Spectral characterization and antibacterial effect of 2-methyl-6-(5-H-Me-Cl-NO <Subscript>2</Subscript>-1<Emphasis Type=Italic>H</Emphasis>-benzimidazol-2-yl)-phenols and some transition metal complexes

2-Methyl-6-(5-H-methyl-chloro-nitro-1H-benzimidazol-2-yl)-phenols( HL _x :x= 1-4)ligands and HL₁ complexes with Fe(NO₃)₃, Cu(NO₃)₂, AgNO₃, Zn(NO₃)₂ have been synthesized and characterized. The structures of the compounds were confirmed on the basis of elemental analysis, molar conductivity, magnetic moment, FT-IR, ¹H-and ¹³C-NMR. Antibacterial activity of the free ligands, their hydrochloride salts and the complexes were evaluated using the disk diffusion method in dimethyl sulfoxide as well as the minimum inhibitory concentration dilution method, against nine bacteria. While HL₁ ligand has not any activity, it’s Ag(I) complex show antibacterial effect toward almost to all the bacteria. Zn(II) complex has antibacterial effect on especially K. pneumoniae, S. epidermidis and S. aureus bacteria.     

Synthesis and amino acid extraction abilities of chiral calix[4]arene triamides containing amino alcohol units

Herein the synthesis and extraction abilities of new d-/l-phenylalaninol substituted p-tert-butylcalix[4]arene triamide derivatives (3 and 4) towards amino acids are reported. These compounds (3 and 4) have been easily synthesized via aminolysis of p-tert-butylcalix[4]arene trimethylester (2) with d-/l-phenylalaninol in methanol-toluen solvent system at one step. The extraction properties of the prepared chiral calix[4]arene triamide derivatives (3 and 4) towards some selected amino acid methylesters are studied by liquid–liquid extraction. Results show that these chiral calix[4]arene triamide derivatives (3 and 4) exhibited a good affinity towards all amino acid species without any remarkably discrimination.     

Sensitive Flow-Injection Electrochemical Determination of Hydrogen Peroxide at a Palladium Nanoparticle-Modified Pencil Graphite Electrode

A novel flow-injection amperometric method was proposed for the sensitive and enzymeless determination of hydrogen peroxide based on its electrocatalytic reduction at a palladium nanoparticle-modified pretreated pencil graphite electrode in a laboratory-constructed electrochemical flow cell. Cyclic voltammograms of the unmodified and modified electrodes were recorded in pH 7.0 phosphate buffer containing 0.10 M KCl at a scan rate of 50?mV s^?1 for the investigation of electrocatalytic reduction of hydrogen peroxide at the palladium nanoparticle-modified pretreated pencil graphite electrode. Cyclic voltammograms of the pretreated pencil graphite electrode revealed an irreversible oxidation peak and a weak reduction peak of hydrogen peroxide at +1100?mV and –450?mV vs. an Ag/AgCl/KCl saturated reference electrode. However, the reduction of hydrogen peroxide was observed at –100?mV with an increase in current in the cyclic voltammograms of the palladium nanoparticle-modified pretreated pencil graphite electrode compared to the unmodified electrode. These results indicate that the palladium nanoparticle-modified pretreated pencil graphite electrode exhibits efficient electrocatalytic activity for the reduction of hydrogen peroxide. A linear concentration range was obtained between .01 and 10.0?mM hydrogen peroxide with a detection limit of 3.0 µM from flow injection amperometric current–time curves recorded in pH 7.0 phosphate buffer at –100?mV and a 2.0?mL min^?1 flow rate. The novelty of this work relies on its use of a laboratory-constructed flow cell constructed for the pencil graphite electrode using these inexpensive, disposable, and electrochemically reactive modified electrodes for the amperometric determination of hydrogen peroxide in a flow injection analysis system.     

Enhanced ethanol sensing properties of WO3 modified TiO2 nanorods

Pristine and WO₃ decorated TiO₂ nanorods (NRs) were synthesised to investigate n-n-type heterojunction gas sensing properties. TiO₂ NRs were fabricated via hydrothermal method on fluorine-doped tin oxide coated glass (FTO) substrates. Then, tungsten was sputtered on the TiO₂ NRs and thermally oxidised to obtain WO₃ nanoparticles. The heterostructure was characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray (EDX) spectroscopy. Fabricated sensor devices were exposed to VOCs such as toluene, xylene, acetone and ethanol, and humidity at different operation temperatures. Experimental results demonstrated that the heterostructure has better sensor response toward ethanol at 200 °C. Enhanced sensing properties are attributed to the heterojunction formation by decorating TiO₂ NRs with WO₃.     

Synthesis,characterization, crystal structure,and antimicrobial studies of 2-morpholinoethyl-substituted benzimidazolium salts and their silver(I)-N-heterocyclic carbene complexes

Research on Chemical Intermediates - This article describes synthesis of N-morpholinoethylbenzimidazole (1), 2-morpholinoethyl-substituted benzimidazolium salts (NHC precursors, 2a–c), and...     

On the lifetime behavior of a discrete time shock model

In this article, we study a shock model in which the shocks occur according to a binomial process, i.e. the interarrival times between successive shocks follow a geometric distribution with mean 1/p$1/p$. According to the model, the system fails when the time between two consecutive shocks is less than a prespecified level. This is the discrete time version of the so-called δ$\delta$-shock model which has been previously studied for the continuous case. We obtain the probability mass function and probability generating function of the system’s lifetime. We also present an extension of the results to the case where the shock occurrences are dependent in a Markovian fashion.     

The maximum surplus in a finite‐time interval for a discrete‐time risk model with exchangeable,dependent claim occurrences

This paper investigates a discrete‐time risk model that involves exchangeable dependent loss generating claim occurrences and compound binomially distributed aggregate loss amounts. First, a general framework is presented to derive the distribution of a surplus sequence using the model. This framework is then applied to obtain the distribution of any function of a surplus sequence in a finite‐time interval. Specifically, the distribution of the maximum surplus is obtained under nonruin conditions. Based on this distribution, the computation of the minimum surplus distribution is given. Asset and risk management–oriented implications are discussed for the obtained distributions based on numerical evaluations. In addition, comparisons are made involving the corresponding results of the classical discrete‐time compound binomial risk model, for which claim occurrences are independent and identically distributed.     

Double-exchange model for molecule-based magnets

We report a detailed study of a double-exchange model proposed for the molecule-based magnets. The model is applied to a two-dimensional periodic complex made of a transition metal and an organic molecule in which the electronic structure is described by effective d orbitals of the transition metal ion at infinite Hund's coupling limit and the lowest unoccupied molecular orbital of the organic molecule, π^∗. Depending on the average electron density of the organic molecules and various superexchange couplings between metal ions' core spins, magnetic states of the complex are investigated. Performing Monte Carlo calculations on a model Hamiltonian for various electron densities of the organic molecule, the average magnetization and critical magnetic ordering temperatures are determined.     

Charge quantization condition withN strings. A new internal quantum number of charge-monopole systems

Dirac theory of magnetic poles is equivalent to a Maxwell electrodynamics in which besides the point singularities (electric charges), extended singularities (e.g. strings) occur. The nature of singularities determine completely the theory, hence Betti numbers of space must occur as quantum numbers. Magnetic charge is one of the fundamental periods of the 2-formF.