Elimination of dispersion-components from high resolution NMR spectra and transverse relaxation times measurement

1997 ◽  
Vol 94 ◽  
pp. 1715-1725
Author(s):  
L Mahi ◽  
JC Duplan ◽  
A Briguet
1969 ◽  
Vol 52 (5) ◽  
pp. 1074-1092 ◽  
Author(s):  
L H Keith ◽  
A L Alford ◽  
A W Garrison

Abstract The high resolution nuclear magnetic resonance spectra of the DDT class of pesticides and related compounds are discussed, including a study of the resonances of the aromatic protons as they are affected by various substiluents. The CCl3 moiety on the α-carbon strongly deshields the ortho protons on the aromatic rings, and this deshielding effect is greatly enhanced by substitution of a chlorine ortho rather than para on the aromatic ring. These deshielding effects are explained by a consideration of the electronegativity of the substituents and the stereochemistry of the molecule. The chemical shifts and coupling constants are tabulated.


1970 ◽  
Vol 13 (2) ◽  
pp. 1106-1111 ◽  
Author(s):  
K. N. Solov'ev ◽  
V. A. Mashenkov ◽  
A. T. Gradyushko ◽  
A. E. Turkova ◽  
V. P. Lezina

1972 ◽  
Vol 26 ◽  
pp. 3678-3684 ◽  
Author(s):  
Per Albriktsen ◽  
P. Steenbøl ◽  
B. Søndergaard Sørensen ◽  
Carl-Gunnar Swahn ◽  
Åke Pilotti

1972 ◽  
Vol 26 ◽  
pp. 2511-2517 ◽  
Author(s):  
P. Albriktsen ◽  
G. Hansen ◽  
Olof Samuelson ◽  
Elisabeth Sjöstrand ◽  
Sigfrid Svensson

1966 ◽  
Vol 45 (10) ◽  
pp. 3567-3570 ◽  
Author(s):  
J. D. Memory ◽  
G. W. Parker ◽  
James C. Halsey

1970 ◽  
Vol 53 (1) ◽  
pp. 157-179 ◽  
Author(s):  
L H Keith ◽  
A L Alford

Abstract The high resolution nuclear magnetic resonance spectra of 35 carbamate pesticides and a major metabolite of one pesticide are discussed. The chemical shifts and coupling constants are tabulated and reproductions of the more complex or unusual spectra are included. A concentration and solvent dependence of both the NH-proton and the NCH3-proton resonances of an N-monosubstituted carbamate is discussed. Hindered rotation is observed in the N,N-dimethylcarbamates, the thiolcarbamates and the dithiocarbamates, but not in the N-methylcarbamates.


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