Relative intensities in the vibrational structure of the Ã1 A u (C 2h )-X 1 + g (D ∞h ) electronic transition of acetylene are calculated. The calculation takes account of the large change of geometry and the change in the normal coordinates (the Dushinskií effect) between the two states. Because co
Visible Wavelength Electronic Spectroscopy of the DCBr ÖX̃ Vibronic Transition
✍ Scribed by Chun-Wei Chen; Tsung-Chuan Tsai; Bor-Chen Chang
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 94 KB
- Volume
- 209
- Category
- Article
- ISSN
- 0022-2852
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✦ Synopsis
The laser excitation and dispersed fluorescence spectra of the DCBr Ã-X vibronic bands between 570 and 600 nm were successfully obtained in a direct current (DC) discharge supersonic free jet expansion. The analysis of the dispersed fluorescence spectra results in information on the vibrational structure of the DCBr X 1 A state for the first time. Perturbations due to the background levels of the ã3 A state can be recognized. The data are consistent with the previously reported triplet-singlet energy gap (the zero-point level energy gap) of 5.73 ± 0.02 kcal/mol for HCBr. We have determined the vibrational frequencies to be 832 cm -1 (bend) and 663 cm -1 (C-Br stretch) for the X 1 A state. In addition to the X state vibrational structure, the Ã(0,6,2) and Ã(0,5,0) levels were also observed for the first time.
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