2‐Pyrazolines from 1,3 ‐ dipolar cycloaddition of diazomethane to arylsulfonylethenes

Novel 2‐pyrazolines were obtained by the cycloaddition of diazomethane to bis(arylsulfonylethenyl)‐sulfones ( 3 ) and 1‐arylsulfonyl‐2‐styrylsulfonylethenes (7). Dehydrogenation of 2‐pyrazolines with chloranil gave pyrazoles.     

A concise review on microbial remediation cells (MRCs) in soil and groundwater radionuclides remediation

Currently, the existing microbial radionuclides transformations processes are not completely understood. Bacteria, however, solubilize radionuclides by direct enzymatic reduction, or indirectly by its metabolites and by facilitating electrochemical redox systems. Microbes exchange electrons from proteins, organelles, metabolites to metals and electrodes have strengthened the novel bioremediation methods. In contrast, MRCs based on this redox behavior has offered considerable value over traditional treatment because of growing renewable and conception of energy incentives methods. Moreover, MRCs provides a flexible platform that enables us to access integrated treatment process of generating power and for recovering valuable resources from the contaminated sites.     

Scattering parameters from an analysis of the hall electron mobility in Ga1−xAlxAs alloys

Hall mobilities in high purity epitaxial layers of n-type Ga_1?xA_xAs alloys with room-temperature electron concentrations in the range (5–10) × 10¹⁵ cm^?3 have been measured at 300 K for alloy compositions in the range 0? x ? 0.78. Models for the variation of various material parameters with composition are developed. The acoustic deformation potentials for the Π and X conduction band minima, the intervalley coupling constants for electron scattering among the X-X and L-X minima and the longitudinal optical phonon temperature for these scatterings and the polar optical scattering in the X minima have been determined from a theoretical fit to the experimental data. The electron mobilities in the Π, L and X minima are found to decrease with the composition in the range 0≦ x ? 0.45, show a minimum at x ? 0.50 and then increase again with composition. These mobility variations are reflected in the minimum in the Hall mobility at x ? 0.5 due to intense non-equivalent electron scattering involving the L and x minima. The minimum in the electron mobilities in the Π and X minima have been identified to occur mainly due to the space charge and intervalley scattering among the L and X minima, respectively. The number of equivalent x minima in Ga_1?x Al_x As alloys are estimated to be three and are, thus, situated at the zone edge.     

Kinetics and mechanism of oxidation of some para-, meta-, and ortho-substituted ethyl S-phenylmercaptoacetates by chloramine-B(CAB)

The kinetics of oxidation of ethyl S-phenylmercapto acetate and several para-, meta-, and ortho-substituted ethyl S-phenylmercaptoacetates by chloramine-B have been studied in 50% (V/V) aqueous ethanol medium containing phosphate buffer. This oxidation is of first order with respect to substrate and zero order with respect to oxidant. A catalytic effect of mercury is observed and the order with respect to mercury is fractional (0.74). The increase in pH decreases the rate of oxidation and the order with respect to H⁺ is 0.05. In general electron-releasing substituents accelerate the rate while electron-attracting groups retard the rate. A good correlation is found to exist between log k ₁ and Hammett constants. Susceptibility of the reaction to the steric effect of ortho-substituents has been analyzed in the light of application of Taft's steric energy parameters. © John Wiley & Sons, Inc.     

Self-assembly of thiacyanine dyes in water for the synthesis of active hybrid nanofibres

Water-soluble self-assembled nanostructures were synthesised by simple counter ion exchange of thiacyanine dyes which helps in the formation of nematic (N) and hexagonal (M) chromonic liquid-crystalline (CLCs) phases. Conjugated double bonds as central spacers connected between two benzothiazole segments affect water solubility and liquid crystal formation. Aggregation-dependent properties characterised by ultraviolet–visible, fluorescence and ¹H nuclear magnetic resonance spectroscopy. Sol–gel reaction of dye aggregates with silica species furnishes entangled nanotubular fibres with constant diameter and their length in excess of micrometres, having templates of pore sizes below the mesoporous range. The π–π stacked chromonic aggregate dyes are also of importance in shape selective catalysis, adsorption, desorption micro-patterned materials, and provide a significant step towards biosensor medical applications because of their water-soluble nature.     

Synthesis and liquid crystalline behaviour of substituted (E)-phenyl-4-(phenyldiazenyl) benzoate derivatives and their photo switching ability

Azobenzene derivatives containing phenyl/4-halogen-phenyl 4-{(E)-[4-(pent-4-en-1-yloxy)phenyl]diazenyl}benzoate group with different electronegative substituent (H, F, Cl, Br and I) at other end was synthesised. These azo-based benzoate derivatives have been characterised by FTIR, ¹H-NMR, ¹³C-NMR, elemental analyser, POM and UV-Vis spectroscopy. Photosaturation at 358 nm obtained after 82 s of UV irradiation and the longest thermal back relaxation time of 45 h recorded by UV-Vis. The azo derivative could be possible photolock under UV light, as observed by the improved thermal back relaxation time. The resulting photolockable chain of azobenzene might prove valuable in the development of optical device application. These azobenzene moieties also exhibit liquid crystalline behaviour with respect to the halogen substitution as an electron withdrawing group shows that strong structure property relationship exists among them.     

Michael adducts‐synthons for pyrazolidinediones,isoxazolidinediones, pyrimidinetriones,and thioxopyrimidinediones

4‐Substituted pyrazolidinediones, isoxazolidinediones, and 5‐substituted pyrimidinetriones, thioxopyrimidinediones were obtained by exploiting gem‐diester functionality in mono‐ and di‐substituted dimethyl malonates. © 2004 Wiley Periodicals, Inc. Heteroatom Chem 15:477–481, 2004; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20053