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Catalytic C-H amination driven by intramolecular ligand-to-nitrene one-electron transfer through a rhodium(iii)
Daiki Fujita1, Hideki Sugimoto, Yoshihito Shiota
1Department of Material and Life Science, Division of Advanced Science and Biotechnology, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan. sugimoto@mls.eng.osaka-u.ac.jp shinobu@mls.eng.osaka-u.ac.jp.
Abstract:
Werner type six-coordinate rhodium(iii) complexes coordinated by a planar trianionic ligand and two axial aniline ligands are synthesised. The trianionic ligand behaves as a redox-active ligand to form a ligand radical species upon one-electron oxidation of the complex. The rhodium(iii) complexes catalyse C-H amination of external substrates such as xanthene with tosylazide as the nitrene source. DFT-calculation and kinetic deuterium isotope effects indicate that a di-radical rhodium(iii) complex formed by one-electron transfer from the redox-active ligand to the nitrene group works as a reactive intermediate to induce aliphatic C-H activation.
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