Year: 2026
Type: article
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.
Source: Chemistry - A European Journal
DOI: 10.1002/chem.70795
Authors: Marc Taillefer, Éric Clot, Alexis Prieto
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,640
OpenAlex ID: W7129618725
