Optical determination of the pitch-dependent diffusion constant in a cholesteric liquid crystal

The concentration profile of a cholesteric compound diffusing into a nematic liquid crystal is observed with optical methods. We propose new experimental initial and boundary conditions which allow a more accurate mathematical solution of the differential equation involved. A numerical approach is applied to compute the concentration profiles with a concentration dependent diffusion constant. Diffusion is found to decrease with the shorter pitch length.     

Optical wave propagation in a cholesteric liquid crystal using the finite element method

Bragg reflections of cholesteric liquid crystals at normal and oblique incidences were investigated using the finite element method (FEM). Detailed FEM derivations together with the consideration of boundary conditions are given. Two methods for achieving broadband Bragg reflection are analysed: one is to use high birefringence liquid crystal in the uniform pitch structure, the other is to use the gradient pitch structure. In each case, the number of cholesteric pitches required for establishing the Bragg reflection was simulated.     

Optical wave propagation in a cholesteric liquid crystal using the finite element method

Bragg reflections of cholesteric liquid crystals at normal and oblique incidences were investigated using the finite element method (FEM). Detailed FEM derivations together with the consideration of boundary conditions are given. Two methods for achieving broadband Bragg reflection are analysed: one is to use high birefringence liquid crystal in the uniform pitch structure, the other is to use the gradient pitch structure. In each case, the number of cholesteric pitches required for establishing the Bragg reflection was simulated.     

Transition radiation in cholesteric liquid crystal

We consider a constant velocity charged particle travelling in an arbitrary direction by a cholesteric liquid crystal. We calculate the time-dependent-induced polarisation in the cholesteric by the electric field generated by the charged particle. Thus, we express the radiation field originated by the induced dipole distribution in the cholesteric in terms of the cholesteric susceptibility. To simplify our procedure, we write Maxwell equations and the constitutive non-local equation for the cholesteric, in the Fourier space since in this representation the equations turn to be simple difference equations. We solve these equations iteratively by assuming small values for the cholesteric birefringence to find the first-order electric field produced by the charge particle immersed in the cholesteric. This allows us to obtain the dominant contributions of the radiation field one of which is the usual Cherenkov effect. We focus in the terms occurring for hypoluminic charged particle and calculate the radiated energy as a function of observing angle, frequency, velocity and direction with respect to the cholesteric axis.     

Optical behaviour of cholesteric liquid crystal cells with novel photoisomerizable chiral dopants

In order to investigate the effect of photoisomerization of E-Z structures on the optical behaviour of cholesteric liquid crystal (ChLC) cells, a series of novel azo derivatives was synthesized. Molecular structures were identified using ¹H NMR, ¹³C NMR, FTIR and elemental analysis. Thermal properties and the specific rotation of the synthesized chiral azo derivatives were estimated. Rubbed polyvinyl alcohol coated on the inner surface of substrates was used to control the liquid crystal alignment in cells. The effect of chiral dopants on the reflection band of ChLC cells was investigated, as well as the dependence of polarizing optical microscope textures on temperature. The stability and reproducibility of the effect of UV irradiation on the cell reflection band and real image recording were confirmed. Real image recording of the ChLC cells fabricated in this investigation was also studied; a photoinduced image through a mask is given. Photoirradiated and non-irradiated areas appear as different reflected colours leading to the formation of an image. Stacking of the ChLC cells was found to intensify the brightness of the reflection band.     

Optical behaviour of cholesteric liquid crystal cells with novel photoisomerizable chiral dopants

In order to investigate the effect of photoisomerization of E–Z structures on the optical behaviour of cholesteric liquid crystal (ChLC) cells, a series of novel azo derivatives was synthesized. Molecular structures were identified using ¹H NMR, ¹³C NMR, FTIR and elemental analysis. Thermal properties and the specific rotation of the synthesized chiral azo derivatives were estimated. Rubbed polyvinyl alcohol coated on the inner surface of substrates was used to control the liquid crystal alignment in cells. The effect of chiral dopants on the reflection band of ChLC cells was investigated, as well as the dependence of polarizing optical microscope textures on temperature. The stability and reproducibility of the effect of UV irradiation on the cell reflection band and real image recording were confirmed. Real image recording of the ChLC cells fabricated in this investigation was also studied; a photoinduced image through a mask is given. Photoirradiated and non‐irradiated areas appear as different reflected colours leading to the formation of an image. Stacking of the ChLC cells was found to intensify the brightness of the reflection band.     

Optical behaviour of photoimageable cholesteric liquid crystal cells with various novel chiral compounds

In theory, both polarity and steric hindrance are basic factors which affect molecular interactions. To investigate the optical properties and steric structures of chiral compounds having different chiral moieties which affect the wavelength of light reflection in liquid crystal (LC) cells, a series of novel chiral compounds and azobenzene derivatives were synthesized. The liquid crystalline phases of the compounds were identified using small angle X‐ray diffraction, differential scanning calorimetry and polarizing optical microscopy. Cholesteric LC cells with various synthesized chiral dopants which selectively reflect visible light were first prepared, the photochemical switching behaviour of colours was then investigated, with special reference to the change in transmittance in cholesteric LC cells containing an azobenzene derivative as a photoisomerizable guest molecule. Reversible isomerization of azobenzene molecules occurred in the cholesteric systems, resulting in a depression of T _ChI and a shift of the selectively reflected wavelength. We discuss the photochemically driven change in the helical pitch of the cholesteric LCs with respect to structural effects involving the chiral moieties. Molecular interactions caused by the added dopants, reliability and stability of the photoisomerization, and UV irradiation effects on the cholesteric LC cells were also investigated. A real image was recorded through a mask on a cholesteric LC cell fabricated in this investigation.     

Optical behaviour of photoimageable cholesteric liquid crystal cells with various novel chiral compounds

In theory, both polarity and steric hindrance are basic factors which affect molecular interactions. To investigate the optical properties and steric structures of chiral compounds having different chiral moieties which affect the wavelength of light reflection in liquid crystal (LC) cells, a series of novel chiral compounds and azobenzene derivatives were synthesized. The liquid crystalline phases of the compounds were identified using small angle X-ray diffraction, differential scanning calorimetry and polarizing optical microscopy. Cholesteric LC cells with various synthesized chiral dopants which selectively reflect visible light were first prepared, the photochemical switching behaviour of colours was then investigated, with special reference to the change in transmittance in cholesteric LC cells containing an azobenzene derivative as a photoisomerizable guest molecule. Reversible isomerization of azobenzene molecules occurred in the cholesteric systems, resulting in a depression of T_ChI and a shift of the selectively reflected wavelength. We discuss the photochemically driven change in the helical pitch of the cholesteric LCs with respect to structural effects involving the chiral moieties. Molecular interactions caused by the added dopants, reliability and stability of the photoisomerization, and UV irradiation effects on the cholesteric LC cells were also investigated. A real image was recorded through a mask on a cholesteric LC cell fabricated in this investigation.     

Polyurethane acrylate-stabilized cholesteric liquid crystal dispersions

Polymer stabilized cholesteric liquid crystals (PSCLCs) have been fabricated based on various structures of polyurethane acrylate (PUA) as well as conventional acrylate polymer, namely poly(1,6-hexanediol diacrylate). For PUA stabilized films, the transmittance spectra of cured films were essentially identical to those of uncured films, with no 'dead' reaction; whereas, using acrylate polymer; reflection greatly decreased upon curing and showed significant 'dead' reaction after the cessations of irradiation. The structure of PUA also had significant effects on the electro-optic performance, and these effects are interpreted in terms of elasticity and interfacial interaction between the polymer and LC.     

Optical properties of frustrated cholesteric liquid crystals

In a previous article, we proposed a model to explain the unwinding transition in an electric field of a frustrated cholesteric liquid crystal sandwiched between two glass plates imposing a homeotropic anchoring. We found that three distinct solutions exist in materials of negative dielectric anisotropy: first, the homeotropic nematic at small thickness and small voltage, second, a translationally invariant configuration (TIC) at large voltage and, third, the cholesteric fingers. In this article, we study some optical properties of these solutions. We show first that the TIC rotates the polarization of light. Its 'apparent' rotatory power is calculated exactly and is compared with the experimental data when the TIC-nematic phase transition is second order. The agreement between theory and experiment is excellent. We show in particular that there exist discrete values of the voltage for which the TIC has a pure rotatory power. We then calculated the optical contrast of the fingers when they are observed between crossed polarizers. The agreement with experiment is still satisfactory, in spite of the approximate form of the director field chosen to describe the topology of the finger.     

Irreversible visual sensing of humidity using a cholesteric liquid crystal

Irreversible optical sensing of humidity by a doped cholesteric liquid crystal is achieved by using a thin film of nematic host E7 with a binaphthylorthosilicate ester as dopant (guest). The film changes its color from blue (to green to orange to red) to colorless when exposed to humidity as the dopant is hydrolyzed.     

Optical activity of a side group cholesteric liquid crystalline silicone

We measured, using a phase modulation technique, the optical rotation in the isotropic and blue phases of a side group cholesteric liquid crystalline silicone polymer. For comparison, similar measurements were performed on cholesteryl nonanoate (CN) and CE6. The polymer has a selective reflection close to that of CE6 and a chiral mesogenic side group chemically similar to CN. The optical activity data for the polymer, unlike those for low molecular mass liquid crystals, does not follow a simple Landau-de Gennes temperature dependence.     

Thermodynamic study of a liquid crystal as a liquid phase in gas-liquid chromatography. II. A cholesteric liquid crystal.

Gas-liquid chromatography is utilized for the determination of thermodynamic solution parameters for various organic solutes at infinite dilution in the meso- and isotropic phases of cholesteryl palmitate. The thermodynamic data and trends in values of the activity coefficients for the solutes are discussed in relation to their structure and to the orientations of the liquid crystal.     

Interface modification of polymer stabilized cholesteric liquid crystal

Films were made by incorporating various quantities of fluoroalkyl acrylate (FA) into the chain termini of polyurethane acrylate oligomer of polymer stabilized cholesteric liquid crystals (PSCLCs). The effects of switching voltage, scanning electron and polarized optical microscope morphologies, texture transition and reversibility, and contact angle of the films were then studied. It was found that the switching voltage of the film decreased with the addition of FA up to 0.8 wt%, beyond which it increased. The decrease and increase were respectively explained in terms of decreased interface energy as noted from the contact angle of the LC on polymer surface, and too small droplet size as noted from the SEM. Copyright © 2008 John Wiley & Sons, Ltd.     

Stability of some structures in a cholesteric liquid crystal layer for tilted anchoring

An analysis of the permitted structures for a cholesteric liquid crystal based on the continuum theory as a function of the anchoring conditions and the thickness of the liquid crystal layer is presented. A new type of bistability is found. The stability domains of various structure types are given.     

Supramolecular self-assembly of a novel hydrogen-bonded cholesteric liquid crystal exhibiting macromolecular behaviour

The mesomorphic, thermoptic and glass-forming properties of 4-[6-((cholesteryloxy) carbonyl)oxy hexyloxy] benzoic acid (Ch-BA) have been investigated as a novel supramolecular hydrogen-bonded cholesteric mesogen. Fourier transform infrared and ¹H nuclear magnetic resonance studies have confirmed the chemical structure and the hydrogen-bond formation between the mesogens. According to polarising optical microscope observations, the compound exhibited smectic and chiral nematic phases. Differential scanning calorimetry indicated an unexpected glass transition (T _g) around 32°C and a liquid crystalline region between 32 and 122°C, in which the cholesteric phase appeared at 80°C. As a result of the glass formation, samples of Ch-BA which were rapidly cooled below the T _g were found to preserve the long-range ordering of the liquid crystalline state and retained the iridescent colours of the cholesteric phase. These results led to the conclusion that the formation of identical dimers by intermolecular hydrogen-bonding of the terminal carboxylic acids accompanying the lateral packing of the rigid cores, built a trimeric arrangement and this was responsible for the macromolecular behaviour of Ch-BA, despite its relatively simple structure and low molecular weight.     

AFM investigations of a glassy cholesteric liquid crystal with hydrophobic aerosil particles

AFM investigations of a glassy heterogeneous system consisting of an oligomeric cholesteric liquid crystal and the hydrophobic aerosil R812 were carried out. With increasing aerosil concentration, a suppression of the characteristic cholesteric surface pattern was observed. Typical separated aerosil aggregates appear in the samples. Their size and form change from small lumps through bigger rod-like entities to large crystallite-like aggregates of aerosil particles. This matches with observations of light scattering of systems with low molecular mass liquid crystals and of the memory effect. The pitch of the cholesteric fingerprint pattern slightly decreases with increase in the aerosil concentration.