H. Krause et Hj. Neusser, DISSOCIATION-ENERGY OF NEUTRAL AND IONIC BENZENE-NOBLE GAS DIMERS BY PULSED-FIELD THRESHOLD IONIZATION SPECTROSCOPY, The Journal of chemical physics, 99(9), 1993, pp. 6278-6286
Delayed pulsed field threshold ionization of clusters excited to high
long-lived Rydberg states is used to study their dissociation behavior
. Benzene-Ar and benzene-Kr dimers are excited by resonance enhanced t
wo-photon ionization to Rydberg levels close to various ionization thr
esholds. The field ionized threshold ions are monitored and separated
from the non-energy-selected ions in a reflecting field mass spectrome
ter with high mass resolution. The appearance of threshold ions at the
daughter ion mass indicates the onset of a dissociation process. Daug
hter ions are first observed for the 16(1)6(1)(3/2) level of the two i
nvestigated dimers. This leads to an upper limit of the dissociation e
nergy of benzene-Ar of 340 cm-1 which is probably higher than the true
dissociation energy. For the first time threshold ions are observed f
or large internal energies of some 5 eV in the core indicating that hi
gh Rydberg states maintain their long lifetime even if the core is ele
ctronically or vibrationally excited by several eV.