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1.
《Liquid crystals》2001,28(5):749-759
A new class of compounds suitable for LCD applications has have synthesized, incorporating a trifluoromethyl group in the terminal alkoxy or alkenyloxy chain. These compounds fulfil many of the specifications for use in TN-LCDs. Compounds containing several aromatic rings were synthesized with a view to producing compounds of high birefringence. This aspect also included the synthesis of compounds containing a carbon-carbon triple bond. Materials with three phenyl rings were also prepared in an attempt to produce nematic liquid crystals with a high clearing point and a high birefringence. Molecules containing a lateral fluoro substituent were synthesized in order to generate a high positive value of the dielectric anisotropy, a low melting point and no smectic mesophases. A series of compounds incorporating a carbon-carbon double bond was prepared in an attempt to produce compounds with a high nematic clearing point and a high birefringence. 相似文献
2.
Goroh Saitoh Toyokazu Nakamura Masayoshi Suzuki Masahiro Satoh Kunikio Yoshio Tetsuya Watanabe 《Liquid crystals》2013,40(6):1753-1761
Abstract New chiral dopants, possessing a trifluoromethyl group, have been synthesized. These dopants have different polar groups, located between the chiral centre and the diphenylacetylene core. The polar part is chosen from ester, methylene ether and ether linkages. Each new chiral dopant was mixed with a non-chiral liquid crystal mixture or a ferroelectric liquid crystal mixture, and their transition temperatures and electrooptic properties measured. The largest spontaneous polarization, 4·1 nC cm?2, was obtained at 25°C for the ferroelectric liquid crystal mixture in which the dopant, with a methylene ether linkage, was incorporated. Molecular orbital calculations (MNDO method) for the dopants show that the calculated dipole moments are correlated with the measured spontaneous polarization, and the calculated results explain the experimental results quite well. In addition, it has been found that the conformation of the chiral part is an important factor which affects the magnitude of spontaneous polarization. 相似文献
3.
Goroh Saitoh Toyokazu Nakamura Masayoshi Suzuki Masahiro Satoh Kunikio Yoshio Tetsuya Watanabe 《Liquid crystals》1993,14(6):1753-1761
New chiral dopants, possessing a trifluoromethyl group, have been synthesized. These dopants have different polar groups, located between the chiral centre and the diphenylacetylene core. The polar part is chosen from ester, methylene ether and ether linkages. Each new chiral dopant was mixed with a non-chiral liquid crystal mixture or a ferroelectric liquid crystal mixture, and their transition temperatures and electrooptic properties measured. The largest spontaneous polarization, 4·1 nC cm-2, was obtained at 25°C for the ferroelectric liquid crystal mixture in which the dopant, with a methylene ether linkage, was incorporated. Molecular orbital calculations (MNDO method) for the dopants show that the calculated dipole moments are correlated with the measured spontaneous polarization, and the calculated results explain the experimental results quite well. In addition, it has been found that the conformation of the chiral part is an important factor which affects the magnitude of spontaneous polarization. 相似文献
4.
New antiferroelectric liquid crystals (AFLCs) with a trifluoromethyl group at the chiral centre were synthesized using optically active 3-(4-methoxyphenyl)-4,4,4-trifluorobutanoic acid. The new AFLCs showed the phase sequence on cooling: isotropic liquid (I)-smectic A (Sa) phase-antiferroelectric (AF) phase-crystal (Cr). In the antiferroelectric phase, a d.c.-threshold, a double hysteresis loop, a small dielectric constant value and two sharp switching-current peaks were observed. These are the first examples that are AFLCs which do not have a carbonyl moiety in the molecule. 相似文献
5.
《Liquid crystals》1998,25(6):733-744
Miscibility phase diagrams of mixtures of side-on side chain liquid crystalline polymers (s-SCLCP) and low molar mass liquid crystals (E48 and E44) have been established by means of polarized optical microscopy and light scattering. E48 and E44 are cyanobiphenyl-based eutectic nematic liquid crystal (LC) mixtures with nematic-isotropic transition temperatures of 93 and 105 C, respectively. The phase diagram of the s-SCLCP/E48 system reveals the coexistence of an isotropic nematic region and a single nematic phase in order of descending temperature. The single nematic phase suggests that the pair is miscible in the nematic region. On the other hand, the s-SCLCP/E44 mixture shows liquid liquid and nematic nematic coexistence phases, suggestive of the immiscibility character of the pair. These nematic phase diagrams of the s-SCLCP/E48 and s-SCLCP/E44 have been analysed in the context of the combined Flory-Huggins (FH) free energy for isotropic mixing and the Maier-Saupe (MS) free energy for nematic ordering of the mesogens. This combined FH/MS theory is capable of predicting the observed nematic phase diagrams consisting of liquid liquid, liquid nematic, nematic nematic, and the pure nematic regions. The change of colour accompanying the appearance and disappearance of the inversion walls may be attributed to the temperature dependence of birefringence. 相似文献
6.
《Liquid crystals》2001,28(3):437-444
The Langmuir films of two liquid crystal materials, 4-octyl-4'-cyanobiphenyl (8CB) and 4-pentyl-4"-cyano-p-terphenyl (5CT), and of their mixtures have been studied by recording surface pressure-area isotherms and Brewster angle microscopy (BAM) images. The pure liquid crystals revealed very different characters of the surface pressure-area isotherms indicating different organization of the molecules and different molecular interactions in the monolayer at the water-air interface. The surface pressure-area isotherms of Langmuir films formed from 8CB/5CT mixtures give evidence for phase separation of the components over the whole range of molar fractions. Similar conclusions have been drawn on the basis of BAM image analysis. 相似文献
7.
The Langmuir films of two liquid crystal materials, 4-octyl-4'-cyanobiphenyl (8CB) and 4-pentyl-4"-cyano-p-terphenyl (5CT), and of their mixtures have been studied by recording surface pressure-area isotherms and Brewster angle microscopy (BAM) images. The pure liquid crystals revealed very different characters of the surface pressure-area isotherms indicating different organization of the molecules and different molecular interactions in the monolayer at the water-air interface. The surface pressure-area isotherms of Langmuir films formed from 8CB/5CT mixtures give evidence for phase separation of the components over the whole range of molar fractions. Similar conclusions have been drawn on the basis of BAM image analysis. 相似文献
8.
Tomoya Kitazume Sadanori Kaneko Takashi YamazakiShoji Watanabe 《Journal of fluorine chemistry》1993,60(2-3):135-140
A practical synthetic route to a series of (R)- or (S)-(1-trifluoromethyl)alkyl 4-hydroxybenzoateshas been developed. These materials were prepared by the reaction of p-hydroxybenzoic acid with (R)- or (S)-1-(trifluoromethyl)alkanols in the presence of p-toluenesulfonic acid under reflux conditions. Further reaction with the acid chloride of4′-alkoxybiphenyl-4-carboxylic acid gave the desired liquid crystals. 相似文献
9.
The discovery of nematic phase in 3-fluoro-4-trifluoromethyl-4?-(4?-alkyl [trans, trans-1,1?-bicyclohexyl]-4-yl) 1,1?-biphenyls (n = 2, 3, 4, 5) is an accidental affair. A convenient method was used for the synthesis of these target compounds. After the preparation of the intermediate with trifluomethyl group, the target compounds were synthesised by Suzuki cross-coupling reaction. Then, these phase transition temperatures were measured by polarising textural observation, which confirmed the existence of single nematic phase. These temperatures were also measured by differential scanning calorimetry, which showed that the clearing point of compound (n = 3) is 267℃. The possible mechanism of occurrence of unique nematic phase was discussed on the basis of the principles of fluorine chemistry. 相似文献
10.
《Liquid crystals》1997,22(3):317-326
A perturbed hard-sphere-chain (PHSC) equation of state is presented to compute nematicisotropic equilibria for thermotropic liquid crystals, including mixtures. The equation of state consists of an isotropic term and an anisotropic term given by the Maier-Saupe theory whose contribution disappears in the isotropic phase. The isotropic contribution is the recently presented PHSC equation of state for normal fluids and polymers which uses a reference equation of state for athermal hard-sphere chains and a perturbation theory for the squarewell fluid of variable well width. The PHSC equation of state gives excellent correlations of pure-component pressure-volume-temperature data in the isotropic region and, combined with the Maier-Saupe theory, correlates the dependence of nematic-isotropic transition temperature on the pressure. Theory also predicts a nematic-isotropic biphasic region and liquid-liquid phase separation in a temperature-composition diagram of binary mixtures containing a nematic liquid crystal and a normal fluid or polymer. Theory and experiment show good agreement for pure fluids as well as for mixtures. 相似文献
11.
Sebastian Gauza Chien-Hui Wen Benjamin Wu Shin-Tson Wu Ania Spadlo Roman Dabrowski 《Liquid crystals》2006,33(6):705-710
High birefringence and low viscosity isothiocyanate liquid crystal single compounds, and eutectic mixtures based solely on unsaturated rigid core structures, are reported. Extraordinarily high values of figure-of-merit were observed at room temperature for the formulated nematic mixtures. Potential applications of such mixtures for laser beam steering at λ = 1.55 µm using optical phased arrays are emphasized. 相似文献
12.
《Liquid crystals》1998,24(2):173-175
Two homologous series with the terminal oxime group are synthesized to evaluate the effect of the oxime group on mesogenic properties of the system. It is observed that oxime formation eliminates the smectic mesophases exhibited by parent homologous series. The nematic phase exhibited by mesogens has higher thermal stability because of intermolecular H-bonding. 相似文献
13.
Three series of liquid crystals based on isothiocyanatotolane core with terminal alkenoxy groups (4A-1?4C-2) have been synthesised via multi-step reactions. Their thermotropic mesophases and physical properties are evaluated by comparison with the alkoxyl analogues (4a-1?4c-2). The results show that the isothiocyanatotolane LCs with alkenoxyl terminals deliver higher birefringence (0.410~0.436), lower melting points, lower melting enthalpies and viscosity. The effects of the alkenoxy terminal groups and the lateral fluoro substituents on the mesomorphic behaviour and physical properties are discussed. The formulation of the mixture containing isothiocyanatotolane liquid crystals with alkenoxyl terminals provides evidence of an useful candidate for liquid crystal photonics. 相似文献
14.
《Liquid crystals》2001,28(8):1171-1176
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. 相似文献
15.
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. 相似文献
16.
In this paper we employ a relatively simple theory to show how a nematic disclination line can act as a nucleation site for the growth of the isotropic phase. With this theory we are able to find analytical expressions for the critical temperature of nucleation and the behaviour of the core radius as a function of temperature. We are then able to compare these results with a previous numerical model of this effect. 相似文献
17.
The behaviour of a nematic liquid crystal when it is spun about an axis orthogonal to a magnetic field is predicted to be controlled by the critical angular velocity, ωc. For spinning speeds below ωc theory shows that the director makes an increasing angle with the field until at ωc this angle is 45°. Above ωc the director should rotate with an angular velocity slightly less than that of the sample. Observation in both regimes allows ωc to be determined; since it depends on the ratio of the diamagnetic anisotropy to the rotational viscosity coefficient of the nematic, this ratio can be measured. However, an experimental investigation by Eastman et al. [1], suggests that the theoretical relationship between ωc and this ratio may be in error by a factor of about four. We have reanalysed their data in an attempt to check this important claim and have found that there is in fact good agreement between theory and experiment. 相似文献
18.
《Liquid crystals》2000,27(10):1301-1304
In this paper we employ a relatively simple theory to show how a nematic disclination line can act as a nucleation site for the growth of the isotropic phase. With this theory we are able to find analytical expressions for the critical temperature of nucleation and the behaviour of the core radius as a function of temperature. We are then able to compare these results with a previous numerical model of this effect. 相似文献
19.
20.
《Liquid crystals》2001,28(9):1389-1402
A complete numerical study of a two-dimensional nematic backflow problem is presented. Nematodynamic equations are reviewed, and characteristic scales are introduced. The relaxation under the application and suppression of a magnetic field is studied in square- and rectangular-shaped cells. Solutions for the flow fields, director fields, and director time derivative fields are given and these are interpreted to gain a qualitative understanding of the problem. The backflow is found to depend critically on the geometry of the cell. The complete solution is compared with the simplified approach in which the backflow is neglected. The discrepancy depends strongly on the cell geometry. 相似文献