Influence of silica gel pretreatment and bonding technique on PAH selectivity of octadecyl bonded phases

Summary The effect of silica gel pretreatment and of different bonding techniques, on the chromatographic properties of octadecyl bonded phases is described. The experiments show that a monomeric octadecyl bonded phase, prepared from silica gel that has not been treated before bonding, has a poor selectivity towards polycyclic aromatic hydrocarbons (PAHs) and shows high adsorption of basic components. Silica gel treatment before the bonding of the monofunctional silane does not give a substantial improvement. Polymeric phases on the other hand show a much better PAH selectivity and a lower adsorptivity towards basic components. Further improvement can be achieved with the polymeric modification if silica gel treatment is carried out before bonding.     

Selective reflection in the cholesteric and blue phases of a chiral-racemic mixture of CE6

Abstract

The reflection spectrum for visible light is examined for the cholesteric and blue phases of chiral CE6. Pronounced side band oscillations are observed. The Bragg wavelength for total reflection diverges towards the smectic phase with an exponent v = 0·71±0·05. Going from the cholesteric phase to BPI, the lattice parameter increases by (2)^1/2. Evidence is given for the existence of a long-lived supercooled blue phase (BPS).     

Investigation of the chirality dependence of thermal properties in chiral-racemic mixtures of the cholesteric ester CE6

Abstract

A scanning adiabatic calorimetric technique has been used to study the thermal properties of the chiral and racemic liquid crystal CE6 and the phase diagram covering the cholesteric phase, the three blue phases and the isotropic phase. The purpose of this investigation is to study thermal properties of liquid crystals as a function of chirality, while all other parameters remain constant. Results for the temperature and the chirality dependence of the enthalpy and of the heat capacity are reported. The latent heats between the cholesteric phase and BPI and between the different blue phases change slightly as a function of the chirality. The total heat of transition at the isotropic phase boundary is independent of the chirality, but with decreasing chirality, we observe a large increase in the latent heat and, correspondingly, a decrease in the pretransitional contribution. These experimental facts are in qualitative agreement with the predictions of a Landau–de Gennes theory for blue phases.     

Electron energy-loss spectroscopy at incommensurately modulated crystalline and glassy Ba2TiGe2O8

Based on cluster molecular orbital calculations, high-energy resolution (ΔE?～ 0.4?eV) Ti–L_2,3 electron energy loss near-edge structures of single-crystalline and glassy Ba₂TiGe₂O₈ are interpreted. The finding that the Ti–L_2,3 near-edge structure of the Ba₂TiGe₂O₈ single crystal possesses less pronounced peaks than the glass under identical experimental conditions can be attributed to distinct distortions of the titanium environment caused by the very strong one-dimensional structural modulation hosted by the Ba₂TiGe₂O₈ crystal lattice. As lattice periodicity is absent in the glass, the titanium environment is more regular in the vitreous surroundings. Moreover, the modulation in crystalline Ba₂TiGe₂O₈ is responsible for the virtually indiscernible O–K near-edge structures of the glassy and crystalline samples.     

Talopyranose Derivatives Suitable for the Planned Synthesis of Teichoic Acids Containing Di-Glycosylated Ribitol Units

ABSTRACT

Easily accessible 1,6-anhydro-2,3-O-(S)-benzylidene-β-D-mannopyranose was converted in four steps to 1,6-anhydro-3,4-di-O-benzyl-β-D-talopyranose. Glycosylation of the latter with ethyl 2,3,4-tri-O-acetyl-1-thio-α-L-rhamnopyranoside gave, after further processing, 1-O-allyl-3,4-di-O-benzyl-2-O-(2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-L-ribitol.