Issue 45, 2025

Pulsed-light-induced photochemical reactions: a case study on trifluoromethylation reactions of 1,3-dimethoxybenzene

Abstract

We develop a novel method for controlling photochemical reactions by changing the frequency of pulsed light. A pulsed-light-induced trifluoromethylation reaction is conducted under simple reaction conditions, wherein we combined dimethoxyarene, anthraquinone, and CF3SO2Na in the absence of additives, oxidants, or reductants. Pulsed light yielded more efficient trifluoromethylation reactions than conventional continuous light, while suppressing undesirable reactions. Interestingly, the reaction yield varied with the frequency of pulsed light—ranging from 10−4 Hz to 105 Hz—at the same total irradiation time (7200 s). Our findings suggest that pulsed light offers a promising avenue for controlling photochemical reactions, and beyond traditional parameters like reagents, solution concentration, and temperature, the method of light irradiation emerges as a critical factor in photochemical processes.

Graphical abstract: Pulsed-light-induced photochemical reactions: a case study on trifluoromethylation reactions of 1,3-dimethoxybenzene

Supplementary files

Article information

Article type
Paper
Submitted
20 Sep 2024
Accepted
23 Oct 2025
First published
24 Oct 2025

New J. Chem., 2025,49, 19523-19528

Pulsed-light-induced photochemical reactions: a case study on trifluoromethylation reactions of 1,3-dimethoxybenzene

M. Maeno, T. Nishida, M. Kitamura and K. Morii, New J. Chem., 2025, 49, 19523 DOI: 10.1039/D4NJ04108A

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