Abstract
η2-Aniline complexes of the π-base pentaammineosmium(II) are synthesized with a variety of different aniline ligands in good yield. Once synthesized, these complexes display ligand-based reactivity with a variety of electrophiles. Reaction with trifluoromethanesulfonic (triflic) acid produces 2H- and 4H-anilinium complexes, species resulting from protonation on the ring. The regioselectivity of protonation depends on a variety of factors, including the aniline substitution pattern, temperature, and solvent. In addition, the η2-aniline complexes undergo regiospecific, chemospecific, and stereospecific reactions with carbon electrophiles such as Michael acceptors, acetals, and ketals. The resulting anilinium complexes are stabilized by a strong metal-to-ligand back-bonding interaction. As a result, these 4H-anilinium complexes may be functionalized further by their reaction with nucleophiles and complete dearomatization of the aniline ligand is thus achieved. The resulting allylamine and imine complexes are oxidatively removed from the metal center to provide organic allyl amine and cyclohexenone products in moderate yield. This methodology is complementary to that based on η6-complexation of an electron-deficient metal center to the aniline.
