Time-resolved fluorescence hscr-induced spectroscopy was used to determine the quencbin~ rates of the vibrations1 Icvets u' = 0,l and 2 of NG(B \*f+ \_,,) bv I& and Ne. For bolt2 quenchers rate constants mz found to base a depcndenoz upon \_ the vibrational escitation of the Ievef. Tlie radiative Ii
Rotational and vibrational relaxation rate constants for N2+(B2Σ, ν' = 0, N') colliding with He
✍ Scribed by A. Plain; J. Jolly
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 363 KB
- Volume
- 135
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
A tunable dye laser was used to populate selectively a single rotational-vibrational state of N 2 ( B 'E , u' = 0, N' = O-l 5 ) . The population changes induced by collisions with He were determined using time-resolved spectroscopy in a flowing afterglow experiment. Total rotational transfer rates form the pumped level were found to vary with N' between 1.6 and 2.5 x lo-"' cm3 s-l. The vibrational quenching of N: (B, v' =O) by He was also determined and found to be as low as 8.0X lo-l2 cm3 s-l.
📜 SIMILAR VOLUMES
Fully converged quantum cross sections for 4He-D2 (u= l,i=O) vibrational reliaxation were determined using the coupled-states method and a modikied version of the Gordon-Secrcst surface. First-order forbidden rotational transitions play a si@fkant role, comparable to that observed previously for the
The rate constants for collisional quenching of Oz(b 'x:) by COz, NzO. NO, NHs\_ HCl and SOz. and of Oz(a '+.I by NO. NH3 and HCl have been measured at room tempera& by studying 'he emissions of singlet moleculx a\pg.en at 762 and 634 nm in D flowing discharge. The rate constant for deactivation of