## Abstract ^15^N chemical shifts were measured in a series of anilinium fluorosulfonate salts and compared with chemical shift data from a comparable series of ^15^N‐enriched aniline derivatives. A smaller overall range of nitrogen chemical shifts was observed for the protonated aniline series com
Substituent effects on 15N NMR chemical shifts in selected N-alkylthiohydroxamic acids. A comparative study
✍ Scribed by Witold Przychodzeń; Leszek Doszczak; Janusz Rachon
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 110 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1497
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✦ Synopsis
Abstract
The ^15^N NMR spectra of three N‐alkyl‐δ‐carbomethoxyvalerothiohydroxamic acids (2) and six synthesized N‐isopropylbenzothiohydroxamic acids (3) were measured and compared with appropriate spectra of structurally similar hydroxylamines (1), benzohydroxamic acids (4), benzamides (5) and thiobenzamides (6). The analysis of the chemical shifts of the thiohydroxamic acids under investigation indicates that the inductive effect of the hydroxyl group rather than steric hindrance is responsible for non‐additivity of the effect of substituents. Additionally, N‐hydroxyl diminishes the effect of aromatic ring substituents on the ^15^N chemical shifts in the thiohydroxamic acids 3 which is approximately half that in the respective thiobenzamides 6. The chemical shift values correlate best with Brown's σ^+^ parameter. Copyright © 2004 John Wiley & Sons, Ltd.
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