Skip to main content

Ab Initio Reaction Kinetics of CH3OĊ(═O) and ĊH2OC(═O)H Radicals

Author(s): Tan, Ting; Yang, Xueliang; Ju, Yiguang; Carter, Emily A

To refer to this page use:
Abstract: The dissociation and isomerization kinetics of the methyl ester combustion intermediates methoxycarbonyl radical (CH3OĊ(═O)) and (formyloxy)methyl radical (ĊH2OC(═O)H) are investigated theoretically using high-level ab initio methods and Rice–Ramsperger–Kassel–Marcus (RRKM)/master equation (ME) theory. Geometries obtained at the hybrid density functional theory (DFT) and coupled cluster singles and doubles with perturbative triples correction (CCSD(T)) levels of theory are found to be similar. We employ high-level ab initio wave function methods to refine the potential energy surface: CCSD(T), multireference singles and doubles configuration interaction (MRSDCI) with the Davidson–Silver (DS) correction, and multireference averaged coupled-pair functional (MRACPF2) theory. MRSDCI+DS and MRACPF2 capture the multiconfigurational character of transition states (TSs) and predict lower barrier heights than CCSD(T). The temperature- and pressure-dependent rate coefficients are computed using RRKM/ME theory in the temperature range 300–2500 K and a pressure range of 0.01 atm to the high-pressure limit, which are then fitted to modified Arrhenius expressions. Dissociation of CH3OĊ(═O) to ĊH3 and CO2 is predicted to be much faster than dissociating to CH3Ȯ and CO, consistent with its greater exothermicity. Isomerization between CH3OĊ(═O) and ĊH2OC(═O)H is predicted to be the slowest among the studied reactions and rarely happens even at high temperature and high pressure, suggesting the decomposition pathways of the two radicals are not strongly coupled. The predicted rate coefficients and branching fractions at finite pressures differ significantly from the corresponding high-pressure-limit results, especially at relatively high temperatures. Finally, because it is one of the most important CH3Ȯ removal mechanisms under atmospheric conditions, the reaction kinetics of CH3Ȯ + CO was also studied along the PES of CH3OĊ(═O); the resulting kinetics predictions are in remarkable agreement with experiments.
Publication Date: 2016
Citation: Tan, Ting, Xueliang Yang, Yiguang Ju, and Emily A. Carter. "Ab Initio Reaction Kinetics of CH3OĊ(═O) and ĊH2OC(═O)H Radicals." The Journal of Physical Chemistry B 120, no. 8 (2016): 1590-1600. doi:10.1021/acs.jpcb.5b07959
DOI: 10.1021/acs.jpcb.5b07959
ISSN: 1520-6106
EISSN: 1520-5207
Pages: 1590 - 1600
Type of Material: Journal Article
Journal/Proceeding Title: The Journal of Physical Chemistry B
Version: Author's manuscript

Items in OAR@Princeton are protected by copyright, with all rights reserved, unless otherwise indicated.