A four-dimensional quantum mechanical state-to-state study of the H2+C2H→H+C2H2 reaction
Author:
Publisher
AIP Publishing
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://aip.scitation.org/doi/pdf/10.1063/1.1367387
Reference37 articles.
1. Four-dimensional quantum mechanical treatment of penta-atomic systems: Case H2+C2H→H+C2H2; total reactive probabilities, cross sections, and rate constants
2. Three‐dimensional quantum mechanical rate constants for the reaction O+O3→2O2, employing a six‐dimensional potential energy surface
3. A three‐dimensional quantum mechanical study of the NH+NO reactions
4. Comparison between Experimental and Three-Dimensional Quantum Mechanical Rate Constants for the NH(D) + NO Reactions
5. Reduced dimensionality theory of quantum reactive scattering
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1. Full-dimensional quantum dynamics study of the H2 + C2H → H + C2H2 reaction on an ab initio potential energy surface;The Journal of Chemical Physics;2016-05-21
2. An investigation of one- versus two-dimensional semiclassical transition state theory for H atom abstraction and exchange reactions;The Journal of Chemical Physics;2016-02-28
3. Reduced-Dimensionality Semiclassical Transition State Theory: Application to Hydrogen Atom Abstraction and Exchange Reactions of Hydrocarbons;The Journal of Physical Chemistry A;2015-07-01
4. Dynamics of alkali ions-neutral molecules reactions: Radio frequency-guided beam experimental cross-sections and direct quasiclassical trajectory studies;AIP Conference Proceedings;2012
5. Kinetic isotope effects for the H2+ C2H ↔ C2H2+ H reaction based on the ab initio calculations and a global potential energy surface;International Journal of Chemical Kinetics;2010-05
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