Intercalated smectic-A structures in a new class of laterally branched substances

X-ray, DSC and optical studies of a new class of substances with aromatic rings in the lateral branches are reported. The thermal behaviour of the substances is discussed. The X-ray measurements lead to a structural model of the SA phases consisting of layer structures with intercalating molecules.     

A multigrid method for predicting periodically fully developed flow

The use of multigrid methods in complex fluid flow problems is still under development. In this paper a full multigrid procedure has been incorporated in a finite volume solution for predicting fully developed fluid flow in a streamwise periodic geometry. Steady computations in two-dimensional body fitted co-ordinates have shown considerable savings in computation time by this multigrid method.     

Raman spectroscopy of carbon fibres

Investigations of coated carbon fibres are reported using Raman spectroscopy. Relationships between different process parameters (for example precursor concentration, reactor temperature and various precursors) and the resulting types of carbon fibres are discussed.     

Stressed states in domain switching of ferroelectric liquid crystal devices

In this paper we show that the director profile of a low pre-tilt surface stabilized ferroelectric liquid crystal passes through quasi-static stressed states during domain switching under direct drive conditions. Using polarized stroboscopic microscopy, we have observed two quasi-static transmission levels during a domain switching transition from dark to light. This is a result of the directors reorienting into stressed profiles both before and after the chevron interface has switched. By modelling the interaction between the elastic forces and the torque from the applied field, we have determined these voltage dependent director profiles and, by calculating their corresponding transmissivities, have shown very good agreement with the experimentally observed values.     

Raman spectroscopic investigations of the structure and phase transitions of liquid crystalline lead(II) alkanoates

Lead(II) alkanoates with even chain lengths from octanoate to octadecanoate have been investigated by Raman spectroscopy. In the low frequency region, transverse and longitudinal acoustical modes (TAM, LAM) have been assigned. It was shown that LAM-1 is the vibration of the double chain with the node of the vibration in the Pb²⁺ layer. A fully extended conformation of the chains in the low temperature phase was confirmed. The frequencies and intensities of the LAMs as compared with those of the alkanes and the fatty acids led to an estimate of the force constant and polarizability of the Pb²⁺ -COO^- bond relative to the C-C bond. The defects at the chain ends were investigated in the ρ(CH₃) and v(CC) region. For the intermediate (CM) phase, both the Pb²⁺ layer distance reduction and the chain length independent enthalpy contributions can be attributed mainly to defects at the chain ends.     

High pressure differential thermal analysis of nematic compounds with different molecular shapes

By means of high pressure differential thermal analysis we measured the pressure/temperature phase diagrams of several nematic compounds with different molecular structures. Using pressures up to about 500 M Pa we found strongly nonlinear clearing curves. This behaviour is interpreted as changes from 'weak' intermolecular potentials to 'hard' potentials, or using thermodynarmic arguments, strong pressure dependence of the volume discontinuity at the clearing transitions.     

Di[2-(4-substituted-phenyl)-3-mercapto-propenato]-nickel(II) complexes. Metallo-mesogens exhibiting broad nematic ranges

Di[2-(4-substituted-phenyl)-3-mercapto-propenato]-nickel(II) complexes have been synthesized and investigated. All of them are mesomorphic; they have nematic phases with wide ranges and typical Schlieren textures.     

Photoinduced electron transfer variables: rigidity or orientation?

The relatives photoreactives of bridged-ring systems 1, 3, 5-X and 6-X (X ≡ Cl or Br) have been studied at 254 nm in acetic acid. The formation of photosolvolysis product was rationalized in terms of photoinduced intramolecular electron transfer (ET) processes. The relative ease of ET in these donor—bridge—acceptor model system was analyzed in terms of known ET variables including free-energy changes, orientation effects and ridigity effects. The observed relative photoreactivities agreed better with the calculated free-energy changes when relative rigidities of the electron acceptor termini were evaluated. In general, the more rigid system were more photoreactive.