Sol–gel synthesis and characterization of conducting polythiophene/tin phosphate nano tetrapod composite cation-exchanger and its application as Hg(II) selective membrane electrode

Nano tetrapod based on conducting polythiophene (PTh) and tin-phosphate (SnP) were synthesized by in situ chemical oxidative polymerization. The morphology of the resulting polythiophene tinphosphate composite was characterized by elemental analysis, fourier transform infrared spectroscopy, thermogravimetric analysis, powder X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The physico-chemical characterization carried out on the composite showed that SnP was modified by conducting PTh with an enhancement of various properties. On the basis of highest distribution coefficient values for Hg(II), the composite was also used for the preparation of Hg(II) selective membrane electrode. The electrode showed working concentration range of 1 × 10^?1 to 1 × 10^?7 with Nernstian slope of 29.29 mV per decade change in concentration and the electrode may be used for wide working pH range of 4–8 having quick response time about 23 s. The life of electrode is 4 months without any notable drift in potential.     

Comparison of HPLC and MEEKC for Miconazole Nitrate Determination in Pharmaceutical Formulation

A simple solid phase extraction (SPE) method coupled with high performance liquid chromatography (HPLC) using UV detector and microemulsion electrokinetic chromatography (MEEKC) has been developed and compared for the quantitative determination of miconazole nitrate in pharmaceutical formulation. For HPLC method, two parameters were optimized, namely, the wavelength and the mobile phases. The optimized condition was at the 225 nm wavelength and the mobile phase of ACN:MeOH (90:10 v/v). There are seven MEEKC parameters that were optimized, in this research, which were applied to voltage, temperature, wavelength, sodium dodecyl sulfate (SDS) concentration, buffer pH, buffer concentration and butan-1-ol concentration. The optimum MEEKC condition was obtained using 86.35 % (w/w) 2.5 mM borate buffer pH 9, 0.25 % (w/w) SDS, 0.8 % (w/w) ethyl acetate, 6.6 % w/w butan-1-ol and 6.0 % (w/w) acetonitrile. The combination of SPE using a diol column with HPLC–UV and the MEEKC methods were successfully applied for the determination of miconazole nitrate in a pharmaceutical formulation with the recovery percentage of 98.35 and 92.50 %, respectively.     

Dye-Sensitized Solar Cell Utilizing TiO<Subscript>2</Subscript> Nanostructure Films: Effect of Synthesis Temperature

This paper is concerned with a study of the influence of synthesis temperature on the properties of TiO₂ films and the performance of dye-sensitized solar cell (DSSC). The TiO₂ film samples synthesized via liquid phase deposition for 5 h at various temperatures, namely, 40, 50, 60, 70 and 80°C. It was found that the morphological shape of the film changes with growth temperature. The optical absorption increases with growth temperature. However, the photoluminescence decreases with growth temperature. These TiO₂ samples were applied in a DSSC of ITO/TiO₂/electrolyte/platinum. The DSSC utilizing the sample grown at 40°C demonstrated the highest photovoltaic parameters with the J_sc, and η of 1.40 mA cm^–2 and 0.44% respectively. This is due to the smallest grain size of TiO₂ films and the smallest bulk resistance of the device.     

Location and associated hyperfine properties of μ+ in La2CuO4

The location of the positive muon used as a probe in highT _c systems is investigated using the unrestricted Hartree-Fock cluster procedure. Our calculations indicate that ⁺ is located in thea–c plane at a distance of 1.08 Å from the apical oxygen at a ⁺-O(a)-Cu angle of 25°. The hyperfine field at this site is also calculated. Our results show the importance of including the local contact and dipolar contributions to the hyperfine field which arise from the unpaired electron spin distribution in the vicinity of the muon.     

Differential pulse polarographic behaviors of p-nitrosodimethylaniline: Application for microdetermination of NADH

The differential pulse polarographic behavior of p-nitrosodimethylaniline has been investigated in Britton-Robinson buffer and phosphate buffer. The peak obtained at pH 8.0 is recommended for the trace determination of this compound, with an experimental detection limit of 18 ppb (1.2 × 10^?7M) in simple aqueous solution. The method is also applied for the indirect microdetermination of NADH. The experimental detection limit of NADH is shown to be 1.05 × 10^?6M.     

Synthesis, Crystal Structure and ab initio Studies of Cyclohexyl N-Phenylcarbamate

Abstract  

Cyclohexyl N-phenylcarbamate, C₁₃H₁₇NO₂ (I), which is a useful target for biotransformations by fungi, has been synthesized and the structure has been solved by X-ray diffraction. The crystals are triclinic, space group P [`1] bar{1} , with a = 5.2581 (2) ?, b = 9.5080 (3) ?, c = 12.6165 (4) ?, α = 70.544 (2)°, β = 89.075 (2)°, γ = 80.447 (2)°, M _r = 219.28, V = 585.96 (3) ?³, Z = 2 and R = 0.065. In the title compound the phenyl ring makes a dihedral angle of 30.68(7)° with the carbamate group The molecules are linked into infinite chains via N–H···O hydrogen bonds along the a axis. These hydrogen-bonded chains are further linked by weaker C–H···π interactions. Quantum-mechanical ab initio calculations for the free molecule reproduce well the observed bond lengths and valency angles but show that the crystal packing might be responsible for the rotation of the phenyl ring out of the carbamate plane in the solid state conformation.     

Microdetermination of benzoylhydrazine and some methoxylated derivatives by using differential pulse polarography

The differential pulse polarographic behaviour of benzoylhydrazine, m-methoxy benzoyl-hydrazine, and o-methoxy benzoylhydrazine has been investigated in Britton-Robinson buffer. The peaks obtained at pH 5 are recommended for the microdetermination of these compounds. The benzoylhydrazine can be obtained with high degrees of accuracy with an experimental detection limit of 4 × 10⁻⁶ M in simple aqueous and aqueous ethanol mixtures.     

Fingerprint chemotaxonomic GC–TOFMS profile of wood and bark of mangrove tree Sonneratia caseolaris (L.) Engl.

The bark and wood of Sonneratia caseolaris (L.) Engl. have been analyzed for chemical profile by GC–TOFMS. Overall thirty-two compounds from bark and twenty-eight compounds from wood have been detected. Sixteen constituents have been found to be common in both the extracts. GC–TOFMS chemical profile may be a significant finger print chemotaxonomic marker as an identity of this plant.