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A detailed x-ray scattering study has been performed in the temperature range of the smectic- A phase for the liquid crystal compounds dodecylcyanobiphenyl (12CB) and octylcyanobiphenyl (8CB) confined in different controlled-pore glasses (CPGs) characterized by their average void radius R . On decreasing the temperature in bulk samples the layer thickness is increasing for 12CB and decreasing for 8CB, respectively. In nontreated CPG samples the layers dilate significantly with respect to the bulk liquid crystal. In order to explain the layer thickness behavior on varying temperature and R , one has to take into account molecular details of the liquid crystalline samples as well as memory effects.

Measurements of the quasistatic and frequency dependent electrical conductivity below 1 MHz were carried out on wet-spun, macroscopically oriented, calf thymus deoxyribonucleic (DNA) and umbilical cord hyaluronic acid (HA) bulk samples. The frequency dependence of the electrical conductivity in the frequency range of approximately 10(-3) - 10(6) Hz of both materials is surprisingly rather similar. Temperature dependence of the quasistatic electrical conductivity above the low temperature saturation plateau can be well described by the activated Arrhenius law with the activation energy of approximately 0.8 eV for both DNA and HA. We discuss the meaning of these findings for the possible conduction mechanism in these particular charged polyelectrolytes.

The high-resolution calorimetric study was carried out on octylcyanobiphenyl liquid crystal (LC) confined to various controlled-pore glass (CPG) matrices with silane-treated surface. The diameter of the voids cross section ranged between 23.7 and 395 nm. The results are compared to those obtained previously on CPG voids nontreated with silane. We found a striking similarity between the shifts in the isotropic to nematic and nematic to smectic-A phase transition temperatures as a function of the void radius in which order parameter variations at the LC-void interface play the dominant role. Weaker temperature shifts are observed in silane-treated samples, where surface ordering tendency is larger. In nontreated samples, a finite-size scaling law in the maximum value of the heat capacity at the nematic to smectic-A transition was observed for void diameters larger than 20 nm. In silane-treated samples, this behavior is considerably changed by surface wetting interactions.

We present a calorimetric study of the phase behavior of octylcyanobiphenyl (8CB) liquid crystal confined to a controlled-pore glass (CPG). We used CPG matrices with characteristic void diameters ranging from 400 to 20 nm. In bulk we obtain weakly first-order isotropic to nematic (I-N) phase transition and nearly continuous character of the nematic to smectic-A (N-SmA) phase transition. In all CPG matrices the I-N transition remains weakly first order, while the N-SmA one becomes progressively suppressed with decreasing CPG pore radius. With decreased pore diameters both phase transition temperatures monotonously decrease following similar trends, but increasing the stability range of the N phase. The heat-capacity response at the weakly first order I-N and continuous N-SmA phase transitions gradually approaches the tricritical-like and three-dimensional XY behavior, respectively. The main observed features were explained using a bicomponent single pore type phenomenological model.