The 13C NMR behaviour of ten acyclic terpene alcohols was examined in the presence of a chiral lanthanide shift reagent (CLSR). For each alcohol, we measured the lanthanide-induced shift (LIS) on the signals of the carbons and the splitting of some signals, which allowed the enantiomeric differentia
Use of lanthanide shift reagents to probe the conformation of fatty acids in solution by 13C NMR
β Scribed by Miquel Pons; Dennis Chapman
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 460 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
The conformational analysis of short polymer chains involves the use of statistical models, and their predictions must be checked against experimental information. Ytterbium-induced shifts in the "C NMR spectra of fatty acids provide a non-perturbing, straightforward method of simultaneously obtaining positional information about all the carbon atoms up to nine bonds away from the complexation point. Experimental results for saturated and unsaturated C-18 fatty acids are compared with the predictions of a restricted isomeric states (RIS) model.
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