Rotational relaxation in the H2CO
1A2 state by transient gain spectroscopy
J. Chem. Phys. 82, 5755 (1985); doi:10.1063/1.448564
Issue Date: 15 June 1985
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A new, pulsed pump–cw probe technique, transient gain spectroscopy, has been used to measure the zero pressure lifetime (279±10 ns) and self-collision depopulation rate (110.5±3.1 µs−1 Torr−1) for the H2CO
1A2 41 JKa,Kc =132,12 level as well as the 122,11
132,12(31±8 µs−1 Torr−1) and 142,13
132,12(40±6 µs−1 Torr−1) rotational relaxation rates. The dominant collisional process is rotational energy transfer, which, for the H2CO(
)+H2CO(
) process examined here, appears to follow dipole–dipole scaling and propensity rules. The 110.5 µs−1 Torr−1 depopulation rate in the
state agrees with the vibrationless
state rate obtained from microwave power broadening scaled by the 1.46 D/2.33 D electric dipole moment ratio. The two strongest a-dipole rotational state-to-state rates account for more than 50% of the total removal rate from H2CO
41 132,12.
The Journal of Chemical Physics is copyrighted by The American Institute of Physics.
132,12(31±8 µs−1 Torr−1) and 142,13
132,12(40±6 µs−1 Torr−1) rotational relaxation rates. The dominant collisional process is rotational energy transfer, which, for the H2CO(| History: | Received 7 March 1985; accepted 8 April 1985 |
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KEYWORDS and PACS
- 33.50.Dq
Molecular spectra and interactions of molecules with photons Fluorescence and phosphorescence; radiationless transitions (intersystem crossing, internal conversion) Fluorescence and phosphorescence spectra - 33.10.Ev
Molecular spectra and interactions of molecules with photons Calculation of molecular spectra Rotational analysis - YEAR: 1985
PUBLICATION DATA
0021-9606 (print)
1089-7690 (online)
REFERENCES (16)
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