## Abstract The ^13^C n.m.r. spectra of the __N__‐methylated mono‐ and diazanaphthalenes have been recorded and analysed. It has been shown that __N__‐methylation as well as __N__‐protonation in cinnoline occur predominantly at the β‐nitrogen atom. __N__‐methylation and __N__‐protonation show a sim
13C n.m.r. investigation on the first and second nitrogen protonation in the diazanaphthalenes
✍ Scribed by Peter van de Weijer; Dirk M. W. van den Ham; Douwe van der Meer
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 403 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^13^C chemical shifts of the diazanaphthalenes have been recorded as a function of the pH value, providing classical titration curves. From these curves the p__K__~1~ and p__K__~2~ values have been determined taking into account the activity coefficients. The changes in ^13^C chemical shift under the influence of nitrogen protonation (Δδ) can be described by two protonation parameter sets.
📜 SIMILAR VOLUMES
## Abstract The pH dependence of the ^13^C chemical shifts (δ) of the diazanaphthalenes has been recorded. From this dependence the p__K__~__a__~ values have been determined using the Henderson‐Hasselbach equation. The change in ^13^C chemical shifts under the influence of nitrogen protonation (Δδ)
## Abstract The ^1^H and ^13^C n.m.r. spectra of __N__‐methylated pyridine, pyridazine, pyrimidine and pyrazine and __N__,__N__‐dimethylated pyrimidine and pyrazine have been recorded and analysed. The change in the ^13^C chemical shifts under the influence of __N__‐methylation (Δδ) in the diazaben
## Abstract The site of hydration for 1,6‐ and 1,7‐naphthyridine has been determined by specific line broadening in the ^1^H n.m.r. spectra on the addition of water. The site of hydration appears to be the same as the site of protonation (β‐nitrogen atom). The site of hydration in quinazoline has b
## Abstract Characteristic differences in multiplet hyperfine structure observed in coupled ^13^C n.m.r. spectra of symmetrical __o__‐disubstituted benzene rings are explained on general grounds. Contrary to earlier proposals, the observation of this effect in unsymmetrical systems is not a suitabl
## Abstract The 1‐NH structure for 3‐azidoindazole has been demonstrated by the observation of ^1^H^1^H and ^13^C^1^H couplings involving the hydrogen atom attached to nitrogen. A comparison between 3‐azidoindazole and indazole shows that both compounds have the same tautomeric structure.