956, Buenos Aires (1 113), Argentina I3C CP/MAS NMR spectra of nitrogen-containing compounds often show complex signals when recorded at low field strengths. This effect is due to the 13C, '"N residual dipolar coupling which is not averaged to zero by magic-angle spinning. Solidstate 13C NMR spectra
Application of deuteriated isotopomers in the analysis of 13C CP/MAS NMR spectra of some azo dyes
✍ Scribed by Jaroslav Straka; Bohdan Schneider; Antonín Lyčka; Josef Jirman
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 520 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C CP/MAS NMR spectra (50.3 MHz) of 4‐[N,N‐bis(2‐hydroxyethyl)amino]azobenzene (1), (N,N‐dimethylamino)azobenzene (2), 4‐methoxyazobenzene (3), 2‐hydroxy‐5‐tert‐butylazobenzene (4) and 4‐hydroxyazobenzene (5) were recorded. The isotopomers of 1, 4 and 5 with pentadeuteriated unsubstituted aromatic rings were also studied. Dipolar dephased spectra of the deuteriated isotopomers were used for chemical shift interpretation in the solid state. The changes in cross‐polarization dynamics caused by deuteration were investigated for 1. The spectra of 1, 2, 3, and 5 were also measured at elevated temperature. It was found that in 1, 2 and 5, rotation of the aromatic rings is induced at elevated temperature.
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## Abstract The ^15^N, ^13^C and ^1^H NMR spectra of 2:1 cobalt(III) complexes of azo dyes and their ^15^N isotopomers, derived from substituted 2‐hydroxyaniline azo coupling products with acetoacetanilide, were measured. It was found that, in contrast to precursors existing fully in their hydrazon
p<:yclodc\trin inclusion complexes of 3-aminobenzonitrile. 4-aminobenzonitrile. and adamantane-I-carbonitrile \\ere studied by means of high-resoiution solid-state CP MAS 13C NMR spectroscopy. The interactions between the host and guest molecules are discussed.