Migration of molecules in p-bromochlorobenzene with vacancies in its structure

Based on polarization measurements of the low-frequency Raman spectra of p-bromochlorobenzene and calculations of the frequency spectra of lattice vibrations by the Dean method it is shown that the structure may contain vacancies. Their presence affects the appearance of additional lines in the low-frequency spectrum, particularly in the vicinity of 70 cm⁻¹, and their positions depend weakly on the orientational disorder of the molecules with respect to the para substituents. The activation energies for diffusion in a randomly disordered p-bromochlorobenzene crystal with vacancies in the structure is calculated from atom-atom potentials. It is shown that the value of the activation energy varies along a selected direction and depends on the arrangement of the p-bromochlorobenzene molecules with respect to the para substituents, in contrast to the results for ordered p-dibromobenzene and p-dichlorobenzene. Fiz. Tverd. Tela (St. Petersburg) 40, 1835–1838 (October 1998)     

Reflection spectrum of a cholesteric liquid crystal with structural defects

An expression is obtained for the reflection coefficient of circularly polarized light normally incident on the film of a cholesteric liquid crystal with a variable helix pitch. It is shown that, in the case of a single defect (local change in the helix pitch), the spectrum of light reflection from a cholesteric acquires a dip corresponding to the defect mode. New qualitative features appear in the reflection spectrum of a cholesteric with two defects as the distance between them varies.     

Electro- and magneto-optical switching of defect modes in one- dimensional photonic crystals

The transmission spectra of polarized light waves in a photonic crystal/liquid crystal (PC/LC) cell placed between crossed polarizers and controlled by an electric or magnetic field have been studied experimentally and theoretically. Electro- and magneto-optical switching based on the interference of polarized defect modes has been demonstrated. The transmission spectra of the PC/LC cell have been calculated as a function of the voltage applied to the LC layer and the magnetic field strength. The results of the calculations agree well with the experimental data.     

One-dimensional photonic crystals with a planar oriented nematic layer: Temperature and angular dependence of the spectra of defect modes

Transmission spectra of a one-dimensional photonic crystal (PC) formed by two multilayer dielectric mirrors and a planar oriented layer of 5CB nematic liquid crystal (LC) that is sandwiched between these mirrors and serves as a structure defect are investigated experimentally. Specific features of the behavior of the spectrum of defect modes as a function of the angle of incidence of light on the crystal are studied for two polarizations: parallel and perpendicular to the director of the LC; the director either lies in the plane of incidence or is perpendicular to it. It is shown that, for the configurations considered, the maxima of the defect modes shift toward the short-wavelength region as the tilt angle of incidence radiation increases; this tendency is more manifest for the parallel-polarized component, when the director lies in the plane of incidence. In the latter case, the width of the photonic band gap (PBG) appreciably decreases. The temperature dependence of the polarization components of the transmission spectra of a PC is investigated in the case of normal incidence of light. The spectral shift of defect modes due to the variation of the refractive index of the LC at the nematic-isotropic liquid phase transition point is measured. It is shown that, in real PCs, the amplitude of defect modes decreases when approaching the center of the band gap, as well as when the number of layers in the dielectric mirrors increases. Theoretical transmission spectra of the PCs calculated by the method of recurrence relations with regard to the decay of defect modes are in good agreement with experimental data.     

Dielectric properties of liquid crystals of the cyano derivative compounds with different fragments in the molecular core

This paper reports on the results of investigations into the influence of variations in the chemical composition of the aromatic core of cyano-containing molecules of liquid crystals on their dielectric properties in the frequency range 1–2000 MHz. It is shown that the dispersion of the longitudinal permittivity is adequately described by the sum of two Debye processes with different weighting factors and relaxation times. The frequency dependence of the transverse permittivity is well approximated by the Debye process with a continuous distribution of relaxation times in a specified range. It is established that the replacement of one benzene ring in the biphenyl core of the 5CB liquid-crystal molecule by a cyclohexane (or bicyclooctane) fragment leads to a considerable decrease in both relaxation times for the longitudinal permittivity, a change in the low-frequency limit of the relaxation time range for the transverse permittivity, and the evolution of the frequency dependence of the dielectric anisotropy.     

A Bandpass Filter Based on Dielectric Layers with a Strip Conductor Subwavelength Grating at Their Interfaces

Doklady Physics - The design of a multilayer bandpass filter has been investigated, in which each of the half-wavelength resonators consists of two dielectric layers with outer strip conductor...     

Mixed crystals of p-dichlorobenzene with p-bromchlorobenzene in the presence of vacancies in the structure

Polarization studies of low-frequency Raman spectra of solid solutions of p-dichlorobenzene with p-bromchlorobenzene (50% p-dichlorobenzene) were carried out. Analysis of the lattice vibration spectra of these mixed crystals shows that vacancies can be present in their structure. The presence of vacancies is responsible for the emergence of additional lines, including those in the 70 cm^?1 region. The calculation of the diffusion activation energy in a mixed crystal proves that its magnitude is determined by the spatial arrangement of p-bromchlorobenzene molecules in the lattice, their orientation relative to parahalides, and (to a lesser extent) temperature variations.