HIGH-RESOLUTION FOURIER-TRANFORM SPECTRA OF THE $NO_{2}$ A-X ELECTRONIC BANDS AROUND 1 $\mu$M

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1997

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Ohio State University

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The strong vibronic interactions between the A and X electronic states lead to a complex structure of the NO2 spectrum in the visible and near-IR. The log-wavelength tail of the spectrum is very weak due to small Franck-Condon factors. In 1965, Douglas and Huberh recorded the first low-resolution spectra of the NO2 bands in the near infrared. In 1975, Brand {et al}i. showed that ``hot” bands are important in this region. In the past, many high-resolution spectra of NO2 were recorded, however no rotationally resolved spectra of this important region were reported up to now. We present high-resolution spectra of the first vibronic bands of NO2 starting around 9740cm−1 and discuss vibrational assignments. The dense rotational structure is very difficult to assign although accurate lower-state energies are available from high-resolution infrared spectra.

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hA.E. Douglas and D.P. Huber, Can. J. Pkys. 43, 74 (1965) iJ. C. D. Brand, W.H. Chan, and J.L. Hardwick, J. Mol. Spectrosc. 56, 309 (1975) jA. Perrin, C. Camy-Peyret, and J. M. Flaud, J. Quant. Spectrosc. Rad. Transfer 48, 645 (1992).


Author Institution: Institute of Environmental Physics, University of Bremen; Institute of Environmental Physics, Grenoble High Magnetic Field Laboratory

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