐carbon and carbon‐halogen bonds. However, frequently‐used photosensitizers such as precious transition metal complexes, or organic dyes have limitations in terms of their potential toxicity and recyclability. Three β‐ketoenamine‐linked covalent organic frameworks (COFs) from 1,3,5‐triformylphloroglucinol and 1,4‐phenylenediamines with variable transient photocurrent and photocatalytic activity have been prepared. A COF bearing electron‐deficient Cl atoms displayed the highest photocatalytic activity toward the ATRA reaction of polyhalogenated alkanes to give halogenated olefins under visible light at room temperature. This heterogeneous photocatalyst exhibited good functional group tolerance and could be recycled without significant loss of activity.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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