Fine-structure branching ratios and Doppler profiles of Cl(2Pj) photofragments from photodissociation of the chlorine molecule near and in the ultraviolet region.

Photofragment chlorine atoms in the 2Pj states from Cl2 at 266–500 nm are measured by a resonance-enhanced multiphoton ionization technique. The measured branching ratio of [Cl*(2P1/2)]/[Cl(2P3/2)] increases monotonically with dissociation wavelengths from (9.5±1.8)×10-3 at 308 nm to (4.7±0.5)×10-1 at 475 nm. At 375 nm≤λ≤475 nm, Doppler profiles of the chlorine atoms indicate adiabatic formation of two Cl(2P3/2) from the 1Π(1u) state of Cl2 and Cl(2P3/2)+Cl*(2P1/2) from the B 3Π(0+u) state. On the other hand, at a shorter wavelength (308 nm), Cl*(2P1/2) is generated from the 1Π(1u) state through nonadiabatic transitions during the dissociation. The relative contribution of the 1Π(1u)←X 1Σ(0+g) and B 3Π(0+u)←X 1Σ(0+g) transitions in the photoabsorption is estimated from the obtained branching ratios at 375 nm≤λ≤475 nm. [ABSTRACT FROM AUTHOR]