Study of the peak effect phenomenon in single crystals of 2H-NbSe2

The weakly pinned single crystals of the hexagonal 2H-NbSe₂ compound have emerged as prototypes for determining and characterizing the phase boundaries of the possible order-disorder transformations in the vortex matter. We present here a status report based on the ac and dc magnetization measurements of the peak effect phenomenon in three crystals of 2H-NbSe₂, in which the critical current densities vary over two orders of magnitude. We sketch the generic vortex phase diagram of a weakly pinned superconductor, which also utilizes theoretical proposals. We also establish the connection between the metastability effects and pinning.     

Shaping Solid-State Supramolecular Cavities: Chemically Induced Accordionlike Movement of gamma-Zirconium Phosphate Containing Polyethylenoxide Pillars

The hydrophilic oxygen atoms of polyethylenoxide chains inserted as pillars in gamma-zirconium phosphate form hydrogen bonds with the acid groups of the host. As a result the pillars are almost perpendicular to the gamma layers. Upon changing the pH level of the supernatant solution the hydrogen bonds are broken and the pillars become almost perpendicular to the layers (shown schematically). Thus there is a reversible enlargement-shortening of the interlayer space.     

The platinum benzole acid blues — a new class of blue platinum compounds

Summary The preparation of platinum blues from Pt(NH₃)₂(H₂O) ₂ ²⁺ and benzoic or phthalic acids is described. The compounds were characterised by e.p.r., u.v./vis. and x-ray photoelectron spectroscopy. Unlike pyrimidine blues, the platinum blues reported here appear to be non-ionic.     

Electrosorptive detection in liquid chromatography of simple charged organic compounds

Summary The applicability of electrosorptive (ES) detection in liquid chromatography to charged organic species, specifically amines, alkanolamines, and alkylsulfonates is demonstrated. Separations can be carried out using ion-pair chromatography, and detection acieved by measuring changes in differential double-layer capacitance (DLC), C_d, brought about by analyte adsorption at potentials either well negative or positive of the potential of zero charge (pzc), depending on whether cationic or anionic forms, respectively, are being determined. The C_d-analyte concentration response curves are linear over a limited range. A welcome feature of the technique is that organic modifiers may be used in the mobile phase without deleterious consequence to the detection. Attempts were also made to detect these charged species as ion pairs by DLC at potentials close to the pzc. This approach, however, appears to have less practical utility.