| Autor: |
Yadav, Ajay Kumar, Mishra, Bhupesh Kumar, Singh, Ashutosh, Gour, Nand Kishor |
| Předmět: |
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| Zdroj: |
Molecular Physics; Jul2022, Vol. 120 Issue 13, p1-9, 9p |
| Abstrakt: |
The mechanism and kinetics of the H-abstractions of ethylvinylketone (CH2=CHCOCH2CH3) with Cl atom have been carried out using density functional theory (DFT). The electronic structures and frequencies of reaction species are carried out at M06-2X/6-31+G(d,p) level. The energy calculation is performed for optimised species at the same functionality but using a 6-311++G(d,p) basis set. We characterised transition states (TSs) in each H-abstraction channel and explored reaction species along with TS involved in CH2=CHCOCH2CH3+Cl reaction on the potential energy diagram. Among the various H-abstraction channels, H-abstraction from the methylene group (–CH2–) of CH2=CHCOCH2CH3 is found to be a more dominant reaction channel which is further confirmed by thermochemical analysis. The rate constants of all H-abstraction reaction channels and overall rate constant are calculated using canonical transition state theory (TST) within the temperature range of 200–400 K. The value of the overall rate constant at 298.15 K and 1atm pressure is found to be 0.94 × 10−10 cm3 mol−1 s−1, which is in close with the experimental reported rate constant value, i.e. (2.91 ± 1.10) × 10−10 cm3 mol−1 s−1. The percentage branching ratios of each H-abstraction reaction channel, as well as the lifetime of the titled compound, are also reported herein. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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