Vibrationally excited ozone, O3†, produced by CO2 laser radiation was found to react with SO significantly faster than thermal ozone via the chemiluminescent reaction process O3+SO→SO2(1B1) +O2(3Σg). The vibrational rate enhancement of this reaction was 2.5±0.6 at 300 K. This represents the utilization of 27% of the available vibrational energy to promote the reaction based on a model assuming involvement of a single vibrational mode. The laser enhanced chemiluminescence measured from 260 to 450 nm was found to exhibit a 630±200 cm−1 blue shift. This is interpreted as a partitioning of the available vibrational energy of O3† in the vibrational manifold of the SO2(1B1) product.
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Kaldor et al. (1974) studied this question.
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