Ozone Photodissociation in the Singlet Channel at 226 nm.
Academic Article
Overview
Identity
Additional Document Info
Other
View All
Overview
abstract
We report the rotational state distribution and vector correlations of the O2(a 1g, v = 0) fragments arising from the 226 nm photodissociation of jet-cooled O3. Consistent with previously reported trends, the rotational distribution is shifted to higher rotational states with decreasing wavelength. We observe highly suppressed odd rotational state populations due to a strong -doublet propensity. The measured rotational distribution is in agreement with classical trajectory calculations for the v = 0 products, although the distribution is slightly narrower than predicted. The spatial anisotropy follows the previously observed trend of decreasing with increasing photon energy with = 0.72 0.14 for v = 0, j = 38. As expected for a triatomic molecule, the v-j correlation is consistent with v perpendicular to j, but the measured correlation is nonlimiting due, in part, to rotational and translational depolarization. The j-dependent line width of the O2(a 1g) REMPI spectrum is also discussed in connection with the lifetime of the resonant O2(d 1g) state due to predissociation via the II 1g valence state.
