M. Allan, EXPERIMENTAL-STUDY OF VIBRATIONAL-EXCITATION OF ALLENE BY SLOW-ELECTRON IMPACT - VIBRONIC COUPLING IN THE SHORT-LIVED NEGATIVE-ION STATES, The Journal of chemical physics, 100(8), 1994, pp. 5588-5596
Vibrational electron energy loss spectra, vibrational excitation funct
ions, and angular dependence of vibrational energy losses were measure
d in relative units for propadiene (allene, H2C=C=CH2) in an incident
energy range up to 16 eV. Resonant excitation via the 2 eV resonance i
s not very selective; symmetric and antisymmetric C-C-C stretch, CH2 t
wist and scissoring, CH stretch, and C-C-C bending are all excited. Th
e antisymmetric C-C-C stretch and CH2 twist are excited by Jahn-Teller
activity of the degenerate 2E resonance, the bending by vibronic coup
ling with higher lying resonances. The essential features of the excit
ation are qualitatively rationalized by a Hartree-Fock (HF)/6-31G ani
on potential energy surface. Unspecific excitation of high vibrational
levels, accompanied by detachment of slow electrons, is also observed
to result from attachment of 2 eV electrons, and is rationalized as a
consequence of temporary trapping of part of the nuclear wave packet
on the bound (not autodetaching) part of the anion potential surface.
Very broad resonance features are observed in the 2-16 eV range, mainl
y in the excitation functions of the C-H stretch and the CH2 scissorin
g vibrations. A moderately broad resonance peak at 11.5 eV, observed i
n the excitation of the symmetric and antisymmetric C-C-C stretch vibr
ations, is assigned to two overlapping sigma shape resonances. Absolu
te elastic cross sections are given for reference.