A 13C-(1H) NMR spectrum of 2,2′-difluoro-4″-hexoxy-4-pentyl-[1,1′: 4′,1″]-terphenyl in the nematic phase has been obtained and analysed to yield a set of partially-averaged dipolar couplings, DijCF, which are used to determine the relative conformation of the two fluorinated rings. The probability distribution for the inter-ring angle is found to be peaked at 47.5 ± 2.5° and 122.5 ± 2.5°. The integrated, normalised probability that the inter-ring angle is less than 90° is 0.43.
The determination of the conformation of the aromatic rings in a lateral fluoro-substituted liquid crystal by 13C NMR spectroscopy
Castiglione F.;
2002-01-01
Abstract
A 13C-(1H) NMR spectrum of 2,2′-difluoro-4″-hexoxy-4-pentyl-[1,1′: 4′,1″]-terphenyl in the nematic phase has been obtained and analysed to yield a set of partially-averaged dipolar couplings, DijCF, which are used to determine the relative conformation of the two fluorinated rings. The probability distribution for the inter-ring angle is found to be peaked at 47.5 ± 2.5° and 122.5 ± 2.5°. The integrated, normalised probability that the inter-ring angle is less than 90° is 0.43.File in questo prodotto:
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