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Vibrationally resolved inelastic scattering and charge transfer in H[sup +]--C[sub 2]H[sub 4] collisions

Journal Article · · Journal of Chemical Physics; (United States)
DOI:https://doi.org/10.1063/1.465230· OSTI ID:5517935
; ; ;  [1];  [2];  [3]
  1. Max-Planck-Institut fuer Stroemungsforschung, Bunsenstr. 10, 3400 Goettingen (Germany)
  2. Center for Molecular Dynamics and Energy Transfer, Department of Chemistry, The Catholic University of America, Washington DC 20064 (United States)
  3. Institut fuer Physikalische Chemie, Universitaet Heidelberg, 6900 Heidelberg (Germany)

Differential cross sections and time-of-flight spectra have been measured in a crossed molecular beam apparatus for inelastic scattering and charge transfer in collisions of 30 eV protons with ethylene. High resolution inelastic time-of-flight spectra reveal peaks corresponding to the fundamentals of at least two of the infrared active antisymmetric vibrational modes of ethylene. In the time-of-flight spectra of H atoms resulting from charge transfer energy loss, peaks corresponding to excitation of two electronic states of the ethylene molecular ion are resolved. The H-atom product angular distributions are consistent with a 2.0 eV potential well in the ground state potential energy surface of the charge transfer reaction. The observations for the antisymmetric vibrational modes are explained in terms of an ion-induced dipole mechanism. Excitation of the symmetric modes is attributed to a vibronic coupling mechanism. An appendix provides a detailed account of the vibronic distributions in idealized low energy, high symmetry collisions leading to stable C[sub 2]H[sub 5][sup +] complexes.

OSTI ID:
5517935
Journal Information:
Journal of Chemical Physics; (United States), Journal Name: Journal of Chemical Physics; (United States) Vol. 99:4; ISSN JCPSA6; ISSN 0021-9606
Country of Publication:
United States
Language:
English