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Title:Ab initio and kinetic study of the reaction of ketones with OH for T="500-2,000" K. Part I: hydrogen-abstraction from H3CC(O)CH(3-x)CH3, x="0-2"
Authors:C-W. Zhou, J. M. Simmie and H. J. Curran, 2011
Abstract: A theoretical study is presented of the mechanism and kinetics of the reactions of the hydroxyl radical with three ketones: dimethyl (DMK), ethylmethyl (EMK) and iso-propylmethyl (iPMK) ketones. CCSD(T) values extrapolated to the basis set limit are used to benchmark the computationally less expensive methods G3 and G3MP2BH&H, for the DMK + ȮH reaction system. These latter methods are then used in computations involving the reactions of the larger ketones. All possible abstraction channels have been modeled. A stepwise mechanism involving the formation of a reactant complex in the entrance channel and a product complex in the exit channel has been recognized in part of the abstracting processes. High-pressure limit rate constants of the title reactions have been calculated in the temperature range of 500–2000 K using the Variflex code including Eckart tunneling corrections. Variable reaction coordinate transition state theory (VRC-TST) has been used for the rate constants of the barrier-less entrance channel. Calculated total rate constants (cm3 mol−1 s−1) are reported as follows: k(DMK) = 1.32 × 10^2 × T^3.30exp(503/T) k(EMK) = 3.84 × 10^1 × T^3.51exp(1515/T) k(iPMK) = 2.08 × 10^1 × T^3.58exp(2161/T) Group rate constants (on a per H atom basis) for different carbon sites in title reactions have also been provided.
ICHEC Project:BurnQuest: Towards a World Class Combustion Chemistry Centre
Publication:Phys. Chem. Chem. Phys., 2011,13, 11175-11192
URL: 10.1039/C0CP02754E
Status: Published

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