Abstract
The 13C and 15N NMR spectra of some ortho-, meta-, and para-substituted dimethanesulphonanilides were recorded. The 13C chemical shifts were analysed utilizing substituent chemical shifts for monosubstituted benzenes and by means of the dual substituent parameter (DSP) and DSP-non linear equations. The results indicate that the -N(SO2Me)2 moiety is an extremely weak electron donor. The 15N chemical shifts of the parasubstituted compounds were also analysed by means of DSP equations and the results compared with those of related compounds. An improved method of preparation of dimethanesulphonanilides is given.
| Original language | English |
|---|---|
| Pages (from-to) | 18-22 |
| Number of pages | 5 |
| Journal | Canadian Journal of Analytical Sciences and Spectroscopy |
| Volume | 42 |
| Issue number | 1 |
| State | Published - 1997 |
Keywords
- C NMR
- Dimethanesulphonanilide
- N NMR
- Substituent effects
ASJC Scopus subject areas
- Analytical Chemistry
- Atomic and Molecular Physics, and Optics
- Spectroscopy
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