Proton Magnetic Resonance Spectra of Some Organosulfur Compounds

1965 ◽  
Vol 19 (4) ◽  
pp. 105-109 ◽  
Author(s):  
J. M. Purcell ◽  
H. Susi

The proton magnetic resonance spectra of various sulfur derivatives of long-chain carboxylic acids have been studied The types of compounds studied include those where the methylene chain is interrupted by a sulfide or a sulfone group and those where the carboxyl group has been replaced by –SO3– or –C(=O)S–. The spectral effects produced by the sulfur-containing groups are discussed. The effect of the sulfur group in sulfides and sulfones is compared with the effect of an oxygen atom in a similar environment. The effect of the –SO3– and –C(=O)S– groups on neighboring methylene groups is compared with the effect of the carboxyl group.

1976 ◽  
Vol 7 (50) ◽  
pp. no-no
Author(s):  
YU. A. USTYNYUK ◽  
G. A. ARTAMKINA ◽  
YU. N. LUZIKOV ◽  
YU. K. GRISHIN ◽  
A. A. AZIZOV ◽  
...  

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.


1968 ◽  
Vol 46 (15) ◽  
pp. 2629-2631 ◽  
Author(s):  
Misbahul Ain Khan ◽  
J. B. Polya ◽  
Brian M. Lynch

9-Hydroxy-9-methyl derivatives of the ring systems named in the title are formed along with the expected 1-(o-acetylphenyl)azoles in the Ullmann condensations of o-bromoacetophenone with imidazole and with 1,2,4-triazole. The structures of these compounds follow from their characteristic proton magnetic resonance spectra.


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