N2B3ng, Y = O-2 and N\*a"v;, Y = 0 were produced by pulsed rodiolysis af nitrogen (100-2000 torr) and fo!lowed by fast kinetic absorption spectroscopy in the second and fifth positive system. T!le rate constants for the denctivation of the species by nitrogen were found to be ~N~A,~ = 1.6i + 0.8; 2.
High-resolution study of collision-induced transitions from N2(A 3Σ+u, ν=10) to N2(B 3Πg, ν=2)
✍ Scribed by R. Bachmann; Ch. Ottinger; A.F. Vilesov
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 458 KB
- Volume
- 203
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
The collision-induced intramolecular energy transfer N2 (A '2: ) + M+N2 (B 'll,) + M was studied under molecular beam conditions using Xe and Nz as the collision partners. Specifically, the near-resonant transfer between the levels A, VI'= 1 O-B, u'= 2 was investigated by means of the product emission, isolated by an interference filter. The rotational and fine structure levels of the A, u"= 10 reactant state were labeled by selective narrow-band laser pumping. The laser was scanned over the whole B, 12+A, 10 band and the subsequent decrease in the collision-induced emission B, 2-A, 0 was recorded. Repeating the scan, the laserinduced fluorescence intensity was recorded. These spectra are similar, showing that there is no significant dependence of the cross section for collision-induced energy transfer on the rotational or fine structure state of the reactant N,( A, d'= IO) molecules.
' Fellow of the Alexander von Humboldt foundation, on leave
📜 SIMILAR VOLUMES
Branching fractions are determined for the product NO (A 'X+, u= 0,l) and NO( B 'II, v= 0) emissions as a function of v' in the energy transfer reaction N,(A 'Z:, v') tNO(X 211n v"=O) in a rapidly pumped discharge-flow reactor operated at a total 2 pressure of TC 2 Torr at % 295 K. Using the NO( A Z