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Angularly resolved rotational energy transfer in highly vibrationally excited states: Na sub 2 ( v =31)--Ne

Journal Article · · Journal of Chemical Physics; (USA)
DOI:https://doi.org/10.1063/1.460611· OSTI ID:5909817
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  1. Fachbereich Physik, Universitaet Kaiserslautern, D-6750 Kaiserslautern, Germany (DE)
The scattering of high vibrationally excited sodium molecules Na{sub 2}({ital v}=31) with Ne atoms at 180 meV collision energy is investigated in a crossed molecular beam arrangement using laser optical methods. Angularly resolved rotationally inelastic and vibrationally elastic cross sections {ital j}{sub {ital i}}{r arrow}{ital j}{sub {ital f}} are measured for {ital j}{sub {ital i}} =5, 7, and 9{le}{ital j}{sub {ital f}} {le}25. Pronounced rotational rainbow maxima are observed, the angular position of which indicates a significantly larger anisotropy of the interaction potential compared to that of Na{sub 2}({ital v}=0)--Ne. Except for the increase of the anisotropy the vibrational excitation has little effect on the dynamics of rotational energy transfer. Good agreement with a new semiempirical Na{sub 2}--Ne potential surface {ital V}({ital r},{ital R},{gamma}) is found.
OSTI ID:
5909817
Journal Information:
Journal of Chemical Physics; (USA), Journal Name: Journal of Chemical Physics; (USA) Vol. 94:6; ISSN JCPSA; ISSN 0021-9606
Country of Publication:
United States
Language:
English