Ra. Brownsword et al., DYNAMICS OF H ATOM FORMATION IN THE PHOTODISSOCIATION OF CHLOROMETHANES AT 193.3 NM, The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 101(29), 1997, pp. 5222-5227
Using the laser photolysis/vacuum-ultraviolet laser-induced fluorescen
ce (LP/VUV-LIF) ''pump-and-probe'' technique the dynamics of H atom fo
rmation after photoexcitation of chloromethanes at 193.3 nm were studi
ed in the gas phase at room temperature under collision-free condition
s. For all chloromethanes, H atoms were detected by (2p(2)P <-- 1s(2)S
)-LIF using tunable narrow-band Lyman-alpha laser radiation (lambda(L
alpha) approximate to 121.6 nm) generated by resonant third-order sum-
difference frequency conversion of pulsed-dye-laser radiation. However
, only in the cases of CH3Cl and CH2Cl2 were the H atoms found to orig
inate from a primary photodissociation step. Absolute quantum yields f
or the formation of primary H atoms were measured by means of a calibr
ation method to be phi(H)(CH3Cl) = (1.2 +/- 0.6) x 10(-2) and phi(H)(C
H2Cl2) = (0.2 +/- 0.1) x 10(-2). From H atom Doppler profiles measured
under single-collision conditions, the average translational energy r
eleased to the H + CH2Cl and H + CHCl2 products in the center-of-mass
system was determined to be: E-T(H-CH2Cl) = (86.6 +/- 14.2) kJ/mol and
E-T(H-CHCl2) = (84.3 +/- 8.9) kJ/mol. On the basis of available therm
ochemical data, the corresponding fraction of the available energy rel
eased as product translational energy was determined to be f(T)(H-CH2C
l) = (0.44 +/- 0.07) and f(T)(H-CHCl2) = (0.41 +/- 0.04). In the CHCl3
photodissociation, primary H atom formation was not observed. The H a
toms detectable after laser irradiation of CHCl3 at 193.3 nm were foun
d to originate from secondary photodissociation of Phe CHCl2 radical.