Dependence of the isotropic hyperfine interaction constant in molecules of nitroxide radicals on the dielectric properties of the solvent

1979 ◽  
Vol 20 (2) ◽  
pp. 241-244 ◽  
Author(s):  
V. I. Baldin ◽  
T. G. Izyumova ◽  
V. P. Putyrskii
1984 ◽  
Vol 22 (10) ◽  
pp. 629-635 ◽  
Author(s):  
V. G. K. M. Pisipati ◽  
N. V. S. Rao ◽  
V. Muralikrishna ◽  
V. S. Murthy ◽  
T. Kesavan

1972 ◽  
Vol 25 (12) ◽  
pp. 2577 ◽  
Author(s):  
RM Golding ◽  
MP Halton

The experimental 14N and 17O n.m.r, results in a series of lanthanide complexes are successfully interpreted from a second-order perturbation treatment of the calculation of (S2), where bonding effects and spin-orbit coupling mixing are incorporated. The isotropic hyperfine interaction constants are shown to be negative for 14N and positive for 17O but both independent of the particular lanthanide ion. We also confirm that the 4f orbitals are not involved in direct bonding with the ligands.


1970 ◽  
Vol 10 (6) ◽  
pp. 885-891 ◽  
Author(s):  
P. V. Schastnev ◽  
G. M. Zhidomirov ◽  
N. D. Chuvylkin

1974 ◽  
Vol 27 (10) ◽  
pp. 2083 ◽  
Author(s):  
RM Golding ◽  
K Lehtonen

From a study of the isotropic proton hyperfine interaction constants for a series of metal dithiocarbamates, and their redox behaviour, it is shown that for iron(111) and manganese(111) dithiocarbamates there is a simple relationship between E1/2 and the NCH2 proton hyperfine interaction constant in the 6Al state. Hence the redox process for these compounds is inferred to take place through the nitrogen atom.


1981 ◽  
Vol 17 (4) ◽  
pp. 235-238 ◽  
Author(s):  
V. G. K. M. Pisipati ◽  
G. Satyanandam ◽  
N. V. S. Rao

1962 ◽  
Vol 17 (3) ◽  
pp. 266-270 ◽  
Author(s):  
Armin Räuber ◽  
Jürgen Schneider

The paramagnetic resonance of Fe3+-ions in cubic synthetic ZnS crystals has been observed after uv-irradiation at 77 °K. The spectrum was analysed withg=2.0194 ± 0.0003 and |α |=0.0128 ± 0.0001 cm-1,where 3 α is the zero-field splitting. The hyperfine interaction constant of the 2.2% isotope Fe57 was found to be |A|= 0.00078 ± 0.00005 cm-1. The splitting of the central fine structure line revealed the existence of submicroscopic twins. Two additional epr-lines have been observed after crushing and after annealing the crystals in zinc vapour.


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