Chemical‐Shift Anisotropy and Nuclear Quadrupole Coupling Constant of14N in Methyl Isocyanide

1970 ◽  
Vol 52 (4) ◽  
pp. 2005-2010 ◽  
Author(s):  
Costantino S. Yannoni
1992 ◽  
Vol 47 (1-2) ◽  
pp. 367-370 ◽  
Author(s):  
A. C. Legon ◽  
P. W. Fowler

AbstractThe 14N-nuclear quadrupole coupling constants χaa(14N<2>) and χaa(14N(1)) for the ground-states of the dimers 14N(2)14N(1) • • • HCCH and 14N(2)14N(1) • • • HC15N have been corrected for zero-point effects and for the electrical effects of the subunit HX to give two estimatesχ(14N) = -5.01 (13) and - 5.07 (8) MHz, respectively, for the coupling constant of the isolated 14N2 molecule


1973 ◽  
Vol 28 (7) ◽  
pp. 1230-1232
Author(s):  
Werner Zeil ◽  
Bernhard Haas

The microwave spectrum of trimethylchlorosilane has been investigated between 8 and 20 GHz. The quadrupole splitting of the K = 0 lines of the transitions J = 2 → 3 and 3 → 4 have been determined. The quadrupole coupling constant of the Cl-35 atom is determined to -34.701 MHz, and the rotational constant is determined to B0 = 2197.382 MHz.


1978 ◽  
Vol 33 (10) ◽  
pp. 1169-1172 ◽  
Author(s):  
G. Winnewisser ◽  
R. A. Creswell ◽  
M. Winnewisser ◽  
M. Winnewisser

Abstract Cyanodiacetylene, H(C ≡ C)2 CN has been produced by a radiofrequency discharge in a mixture of acetylene, HCCH, and hydrogen cyanide, HCN. This reaction is of astrophysical importance, since it lends support to the possibility of the ion-molecule formation scheme of producing long carbon chain molecules in interstellar sources. From a measurement of the J = 4←3 transition of HC5N the nuclear quadrupole coupling constant eqQ = - 4.242 (30) MHz was determined.


1987 ◽  
Vol 65 (6) ◽  
pp. 1332-1335 ◽  
Author(s):  
Donald R. Eaton ◽  
Richard J. Buist ◽  
Brian G. Sayer

The solid state 59Co nmr spectra of a number of octahedral complexes are reported. In the case of sodium hexanitrocobaltate(III) the spectra have been obtained at several different field strengths and the results are analysed to give a quadrupole coupling constant of 9.4 MHz, an asymmetry parameter of zero and an axial chemical shift tensor with an anisotropy of 180 ppm. Several other complexes have been examined at high field (11.8 T) to minimize the effects of quadrupole coupling and maximize the influence of chemical shift anisotropy. The results are, where possible, compared with single crystal X-ray and low field nmr data. It is concluded that high fields are necessary to obtain reliable chemical shift anisotropy values. The conditions necessary for obtaining reasonable quality spectra from polycrystalline samples containing quadrupolar nuclei are discussed.


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