Design and synthesis of nematic liquid crystals with negative dielectric anisotropy

Axially fluorinated cyclohexane derivatives are a promising new type of liquid crystals with negative dielectric anisotropy. Up to now, the technical application of these materials in LCDs was impeded by their strong tendency to form smectic B mesophases. We present a convenient synthetic pathway leading to new homologues carrying alkenyl side chains which induce nematic phases.     

Kerr effect of low melting nematic liquid crystals with negative dielectric anisotropy

The two low melting nematic liquid crystals, 2-chloro-4-heptylphenyl 4-pentylbicyclo[2,2,2]octane-1-carboxylate (7CP5BOC) and 2-chloro-4-heptylphenyl 4-heptylbicyclo[2,2,2]octane-1-carboxylate (7CP7BOC) have been investigated to determine their electro-optical behaviour and third order non-linearity by the static Kerr effect method. Both liquid crystals are laterally substituted by a single chlorine atom located close to the ester linking group. The temperature dependence of the electric Kerr constant in the isotropic phase and the pretransitional behaviour have been investigated for these low birefringence nematic liquid crystals in the isotropic phase. Both the compounds, with negative dielectric anisotropy, have a positive Kerr constant. The Landau-de Gennes model was obeyed for these compounds.     

Electrical orientation behaviour of a nematic liquid crystal with negative dielectric anisotropy above the microelectrodes

Factors for the electrical orientation on interdigitated microelectrodes deposited on a substrate, a microdielectrometric sensor (or a sensor), were discussed experimentally using a model nematic liquid crystal with negative dielectric anisotropy. The electrical orientation behaviour of the nematic liquid crystal was investigated using microdielectrometry and polarised optical microscopy. The experimental results were discussed in relation to electric-field line, surface topology, anchoring of the liquid crystalline molecules to the microelectrodes, and transversal rotation of a rode-like molecule of the liquid crystal with negative dielectric anisotropy.     

Transverse dipole association and negative dielectric anisotropy of nematic liquid crystals

Measurements are reported of the dielectric properties of three laterally substituted dicyano compounds with large molecular dipole moments perpendicular to the long molecular axis. Results are given for the materials in solution, in the isotropic liquid state, and for one compound in the nematic state. There is evidence of a high degree of local ferroelectric order in all phases, and dipole correlation factors in excess of 3 were obtained. The significance of these observations for macroscopic ferroelectrically ordered and biaxial liquid-crystalline phases is considered.     

Plateau instability of a liquid crystalline cylinder in a magnetic field

The capillary instability of a liquid crystalline cylinder in magnetic field is considered using an energy approach. The boundary problem is solved in the linear approximation of the anisotropy chi(a) of the magnetic susceptibility chi. The effect of anisotropy, in the region 1> chi > chi(a) > chi2, can be strong enough to counteract and even reverse the tendency of the field to enhance stabilization by enlarging the cutoff wave number k(s) beyond the conventional one set by Rayleigh.     

Synthesis and characterization of a semiflexible liquid crystalline polyester with a broad nematic region

In this paper, we report on the synthesis and detailed characterization of a new semiflexible nematic liquid crystalline polyester which could serve as a 'model' polyester for a variety of physical and physico-chemical investigations. The polymer is a nematic liquid over a wide temperature range-from the glass transition temperature at ∼95°C to the isotropic transition at ∼240°C. We expect this polyester to be particularly useful for studying the effect of flow on the orientation of liquid crystalline polymers, as well as the production and removal of disclinations.     

Dielectric and electro-optical properties of a nematic liquid crystalline material with gold nanoparticles

ABSTRACT

We have prepared the composites of a room temperature nematic liquid crystalline material namely 4-(trans-4′-n-hexylcyclohexyl) isothiocyanatobenzoate (6CHBT) and gold nanoparticles (GNPs). Thermodynamic, electro-optical and dielectric properties have been investigated. Effect of dispersion of GNPs on various electro-optical and display parameters of host liquid crystalline material have been studied. Physical parameters such as threshold voltage, dielectric anisotropy and splay elastic constant have altered for composite systems. Due to the dispersion of GNPs, nematic to isotropic transition temperature is significantly increased. Relaxation frequency corresponding to flip-flop motion of the 6CHBT molecules about their short axes has increased due to the presence of GNPs.     

Visco-elastic properties of reentrant nematic liquid crystalline mixtures

The visco-elastic properties for binary mixtures of 4-n -hexyloxy-4′-cyanobiphenyl (6OCB) and 4-n-octyloxy-4′-cyanobiphenyl (8OCB) are investigated in detail by a light scattering technique. The mixtures exhibit a reentrant nematic (RN) phase between the smectic A (SmA) and crystal phases in the range 22.0–29.5 wt % of 6OCB. The viscosity and the elastic constant increase with cooling in both the nematic and reentrant nematic phases. It is also found that the mixtures exhibit anomalously large values of viscosity and elastic constant near the phase transition, i.e. a pretransitional phenomenon can be observed. The activation energy for viscosity is smaller in the RN phase than in the ordinary nematic phase appearing at higher temperatures, while the normalized elastic constant (defined as the ratio of the elastic constant to the square of the dielectric anisotropy) is larger. Moreover, the visco-elastic behaviour depends on the specific time during which the sample has been kept in the SmA phase. These results confirm that the SmA phase has a strong influence on the formation of molecular aggregates, which plays an important role in the reentrant phenomenon of these systems.     

Visco-elastic properties of reentrant nematic liquid crystalline mixtures

The visco-elastic properties for binary mixtures of 4- n -hexyloxy-4'-cyanobiphenyl (6OCB) and 4- n -octyloxy-4'-cyanobiphenyl (8OCB) are investigated in detail by a light scattering technique. The mixtures exhibit a reentrant nematic (RN) phase between the smectic A (SmA) and crystal phases in the range 22.0-29.5 wt % of 6OCB. The viscosity and the elastic constant increase with cooling in both the nematic and reentrant nematic phases. It is also found that the mixtures exhibit anomalously large values of viscosity and elastic constant near the phase transition, i.e. a pretransitional phenomenon can be observed. The activation energy for viscosity is smaller in the RN phase than in the ordinary nematic phase appearing at higher temperatures, while the normalized elastic constant (defined as the ratio of the elastic constant to the square of the dielectric anisotropy) is larger. Moreover, the visco-elastic behaviour depends on the specific time during which the sample has been kept in the SmA phase. These results confirm that the SmA phase has a strong influence on the formation of molecular aggregates, which plays an important role in the reentrant phenomenon of these systems.     

Changing liquid crystalline phase with field

Since 1888, the liquid crystal display (LCD) industry is facing a fierce competition due to serious limitations such as poor contrast ratio and response time. Although some new materials have offered new applications and opened new markets for LCDs, materials with improved contrast ratio are highly desirable in LCD industry to sustain in the current market. This work reports a new behaviour in nano-material-doped liquid-crystal composite which is suitable for eradicating limitations of contrast ratio. Here, a high concentration of carbon nanotubes (CNTs) is doped in liquid crystal (LC) materials wherein the CNTs form aggregates in the LC composition. In these heavily doped samples, the phase change takes place with application of bias. This reversible process improves the contrast ratio as the material oscillates between crystalline and LC phases with field.     

End-chain ordering and even-odd effects in nematic thermotropic liquid crystalline mesophases studied by deuterium magnetic resonance

Deuterium quadrupole splittings are reported for the nematic mesophases of all isomers of 4,4′-di-n-octyl-d₄(d₆)-oxyazoxybenzene with CD₂(CD₃) groups at corresponding segments in the two end chains. These splittings do not decrease monotonically with increasing separation of the chain segment from the aromatic core as has previously been assumed. Comparison with similar measurements for 4,4′-di-n-heptyloxyazoxybenzene reveals an “even—odd” effect in the chain ordering, but only in so far as to reflect differences in the molecular order in the two mesophases. The results are used to test earlier theoretical calculations by Mar?elja.     

Texture dependence of capillary instabilities in nematic liquid crystalline fibres

Static and dynamic linear analyses of axisymmetric capillary instabilities in textured nematic liquid crystalline fibres are performed using the equations of nemato-statics and inviscid nemato-dynamics. Three representative textures, viz. axial, onion, and radial, are analysed to show all possible effects of Frank gradient elasticity on the wavelength selection and growth rate of peristaltic modes driven by surface area reduction. It is found that Frank elasticity may tend to stabilize or destabilize the fibre, depending on the initial fibre texture. Axial textures tend to stabilize the fibre through the director splay-bend distortions driven by surface tilting. Onion textures are destabilized by decreasing azimuthal bend elastic energy caused by surface displacement. Radial textures exhibit a stabilizing tilt mechanism due to bend modes and a destabilizing displacement mechanism due to splay modes, but the former is predicted to be dominant. The static analysis provides good estimates of the instability thresholds while the transient energy balance provides information on the fastest growing modes. The static and dynamic results are compared and shown to be fully consistent. The couplings between splay and/or bend distortions, surface tilting, and surface displacement in nematic fibres are characterized and used to explain the deviations from the classical Rayleigh instability.     

Photoinduced anisotropy and photoalignment of nematic liquid crystals by a novel polymer liquid crystal with a coumarin-containing side group

A new type of photo-crosslinkable methacrylate polymer liquid crystal (PLC) with a coumarincontaining mesogenic side group was synthesized and applied as the photoalignment layer for low molecular mass nematic liquid crystals. Linearly polarized ultraviolet light was directed onto a thin film of PLC under various exposure conditions. When a film was irradiated at room temperature, a small negative optical anisotropy was generated due to angular-selective photo-crosslinking. In contrast, when the film was exposed near the clearing temperature of the PLC, the induced anisotropy was positive due to thermally enhanced photoinduced reorientation of the side groups. The aggregation of the mesogenic groups was also observed when the irradiation was carried out in the liquid crystalline temperature range of the PLC. The LC alignment on the photoreacted film was greatly dependent on these irradiation conditions. It was made clear that the LC alignment was regulated by the interaction among the LC, the photo-crosslinked side groups and the remaining mesogenic side groups, and that the aggregated mesogenic groups inhibited the LC alignment.     

Fast spatially localised electrooptical mode in vertically aligned nematic LCs with negative dielectric anisotropy

ABSTRACT

Electro-optical switching and the liquid crystal (LC) director distribution are studied in spatially periodic electric field for vertically aligned LC with negative dielectric anisotropy. Two electro-optical switching modes characterised by different switching times are observed. These modes are well distinguished optically by choosing proper geometry for the polarisers axes orientation. One of these modes is significantly faster as compared to the other. The fast switching is explained in terms of localised near-to-surface director reorientation. The 3D-numerical simulation shows very good agreement with the experiment: it points out the existence of the disclination lines and field-stabilised walls responsible for the localised director field switching and its relaxation. Possibilities of enhancing the fast mode for high-speed light modulators are discussed.     

Photoinduced anisotropy and photoalignment of nematic liquid crystals by a novel polymer liquid crystal with a coumarin-containing side group

A new type of photo-crosslinkable methacrylate polymer liquid crystal (PLC) with a coumarincontaining mesogenic side group was synthesized and applied as the photoalignment layer for low molecular mass nematic liquid crystals. Linearly polarized ultraviolet light was directed onto a thin film of PLC under various exposure conditions. When a film was irradiated at room temperature, a small negative optical anisotropy was generated due to angular-selective photo-crosslinking. In contrast, when the film was exposed near the clearing temperature of the PLC, the induced anisotropy was positive due to thermally enhanced photoinduced reorientation of the side groups. The aggregation of the mesogenic groups was also observed when the irradiation was carried out in the liquid crystalline temperature range of the PLC. The LC alignment on the photoreacted film was greatly dependent on these irradiation conditions. It was made clear that the LC alignment was regulated by the interaction among the LC, the photo-crosslinked side groups and the remaining mesogenic side groups, and that the aggregated mesogenic groups inhibited the LC alignment.     

Interpretation of cw-ESR spectra of p-methyl-thio-phenyl-nitronyl nitroxide in a nematic liquid crystalline phase

In this paper we report on the characterization by continuous wave electron spin resonance spectroscopy (cw-ESR) of a nitronyl nitroxide radical in a nematic phase. A detailed analysis is performed by exploiting an innovative modeling strategy alternative to the usual spectral simulation approach: most of the molecular parameters needed to calculate the spectrum are evaluated a priori and the ESR spectrum is obtained by direct application of the stochastic Liouville equation. Allowing a limited set of fitting parameters it is possible to reproduce satisfactorily ESR spectra in the temperature range 260 K-340 K including the nematic-to-isotropic phase transition (325.1 K). Our results open the way to a more quantitative understanding of the ordering and mobility of nitronyl nitroxide radicals in nanostructured environments.     

Investigation of fracture mechanism on liquid crystalline epoxy networks arranged by a magnetic field

A liquid crystalline epoxy resin was cured under non‐ and 10T‐magnetic fields, and polydomain and monodomain networks were obtained, respectively. The fracture toughness of these systems was evaluated and it was clarified that the toughness of the magnetic field system showed a higher value. To investigate the toughening mechanism, polarized micro FTIR measurements were carried out. As a result, it was clarified that their mechanisms were quiet different. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1406–1412, 2006     

Helical twisting power and compatibility in twisted nematic phase of new chiral liquid crystalline dopants with various liquid crystalline matrices

ABSTRACT

Four chiral dopants exhibiting smectic LC phases themselves were prepared and their helical twisting power (HTP) and thermal phase behaviour in mixtures with four various LC hosts were studied. The influence of host liquid crystal on HTP was evaluated and generally higher values were found for hosts with high birefringence. Unexpectedly, high enhancement was found for an LC-chiral dopant pair, both having a similar aromatic core – biphenyl ring substituted with polar group. All studied chiral dopants exhibited limited compatibility with the LC hosts in twisted nematic phase at room temperature. For one of the studied mixtures, it was able to obtain single twisted nematic phase with selective light reflection band with maximum at wavelength about 1.0 µm. Carboxylic acid-type dopants exhibited total compatibility with the studied host in single twisted nematic phase at elevated temperatures, allowing preparation of mixtures with reflection band in the visible range. In case of the carboxylic acid dopants, blue phases for optimised compositions were observed. Intermolecular hydrogen bonding between carboxylic acid proton and pyridine nitrogen of chiral dopants was found. Doping the LC host with these dopants led to slight enhancement of HTP value and higher solubility in the LC host.