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  • Title: Experimental and Multireference ab Initio Investigations of Hydrogen-Atom-Transfer Reactivity of a Mononuclear MnIV-oxo Complex.
    Author: Rice DB, Massie AA, Jackson TA.
    Journal: Inorg Chem; 2019 Oct 21; 58(20):13902-13916. PubMed ID: 31583881.
    Abstract:
    A combined experimental-computational study of hydrocarbon oxidation by the MnIV-oxo complex of the neutral, pentadentate N4py ligand [N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine] offers support for a complex reaction coordinate involving multiple electronic states. Variable-temperature kinetic investigations of ethylbenzene oxidation by [MnIV(O)(N4py)]2+ yield experimental activation parameters that were used to evaluate computationally predicted energy barriers. Both density functional theory (DFT) and multireference complete-active-space self-consistent-field (CASSCF) computations with n-electron valence state perturbation theory (NEVPT2) corrections were employed to investigate the hydrogen-atom-transfer reaction barriers for the 4B1 and 4E states. The 4B1 state is the ground state in the absence of substrate, and the 4E state is related to the ground state by a one-electron MnIV e(dxz,3dyz) to MnIV b1(dx2-y2) excitation. A comparison of the DFT, CASSCF/NEVPT2, and experimental results shows that the B3LYP-D3 method underestimates the activation barriers of both electronic states by ca. 10 kcal mol-1. In contrast, the enthalpic barrier predicted for the 4E state by the CASSCF/NEVPT2 method is within 2 kcal mol-1 of the experimental value. The 4E state is early, with dominant structural distortions in the Mn-Nequatorial distances and perturbations to Mn═O bonding that lead to strong electronic stabilization of interactions between the MnIV-oxo unit and substrate C-H bond. While previous DFT studies were qualitatively correct in their ordering of the 4B1 and 4E transition states, this combined use of experimental and CASSCF/NEVPT2 methods provides an ideal means of assessing the two-state reactivity model of MnIV-oxo complexes.
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