Non-innocent Radical Ion Intermediates in Photoredox Catalysis: Parallel Reduction Modes Enable Coupling of Diverse Aryl Chlorides

We describe a photocatalytic system that elicits potent photoreductant activity from conventional photocatalysts by leveraging radical anion intermediates generated in situ. The combination of an isophthalonitrile photocatalyst and sodium formate promotes diverse aryl radical coupling reactions from abundant but difficult to reduce aryl chloride substrates. Mechanistic studies reveal two parallel pathways for substrate reduction both enabled by a key terminal reductant byproduct, carbon dioxide radical anion.

Automated summary

This photocatalytic system utilizes radical anion intermediates to enhance photoreductant activity, enabling diverse aryl radical coupling reactions. Mechanistic studies reveal two parallel pathways for substrate reduction, both facilitated by the key terminal reductant byproduct, carbon dioxide radical anion.