Determination of the dipole moment function of an ozone molecule on the basis of vibrational transition probabilities

1983 ◽  
Vol 26 (9) ◽  
pp. 866-869
Author(s):  
O. K. Voitsekhovskaya ◽  
Yu. S. Makushkin ◽  
O. N. Sulakshina
2000 ◽  
Vol 113 (23) ◽  
pp. 10572-10582 ◽  
Author(s):  
O. N. Sulakshina ◽  
Yu. G. Borkov ◽  
Vl. G. Tyuterev ◽  
A. Barbe

Certain intensity changes arising in the spectrum of the nitrogen afterglow are attributed to collisional energy exchanges between the molecules. A method is described by which the probabilities of such exchanges can be derived from precise measurements of the intensity variations. For N 2 ( B 3 Π g )—N 2 collisions, the probability of a vibrational transition is found to be of the order of 10 -2 per gas-kinetic collision.


1983 ◽  
Vol 26 (4) ◽  
pp. 403-405
Author(s):  
O. K. Voitsekhovskaya ◽  
O. N. Sulakshina

1989 ◽  
Vol 90 (10) ◽  
pp. 5455-5465 ◽  
Author(s):  
David D. Nelson ◽  
Aram Schiffman ◽  
David J. Nesbitt

1984 ◽  
Vol 62 (12) ◽  
pp. 1579-1585 ◽  
Author(s):  
C. Chackerian Jr. ◽  
R. Farrenq ◽  
G. Guelachvili ◽  
C. Rossetti ◽  
W. Urban

Experimental intensity information is combined with numerically obtained vibrational wave functions in a nonlinear least-squares fitting procedure to obtain the ground electronic state electric dipole moment function of carbon monoxide valid in the range of nuclear oscillation (0.87–1.91 Å) of about the V = 38th vibrational level. Vibrational transition matrix elements are computed from this function for ΔV = 1, 2, 3 with V ≤ 38.


2016 ◽  
Author(s):  
O. V. Egorov ◽  
O. K. Voitsekhovskaya ◽  
D. E. Kashirskii

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