Generation of a Ground‐State Electron Donor Utilizing Stored Light Energy

This study presents a process for generating potent ground-state electron donors using chemically stored light energy. Our strategy leverages light energy through high-energy vicinal diols produced by the photodimerization of diaryl ketones. Under basic conditions, these diols can produce dianions with potentials near -2.7 V, which further act as strong organic reductants. These reductants demonstrate a high capacity for effectively reducing recalcitrant substrates at room temperature, including electron-rich aryl bromides, alkyl iodides, and sulfonamide compounds. Mechanistic investigations, supported by density functional theory (DFT) calculations, confirm both the formation of these dianions and their exceptional electron-donating properties.

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Publication Details

Journal
Chemistry - A European Journal
Published
2026-02-17
DOI
https://doi.org/10.1002/chem.70795
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Generation of a Ground‐State Electron Donor Utilizing Stored Light Energy

Eric Clot, Marc Taillefer
Chemistry - A European Journal
Radical Photochemical Reactions
article

Generation of a Ground‐State Electron Donor Utilizing Stored Light Energy

Eric Clot, Marc Taillefer
article en

Abstract

This study presents a process for generating potent ground-state electron donors using chemically stored light energy. Our strategy leverages light energy through high-energy vicinal diols produced by the photodimerization of diaryl ketones. Under basic conditions, these diols can produce dianions with potentials near -2.7 V, which further act as strong organic reductants. These reductants demonstrate a high capacity for effectively reducing recalcitrant substrates at room temperature, including electron-rich aryl bromides, alkyl iodides, and sulfonamide compounds. Mechanistic investigations, supported by density functional theory (DFT) calculations, confirm both the formation of these dianions and their exceptional electron-donating properties.

Chemistry - A European Journal
École Nationale Supérieure de Chimie de Montpellier (FR), Centre National de la Recherche Scientifique (FR), Université de Montpellier (FR)
Centre National de la Recherche Scientifique, Université de Montpellier
Affordable and clean energy
Openalex Percentile: Top 50%
Radical Photochemical Reactions
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