Ge. Hall et al., TIME-RESOLVED FOURIER-TRANSFORM INFRARED STUDY OF THE PHOTODISSOCIATION OF 1,1-DIFLUOROETHENE AT 193-NM, The Journal of chemical physics, 101(5), 1994, pp. 3679-3687
We have measured vibrational and rotational population distributions f
or the excited HF product of the 193 nm photolysis of CH2CF2. Approxim
ately 15% of the available energy is released as vibrational energy of
HF, and the estimated nascent HF rotational energy corresponds to abo
ut 10% of the total available energy. The relative vibrational populat
ions can be fit to a linear surprisal. We have compared the vibrationa
l distribution to that observed from this reaction with different amou
nts of available energy, and to the HF vibrational distributions produ
ced in the dissociation of other fluoroethenes. While results differ a
mong the various experiments considered, overall more than the amount
of vibrational energy expected statistically is deposited in HF. The r
otational population distributions we observe fit both a Boltzmann dis
tribution and an information theoretic model corresponding to a nearly
statistical energy distribution.