Abstract
The room-temperature gas-phase ultraviolet absorption spectrum and cross-sections of vinyl (C 2H 3) radicals have been determined in the spectral range 225–238 nm, employing cavity ring-down absorption spectroscopy. Vinyl radicals in these experiments were produced from the 193 nm excimer laser photolysis of methyl vinyl ketone (CH 3COC 2H 3) and vinyl bromide (C 2H 3Br). The spectra obtained from the two systems were nearly identical. The observed spectrum exhibits a relatively broad and featureless absorption with a cross-section of 5.3×10 −18 cm 2 molecule −1 at 230 nm. A combined uncertainty of ∼25% for cross-section values has been assessed. The electronic transitions in the vinyl radical have been calculated by ab initio quantum chemical methods at the CIS, EOM-CCSD, CASSCF and CASPT2 levels of theories which assign the new observed band to the highly allowed and `in plane' π *(2a″) ← π(1a″) transition.
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