Rotational level dependence in the collisional removal of CH/D(A2Δ)
Author:
Publisher
Elsevier BV
Subject
General Physics and Astronomy,General Chemical Engineering,General Chemistry
Reference26 articles.
1. Rotational‐level‐dependent quenching of A 2Σ+ OH and OD
2. Rotational and translation effects in collisions of electronically excited diatomic hydrides
3. Electronic quenching of methylidyne(A2.DELTA.), imidogen(A3.PI.), imidogen(c1.PI.), and phosphinidene(A3.PI.) between 240 and 420 K
4. Collisional quenching of OH (A2Σ+, ′=0) by N2, O2 and CO2 between 204 and 294 K. Implications for atmospheric measurements of OH by laser-induced fluorescence
5. Electronic quenching of between 300 and 950 K
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1. Star-Lif: State-Resolved Laser-Induced Fluorescence Modeling for Diatomic Molecules;2024
2. The effects of energy-level resonance on collision-induced electronic energy transfer: CD (A 2Δ ↔ B 2Σ−) coupling;Phys. Chem. Chem. Phys.;2007
3. Collision-Partner Dependence of Energy Transfer between the CH A2Δ and B2Σ- States;The Journal of Physical Chemistry A;2005-01-05
4. Fate of isolated CH(B2Σ−,v=0,J) states in inelastic collisions with CO;The Journal of Chemical Physics;2002-12-22
5. Rotationally resolved quenching and relaxation of CH(A2Δ,v=0,N) in the presence of CO;The Journal of Chemical Physics;2002-02-15
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