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Photo-Induced Vibrational Predissociation of Van Der Waals Molecules

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Advances in Laser Chemistry

Part of the book series: Springer Series in Chemical Physics ((CHEMICAL,volume 3))

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

  1. W. Klemperer, Ber. Bunsenges. 78, 128 (1974)

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  2. J.A. Beswick and J. Jortner, Chem. Phys. Letters 49, 13 (1977)

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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

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-67056-5

  • Online ISBN: 978-3-642-67054-1

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