Carbon-oxygen bond formation via organometallic Baeyer-Villiger transformations: a computational study on the impact of metal identity.

Metal-mediated formation of C-O bonds is an important transformation that can occur by a variety of mechanisms. Recent studies suggest that oxygen-atom insertion into metal-hydrocarbyl bonds in a reaction that resembles the Baeyer-Villiger transformation is a viable process. In an effort to identify promising new systems, this study is designed to assess the impact of metal identity on such O-atom insertions for the reaction [(bpy)(x)M(Me)(OOH)](n) → [(bpy)(x)M(OMe)(OH)](n) (x = 1 or 2; bpy = 2,2'-bipyridyl; n is varied to maintain the d-electron count at d(6) or d(8)). Six d(8)-square-planar complexes (M = Pt(II), Pd(II), Ni(II), Ir(I), Rh(I), and Co(I)) and eight d(6)-octahedral systems (M = Ir(III), Rh(III), Co(III), Fe(II) Ru(II), Os(II), Mn(I), and Tc(I)) are studied. Using density functional theory calculations, the structures and energies of ground-state and transition-state species are elucidated. This study shows clear trends in calculated ΔG(++)'s for the O-atom insertions. The organometallic Baeyer-Villiger insertions are favored by lower coordination numbers (x = 1 versus x = 2), earlier transition metals, and first-row (3d) transition metals.