Analyse Rotationnelle de la Bande (0,0) du Système Orange de ScO

1972 ◽  
Vol 50 (4) ◽  
pp. 395-403 ◽  
Author(s):  
R. Stringat ◽  
C. Athénour ◽  
J. L. Féménias

The orange system of ScO has been reanalyzed as a 2Π → 2Σ transition. We have observed all the branches which are compatible with the selection rules ΔJ = 0, ± 1. We have not detected the hyperfine structure in the excited state, the coupling case being therefore aβ. The magnetic hyperfine interaction inducing the ground state doubling is the only one which appears; it has been analyzed by other authors who have shown that the coupling case for this state is of the type bβS.The use of an alloy hollow-cathode lamp, cooled with liquid nitrogen, has enabled us to improve the frequency measurements. The values of the constants have been obtained by a method by which, working directly with the Hamiltonian, the introduction of each parameter can be justified. The study of the Λ doubling in 2Π3/2 and 2Π1/2 levels leads us to values of ξ and η very close to those predicted for a pure precession case.

1967 ◽  
Vol 45 (7) ◽  
pp. 2249-2251 ◽  
Author(s):  
L. O. Dickie ◽  
F. M. Kelly

The hyperfine structure of the 2D3/2 and 2P1/2 levels of the 6p3 ground configuration of Bi I has been determined from the h.f.s. of the λ 4 722 Å and λ 4 121 Å lines of the arc spectrum. The spectrum was excited in a liquid nitrogen cooled hollow cathode source and the structure resolved with a Fabry–Pérot interferometer. The hyperfine interaction constants and the quadrupole moment have been calculated as follows: for 2D3/2,[Formula: see text]


1972 ◽  
Vol 50 (12) ◽  
pp. 1402-1408 ◽  
Author(s):  
S. M. Japar

The 2800 Å band system of p-dibromobenzene has been photographed under high resolution and an extended vibrational analysis has been carried out. The analysis is not inconsistent with the assignment of the system to a 1B2u ← 1Ag transition, by analogy with other p-dihalogenated benzenes. The observed spectrum can be explained in terms of a number of strong type-B vibronic bands and a considerably smaller number of type-A vibronic bands. The extensive sequence structure is adequately accounted for, and can be related to observations on other halogenated benzene molecules. Thirteen ground state and nine excited state fundamental vibrational frequencies have been assigned.


2018 ◽  
Vol 16 (3) ◽  
pp. 033001
Author(s):  
Pengyuan Chang Pengyuan Chang ◽  
Bo Pang Bo Pang ◽  
Yisheng Wu Yisheng Wu ◽  
Jingbiao Chen Jingbiao Chen

1991 ◽  
Vol 8 (4) ◽  
pp. 172-175 ◽  
Author(s):  
Jia Liejuan ◽  
Jing Chunyang ◽  
Lin Fucheng

2001 ◽  
Vol 79 (2-3) ◽  
pp. 479-482 ◽  
Author(s):  
D B Braund ◽  
A RH Cole

The spectrum of trans-glyoxal has been recorded at a resolution of about 0.004 cm–1 in the region from 2770 to 2900 cm–1. 1549 lines have been assigned to the type B band due to the υ9 (bu) fundamental (antisymmetric C–H stretching vibration). The ground-state rotational constants confirm earlier values and new constants are determined for the excited state of υ9. PACS No.: 33.20E


1999 ◽  
Vol 61 (1) ◽  
Author(s):  
A. Nagel ◽  
C. Affolderbach ◽  
S. Knappe ◽  
R. Wynands

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