scholarly journals Axial asymmetry in the nuclear magnetic resonance spectra of deuterated methyl groups: An alternative explanation

1994 ◽  
Vol 101 (1) ◽  
pp. 231-237 ◽  
Author(s):  
Mieng‐Hua Wann ◽  
Gerard S. Harbison
1963 ◽  
Vol 41 (3) ◽  
pp. 711-713 ◽  
Author(s):  
E. Bullock

The nuclear methyl groups and ring protons in nitro- and dimethylamino-durenes and -mesitylenes show considerable chemical shifts relative to the parent hydrocarbons. The shifts are generally in the direction expected from a mesomeric effect, despite the lack of coplanarity between the aromatic ring and the substituent.


1967 ◽  
Vol 45 (21) ◽  
pp. 2529-2535 ◽  
Author(s):  
T. E. Gough ◽  
W. S. Lin ◽  
R. G. Woolford

The nuclear magnetic resonance spectra are reported for a series of α-substituted 3-pentanones. Magnetically nonequivalent methylene hydrogens are observed whenever the substituent group is diamagnetically anisotropic. The results are discussed in terms of the possible conformations of the molecules; the most stable conformations are those with the C=O bond essentially eclipsed by the terminal methyl groups.


1961 ◽  
Vol 39 (11) ◽  
pp. 2262-2273 ◽  
Author(s):  
F. A. L. Anet

The N.M.R. spectra of compounds containing various types of C-methyl groups are discussed with special reference to the effects of spin coupling. Particular attention is given to compounds containing the CHCH3 group in saturated systems. It is pointed out that the observed splitting of the methyl band is not always equal to the coupling constant between the methyl protons and the adjacent proton, even when the chemical shift between the two groups of protons is large.


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