Proton magnetic resonance spectra of some β-methylstyrenes, β,β-dimethylstyrenes, and α-methylstilbenes; and a discussion of long-range shieldingand coupling effects in these and related systems

1965 ◽  
Vol 18 (11) ◽  
pp. 1759 ◽  
Author(s):  
H Rottendorf ◽  
S Sternhell ◽  
JR Wilmshurst

The preparation of some new β,β-dimethylstyrenes and α-methylstilbenes is described and their p.m.r. spectra are reported. The long-range shielding effects in β,β-dimethylstyrenes and other styrene derivatives are discussed. The differences between the cisoid and transoid allylic coupling constants in β,β-dimethylstyrenes are much smaller than the corresponding differences in simple propenes. No appreciable (J ≥ 0.3 c/s) coupling between the non-equivalent methyl protons in β,β-dimethylstyrenes has been observed. Long-range coupling in the compounds investigated appears to be independent of ring substitution. Some general features of allylic coupling are discussed.

1971 ◽  
Vol 24 (9) ◽  
pp. 1949 ◽  
Author(s):  
FHC Stewart

The proton magnetic resonance spectra of various N-nitroso derivatives of sarcosine, L-proline, and iminodiacetic acid, including some protected dipeptides, have been obtained. Magnetic non-equivalence and conformational isomerism arising from restricted rotation of the nitroso group are discussed in relation to the reported behaviour of other nitrosamines. Long-range shielding effects on protons at a considerable distance from the anisotropic nitrosamino centre were readily detected with these compounds.


1965 ◽  
Vol 18 (5) ◽  
pp. 707 ◽  
Author(s):  
PJ Black ◽  
ML Heffernan

The proton magnetic resonance spectra of the four isomeric diazanaphthalenes, quinoxaline, phthalazine, quinazoline, and cinnoline, all as dilute solutions in carbon tetrachloride and acetone, have been investigated at 100 Mc/s. The chemical shifts and coupling constants have been obtained by direct calculation or, where appropriate, by an iterative procedure. Long-range coupling constants between protons separated by five and six bonds have been observed.


1964 ◽  
Vol 17 (10) ◽  
pp. 1128 ◽  
Author(s):  
PJ Black ◽  
ML Heffernan ◽  
LM Jackman ◽  
QN Porter ◽  
GR Underwood

The proton magnetic resonance spectra of indolizine, indolizine-1,3-d2, 1- and 2-methylindolizine, 2,3-, 2,5-, 2,6-, and 2,7-dimethylindolizine and 1-, 2-, and 3-azaindolizine have been determined at 100 and/or 60 Mc/s. Unequivocal assignments have been made to all protons and the coupling constants and chemical shifts for indolizine and its aza analogues have been obtained by an iterative procedure. Long-range coupling constants involving protons separated by five and six bonds have been observed.


1966 ◽  
Vol 19 (10) ◽  
pp. 1813 ◽  
Author(s):  
ML Heffernan ◽  
AJ Jones

The high-resolution proton magnetic resonance spectra of 6- phenylfulvene, 6-methyl-6-phenylfulvene, and 6-dimethylaminofulvene have been studied in detail. The aromatic character of the fulvenes is discussed in terms of the derived parameters, and observations, in general, indicate that these compounds should be regarded as cyclic dienes. Long-range coupling constants involving protons separated by five and six bonds have been observed.


1970 ◽  
Vol 48 (7) ◽  
pp. 1046-1053 ◽  
Author(s):  
C. J. Macdonald ◽  
W. F. Reynolds

Complete analyses of the proton magnetic resonance spectra of propylene oxide, epifluorohydrin, epibromohydrin, and epiiodohydrin shows that in all cases the cisoid coupling constants over four bonds are negative, and the transoid coupling constants positive. Dipole moments, together with the vicinal coupling constants of the CH—CH2X moiety, are used to establish the probable conformations for all the epihalohydrins. Conformational factors appear to obscure any possible relationship between substituent electronegativity and long-range coupling constants.


1969 ◽  
Vol 22 (6) ◽  
pp. 1157 ◽  
Author(s):  
DN Ford ◽  
W Kitching ◽  
PR Wells

Iodo lactones and chloromercuri lactones derived from a number of 2- and 3-methyl-5-norbornene-2-endo-carboxylic acids have been prepared and characterized. Analyses of 60-MHz and 100-MHz proton magnetic resonance spectra have estab- lished their configurations, which conform to a general pattern of trans-addition. Criteria for stereochemical assignments in this system can be based upon identifiable vicinal, geminal, and some long-range 1H-1H and 1H-199Hg coupling constants. These criteria are used to establish that 5-norbornene-2-endo,3-endo-dicarboxylic acid and its derivatives do not follow the cis-oxymercuration route previously suggested.


1968 ◽  
Vol 21 (7) ◽  
pp. 1853 ◽  
Author(s):  
B Caddy ◽  
M Martin-Smith ◽  
RK Norris ◽  
ST Reid ◽  
S Sternhell

N.m.r. data for 19 5-substituted and 13 polysubstituted benzo[b]thiophens are tabulated. The influence of the substituents at C5 on the chemical shifts of H4 and H6 is discussed. Long-range interproton spin-spin coupling between H3 and H7, and between H2 and H6, is general in benzo[b]thiophens. The vicinal coupling J6,7 in 5-substituted benzo[b]thiophens varies directly and linearly with the electronegativity of the substituents at C5.


1965 ◽  
Vol 20 (10) ◽  
pp. 948-956 ◽  
Author(s):  
Harald Günther

The proton magnetic resonance spectra of 1.6-methano- and 1.6-oxido-cyclodecapentaene are described and analyzed in terms of chemical shifts and coupling constants. The results are discussed in connection with the structure and possible aromatic character of these compounds. Measurements of the concentration dependence of the chloroform resonance signal in solutions of both compounds give additional support for the presence of a delocalized 10 π-electron system.


1976 ◽  
Vol 54 (23) ◽  
pp. 3666-3671 ◽  
Author(s):  
Ted Schaefer ◽  
J. B. Rowbotham ◽  
Kalvin Chum

The proton magnetic resonance spectra in the absence of intermolecular proton exchange for 0.27, 0.59, and 0.79 M solutions of phenol in CCl4 are analyzed. The long-range coupling over five bonds between the hydroxyl and ring protons is estimated as 0.33 Hz in the monomer and as 0.20 Hz in the trimer of a monomer–trimer model. Support for the decrease in the coupling on trimerization is found in CNDO/2 and INDO MO FPT calculations. The long-range coupling over six bonds is unobservable, consistent with conformations of the trimer in which the phenol molecules remain planar. Water catalyzes the intermolecular proton exchange and, in its absence, the transfer of hydroxyl protons from molecule to molecule within the associated species is inefficient.


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