Measurements of vibronic term values in excited electronic states of NO2 have been performed with cw dye lasers over the whole spectral range from 12117 cm−1 to 24563 cm−1. The low rotational temperatures, achieved by adiabatic cooling of NO2 seeded in a supersonic argon beam, allow the separation of closely lying bands as well as a distinction between transitions to the 2B1 state and the vibronically coupled 2B2 – 2A1 states. The statistical analysis of the distribution P(S), where S is the energy separation between adjacent vibronic levels and of the intensity distribution of all measured bands, suggests that a short range correlation exists between the excited levels. Whether also a long range correlation exists is still under investigation. A definite answer requires an unambiguous determination of all bands even with low intensities and a safe assignment of all hot bands. These points are discussed in detail.
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Persch et al. (1988) studied this question.
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