4.7 Article

The elusive active species in nickel(ii)-mediated oxidations of hydrocarbons by peracids: a NiII-oxyl species, an aroyloxy radical, or a NiII-peracid complex?

Journal

DALTON TRANSACTIONS
Volume 52, Issue 25, Pages 8676-8684

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3dt01276j

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The novel free radical chain mechanism of the Ni(II)-mediated oxidation of cyclohexane by mCPBA is investigated using density functional theory calculations. The involvement of a long speculated Ni-II-oxyl species is ruled out, and it is found that an aroyloxy radical (mCBA) and a Ni-III-hydroxyl species formed by O-O homolysis of a Ni-II-mCPBA complex are the active species in the C-H bond activation. These mechanistic findings support the free radical chain mechanism and enrich the mechanistic knowledge of metal-peracid oxidation systems containing transition metals after group 8.
Nonheme nickel(ii)-mediated oxidations of hydrocarbons by meta-chloroperbenzoic acid (mCPBA) show promising activity and selectivity; however, the active species and the reaction mechanism of these reactions are still elusive after decades of efforts. Herein, a novel free radical chain mechanism of the Ni(ii)-mediated oxidation of cyclohexane by mCPBA is investigated using density functional theory calculations. In this study, we rule out the involvement of a long speculated Ni-II-oxyl species. Instead, an aroyloxy radical (mCBA) and a Ni-III-hydroxyl species formed by a rate-limiting O-O homolysis of a Ni-II-mCPBA complex are active species in the C-H bond activation to form a carbon-centered radical R, where mCBA is more robust than the Ni-III-hydroxyl species. The nascent R radical either reacts with mCPBA to form a hydroxylated product and a mCBA radical to propagate the radical chain or reacts with the solvent dichloromethane to form a chlorinated product. In addition, the Ni-II-mCPBA complex is found for the first time to be a robust oxidant in hydroxylation of cyclohexane, with an activation energy of 13.4 kcal mol(-1). These mechanistic findings support the free radical chain mechanism and enrich the mechanistic knowledge of metal-peracid oxidation systems containing transition metals after group 8 in periodic table of elements.

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