15N, 1 7 0 and 33S N M R chemical shifts were determined for some aliphatic and aromatic sulphonamides, sulphinamides, sulphenamides and related sulphones and sulphoxides. The 1 7 0 and NMR chemical shifts change only slightly for the sulphonyl compounds. In the sulphinyl componnds, on the other han
Sulphur-33 and oxygen-17 NMR studies of sulpholane in acetic acid and related solvents
✍ Scribed by Ahmed A. M. Ali; Robin K. Harris; Peter S. Belton
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 552 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Sulphur‐33 NMR spectra were obtained for sulpholane in acetic acid, trifluoroacetic acid, methyl acetate and methyl trifluoroacetate over the entire solution range and at a variety of temperatures. Oxygen‐17 NMR spectra were recorded for both components of each solution. The line width and chemical shift data are discussed in terms of molecular interactions and viscosity variations. Some variable‐temperature measurements are included, as are some values of ^13^C spin‐lattice relaxation times. It is concluded that there is an interaction, probably protonation, between sulpholane and trifluoroacetic acid, although occurring to only a small extent, which is not shown by the other solutions. The ^33^S and ^17^O line widths of sulpholane are peculiarly sensitive to the interaction.
📜 SIMILAR VOLUMES
## Abstract The ^17^O‐NMR. line widths of the enriched amino acids glycine, aspartic acid, glutamic acid and, for comparative reasons, acetic acid were measured in aqueous solution between pH 1 and 14. The ^17^O‐NMR. line‐width maxima of glycine at pH≈︁11 and acetic acid at pH≈︁5 are shown to arise
## Abstract The ^17^O‐NMR. chemical shifts of the enriched amino acids glycine, aspartic acid and glutamic acid were measured in aqueous solution as a function of pH. High magnetic fields are necessary to resolve the α, β‐ and α, γ‐carboxyl resonances of aspartic acid and glutamic acid, respectivel