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- W2079384612 abstract "The orientational ordering of a series of ferroelectric liquid crystals 4'-[(2S, 3S)-3-methyl- 2-halopentanoyloxy]-4-hexyloxybiphenyls (3M2XPHOB, X=F for fluorine, C for chlorine, B for bromine) and their racemates have been studied by two-dimensional carbon-13 separated local field spectroscopy combined with off-magic-angle spinning. All carbons are well-resolved in the carbon-13 NMR spectrum so that carbon-proton dipolar coupling constants for all carbons in the liquid crystal molecule can be determined, giving detailed segmental orienta- tional ordering information. (The order parameters of the biphenyl core segments and each carbon-proton bond in the aliphatic chains were measured as a function of temperature.) The results show that the substitution of different halogens on the chiral chain affects the carbon- proton bond orientational ordering of the entire chiral chain, while the orientational ordering of the rest of the liquid crystal molecule (core and achiral chain) remains unchanged. For the fluoro-substituted liquid crystals, carbon-fluorine dipolar couplings are also observed. At the SmA-to-SmC* transition, there is a discontinuous change in the magnitudes of all C-H bond order parameters. However, the aliphatic ordering relative to the core ordering is unchanged, suggesting that there is a negligible change in the mesogen conformation and the environment of the aliphatic chain at this transition, i.e. there is no evidence for substantial 'chiral interactions' in the SmC* phase." @default.
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- W2079384612 date "1998-02-01" @default.
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- W2079384612 title "Ferroelectric liquid crystals derived from isoleucine II. Orientational ordering by carbon-13 separated local field spectroscopy" @default.
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- W2079384612 doi "https://doi.org/10.1080/026782998207433" @default.
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