Strong energy dependence of collisional vibrational relaxation between 2500 and 5400 cm−1 in T1 pyrazine
Author:
Publisher
AIP Publishing
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://aip.scitation.org/doi/pdf/10.1063/1.457726
Reference18 articles.
1. State-to-state vibrational transfer in atom-molecule collisions. Beams vs. bulbs
2. The collisional flow of vibrational energy into surrounding vibrational fields within S1 benzene
3. Level dependence of vibrational relaxation rates inS0p‐difluorobenzene in the range εvib=1500–3300 cm−1: Large efficiencies with He as a collision partner
4. Vibrationally excited formaldehyde. The relationship between vibrational structure and collisional properties
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1. Competition between Photochemistry and Energy Transfer in UV-Excited Diazabenzenes. 4. UV Photodissociation of 2,3-, 2,5-, and 2,6-Dimethylpyrazine;The Journal of Physical Chemistry A;2007-11-30
2. Classical Trajectory Study of Energy Transfer in Pyrazine−CO Collisions;The Journal of Physical Chemistry A;2001-03-01
3. Competition between Photochemistry and Energy Transfer in Ultraviolet-Excited Diazabenzenes. 3. Photofragmentation and Collisional Quenching in Mixtures of 2-Methylpyrazine and Carbon Dioxide;The Journal of Physical Chemistry A;2000-10-19
4. Monte Carlo analysis of T1 pyrazine collisional vibrational relaxation: Evidence for supercollisions;The Journal of Chemical Physics;2000-06-15
5. Competition between photochemistry and energy transfer in ultraviolet-excited diazabenzenes. I. Photofragmentation studies of pyrazine at 248 nm and 266 nm;The Journal of Chemical Physics;2000-04
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