Photoredox manifold for dehydrogenative coupling using protons as oxidants

05 January 2026, Version 1
This content is an early or alternative research output and has not been peer-reviewed by Cambridge University Press at the time of posting.

Abstract

The direct coupling of two unfunctionalized molecules under mild conditions embodies an ideal in synthetic chemistry. In this study, we report a metal-free photocatalytic process for arene C-H functionalization that employs an acridinium-type catalyst and produces dihydrogen as the only by-product. Throughout the catalytic cycle, the catalyst acts as an oxidizing agent, a hydrogen atom transfer agent, and a proton-reducing agent, enabling a cross-dehydrogenative transformation without the need for external oxidants. The reaction is conveniently performed using visible light, and the high oxidation potential of the catalyst allows it to engage even electron- deficient arene substrates. The catalytic mechanism disclosed herein can become a general logic for developing various cross-dehydrogenative reactions adaptable for pharmaceutical and material sciences.

Keywords

acridinium
photoredox
cross-dehydrogenative transformation
C-H activation
organic hydrides

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