Theoretical study of the reaction kinetics of atomic bromine with tetrahydropyran
KAUST DepartmentClean Combustion Research Center
Physical Sciences and Engineering (PSE) Division
Mechanical Engineering Program
Chemical Kinetics & Laser Sensors Laboratory
Permanent link to this recordhttp://hdl.handle.net/10754/564056
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AbstractA detailed theoretical analysis of the reaction of atomic bromine with tetrahydropyran (THP, C5H10O) was performed using several ab initio methods and statistical rate theory calculations. Initial geometries of all species involved in the potential energy surface of the title reaction were obtained at the B3LYP/cc-pVTZ level of theory. These molecular geometries were reoptimized using three different meta-generalized gradient approximation (meta-GGA) functionals. Single-point energies of the stationary points were obtained by employing the coupled-cluster with single and double excitations (CCSD) and fourth-order Møller-Plesset (MP4 SDQ) levels of theory. The computed CCSD and MP4(SDQ) energies for optimized structures at various DFT functionals were found to be consistent within 2 kJ mol-1. For a more accurate energetic description, single-point calculations at the CCSD(T)/CBS level of theory were performed for the minimum structures and transition states optimized at the B3LYP/cc-pVTZ level of theory. Similar to other ether + Br reactions, it was found that the tetrahydropyran + Br reaction proceeds in an overall endothermic addition-elimination mechanism via a number of intermediates. However, the reactivity of various ethers with atomic bromine was found to vary substantially. In contrast with the 1,4-dioxane + Br reaction, the chair form of the addition complex (c-C5H10O-Br) for THP + Br does not need to undergo ring inversion to form a boat conformer (b-C4H8O2-Br) before the intramolecular H-shift can occur to eventually release HBr. Instead, a direct, yet more favorable route was mapped out on the potential energy surface of the THP + Br reaction. The rate coefficients for all relevant steps involved in the reaction mechanism were computed using the energetics of coupled cluster calculations. On the basis of the results of the CCSD(T)/CBS//B3LYP/cc-pVTZ level of theory, the calculated overall rate coefficients can be expressed as kov.,calc.(T) = 4.60 × 10-10 exp[-20.4 kJ mol-1/(RT)] cm3 molecule-1 s-1 for the temperature range of 273-393 K. The calculated values are found to be in excellent agreement with the experimental data published previously.
SponsorsThe computations described in this work were performed on the computing facilities of the department of Academic Information and Communication Technologies (AICT) and the High-Performance Computing (HPC) facilities within the research computing services of the University of Calgary and the Western Canada Research Grid. We are grateful to Dr. Matthias Olzmann for helpful discussions and also for providing the program script for the SACM calculations. The work of KAUST authors was supported by funding from King Abdullah University of Science and Technology.
PublisherAmerican Chemical Society (ACS)
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