Aromatic C–H σ-Bond Activation by Ni0, Pd0, and Pt0 Alkene Complexes: Concerted Oxidative Addition to Metal vs Ligand-to-Ligand H Transfer Mechanism

Shuwei Tang, Odile Eisenstein, Yoshiaki Nakao, Shigeyoshi Sakaki

doi:10.1021/acs.organomet.7b00256

C–H σ-bond activation of arene (represented here by benzene) by the Ni0 propene complex Ni0(IMes)(C3H6) (IMes = 1,3-dimesitylimidazol-2-ylidene), which is an important elementary step in Ni-catalyzed hydroarylation of unactivated alkene with arene, was investigated by DFT calculations. In the Ni0 complex, the C–H activation occurs through a ligand-to-ligand H transfer mechanism to yield NiII(IMes)(C3H7)(Ph) (C3H7 = propyl; Ph = phenyl). In Pd0 and Pt0 analogues, the activation occurs through concerted oxidative addition of the C–H bond to the metal. Analysis of the electron redistribution during the C–H activation highlights the difference between the two mechanisms. In the ligand-to-ligand H transfer, charge transfer (CT) occurs from the metal to the benzene. However, the atomic population of the transferring H remains almost constant, suggesting that different CT simultaneously occurs from the transferring H to the LUMO of propene. The electron redistribution contrasts significantly with that found for ...

Aromatic C–H σ-Bond Activation by Ni<sup>0</sup>, Pd<sup>0</sup>, and Pt<sup>0</sup> Alkene Complexes: Concerted Oxidative Addition to Metal vs Ligand-to-Ligand H Transfer Mechanism

Search this article

Description

Journal

Citations (10)*help

References(90)*help

Related Projects

Details 詳細情報について

Export

Report a problem