Abstract
A van der Waal’s molecule formed between diatomic or polyatomic molecules will, in general, have at least one vibrational frequency for which the associated quantum is greater than the well-depth of the van der Waal’s bond. Excitation of this frequency will, therefore, raise the internal energy to a level above that, required for dissociation of the van der Waal’s bond. In 1974 Klemperer suggested [1] that (HF)2 might be produced in, a supersonic molecular beam and detected with a mass spectrometer: excitation of the HF stretching frequency of (HF)2, if followed by dissociation of the dimer, should lead to a decrease in the mass spectrometer output.
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References
W. Klemperer, Ber. Bunsenges. 78, 128 (1974)
J.A. Beswick and J. Jortner, Chem. Phys. Letters 49, 13 (1977)
M.S. Child, Faraday Disc. Chem. Soc. 62, 307 (1977)
R.E. Smalley, D.H. Levy, and L. Wharton, J. Chem. Phys. 64, 3266 (1976)
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L. Mannik, J.C. Stryland, and H.L. Welsh, Can. J, Phys. 49, 3056 (1971).
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© 1978 Springer-Verlag Berlin Heidelberg
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Gough, T.E., Miller, R.E., Scoles, G. (1978). Photo-Induced Vibrational Predissociation of Van Der Waals Molecules. In: Zewail, A.H. (eds) Advances in Laser Chemistry. Springer Series in Chemical Physics, vol 3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-67054-1_42
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DOI: https://doi.org/10.1007/978-3-642-67054-1_42
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