Microwave Spectrum of Methylhydrazine; Rotational Isomerism, Internal Motions, Dipole Moments, and Quadrupole Coupling Constants

1970 ◽  
Vol 53 (12) ◽  
pp. 4575-4583 ◽  
Author(s):  
Robert P. Lattimer ◽  
Marlin D. Harmony
1996 ◽  
Vol 176 (1) ◽  
pp. 17-22 ◽  
Author(s):  
Masao Onda ◽  
Tsuaki Odaka ◽  
Hideya Miyazaki ◽  
Masayoshi Mori ◽  
Ichiro Yamaguchi ◽  
...  

1978 ◽  
Vol 33 (5) ◽  
pp. 549-558 ◽  
Author(s):  
Anil Kumar ◽  
John Sheridan ◽  
Otto L. Stiefvater

The dipole moments and the quadrupole coupling constants of the normal and the three mono-deuterated species of oxazole have been measured. The dipole moment of 1.50 ± 0.03 D is found to deviate by 10.8° from the external bisector of the CNC angle towards the C(2) carbon atom. The principal values of the quadrupole coupling tensor are determined as Xzz = -4.04 ± 0.02 MHz and Xxx - 1-66 ± 0.02 MHz along the axes in the molecular plane, so that the gradient perpendicular to this plane is Xyy = 2.38 MHz. The direction of the largest gradient deviates by 5.7° from the external bisector of the CNC angle towards the carbon atom C(4).An attempt is made to correlate these results and the geometry of oxazole with the electron distribution in this molecule


1967 ◽  
Vol 1 (9) ◽  
pp. 379-381 ◽  
Author(s):  
G.L. Blackman ◽  
R.D. Brown ◽  
F.R. Burden ◽  
J.E. Kent

1987 ◽  
Vol 42 (2) ◽  
pp. 197-206 ◽  
Author(s):  
M. Meyer ◽  
U. Andresen ◽  
H. Dreizler

The microwave spectrum of 2-chloropyridine, 2-Cl(C5H4N), has been studied to determine the 35Cl, 37Cl and 14N nuclear quadrupole coupling constants. The results are discussed within a simple MO theory. We propose an approximate r0-structure under certain assumptions. In addition to the ground state we observed one vibrationally excited state of both chlorine isotopic species of 2-chloropyridine.


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