Issue 11, 2022

Photocatalytic conversion of arylboronic acids to phenols by a new 2D donor–acceptor covalent organic framework

Abstract

Covalent organic frameworks (COFs) are a kind of promising crystalline material for photocatalytic organic conversion. The introduction of electron donor–acceptor (D–A) units into its structure can reasonably adjust the photoelectric properties and energy bandwidth of COFs. In this research, we designed and synthesized a two-dimensional (2D) D–A type COF (BTT-BTDDA-COF) based on alternating connections of benzotrithiophene (BTT) and 4,4’-(2,1,3-benzothiadiazole-4,7-diyl)dianiline (BTDDA) units, with a wide visible light absorption range and good photoelectric response characteristics. In the photocatalytic conversion of arylboronic acid to phenol, BTT-BTDDA-COF exhibits high catalytic activity, wide substrate applicability and good recoverability. The high-efficiency photocatalytic activity of BTT-BTDDA-COF is reasonably attributed to the electron push–pull effect between the donor and acceptor units, which significantly improves the transfer and separation of carriers, which leads to the expansion of the visible light absorption range. The above results show the practicability of COFs material design and provide a new idea for the application of the new D–A COF catalyst in photocatalytic organic conversion.

Graphical abstract: Photocatalytic conversion of arylboronic acids to phenols by a new 2D donor–acceptor covalent organic framework

Supplementary files

Article information

Article type
Paper
Submitted
01 Mar 2022
Accepted
09 Apr 2022
First published
11 Apr 2022
This article is Open Access
Creative Commons BY license

Mater. Adv., 2022,3, 4699-4706

Photocatalytic conversion of arylboronic acids to phenols by a new 2D donor–acceptor covalent organic framework

B. Luo, Y. Zhang, Y. Chen and J. Huo, Mater. Adv., 2022, 3, 4699 DOI: 10.1039/D2MA00237J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements