Kinetic energy dependence of cross sections for state‐to‐state vibrational excitation in collisions of S0 aniline with He
Author:
Publisher
AIP Publishing
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://aip.scitation.org/doi/pdf/10.1063/1.447106
Reference13 articles.
1. Collisional deactivation of a selected energy level inS0p‐difluorobenzene embedded in a dense vibrational field: Absolute rate constants for a variety of collision partners
2. Collisional deactivation of a selected energy level inS0p‐difluorobenzene embedded in a dense vibrational field: Absolute rate constants for a variety of collision partners
3. Collisional deactivation of a selected energy level inS0p‐difluorobenzene embedded in a dense vibrational field: Absolute rate constants for a variety of collision partners
4. Mode‐to‐mode energy transfer in1B2aniline induced by very low energy collisions with He
5. Mode‐to‐mode energy transfer in1B2aniline induced by very low energy collisions with He
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2. State-to-state differential cross sections for rotationally inelastic collisions of NO(2Π1/2,j⩽2.5) with CO(1Σ+) and O2(3Σg−) at a kinetic energy of 442 cm−1;The Journal of Chemical Physics;1998-02-22
3. Differential cross sections for rotationally inelastic collisions of NO(2Π1/2, j′⩽2.5) with NO(2Π1/2, j′⩽2.5) at a kinetic energy of 442 cm−1;The Journal of Chemical Physics;1997-01-22
4. State‐to‐state differential cross sections for rotationally inelastic collisions of NO(2Π1/2,j=0.5) with Ar at kinetic energies between 117 cm−1 and 1694 cm−1;The Journal of Chemical Physics;1996-10
5. Vibrational energy transfer from four levels below 410 cm−1 in S1 p‐difluorobenzene. I. A strong collision partner dependence in state‐to‐state transfer by monatomics;The Journal of Chemical Physics;1996-05-15
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