This paper describes nonlinear ion transport properties of liquid and solid electrolytes. Typically, the relation between ionic current density and electric field becomes nonlinear at electric fields above 50–100?kV/cm. We review the 1st and 2nd Wien effect found in classical strong and weak electrolyte solutions as well as the strong nonlinear ion transport effects observed for inorganic glasses and for polymer electrolytes. Furthermore, we give an overview over models describing nonlinear ion transport in electrolyte solutions, in glasses and in polymers. Recent results are presented for the nonlinear ionic conductivity of supercooled ionic liquids. We show that supercooled ionic liquids exhibit anomalous Wien effects, which are clearly distinct from the classical Wien effects. We also discuss the frequency dependence of higher-order conductivity and permittivity spectra of these liquids. 相似文献
The free radical scavenging properties and possible antioxidant activity of 1,3-diphenylpropane-1,3-dione (1) are reported.
Pulse radiolysis technique was employed to study the one-electron oxidation of 1 with various radicals viz. CCl3O2•, N3• and•OH in homogeneous aqueous solution. All these radicals reacted with 1 under ambient conditions at almost diffusion controlled
rates producing transient species with an absorption maximum around 420 nm that decayed at first order rates. The transient
absorption peak was shifted in the case of CCl3OO• radical reaction with 1 due to change in the polarity of the medium. Formation of a stable product with a broad absorption
band starting from 400 nm and cut off at 230 nm was observed in the oxidation of 1 with•OH and•N3 radicals. In a biological system also, 1 showed significant inhibitory activity against Fe2+-mediatedlipidperoxidation. Based on these observations, a suitable mechanism for the oxidation of 1 has been proposed. 相似文献
In wireless multi-hop and ad-hoc networks, minimizing power consumption and at the same time maintaining desired properties
of the network topology is of prime importance. In this work, we present a distributed algorithm for assigning minimum possible
power to all the nodes in a static wireless network such that the resultant network topology is k-connected. In this algorithm, a node collects the location and maximum power information from all nodes in its vicinity,
and then adjusts the power of these nodes in such a way that it can reach all of them through k optimal vertex-disjoint paths. The algorithm ensures k-connectivity in the final topology provided the topology induced when all nodes transmit with their maximum power is k-connected. We extend our topology control algorithm from static networks to networks having mobile nodes. We present proof
of correctness for our algorithm for both static and mobile scenarios, and through extensive simulation we present its behavior. 相似文献
The nucleoside triphosphates of N6-(2-deoxy-alpha,beta-d-erythro-pentofuranosyl)-2,6-diamino-4-hydroxy-5-formamidopyrimidine (Fapy.dGTP) and its C-nucleoside analogue (beta-C-Fapy.dGTP) were synthesized. The lability of the formamide group required that nucleoside triphosphate formation be carried out using an umpolung strategy in which pyrophosphate was activated toward nucleophilic attack. The Klenow fragment of DNA polymerase I from Escherichia coli accepted Fapy.dGTP and beta-C-Fapy.dGTP as substrates much less efficiently than it did dGTP. Subsequent extension of a primer containing either modified nucleotide was less affected compared to when the native nucleotide is present at the 3'-terminus. The specificity constants are sufficiently large that nucleoside triphosphate incorporation could account for the level of Fapy.dG observed in cells if 1% of the dGTP pool is converted to Fapy.dGTP. Similarly, polymerase-mediated introduction of beta-C-Fapy.dG could be useful for incorporating useful amounts of this nonhydrolyzable analogue for use as an inhibitor of base excision repair. The kinetic viability of these processes is enhanced by inefficient hydrolysis of Fapy.dGTP and beta-C-Fapy.dGTP by MutT, the E. coli enzyme that releases pyrophosphate and the corresponding nucleoside monophosphate upon reaction with structurally related nucleoside triphosphates. 相似文献
6-Halo-2-cyclopropyl-3-(pyridyl-3-ylmethyl) quinazolin-4(3H)-one derivatives have been synthesized and utilized for amination reactions with aryl, heteroaryl and alkyl amines. Optimization of reaction conditions with different catalysts, ligands, bases, and solvents was conducted. The combination of Pd2(dba)3 with DavePhos (L3) proved to be best for these conversions in the presence of NaOtBu in 1,4-dioxane at 100 °C. The relative reactivities of 6-bromo and 6-chloro-2,3-disubstitued quinazolinones with p-toluidine were conducted and as anticipated the 6-bromo analogue was totally consumed and 6-chloro derivative was completely unreactive. 相似文献
Journal of Solid State Electrochemistry - This review article presents the use of mechanical milling technique for the synthesis of a variety of fast fluoride ion conducting materials for different... 相似文献
Optimizing the current distribution of an evenly spaced antenna array has shown to be an efficient approach for reducing side lobe levels. In this article, the Tchebyscheff distribution-based antenna array synthesis approach is combined with an adaptive signal processing algorithm for beamforming and side lobe level reduction in smart antennas in various fading situations. The performance of smart antennas in uniformly spaced linear, planar, circular, and semi-circular arrays are evaluated. The presence of Rayleigh and Rician channels is examined in the network. The least mean square (LMS) and normalised least mean square (NLMS) algorithms are applied as adaptive algorithms. In fading environments, the NLMS algorithm with Tchebyscheff distribution outperforms than the LMS algorithm with Tchebyscheff distribution, with a side lobe level decrease of 11.23 dB. The lowest side lobe achieved with the NLMS algorithm with Tchebyscheff distribution is???45.59 dB for uniform planar array.
An efficient and eco-friendly method for the synthesis of substituted pyrroles has been developed via ruthenium-catalyzed multicomponent reaction of ketone, amine, and ethylene glycol in PEG-400 as solvent medium without using any external ligand. The catalytic system and solvent can be recycled with the same, as well as different, ketones with minimum loss of Ru-catalyst activity. 相似文献