Stereodynamic Control of Collision-Induced Nonadiabatic Dynamics of NO (A2Σ+) with H2, N2, and CO: Intermolecular Interactions Drive Collision Outcomes
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, California State University—Fullerton, Fullerton, California 92834-6866, United States
2. Department of Chemistry, The College of William and Mary, Williamsburg, Virginia 23187-8795, United States
Funder
Virginia Space Grant Consortium
American Chemical Society Petroleum Research Fund
National Science Foundation
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.1c05653
Reference43 articles.
1. Fully State-Resolved Differential Cross Sections for the Inelastic Scattering of the Open-Shell NO Molecule by Ar
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3. Infrared Spectroscopy of OH··CH3OH: Hydrogen-Bonded Intermediate Along the Hydrogen Abstraction Reaction Path
4. Nonadiabatic Events and Conical Intersections
5. Role of Conical Intersections in Molecular Spectroscopy and Photoinduced Chemical Dynamics
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3. Theoretical Study of the Photochemical Mechanisms of the Electronic Quenching of NO(A2Σ+) with CH4, CH3OH, and CO2;The Journal of Physical Chemistry A;2023-08-08
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