## Abstract ^15^N Chemical shifts of __cis__‐decahydroquinoline, __N__‐methyl‐__cis__‐decahydroquinoline, and of 19 methyl substituted NH‐ and NCH~3~‐__cis__‐decahydroquinolines are reported. Shift values of conformationally homogeneous compounds can be used to determine the chemical shifts of the
Nitrogen nuclear magnetic resonance spectroscopy. Nitrogen-15 and proton chemical shifts of methylanilines and methylanilinium ions
✍ Scribed by Linda Psota; Marcia Franzen-Sieveking; Jocelyne Turnier; Robert L. Lichter
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 418 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Nitrogen and carbon electron densities of the toluidines and xylidines have been recalculated by the INDO method; previously published errors have been corrected. Although the nitrogen‐15 chemical shifts of these compounds still display the earlier suggested correlation with σ and total electron densities, the calculated inverse correlation with proton electron densities has been shown to be incorrect. Methyl proton chemical shifts of these compounds display no meaningful correlation with the nitrogen shifts. The nitrogen chemical shifts of the toluidinium and xylidinium ions correlate moderately well with the ^13^C chemical shifts of the analogous di‐ and tri‐methylbenzenes.
📜 SIMILAR VOLUMES
## Abstract Nitrogen‐15 chemical shifts of alkylthioureas in dimethylsulphoxide and pyridine are reported.
## Abstract Measurements are reported of NH exchange rates of urea, thiourea, acetamide and thioacetamide, using line‐shape analysis with natural‐abundance ^15^N NMR spectra. Base‐catalyzed NH‐proton exchange of thiourea is 30–40 times faster than for urea, while the corresponding acid‐catalyzed ex
## Abstract Nitrogen‐15 NMR spectra of 11 ketenimines have been taken both at the natural‐abundance level of ^15^N and with the aid of ^15^N‐labeling. The nitrogen chemical shifts are substantially different from those of neutral imines and are upfield, more like those of protonated imines. The res
## Abstract Nitrogen‐15 chemical shifts of 1,2‐diaminobenzenes, 1,8‐diaminonaphthalenes and their monoprotonated species are reported.