Copper(II) complex of 3-cinnamalideneacetylacetone: Synthesis and characterisation

A bidentate ligand derived from cinnamaldehyde and acetylacetone and its copper(II) complex have been synthesized and characterized by elemental analysis, UV-Vis, IR, ESR and magnetic susceptibility measurements. Magnetic susceptibility measurements, ESR and electronic spectral data indicate the presence of six coordinated Cu(II) ion. The ligand and complex are tested for antibacterial activity againstPseudomonas aeroginosa. They are found to show the antibacterial activity.     

Some compactifications of a semitopological semigroup

Let S be a semitopological semgroup and let C_b (S) denote the B^*-algebra of all continuous bounded complex-valued functions on S. In this paper, we consider a left m-introverted and translation invariant B^*-subalgebra F of C_b(S) containing the constant functions. Our concern is with ΔF, the maximal ideal space of F up to an isomorphic homeomorphism, when it is made into a compact right topological semigroup containing a dense continous homomorphic image of S under the Gelfand topology and a suitably chosen binary operation. We establish a representation of the closed left ideals of ΔF and study its centre and ideal structure in some special cases.     

The Nonchiral Fusion Rules in Rational Conformal Field Theories

We introduce a general method in order to construct the nonchiral fusion rules which determine the operator content of the operator product algebra for rational conformal field theories. We are particularly interested in the models of the complementary D-like solutions of the modular invariant partition functions with cyclic center Z _N . We find that the nonchiral fusion rules have a Z _N -grading structure.     

Comparison of Two Stability-Indicating Chromatographic Methods for the Determination of Mirabegron in Presence of Its Degradation Product

Mirabegron is a novel β₃-adrenoceptor agonist containing an amide group. It was subjected to stress conditions of acidic and alkaline hydrolyses. The hydrolytic degradation product was isolated and its structure was confirmed using mass and IR spectrometry. Two stability-indicating chromatographic methods have been proposed for the determination of mirabegron. TLC method was applied using silica gel as stationary phase and chloroform–methanol–ammonia (9.0:1.0:0.1 by volume) as the mobile phase, and chromatograms were scanned at 250 nm. Accurate determination of the drug was achieved over the concentration range of 2–12 μg per band. In addition, an isocratic HPLC method was developed on Agilent C18 column (150 mm × 4.5 mm I.D., particle size 5 µm) using ethanol-phosphate buffer pH 2.5 (30:70, by volume) as a mobile phase with flow rate of 1 mL min^?1.The intact drug was detected at 250 nm with running time less than 5 min. Mirabegron was determined accurately in a concentration range of 1–25 µg mL^?1. The proposed chromatographic methods were applied successfully for the assay of mirabegron in pharmaceutical dosage form and both methods were validated as per the International Conference on Harmonization guidelines and statistically compared with a reported gradient HPLC method.     

Studies on electron transfer reactions: reduction of heteropoly 10-tungstodivanadophosphate by <Emphasis Type="SmallCaps">l</Emphasis>-cysteine in aqueous acid medium

l-cysteine undergoes facile electron transfer with heteropoly 10-tungstodivanadophosphate, [ \textPV^\textV \textV^\textV \textW _{1 0} \textO _{4 0} ]^{5 -} , \left[ {{\text{PV}}^{\text{V}} {\text{V}}^{\text{V}} {\text{W}}_{ 1 0} {\text{O}}_{ 4 0} } \right]^{5 - } , at ambient temperature in aqueous acid medium. The stoichiometric ratio of [cysteine]/[oxidant] is 2.0. The products of the reaction are cystine and two electron-reduced heteropoly blue, [PV^IVV^IVW₁₀O₄₀]⁷⁻. The rates of the electron transfer reaction were measured spectrophotometrically in acetate–acetic acid buffers at 25 °C. The orders of the reaction with respect to both [cysteine] and [oxidant] are unity, and the reaction exhibits simple second-order kinetics at constant pH. The pH-rate profile indicates the participation of deprotonated cysteine in the reaction. The reaction proceeds through an outer-sphere mechanism. For the dianion ⁻SCH₂CH(NH₃ ⁺)COO⁻, the rate constant for the cross electron transfer reaction is 96 M⁻¹s⁻¹ at 25 °C. The self-exchange rate constant for the ^- \textSCH₂ \textCH( \textNH₃ ⁺ )\textCOO ^- \mathord

Evaluation of a Vancomycin-Based LC Column in Enantiomeric Separation of Atenolol: Method Development, Repeatability Study and Enantiomeric Impurity Determination

An LC method was developed and validated for the enantioselective separation and enantiomeric impurity quantitation of atenolol. Separation of the atenolol enantiomers on the Chirobiotic V2 (150 mm × 4.6 mm, 5 μm) column was best achieved using a ternary mobile phase of methanol–acetonitrile-triethylamine acetate 0.5% (w/v), pH 4.5 in a ratio of (45:50:5; v/v/v). Good resolution value of R _s  = 3 was obtained at a flow rate of 1 mL min^?1 within a total run time of less than 40 min. Peak identification was achieved using the standard reference of individual enantiomers. The peak of the impurity was eluted in front of the peak of the main enantiomer. Detection was performed by UV at 226 nm. Within and between day’s repeatabilities for both retention time and peak area were investigated at three concentration levels and found to be low. The method was also found to be efficient for the determination of atenolol enantiomeric impurity. An impurity quantitation level of (R)-atenolol down to 0.08% relative to the main enantiomer (S)-atenolol was found possible.     

An unusual bioactive oleanane triterpenoid from Rhododendron campanulatum D.Don

An unusual oleanane triterpene(1) was isolated from aerial parts of Rhododendron campanulatum.The compound had shown prominent antibacterial and immunomodulatory activities.The structure of the compound was determined by spectroscopic data including 1D and 2D NMR spectral analysis.