Kinetic C-H oxidative addition vs thermodynamic C-X oxidative addition of chlorobenzene by a neutral Rh(I) system. A density functional theory study.
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abstract
Density functional theory (DFT) is used to explore competitive C-H and C-Cl oxidative additions (OA) of chlorobenzene by the neutral Rh(I) complex: (PNP)Rh(I) [PNP = bis(Z-2-(dimethylphosphino)vinyl)amino]. Consistent with experimental results, our calculation shows that C-Cl OA (DeltaG(double dagger) = 16.0 kcal x mol(-1)) is kinetically competitive with C-H OA (DeltaG(double dagger) = 16.7 kcal x mol(-1)) and that the C-Cl OA is thermodynamically preferred by 28.3 kcal x mol(-1) over the most stable C-H OA product. Hence, the only experimentally observed product was from C-Cl OA.
