The absorption cross-sections of vibrationally excited FSO3 radicals h
ave been measured over the 340-470 nm wavelength range at 295 K. The r
adicals are formed following the electronic quenching of the FSO3(B(2)
E) radicals initially generated in the photolysis of F2S2O6 at 193 nm.
Using previously obtained relaxation rate coefficients, a modelling o
f the double-exponential decay of the vibrationally excited FSO3 with
a consecutive first-order mechanism allows the determination of the ab
sorption cross-sections for these species. Evidence is presented which
suggests that these phenomenological cross-sections correspond to low
-lying manifolds of vibrational states.