One-pot synthesis of symmetrical and unsymmetrical acridine sulfonamide derivatives catalyzed by p-TSA

Research on Chemical Intermediates - Synthesis of a series of symmetrical and unsymmetrical 1,8-dioxo-octahydroacridine benzenesulfonamide derivatives has been achieved by one-pot, multicomponent...     

Dielectric studies on pure and doped sr (NO3)2

Single crystals of pure and Na⁺-doped strontium nitrate were grown by slow evaporation of aqueous solution. Systematic measurement of dielectric constant (ϵ) and loss (tan δ) have been carried out in the frequency range of 100 Hz to 100 kHz at temperatures ranging from room temperature to 420 °C. A.C. conductivity (σ) is obtained from the data on ϵ and tan δ, ϵ, and σ were found to show anomalies around 300 °C. The results are discussed in the context of order-disorder phase transition.     

Influence of thermal history and humidity on the ionic conductivity of nanoparticle‐filled solid polymer electrolytes

The crystallinity and conductivity of nanoparticle‐filled solid polymer electrolytes (SPEs) are investigated as a function of thermal history and water content. Our objective is to evaluate how performance is affected by the conditions under which the SPEs are handled and tested. The samples consist of polyethylene oxide (PEO), LiClO₄, and Al₂O₃ nanoparticles. At low humidity, SPEs at ether oxygen to lithium ratios of 8:1 do not crystallize immediately; instead, 3 days are required for crystallization to occur, and this does not depend strongly on the presence of nanoparticles. The conductivity is improved by the addition of nanoparticles at low humidity, but only at an ether oxygen to lithium ratio of 10:1, which corresponds to the eutectic concentration. At high humidity, the recrystallization time is delayed for 3 weeks, and the conductivity increases in both filled and unfilled SPEs beyond that of the low humidity samples. Although we observe that water amplifies the influence of nanoparticles on conductivity, we also find that nanoparticles inhibit water uptake—but only in the presence of lithium. Because Li⁺ strongly absorbs water, this result suggests that nanoparticles may interact directly with Li⁺ ions to prevent water uptake. In filled samples at the eutectic concentration (10:1), more water is absorbed compared to the nanoparticle‐filled 8:1 samples, even though less lithium is present. This suggests that nanoparticles may segregate to lithium‐poor regions in the 10:1 samples, and this scenario is supported by the morphology that would be expected at the eutectic concentration. © 2011 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 49: 1496–1505, 2011     

Mesoscale simulation of morphology in hydrated perfluorosulfonic acid membranes

Current fuel cell proton exchange membranes rely on a random network of conducting hydrophilic domains to transport protons across the membrane. Despite extensive investigation, details of the structure of the hydrophilic domains in these membranes remain unresolved. In this study a dynamic self-consistent mean field theory has been applied to obtain the morphologies of hydrated perfluorosulfonic acid membranes (equivalent weight of 1100) as a model system for Nafion at several water contents. A coarse-grained mesoscale model was developed by dividing the system into three components: backbone, side chain, and water. The interaction parameters for this model were generated using classical molecular dynamics. The simulated morphology shows phase separated micelles filled with water, surrounded by side chains containing sulfonic groups, and embedded in the fluorocarbon matrix. The size distribution and connectivity of the hydrophilic domains were analyzed and the small angle neutron scattering (SANS) pattern was calculated. At low water content (lambda<6, where lambda is the number of water molecules per sulfonic group) the isolated domains obtained from simulation are nearly spherical with a domain size smaller than that fitted to experimental SANS data. At higher water content (lambda>8), the domains deform into elliptical and barbell shapes as they merge. The simulated morphology, hydrophilic domain size and shape are generally consistent with some experimental observations.     

A note on duality of generalized equilibrium problem

The main aim of this note is to extend the dual (in the form of an optimization problem) given for equilibrium problem by Martinez-Legaz and Sosa (in J Glob Optim 35:311–319, 2006) for a generalized equilibrium problem in finite dimensional setting and to establish its equivalence with the dual derived by Bigi et al. (in J Math Anal Appl 342:17–26, 2008) (in the form of inclusion conditions) under a mild condition.     

Carbon-carbon bond forming reactions via Pd-catalyzed detellurative homocoupling of diorganyl tellurides

A simple and highly efficient method for the constructions of Csp-Csp, Csp²-Csp² and Csp³-Csp³ bonds is reported. The symmetrical diaryl tellurides undergo detellurative homocouplings to afford symmetrical biaryl products. The reactions are carried out at ambient temperature using PdCl₂ as a catalyst in the presence of Ag₂O and Na₂CO₃. Similarly, the detellurative homocouplings of dibenzyl telluride and bis(phenylethynyl)telluride give bibenzyl and the conjugated diyne, respectively.     

Cyanuric chloride catalyzed metal-free mild protocol for the synthesis of highly functionalized tetrahydropyridines

An environmentally benign, facile and elegant synthetic approach for the convenient access of a series of diverse 2,6-diaryl-tetrahydropyridine-3-carboxylates via a one-pot, pseudo five-component condensation of ethyl acetoacetate, anilines and aromatic aldehydes under mild reaction conditions has been described. This domino strategy allows rapid cyclization in the presence of 10 mol% of cyanuric chloride as a source of hydrochloric acid to afford the desired target skeletons in excellent yields. The present protocol offers prominent advantages of simple operational procedure, metal-free organocatalyst, practically robust and extensive substrate scope.