Redox-active and Brønsted basic dual sites for photocatalytic activation of benzylic C–H bonds based on pyridinium derivatives-Reference-Cited by-同舟云学术

Redox-active and Brønsted basic dual sites for photocatalytic activation of benzylic C–H bonds based on pyridinium derivatives

Published:2022 Issue:6 Volume:24 Page:2492-2498
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Ma Shuai¹,Ma Jin-Ming²,Cui Jing-Wang¹,Rao Cai-Hui¹,Jia Meng-Ze¹,Zhang Jie¹^ORCID

Affiliation:

1. MOE Key Laboratory of Cluster Science, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 102488, P. R. China

2. Hebei Key Laboratory of Applied Chemistry, School of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, P. R. China

Abstract

A mild and efficient photocatalytic C–H bond activation strategy has been developed by combining redox-active and Brønsted basic dual sites to offer a concerted pathway for H abstraction through concomitant proton and electron transfer.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/GC/D1GC04370F

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1. Solvent-Free Oxidation of Primary Carbon-Hydrogen Bonds in Toluene Using Au-Pd Alloy Nanoparticles

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