Herein, we describe a dual photocatalytic system to synthesize phenol–pyridinium salts using visible light. Utilizing both electron donor–acceptor (EDA) complex and iridium(III) photocatalytic cycles, the C–N cross-coupling of unprotected phenols and pyridines proceeds in the presence of oxygen to furnish pyridinium salts. Photocatalytic generation of phenoxyl radical cations also enabled a nucleophilic aromatic substitution (SNAr) of a fluorophenol with an electron-poor pyridine. Spectroscopic experiments were conducted to probe the mechanism and reaction selectivity. The unique reactivity of these phenol–pyridinium salts were displayed in several derivatization reactions, providing rapid access to a diverse chemical space.
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Carson et al. (2024) studied this question.
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