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The (Z)/(E)-configurational analysis of isolated double bonds in pheromones and unsaturated fatty acids. The use of 1D and 2D J-resolved 1H CW off-resonance techniques in 13C NMR spectroscopy

✍ Scribed by Reiner Radeglia; Helmut Poleschner; Matthias Heydenreich


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
494 KB
Volume
29
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

The ^1^H CW off‐resonance decoupled ^13^C NMR spectra of pheromones and unsaturated fatty acids were measured for the determination of the configuration of double bonds of the type CH~2~CH  CHCH~2~. The decoupling frequency corresponded to the resonance frequency of the CH~2~ protons. The 2nd order splittings in the observed multiplets of the olefinic carbon atoms allow an approximate determination of the vicinal coupling constant between the olefinic protons, and the configurational assignment of the double bond.