INFRARED INFRARED DOUBLE-RESONANCE SPECTROSCOPY OF AR-HF - INTERMOLECULAR STATE DEPENDENCE OF THE DIPOLE-MOMENT AND VIBRATIONAL PREDISSOCIATION IN VHF=2
Pa. Block et Re. Miller, INFRARED INFRARED DOUBLE-RESONANCE SPECTROSCOPY OF AR-HF - INTERMOLECULAR STATE DEPENDENCE OF THE DIPOLE-MOMENT AND VIBRATIONAL PREDISSOCIATION IN VHF=2, Chemical physics letters, 226(3-4), 1994, pp. 317-324
Stark spectra have been measured for Ar-HF in several excited intermol
ecular bending and stretching states associated with upsilon(HF)=1. Th
e resulting dipole moments are compared with those calculated using th
e most recent potential energy surface. Infrared-infrared double reson
ance spectroscopy is used to access the corresponding states in upsilo
n(HF)=2 where, in the absence of intermolecular excitation, dissociati
on occurs before the molecules can reach the detector. Simultaneous ex
citation of the SIGMA or PI bending vibrations, which have the effect
of making the hydrogen atom point away from argon atom on average, res
ults in lifetimes in excess of the molecular flight time (0.3 ms).