Visible light induced reactions of quinones

Abstract

This review covers the visible light induced reactions of quinones such as benzoquinone, naphthoquinone, and anthraquinone. These quinones are distinguished by their fully conjugated structures, which feature minimal energy gaps, and nonbonding electron pairs on the oxygen atoms. Such structural attributes facilitate np → π* transition, allowing for easy access to excited states and rendering quinones highly reactive under visible‐light irradiation. We describe three primary types of reactions facilitated by these electronic characteristics: Paternò–Büchi (PB) reactions, which entail [2 + 2] photocycloaddition between the carbonyl groups of quinones and alkenes or alkynes; CH activation processes, which showcase quinones' versatility in functionalizing hydrocarbons; and the formation of electron donor–acceptor complexes, demonstrating quinones' capability to engage in charge transfer interactions. Through this review, we highlight the critical role quinones play in photochemistry, their unique electronic properties, and their broad applicability in synthetic organic chemistry.