Barrierless unimolecular association reactions are prominent in atmospheric and combustion mechanisms but are challenging for both experiment and kinetics theory. A key datum for understanding the pressure dependence of association and dissociation reactions is the high-pressure limit, but this is often available experimentally only by extrapolation. Here we calculate the high-pressure limit for the addition of a chlorine atom to acetylene molecule (Cl + C2H2→C2H2Cl). This reaction has outer and inner transition states in series; the outer transition state is barrierless, and it is necessary to use different theoretical frameworks to treat the two kinds of transition state. Here we study the reaction in the high-pressure limit using multifaceted variable-reaction-coordinate variational transition-state theory (VRC-VTST) at the outer transition state and reaction-path variational transition state theory (RP-VTST) at the inner turning point; then we combine the results with the canonical unified statistical (CUS) theory. The calculations are based on a density functional validated against the W3X-L method, which is based on coupled cluster theory with single, double, and triple excitations and a quasiperturbative treatment of connected quadruple excitations [CCSDT(Q)], and the computed rate constants are in good agreement with some of the experimental results. The chlorovinyl (C2H2Cl) adduct has two isomers that are equilibrium structures of a double-well C≡C-H bending potential. Two procedures are used to calculate the vibrational partition function of chlorovinyl; one treats the two isomers separately and the other solves the anharmonic energy levels of the double well. We use these results to calculate the standard-state free energy and equilibrium constant of the reaction.
|Original language||English (US)|
|Number of pages||7|
|Journal||Proceedings of the National Academy of Sciences of the United States of America|
|State||Published - Mar 17 2020|
Bibliographical noteFunding Information:
This work was supported in part by the US Department of Energy, Office of Basic Energy Sciences, under Grant DE-SC0015997, and by the National Natural Science Foundation of China under Grant 51536002. L.Z. was supported by a scholarship from the China Scholarship Council (201706120185).
ACKNOWLEDGMENTS. This work was supported in part by the US Department of Energy, Office of Basic Energy Sciences, under Grant DE-SC0015997, and by the National Natural Science Foundation of China under Grant 51536002. L.Z. was supported by a scholarship from the China Scholarship Council (201706120185).
© 2020 National Academy of Sciences. All rights reserved.
- Direct dynamics
- Electronic structure
- Rate constant
- Transition state