1971
DOI: 10.1080/15421407108083221
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Characterization of Molecular Role in Pitch Determination in Liquid Crystal Mixtures

Abstract: Pitch versus composition data in a binary mixture of a cholesteric and a room-temperature nematic are used to demonstrate that molecular influence in pitch determination is more linear when credited according to weight percent than when credited according to mole 7'0. It is also shown that the effective rotary power of cholesteryl iodide is influenced by its environment to the extent that it exhibits the chirality of the other constituent in a binary mixture.

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Cited by 48 publications
(4 citation statements)
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“…These numerical results are consistent with the experimental results. 2,8,[11][12][13] The pitch strongly depends on the chiral interaction parameter x between a polymer and a liquid crystal.…”
Section: A Cholesteric Pitch Depending On Concentration and Temperaturementioning
confidence: 99%
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“…These numerical results are consistent with the experimental results. 2,8,[11][12][13] The pitch strongly depends on the chiral interaction parameter x between a polymer and a liquid crystal.…”
Section: A Cholesteric Pitch Depending On Concentration and Temperaturementioning
confidence: 99%
“…[7][8][9][10] The pitch and the physical properties of cholesterics can be controlled by mixing cholesteric liquid crystals and polymer chains, or photo reactive molecules. 2,[11][12][13] It has been shown both experimentally [14][15][16][17] and theoretically [18][19][20][21][22][23][24][25] that in mixtures of a polymer and a liquid crystal (so-called polymer dispersed liquid crystals: PDLCs), phase separations between an isotropic and a nematic or a smectic phase appears below the nematic-isotropic phase transition (NIT) temperature of the pure liquid crystal. 2 For strong anisotropic (attractive) interactions between polymers and liquid crystals, it has been recognized that a smectic phase can be induced in a nematic liquid crystal mixture.…”
Section: Introductionmentioning
confidence: 99%
“…In a chiral nematic phase with a chiral dopant, helical pitch ( p ) is given by p 1 = β c where β is helical twisting power (HTP), c is a molar fraction of the chiral dopant, and the signs “+” and “–” of p and β represent right- and left-handedness of helical mesostructures, respectively. In a chiral nematic system with multiple chiral components, an additive law is often applied: p 1 = i β i c i where β i and c i denote the HTP and molar fraction of the i th component, respectively. Azobenzenes with chirality can be used as dopants in LCs, of which HTP can be switched through the trans – cis isomerization of the azobenzene moieties. Photoinduced change in HTP has been applied to control reflection wavelength of chiral nematic LCs in planar alignment. , Furthermore, transparent–scattering transition has been achieved by using LCs containing both azobenzene and photoinert chiral dopants with the opposite signs of HTP to each other. These compensated nematic LCs with p –1 = 0 show transparent states in homeotropic alignment, whereas photoisomerization leads to the change in HTPs of chiral azobenzenes and results in the transition to scattering states with chiral nematic mesostructure.…”
Section: Introductionmentioning
confidence: 99%
“…The concentration of chiral compounds in nematic LC-1289 was taken 0.01-0.02 mole fraction. For practical use HTP values are also expressed in mass fractions.The cholesteric helix handedness (twisting sign) was determined according to Adams-Haas method[26]. For cases when the cholesteric helix handedness was notdetermined, HTP values are given as absolute values.…”
mentioning
confidence: 99%