Narrow Results

The mesogenic behavior and electronic properties of hydrogen bond ferroelectric liquid crystal (HBFLC) complex are studied using experimental and theoretical techniques. HBFLC complex is synthesized from mesogenic 4-hexyloxy benzoic acid (6O BA) as the proton donor and nonmesogenic chiral DL-tartaric acid (DLTA) as the proton acceptor through intermolecular hydrogen bonding. Molecular geometry of DLTA+6O BA HBFLC complex is optimized by density functional theory (DFT) calculation. An interesting observation is that polarizing optical microscope (POM) study confirms that the HBFLC complex exhibits thermochromic behavior in chiral nematic (N${}^{\ast })$ along with induced nontitled smectic G^* phases. Another noteworthy observation is the manifestation of tripartite temperature stages. Fourier-transform infrared spectroscopy (FTIR) and natural bond orbital (NBO) analysis elucidate the intermolecular hydrogen bond between mesogenic (6O BA) and nonmesogenic (DLTA) compounds. Further, frontier molecular orbital (FMO) study and electrostatic potential (ESP) analysis explore the reactivity sites, intermolecular charge transfer and electronic behavior of HBFLC complex.

In this work, the effect of thin films on the orientational, thermotropic and optical properties and on the peculiarities of the nematic–isotropic liquid phase transition has been carried out.

The planar textures of MBBA+EBBA eutectic mixture on the surfaces coated with Al₂O₃ and ZrO₂ thin films have been obtained. The optical and thermodynamical parameters of the obtained, oriented textures have been determined. The effect of thin films on the temperature width of heterophase region and on the nematic–isotropic liquid phase transition temperatures has been investigated. The shift of the phase transition temperatures and the change of the temperature width of the heterophase region have been revealed.

For the analysis of peculiarities of the nematic–isotropic liquid phase transition and the heterophase regions of this transition, the mean field theory has been used.

A new series of thermotropic polyurethanes containing biphenyl units was synthesized by polyaddition reaction of diisocyanates such as 2,6-tolylene diisocyanate, 2,5-tolylene diisocyanate, 2,4-tolylene diisocyanate, and 1,4-phenylene diisocyanate, with 4,4□-bis(9-hydroxynonoxy)biphenyl (BP9). Structures of the monomer and the corresponding polymers were identified using FT-IR and ¹H NMR spectroscopic methods. BP9 exhibited a smectic type mesophase, however, nematic phase was found for all synthesized liquid crystalline polyurethanes except for 1,4-phenylene diisocyanate/BP9 based polyurethane. Their phase transition temperatures and thermal stability were investigated by differential scanning calorimetry (DSC), optical polarizing microscopy, and X-ray scattering. The infrared study indicated that the hydrogen bonding among urethane linkages attributed to the mesomorphism. Thermal gravimetric analysis (TGA) of synthesized polyurethanes showed that no weight loss of the polymers observed up to 280°C.

In this work, effect of thickness of the liquid crystalline layer on the morphologic, thermotropic and thermodynamical properties of the nematic–isotropic liquid and isotropic liquid–nematic phase transitions in Shiff based liquid crystals has been investigated.

The shift of temperatures of the nematic–isotropic liquid and isotropic liquid–nematic phase transitions to the lower temperatures and the widening of linear and temperature widths of the heterophase regions of these phase transitions by the increase in the thickness of liquid crystalline layer have been found.

The effect of thickness of liquid crystalline layer on morphologic, thermotropic and thermodynamical properties of liquid crystals under investigations is connected with change of interaction energy between liquid crystalline molecules and reference surfaces.