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.     

Energy and Acid-Base Characteristics of the Surface of Nitramine Fillers for Polymeric Composites

Single crystals of nitramine fillers for special-purpose polymeric composites are characterized by the surface energy and its constituents and also by the acidity of their surface.     

Numerical simulation of achromatic deflecting systems

A deflecting system formed by two parallel-plate capacitors on opposite sides of an optoelectronic element that alters the energy of a beam of charged particles, is calculated numerically. The conditions for correcting the chromatic beam spreading in the plane of the target are found. Good agreement with the results of an approximate analytical calculation is demonstrated. Zh. Tekh. Fiz. 67, 86–88 (December 1997)     

Reactions of cyclammonium cations

The reaction of 1,2-diaminopyridinium salts with -dicarbonyl compounds or -halogeno ketones forms pyrido[1,2-b][1,2,4]triazinium salts. A methyl group present in position 2 of one of these salts condenses with aldehydes, giving styryl derivatives and reacts with orthoesters to give cyanines.For Communication XXII, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1266–1270, September, 1973.     

Lactones ofFerula gigantea

The following substances have been isolated from an acetone extract ofFerula gigantea B. Fedtsch.: a coumarin — umbelliferone, C₉H₆O₂, mp 230–233°C; and sesquiterpene lactones — talassin A, C₂₅H₃₀O₇, mp 188–191°C; malaphyllinin, C₂₄H₂₄O₇, mp 231–235°C; malaphyll, C₂₉H₃₂O₉, mp 212–213°C; and malaphyllin, C₂₆H₂₈O₉, mp 216–218°C. Structures have been proposed for three new sesquiterpene lactones on the basis of an analysis of their spectral characteristics.All-Union Scientific-Research Institute of Medicinal Plants, Moscow. M. V. Lomonosov Moscow State University, Botanical Garden, Moscow. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 490–495, July–August, 1979.     

Visual investigation of the intermediate state in the region of metamagnetic phase transition in ErFeO3

We carried out the first observation of the intermediate state (IS) in the region of metamagnetic phase transition (MPT) in ErFeO₃: an external magnetic field H∥c (H=0–4 kOe), the temperature range 2.15–1.6 K. The ranges of the IS existence and the domain structure (DS) features were determined. Likely mechanisms of the IS thermodynamic stabilization and conditions for its visualization in ErFeO₃-plates with various crystallographic orientations were analyzed. The thermodynamic model of IS was offered: the intermediate state was stabilized by the mechanical stress that accompanies MPT. Excellent agreement with experiment was achieved.     

Electrochemical behavior of silver thin films interfaced with yttria-stabilized zirconia

Thin silver films (100–800 nm) were deposited by physical vapor deposition (PVD) on yttria-stabilized zirconia solid electrolyte. The electric percolation as a function of the film thickness was studied during deposition and annealing using a two-electrode in-situ resistance measurement technique. Electrical percolation was achieved in as-deposited films greater than 5.4?±?0.4 nm; however, thermal treatment (550 °C in air) resulted in film dewetting for Ag films as thick as 500 nm and formation of electronically isolated Ag nanoparticles, as was confirmed by SEM and XPS. In thermally treated samples, stable electronic conductivity associated with a continuous percolated network was only observed in samples greater than 600 nm in thickness. The effect of polarization on the electrochemical reactions at the three-phase (electrode-gas-electrolyte) and two-phase (electrode-electrolyte) boundaries of the electrode was investigated by solid electrolyte cyclic voltammetry (SECV) at 350 °C and P _O2?=?6 kPa. With the application of positive potential, silver oxide (Ag₂O) was found to form along the three-phase boundary and then extends within the bulk of the electrode with increasing anodic potentials. By changing the hold time at positive potential, passivating oxide layers are formed which results in a shift in favor of the oxygen evolution reaction at the working electrode. This oxide forms according to a logarithmic rate expression with thick oxides being associated with decrease in current efficiency for subsequent oxide formation.     

Improved cylindrical mirror energy analyzer

A study has been carried out of the electron-optical properties of improved design of the cylindrical mirror energy analyzer. Both external and internal electrodes of the analyzer are divided into three isolated parts, whereby the potentials on the individual parts can be regulated independently from each other. In symmetric operating mode at identical potentials on the side parts of the electrodes, a significant increase has been obtained in resolving power and light-gathering power of the analyzer compared to the standard design of the cylindrical mirror. In asymmetric operating mode, which is implemented in a linear potential distribution on the external electrode, the conditions have been found under which the linear dispersion of the analyzer increases several times.