Study of organomercury compounds by high-resolution NMR. VIII. Solvation of symmetrical organomercury compounds

1983 ◽  
Vol 23 (5) ◽  
pp. 673-681
Author(s):  
L. A. Fedorov
Keyword(s):  
High Resolution ◽  
High Resolution Nmr ◽  
Organomercury Compounds

Study of organomercury compounds by high-resolution NMR

1979 ◽  
Vol 19 (4) ◽  
pp. 549-554 ◽  
Author(s):  
L. A. Fedorov ◽  
B. A. Faingor ◽  
L. S. Golovchenko ◽  
D. N. Kravtsov
Keyword(s):  
High Resolution ◽  
High Resolution Nmr ◽  
Organomercury Compounds

Investigation of organomercury compounds by high-resolution NMR method

1975 ◽  
Vol 15 (6) ◽  
pp. 943-949 ◽  
Author(s):  
L. A. Fedorov ◽  
Z. A. Stumbrevichyute ◽  
�. I. Fedin
Keyword(s):  
High Resolution ◽  
Nmr Method ◽  
High Resolution Nmr ◽  
Organomercury Compounds

The High Resolution NMR Spectra of Pesticides. II. The DDT-Type Compounds

1969 ◽  
Vol 52 (5) ◽  
pp. 1074-1092 ◽  
Author(s):  
L H Keith ◽  
A L Alford ◽  
A W Garrison
Keyword(s):  
Nuclear Magnetic Resonance ◽  
High Resolution ◽  
Nmr Spectra ◽  
Chemical Shifts ◽  
Coupling Constants ◽  
Aromatic Rings ◽  
Nuclear Magnetic Resonance Spectra ◽  
High Resolution Nmr ◽  
Related Compounds ◽  
Deshielding Effect

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.

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