Two- and three-dimensional analysis of bose-einstein correlations inπ +/K+p interactions at 250 GeV/c

The NA22 data onπ ^? π ^? correlations are analyzed in terms of a number of two- and three-dimensional parametrizations (Gaussian space-time, Goldhaber, Bowler string-like, Bertsch hydrodynamical, Kopylov-Podgoretskii, etc.). Contrary to the results obtained for e⁺e^? andµp collisions, the Goldhaber parametrization, as well as string-like models, fail in describing the hadron-hadron data. Better fits are obtained in the framework of surface-emitting fireball-like models, both when including and excluding hydrodynamical expansion of nuclear matter. Our results indicate that pion radiation occurs at earlier stages of matter evolution than in nuclear collisions.     

Structure and electronic spectra of 2-phenylbenzimidazoles. Quantum chemical analysis of the intramolecular hydrogen bond

Institute of High-Molecular-Weight Compounds, Russian Academy of Sciences. Leningrad State University Translated from Zhurnal Strukturnoi Khimii, Vol. 33, No. 5, pp. 20–27, September–October, 1992.     

Logarithmic corrections for dilute uniaxial ferromagnets at the critical dimension

The leading logarithmic corrections to the critical behavior of a dilute uniaxial (Ising) ferromagnet in the disordered phase are derived using renormalization group methods. The values of the exponents in the logarithmic terms differ from those given by previous authors.     

Electrooxidation of carbo/thiocarbohydrazide and their hydrazone derivatives at a glassy carbon electrode

Electrochemical oxidation of thio/carbohydrazide and their hydrazone derivatives Benzaldehyde thiocarbohydrazone [BTCH] diacetylene thiocarbohydrazone [DATCH] have been studied in Brit-ton Robinson buffer in aqueous and nonaqueous media at a glassy carbon electrode. The effects of pH, sweep rate, concentration, temperature and surfactants have been studied. The complex bis (carbo/thiocabohydrazide) Zn(II) chloride was also subjected to voltammetric analysis in order to understand the reactivity both in free and metal bound states. The reaction conditions were optimized for the determination of above compounds in micrograms quantities by differential pulse voltammetry, analytical utility of this investigation is also highlighted.     

Cationic poly(methacryl oxyethyl trimethylammonium) and its poly(ethylene glycol)‐grafted analogue as capillary coating materials in electrophoresis

Cationic polyelectrolytes were synthesized and used as semipermanent coating materials for capillaries in electrophoresis. The polyelectrolytes used were a homopolymer of poly(methacryl oxyethyl trimethylammonium chloride) (PMOTAC) and its poly(ethylene glycol) (PEG)‐grafted analogue. Two PMOTAC polyelectrolytes, with molar masses of 85,000 and 300,000 g/mol, and PEG‐grafted PMOTAC with a molar mass of 280,000 g/mol were synthesized and then characterized by size exclusion chromatography (SEC) and nuclear magnetic resonance (NMR) spectroscopy. Attachment of the polyelectrolytes to the wall of the fused silica capillary for electrophoresis caused the electroosmotic flow (EOF) to reverse. The polyelectrolyte coatings were tested over the pH range 2–11 at different buffer ionic strengths, and the most stable and strongest anodic EOFs were obtained at acidic pH values with low ionic strength buffers. Between runs the capillary is merely rinsed for 2 or 3 min with the background electrolyte solution. With the PMOTAC coatings at pH values ≤5, the RSDs of the EOFs were less than 2.9% after 60 injections. The effects of the molar mass of the polycation and of PEGylation of PMOTAC on the interactions between the polycations and basic proteins were studied at acidic pH values. The differences in the effective electrophoretic mobilities, resolution values, and plate numbers of the proteins with the different coatings were due to the EOF, as demonstrated through calculations of reduced mobilities, relative resolution values, and relative plate numbers. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 2655–2663, 2007     

Protonation constant of salicylidene (N-benzoyl)glycyl hydrazone and its coordination behaviour towards some bivalent metal ions

Protonation constant of an unsymmetrical Schiff base, salicylidene(N-benzoyl)glycyl hydrazone (SalBzGH), and formation constants of its complexes have been determined potentiometrically at different temperatures in aqueous dioxane medium. Complexes of SalBzGH with VO(IV), Mn(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Hg(II) have been prepared. Elemental analyses, pH-metric, molar conductance, magnetic susceptibility, electronic, IR, ESR, XRD (powder) and NMR studies have been carried out to study the coordination behaviour of SalBzGH toward these metal ions. pH-metric and 1H NMR studies show the presence of two dissociable protons in the ligand. IR and NMR spectra suggest the tridentate nature of the ligand, coordinating as a uninegative species in the Mn(II) complex and as a dinegative species in all the other complexes. Presence of two different conformers of the ligand at room temperature and stabilization of a single conformer upon complex formation have been established from¹H NMR spectra of the metal-free ligand, Zn(II) and Hg(II) complexes recorded at 296 K. Electronic and ESR spectra indicate highly distorted tetragonal geometry for VO(IV) and Cu(II) complexes. XRD powder patterns of the Zn(II) complexes are indexed for an orthorhombic crystal system.     

A Miura of the Painlevé I Equation and Its Discrete Analogs

We present Miura transformations for the continuous and several discrete Painlev\'e I equations. In the case of the continuous P_I, we use the Hamiltonian formulation of the Painlev\'e equations and show that there exists a Miura transformation between P_I and the binomial, second degree, equation of Cosgrove SD_V. In the case of the discrete P_I's we obtain two different kinds of Miuras. One kind relates a d-P_I to some other d-P_I while the other leads to discrete four-point equations which are the discrete analogs of the derivative of Cosgrove's equation SD_V.