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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

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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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