Evidence for the existence of an electric field effect from the vinyl proton magnetic resonance spectra of 4-substituted styrenes

1968 ◽  
Vol 46 (24) ◽  
pp. 3813-3820 ◽  
Author(s):  
G. K. Hamer ◽  
W. F. Reynolds

Vinyl proton chemical shifts of styrene and six 4-substituted styrenes have been determined at infinite dilution in cyclohexane. It is shown that changes in the chemical shift difference of the β protons, Δ(δC − δB) can be accounted for by electric field effects. Reasonable values of the constant in the Buckingham equation of(−3.11 ± 0.50) × 10−12 and (−4.77 ± 0.83) × 10−12 are obtained from two different types of field effect calculations. Residual chemical shift changes for β protons after correction for electric field effects can be explained in terms of mesomeric and possibly inductive mechanisms. α-Proton chemical shift values cannot be satisfactorily rationalized. Small concentration effects are noted, usually resulting in high field shifts with increasing concentration. Previous results are reexamined in order to resolve a conflict in the literature.

1977 ◽  
Vol 55 (3) ◽  
pp. 530-535 ◽  
Author(s):  
Robert H. Kohler ◽  
William F. Reynolds

Correlations of cyclopropyl proton chemical shifts for 4-substituted (2,2-dichlorocyclopropyl)-benzenes with σI and σR0 provide evidence that these chemical shifts reflect direct field effects and weak phenyl–cyclopropyl conjugative interactions. Corrections for variable ring current effects due to substituent-induced changes in conformation improve the individual correlations but do not alter the basic pattern of results. Correlation of the β cyclopropyl 1H chemical shift difference with σI with calculated hydrogen electron densities, and with calculated electric field components provides further strong evidence for a field effect on 1H chemical shifts.


1971 ◽  
Vol 49 (9) ◽  
pp. 1335-1338 ◽  
Author(s):  
J. W. ApSimon ◽  
H. Beierbeck ◽  
D. K. Todd ◽  
P. V. Demarco ◽  
W. G. Craig

The calculation of chemical shift values by the method used in parts I–V (1–5) has been extended to a derivation of the shielding effects of the ethylene–ketal and −thioketal groups. For these studies ketal and thioketal derivatives of monoketoandrostanes were prepared. The chemical shifts of the C-18 and -19 methyl protons in these compounds are reported for the solvents CDCl3, CCl4 and benzene.Representing both groups by point dipoles, values for the anisotropies and for K, a parameter descriptive of the electric field effect, were derived for various, coincidental, locations of the magnetic and electric dipoles along the symmetry axes of the two groups.


1995 ◽  
Vol 73 (7-8) ◽  
pp. 440-443 ◽  
Author(s):  
L. I. Dorman ◽  
I. V. Dorman

Experimental data on the atmospheric electric field effect in the cosmic-ray muon component are discussed on the basis of the general theory of cosmic-ray meteorological effects. In this framework, we develop the theory of atmospheric electric field effects in the hard- and soft-muons of secondary cosmic rays and in the neutron-monitor counting rates as well. We show that the experimental results can be understood on the basis of this theory. We also show that a sufficient atmospheric electric field effect in the cosmic-ray neutron component is to be expected because the neutron monitors work as analyzers of soft muons and really detect only negative muons as well as neutrons.


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