A Polyester Forming a Thermotropic Cholesteric Phase

Mesomorphic polyesters were synthesized from 4, 4′-dihydroxy-α-methylstilbene and adipic acid (P-6) or (+)-3-methyl adipic acid (P-6M). P-6 forms a thermotropic nematic phase and P6-M a thermotropic cholesteric phase. The nematic phase of P-6 could easily be identified by optical microscopy. For both polymers we observed a biphasic region in which the isotropic and liquid crystalline phases coexist. Bright colors were obtained by increasing the pitch of P6-M by admixture with either a low molecular weight nematogen or with polymer P-6, and also by synthesizing a copolymer containing the two dibasic acids. The copolymeric cholesteric phase, which is stable between 199 and 282[ddot]C, had a predominately planar texture, and these features could be retained in the solid state by quenching to produce a film having a deep blue color at room temperature. The role of the degree of polymerization upon the development of organization, and parameters, of the mesophase is discussed.     

Nano Molecular Self Assembly in the Formation of Induced Mesomorphism in Mixture of ChCl,DTAC, and EG

The multi-component system of cholesteryl chloride (ChCl), dodecyl trimethylammonium chloride (DTAC), and ethylene glycol (EG) exhibits very interesting liquid crystalline mesophases like cholesteric and SmA, SmC, and SmB phases sequentially when the specimen is cooled from its isotropic phase. These phases have been characterized by employing optical and X-ray studies. Pitch of the cholesteric phase has been calculated and discussed. Variation of pitch from the cholesteric phase to smectic phase is smooth and continuous. The temperature variation of optical anisotropy and electrical-conductivity has also been discussed. It has been found that wherever there is a phase transition, the value of electrical susceptibility changes appreciably.     

Chiral Gay–Berne model for molecular dynamics computer simulations

Abstract

We have extended the chiral Gay–Berne (GB) pair potential of Memmer and co–workers [Liq. Cryst. (15), 345 (1993)] to the general case of biaxial ellipsoids, and we provide explicit expressions for the gradient and the torques to be used in molecular dynamics (MD) codes. To test our results against published results we have performed MD simulations of samples formed by N?=?1024 uniaxial GB ellipsoids with constant volume, and we have studied how the thermotropic behavior is affected by particle chirality. We have run temperature scans starting from isotropic samples and found clear signatures of the spontaneous formation of both lower temperature blue and cholesteric phases.     

Tolanes derivatives

The phase behavior for each of two linear thermotropic liquid crystalline polyesters with a corresponding low molecular weight liquid crystal of similar structure have been investigated. Two distinct types of phase diagrams have been obtained for binary mixtures of a polymer, one containing an in-chain azoxybenzene moiety mixed with para-azoxyanisole and one containing a naphthalene unit mixed with a dimethylester liquid crystal. These phase diagrams were studied by DSC, polarized light microscopy and x-ray diffraction. From this understanding of the physical mixtures a transesterification reaction incorporating the bifunctional low molecular weight liquid crystal by a solid-state reaction into the naphthalene-containing polyester was undertaken. This reaction may be viewed as a potential new processing technique for polymers. The thermal stability of an interreacted blend was shown to be superior to that of either individual component by thermogravimetric analysis. Thus, the potential new processing technique features a lower melting, lower viscosity blend followed by the incorporation of the dimethylester liquid crystal into the polyester main chain producing a more rigid, more stable polymer backbone.     

Synthesis and mesomorphic behavior of symmetrical chiral liquid crystal dimers incorporating ester linked biphenyl- naphthyl cores and terminal vinyl group

A series of symmetrical chiral, liquid crystal dimeric molecules possessing ester- linked, biphenyl-naphthyl cores with varied spacer lengths and terminal vinyl groups have been synthesized using Naproxen as the synthetic precursor. The synthesized symmetrical chiral dimers were characterized by 1H NMR spectroscopy, and their liquid crystalline behavior was confirmed by DSC and HOPM studies. Structural effects on the mesomorphic and physicochemical properties were investigated in terms of variation of chiral chain length. The synthesized dimeric compounds exhibited SmX^*, SmC^*, SmA^*, N^*, BPI^*, and BPII^* mesophase sequences. An odd-even effect was observed in the dimers and the duration of the mesophase decreased with increasing spacer length. The synthesized vinyl substituted liquid crystalline dimers are particularly useful in understanding liquid crystal polymorphism and act as model compounds for liquid crystal polymers.     

Effect of various external factors and pretransitional phenomena on structural transformations in cholesteric liquid crystals

The publications on low-molecular thermotropic liquid crystals with cholesteric structures have been reviewed. The effect of an applied electric field on cholesteric structures is studied. Bistability of the cholesteric-nematic transition, electric field-induced color textures of cholesteric mixtures, and electro-optics of amorphous cholesteric structures are considered as well as pretransitional (blue and TGB) phases, discotic cholesterics, PDLC films, flexoelectric electro-optics, and photostimulated switching in cholesterics.     

In situ composites based on blends of PEEK and thermotropic liquid crystalline polymer

A series of blends were prepared by mixing pellets of the thermotropic liquid crystalline polymers (TLCP) with poly (ether ether ketone)(PEEK) in the dry state under injection mouldingmolding conditions. The mechanical properties of blends were measured, and it is proved that the mechanical properties of blends are better than those of their matrix. Compared with the thermoplastic matrix, the tensile modulus and strength of the blends increased obviously, with the addition of only 2 wt% LCP. At the same time, the addition of TLCP decreased the melt viscosity of the blends.     

Investigation of the Homologous Series of 4-Acetyl-4′-n-Alkanoyloxyazobenzenes by X-ray Diffraction

This paper reports an investigation by X-ray diffraction of the homologous series of liquid crystalline 4-acetyl-4′-n-alkanoyloxyazobenzenes. By using two independent parameters, namely the temperature and the paraffinic chain length, it was possible to obtain some structural information on two solid phases for comparison with a previously reported model for the S_A phase of the same series. In particular, the molecular layer thickness and, by using previously reported dilatometric data, the aromatic sublayer thickness, the methylene group thickness, the molecular area and the aromatic stem inclination angle were obtained for the different phases.     

X-Ray Diffraction Studies of Liquid Crystalline Polymers

Thermotropic liquid crystalline copolyesters display an ordered fluid phase at elevated temperatures which permits the development of unusually high orientation at ambient temperatures. The transition which occurs upon cooling the high temperature nematic liquid crystalline phase very rapidly (e.g. fiber spinning) results in a polymeric glass with nematic structural order. Annealing increases structural order from the nematic glass toward ideal three dimensional crystalline order. Precision X-ray diffractometry has been used to directly observe changes in structural correlations which occur with annealing. Structural transitions range in character in these copolyesters from no change upon annealing to a transition from fully two dimensional to fully three dimensional structural order. Increased three dimensional order also results in substantially increased first order character of the high temperature phase transition. The chemical structure of co-monomers determines, in part, the final degree of dimensionality.     

Main-chain biodegradable liquid crystal based on diosgenyl end-capped poly(trimethylene carbonate)

Main-chain biodegradable liquid crystal based on c diosgenyl end-capped poly(trimethylene carbonate) [Dios-(TMC)n] was investigated. The novel liquid crystal was synthesized through ring-opening polymerization of trimethylene carbonate initiated by diosgenin, without adding any catalyst. The chemical structure of resulting polymers was confirmed by ¹H NMR. The liquid crystalline properties were validated by X-ray diffraction, differential scanning calorimetry, and polarising optical microscopy. The results showed that the synthesized Dios-(TMC)n exhibited liquid crystallinity in particular temperature ranges because of the incorporation of the diosgenin moieties.     

Phase transition and thermal stability of reentrant smectic phase in mixture of liquid crystalline materials

In the present work, our investigation is to study the optical and thermal properties of the binary mixture of cholesteric and nematic compounds namely, decyloxy benzoic acid (DBA), and cholesteryl chloride (ChCl), which exhibits different liquid crystalline phases with reentrant smectic-A phase. The reentrant smectic-A phase has been observed at different concentrations and at different temperatures. The existence of reentrant smectic-A phase has been observed by optical microscopic studies. The temperature variation of optical anisotropy, X-ray and helical pitch of the cholesteric (N^*) phase has also been discussed.     

Optical Rotatory Dispersion Measurements of the Liquid Crystalline Blue Phases in Thick Layers

The results of optical rotatory dispersion (ORD) measurements in liquid crystalline blue phases (BP) are reported for pure compounds and mixtures. They have been performed on polycrystalline samples (thick layers). Two features distinguish their spectra from those obtained from liquid single crystals:

(1) The magnitude of the rotation is much smaller, and

(2) no sharp anomalous ORD region is present.

The spectra possess a weak, broad anomalous region. Their sign and wavelength dependence follows the sense and pitch of the cholesteric helix. ORD experiments with mixtures of the same cholesteric esters with a nematic substance yield results typical of well oriented samples. The spectra exhibit larger rotation angles and a significantly smaller anomalous region.     

New chiral liquid crystal materials based on menthol: Synthesis and phase behavior

To study structure-mesomorphism relationships of chiral materials based on menthol, a series of chiral compounds containing menthyl group were synthesized. Their chemical structures, formula, and the purity were characterized by Fourier transform infrared (FTIR), proton nuclear magnetic resonance (¹H NMR), and elemental analyses. The corresponding phase behavior was investigated with differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). The effect of the mesogenic core, flexible spacer, and terminal groups on the mesophase formation and type was discussed. The compound 4-menthyloxyacetoxybenzoyloxy-4′- (6-bromohexyloxy)biphenyl showed the smectic A (S_A) and cholesteric phases on heating cycle, and a cubic Blue Phase, chiral smectic C (S_C^*), S_A and cholesteric phases on cooling cycle. However, the compound 4-menthyloxyacetoxybenzoyloxy-4′-(4-bromobutoxy)biphenyl showed enantiotropic S_C^*, S_A and cholesteric phases, moreover, the platelet texture of a cubic Blue Phase was also observed on cooling cycle. The methacrylate monomer with six flexible methylene units and three phenyl rings as mesogenic core only showed cholesteric phase, while the methacrylate monomer with four methylene unit and three phenyl rings showed the S_C^* and cholesteric phases. However, when the terminal methacryloyloxy groups in the monomers were substituted by thiophenylacryloyloxy groups, the corresponding monomers all show no mesophase. With increasing the rigidity of mesogenic core or decreasing the flexible methylene spacer length, the corresponding melting temperature (T_m) or isotropic temperature (T_i) increased.     

Thermotropic Liquid-Crystalline Polymers,Re-Entrant and Discotic Liquid Crystals. A Bibliography for 1977–1984

This bibliography contains bibliographic data of books and papers concerning the thermotropic liquid-crystalline polymers, re-entrant and discotic liquid crystals for 1977–1984 years. The bibliography of the thermotropic liquid-crystalline polymers contains also bibliographic data of papers describing both the thermotropic and lyotrophic behavior of the liquid-crystalline polymers, liquid-crystalline melts, solutions of thermotropic liquid-crystalline polymers, solutions of polymer chains in a nematic solvent and some polymerization problems. In this bibliography are included also bibliographic data of papers which according to the citation in the literature are important for the study of both the thermotropic and lyotropic liquid-crystalline polymers. In the bibliography of the re-entrant liquid crystals (at atmospheric pressure) are included the papers published after the first work in this field of Cladis (Phys. Rev. Lett. 35, 48–51 (1975)) up to the end of 1984 year. Similarly, in the bibliography of the discotic liquid crystals are included the papers published after the first work of Chandrasekhar, Sadashiva and Suresh (Pramana 9, 477–480, (1977)) also up to the end of 1984 year.     

Liquid Crystal Auto-Induction and Amplification Function for Circularly Polarized Luminescence (CPL) with High gem-Value,and Dynamically Controllable CPL Devices

Optically active phenylenevinylene derivatives with fluorescence are employed for preparation of a cholesteric liquid crystal based circularly polarized light (CPL) emission device. The device shows intense CPL with a quite large value of the g_em-factor (= 0.6) and quick CPL light switching driven by cholesteric-nematic transition with a homeotropic alignment. This research develops the auto-induction of fluorescent chiral inducers in host liquid crystal for formation of a helical structure with CPL amplification. The present research applies a classical LC light-scattering system using chiral technology as a new method for obtaining CPL dynamic control with an intense g_em-factor.     

The Preparation and Properties of the α,ω-bis(4,4′-Cyanobiphenyloxy)Alkanes: Nematogenic Molecules with a Flexible Core

The first twelve members of the homologous series of α,ω-bis(4,4′-cyanobiphenyloxy) alkanes have been synthesised. The compounds are nematogenic, although the mesophases for the first and third members of the series are monotropic. Both the nematic-isotropic transition temperature and the entropy of transition exhibit a pronounced dependence on the length of the flexible core; this is analogous to that found for main chain thermotropic liquid crystal polymers.     

Topology of a Surface of the Phase Diagram of the Cholesteric Lyotropic Mesophase: Potassium Laurate/1-Decanol/Water/I-N-Lauroyl Potassium Alaninate

A surface of the phase diagram of the lyotropic cholesteric mesophase of potassium laurate/1-decanol/H₂O/l-N-lauroyl potassium alaninate (l-LAK) is studied by optical microscopy and X-ray diffraction as a function of the relative molar concentration of l-LAK and temperature. Cholesteric discotic and calamitic phases are observed and also a large domain of biaxial cholesteric phase. The inverse pitch as a function of the l-LAK relative molar concentration presents a linear behavior in the doping range studied. The l-LAK doping and its influence in favoring cholesteric calamitic phase formation are discussed in terms of the packing of the l-LAK amphiphile in the bilayer and the orientational fluctuations of the intrinsically biaxial correlation volumes.     

Chiral Induction in Liquid Crystals with Dopants Derived from 1-Phenyl-2-Aminoalcohols

New chiral additives derived from 1-phenyl-2-aminoalcohols have been prepared and tested. Especially ephedrine and pseudoephedrine as chiral auxiliaries with two asymmetric C atoms offer functional groups of divergent reactivity. Dopants prepared by acylation with promesogenic agents can be used in various electro-optic devices. A specific utilization concerns bistable cholesteric liquid crystal displays with stacked double layer construction in order to enhance the luminance of reflected light. Further, the solubility in nematic mixtures, the long term phase behavior, the dopant's impact on textures and phase behavior, the electro-optic response and the photostability of cholesteric mixtures have been investigated.     

Alkyloxy azo-cinnamate ester based thermotropic liquid crystals and their photophysical investigations

Two series of rod shaped Schiff base containing azo-cinnamate thermotropic liquid crystalline compounds were synthesized and characterized. These molecules have four different alkyl spacers (n = 6, 8, 10, and 12) at one end and a dodecyloxy chain at another end (n = 12) which influence their liquid crystalline properties. Liquid crystallinity commence from six methylene spacer onwards in the series exhibiting with Nematic to Smectic-C mesophases. Analytical data confirm the molecular structures of homologues series of compounds. The characteristic texture of liquid crystalline phases obtained using polarizing‐light microscope with a heating stage. The structural transformation of these liquid crystals was confirmed by differential scanning calorimetry. All the compounds exhibited various calamitic mesophases with wide mesomorphic temperature ranges. The relationship between structure and mesomorphic properties was discussed in framework of geometrical configuration of central unit, linking part, and length of alkoxy chains. Photosensitive azobenzene group undergoes photoisomerization under UV light and monitored by UV-Visible spectroscopy.     

Nano segregation and thermal stability of TGB and re-entrant smectic-A phases in a ternary mixture of liquid crystalline materials

The ternary system of 4’-n-octyloxy-4-cyanobiphenyl (8OCB), 4-cyano-4’-Pentyl teraphenyl (5CT), and cholesteryl nonanoate (CN) exhibits very interesting unusual liquid crystalline phase of N^* (cholesteric), twisted grain boundary (TGB) phase, and re-entrant smectic-A (ReSmA) phases and it is obtained sequentially when the specimen is cooled from isotropic phase. These phases have been characterized by using X-ray and optical texture studies. The temperature variations of electrical conductivity have been discussed.