Synthesis of Phenol-Pyridinium Salts Enabled by Tandem Electron Donor-Acceptor Complexation and Iridium Photocatalysis.
Matthew C CarsonCindy R LiuMarisa C KozlowskiPublished in: The Journal of organic chemistry (2024)
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 (S N Ar) 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.
Keyphrases
- visible light
- ionic liquid
- solar cells
- electron transfer
- ms ms
- liquid chromatography tandem mass spectrometry
- electron microscopy
- simultaneous determination
- gas chromatography mass spectrometry
- mass spectrometry
- amino acid
- gold nanoparticles
- gas chromatography
- molecular dynamics simulations
- tandem mass spectrometry
- loop mediated isothermal amplification
- ultra high performance liquid chromatography