Restricted Hartree-Pock functions for NO X\*11 and A2CC have been calculated using a large, Slater-type basis set. Several molecular properties, including hyperfine constants, have been computed and are found to agree rather weit with experimental values
First experimental observation of vibrationally excited NO2+(X 2Σ+, A 2Π)
✍ Scribed by M. Hamdan; A.G. Brenton
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 282 KB
- Volume
- 155
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Transitions among the three lowest X 'Z+, A % and B 'Z+ bound states of NO'+ are investigated by means of high-resolution (0.08-0.35 eV fwhm) translational energy spectroscopy (TES). As well as electronic transitions between the ground and the two lowest electronic excited states, the spectra clearly show two distinct groups of vibrational transitions hating average vibrational spacings of 0.22 and 0.17 eV respectively. The two groups of vibrational levels are assigned to transitions involving NO*+ (X 'I;', 7 > VP 3 @ 0~0) and (A zll, 6 > Y+ 3tu= 0. The measured vibrational spacings are in accord with the values of 0.159 and 0.242 eV predicted by the latest ab initio calculations.
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