## Abstract The eluotropic strength of binary mobile phases was calculated for three homologous series of __cis__, __trans__, and __cis__‐__cis__ unsaturated fatty acid methyl esters (FAMEs). Binary mobile phases with chloroform, dichloromethane, or tetrahydrofuran as strong solvent and methanol or
13C-NMR of double and triple bond carbon atoms of unsaturated fatty acid methyl esters
✍ Scribed by Jan Bus; Izaäk Sies; Marcel S.F. Lie Ken Jie
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- English
- Weight
- 562 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0009-3084
No coin nor oath required. For personal study only.
✦ Synopsis
Fhe carbon magnetic resonance spectra of many fatty acid methyl esters with cis and trans double bonds and triple bonds at various positions and in many different combinations have been investigated.
The influence of the ester group on double and triple bonds in the fatty acid chain depends strongly on the positions of these bonds. For a given position the influence is constant, even if one or more other double or triple bonds are present.
Together with the evaluated chemical shift parameters for the effects of double and triple bonds on each other, complete assignments are possible and spectra of various types of unsaturated esters can be predicted with high accuracy (± 0.1 ppm).
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