The electronic spectrum of NiCN in the 500-630 nm region has been observed by laser-induced fluorescence, following the reaction of laser-ablated nickel atoms with cyanogen under free jet expansion conditions. Seven electronic states have been identified. Three of these, X1 2 5/2 , X2 2 3/2 , and W1
The Electronic Spectrum of Jet-Cooled FeC in the Visible Region
β Scribed by Kosuke Aiuchi; Kazuhiko Shibuya
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 275 KB
- Volume
- 209
- Category
- Article
- ISSN
- 0022-2852
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β¦ Synopsis
The iron monocarbide radical (FeC) has been produced by the reaction of laser ablated Fe atoms with CH 4 , and its laserinduced florescence spectrum has been recorded in the region 15 000 to 23 800 cm -1 at a resolution of 0.04 to 0.06 cm -1 under supersonic jet-cooled conditions. Rotational analyses have been carried out for about 46 vibronic bands. About 35 bands have been observed for the first time, while the other 11 bands were previously recorded at 0.2 cm -1 resolution by Balfour et al. (J. Chem. Phys. 103, 4046 (1995)). The classification of the band systems has been made based on the 56 Fe 12 C/ 56 Fe 13 C isotope shifts, the dispersed fluorescence spectra, and the excited level lifetimes. The energy separation between the = 3, 1 spin components of the X 3 i state has been determined to be 719.56 cm -1 with an upper state rotational perturbation. In the visible spectrum, we could characterize five electronic states for which the Hund's case (a) labels are possible, namely, three 3 , one 3 , and one 1 state. The 3 i , state of which the 3 3,2,1 substates lie at 20 274, 20 455, and 20 845 cm -1 , respectively, has been shown to have very irregular spin-orbit splittings due to the spin-orbit interaction with the nearby 1 state.
π SIMILAR VOLUMES
The infrared spectrum of HCFC-142b, CH 3 CF 2 Cl, has been recorded at high and low resolution using a supersonic jet-FTIR spectrometer system. Molecular parameters for a number of vibrational states have been obtained from rovibrational analyses of the C-type bands n 14 (1192 cm 01 ) and n 15 (967
The 3 A 2 (nΟ \* ) β 1 A 1 X (T 1 β S 0 ) phosphorescence excitation spectrum of jet-cooled xanthione was investigated in the region 14 920-17 600 cm -1 . The structure observed is shown to be due to the T 1 β S 0 absorption and an assignment in terms of the vibronic structure of that band is propos