1980
DOI: 10.1002/pol.1980.130180810
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A novel technique for characterizing the sense of twisting in cholesteric liquid crystals

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Cited by 18 publications
(6 citation statements)
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“…The DCE.solution thus has negative rotatory power and left-handed cholesteric twisting. 6 The sense of distortion in the depolarized "cholesteric scattering pattern" depends not only Polymer J., Vol. 13, No.7, 1981 on the solvent but also on temperature as dem-.…”
Section: Resultsmentioning
confidence: 99%
“…The DCE.solution thus has negative rotatory power and left-handed cholesteric twisting. 6 The sense of distortion in the depolarized "cholesteric scattering pattern" depends not only Polymer J., Vol. 13, No.7, 1981 on the solvent but also on temperature as dem-.…”
Section: Resultsmentioning
confidence: 99%
“…For example the scattering maximum in the large-angle region occurs at the scattering angle reciprocally related to the identity period S of the alternating bright and white stripes in the micrograph shown in Figure 9(a), i.e., half the distance of the cholesteric pitch.1S. 16 Figure l 0 shows the micrographs under crossed polarizers corresponding to the scattering patterns shown in Figure 4 for the solutions enclosed in a cell. The polarization directions are set vertically and horizontally.…”
Section: Supramolecular Structure In Concentrated Solutionsmentioning
confidence: 99%
“…The effect of the optical rotation on the "ring" scattering, i.e., the scattering maximum arising from the cholesteric twisting will be described in detail in a subsequent paper. 15 Polymer J., Vol. 12, No.…”
Section: O• Kd=0°mentioning
confidence: 99%
“…This sample had spherical morphology44 (at +s = 0.265) which, being favored over planar morphology, should have a higher T, than calculated here. Finally, an adjustment of SS -SE to 0.88from 0.80, inferred5 from using the Step profile-would lead the present model to match the Roe result when the q = 5 profile is used.Discussion of the tapered SI copolymer of Hashimoto et al39 is not easy in the context of the present theory for distinct-block molecules. Qualitatively, however, that result is understandable in the sense that tapering makes the two ends of the molecule more compatible than would be so for SI blocks described by the theory.…”
mentioning
confidence: 99%