## Abstract The high‐resolution proton‐coupled ^13^C NMR spectra of 2‐chloro‐ and 2‐phenyl‐4‐methyl‐1,3,2‐dithiarsolane and 2‐chloro‐ and 2‐phenyl‐1,3,2‐dithiarsolane have been obtained and completely analysed. The spectral analysis has provided all the ^13^C chemical shifts and ^13^C^1^H coupling
Proton-coupled carbon-13 NMR spectra of butadienes
✍ Scribed by Robin K. Harris; Soon Ng; Alan Connelly
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 434 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Proton‐coupled ^13^C NMR spectra were obtained for three methyl‐substituted butadienes, namely 2‐methylbuta‐1,3‐diene, trans‐2‐methylpenta‐1,3‐diene and 2,4‐dimethylpenta‐1,3‐diene. The second‐order spectra were analysed by computer, using some new ^1^H NMR data, and the resulting chemical shifts and coupling constants are reported. The parameters are related to conjugation (and, in turn, to conformation) of the compounds, and to the influence of σ and π pathways for coupling.
📜 SIMILAR VOLUMES
## Abstract The application of selective population inversion (SPI) to the assignment of ^13^C resonances and to the determination of the relative sign of ^13^C^1^H coupling constants is demonstrated for 1‐phenyl‐1,2‐dibromo‐2‐nitroethane. A negative sign for the geminal C‐2H‐1 coupling constant
## Abstract ‘Unexpected’ second‐order effects encountered in proton‐coupled ^13^C NMR spectra where relative proton shifts are large compared to proton‐proton coupling constants are illustrated. The observed phenomenon is explained, with reference to the ABX spin system as a model, as being due to
## Abstract Carbon‐13 chemical shifts of three arylmethyl carbanions have been determined by changing solvents and counter ions. The charge distributions in the carbanions are discussed and compared with those obtained from the ^1^H chemical shifts.