Hetarylpyrazoles. IV. Synthesis and reactions of 1,5′-bipyrazoles

A number of 1, 5′-bipyrazoles were obtained from the condensation of pyrazol-5-ylhydrazine and 1, 3-dicarbonyl compounds. Electrophilic substitution reactions of these 1, 5′-bipyrazoles occur at the four position of the pyrazole ring.     

1H-pyrazolo[3,4-d]thieno[2,3-b]pyridine and its derivatives

The synthesis of the parent ring system and some of the derivatives of 1H-pyrazolo[3,4-d]thieno[2,3-b]pyridine are described.     

Ruthenium(II) complexes with mono and ditertiary arsines and phosphines and their reaction with small molecules

Dichlorotetrakis(dimethylsulphoxide)ruthenium(II) reacts with AsPh₃ AsMePh₂, AsMe₂Ph and SbPh₃ in ethanolic hydrochloric acid solution to yield the complexes RuCl₂(DMSO)₂(AsPh₃)₂, RuCl₂(DMSO) L₂ (L = AsMePh₂, AsMe₂Ph, SbPh₃) respectively. The treatment of ruthenium(II) blue solution with AsMePh₂, AsMe₂Ph and SbPh₃ in alcohol resulted in the formation of the complexes; RuCl₂L₃ (L = AsMePh₂, AsMe₂Ph and SbPh₂), respectively. The reaction of RuCl₂(DMSO)₄ with the bidentate ligands 1,2 bis (diphenylarsino)methane (DPAM), 1,2 bis(diphenylarsino)ethane (DPAE) and 1,2 bis (diphenylphosphino)methane (DPPM). 1,2 bis(diphenylphosphino)ethane (DPPE), in ethanol gave the complexes RuCl₂(DPAM)₂, RuCl₂(DPAE)₂, RuCl₂ (DPPM)₂ RuCl₂(DPPE)₂, respectively. The complexes thus obtained undergo reaction with carbon monoxide, hydrogen, molecular nitrogen and nitric oxide to yield a variety of mixed ligand complexes.     

Multiswitching compound antisynchronization of four chaotic systems

Based on three drive–one response system, in this article, the authors investigate a novel synchronization scheme for a class of chaotic systems. The new scheme, multiswitching compound antisynchronization (MSCoAS), is a notable extension of the earlier multiswitching schemes concerning only one drive–one response system model. The concept of multiswitching synchronization is extended to compound synchronization scheme such that the state variables of three drive systems antisynchronize with different state variables of the response system, simultaneously. The study involving multiswitching of three drive systems and one response system is first of its kind. Various switched modified function projective antisynchronization schemes are obtained as special cases of MSCoAS, for a suitable choice of scaling factors. Using suitable controllers and Lyapunov stability theory, sufficient condition is obtained to achieve MSCoAS between four chaotic systems and the corresponding theoretical proof is given. Numerical simulations are performed using Lorenz system in MATLAB to demonstrate the validity of the presented method.     

Oscillations in radioactive exponential decay

Several older and recent reports provided evidence for the oscillatory character of the exponential decay law in radioactive decay and attempted to explain it with basic physics. We show here that the measured effects observed in some of the cases, namely in the decay of ²²⁶Ra, ³²Si in equilibrium, and ³⁶Cl, can be explained with the temperature variations.     

Shape- and Size-Selective Preparation of Hectorite-Supported Ruthenium Nanoparticles for the Catalytic Hydrogenation of Benzene

The cationic organometallic aqua complexes formed by hydrolysis of [(C₆H₆)₂RuCl₂]₂ in water, mainly [(C₆H₆)Ru(H₂O)₃]²⁺, intercalate into white sodium hectorite, replacing the sodium cations between the anionic silicate layers. The yellow hectorite thus obtained reacts in water with molecular hydrogen (50 bar, 100 °C) to give a dark suspension containing a black hectorite in which large hexagonally shaped ruthenium nanoparticles (20–50 nm) are intercalated between the anionic silicate layers, the charges of which being balanced by hydronium cations. If the reduction with molecular hydrogen (50 bar, 100 °C) is carried out in various alcohols, spherical ruthenium nanoparticles of smaller size (3–38 nm depending on the alcohol) are obtained. In alcohols other than methanol, the reduction also works without H₂ under reflux conditions, the alcohol itself being the reducing agent; the ruthenium nanoparticles obtained in this case are spherical and small (2–9 nm) but tend to aggregate to form clusters of nanoparticles. Whereas the ruthenium nanoparticles prepared by reduction of the yellow hectorite in refluxing alcohols without hydrogen pressure are almost inactive, the nanoparticles formed by hydrogen reduction catalyze the hydrogenation of benzene to give cyclohexane under mild conditions (50 °C) with turnover frequencies up to 6500 catalytic cycles per hour, the best solvent being ethanol. Dedicated to Professor C. N. R. Rao, pioneer of nanocluster chemistry, on the occasion of his 75th birthday.     

Determination of glimepiride in pharmaceutical formulations using HPLC and first-derivative spectrophotometric methods

Two validated analytical methods have been developed to determine glimepiride in pharmaceutical formulations using HPLC and 1st order derivative spectrophotometric techniques. Employing reverse phase HPLC method, the drug was analyzed by pumping a mixture of acetonitrile and 2% formic acid solution, pH 3.5 (80: 20 v/v) through a C₁₈ column (250 × 4.6 mm, 5 μm) and detecting the eluents at 228 nm. The linearity range was found to be 20–140 μg/mL with mean recovery of 100.52 ± 0.33%. The second method was based on the formation of a complex of the drug with 2,3,5-triphenyl-2H-tetrazolium chloride in basic media. 1st order derivative spectrum made it possible to detect the complex at 413.5 nm. The linearity range was found to be 40–160 μg/mL, with mean recovery of 100.33 ± 0.47%. Both the proposed methods can reliably be used for routine analysis of glimepiride in raw material as well as in pharmaceutical formulations. The article is published in the original.     

The effect of delocalization on the exchange energy in meta- and para-linked Pt-containing carbazole polymers and monomers

A series of novel platinum-containing carbazole monomers and polymers was synthesized and fully characterized by UV-VIS absorption, luminescence, and photoinduced absorption studies. In these compounds, a carbazole unit is incorporated into the main chain via either a para- or a meta-linkage. We discuss the effects of linkage and polymerization on the energy levels of S1, T1, and Tn. The S1-T1 splitting observed for the meta-linked monomer (0.4 eV) is only half of that in the para-linked monomer (0.8 eV). Upon polymerization, the exchange energy in the para-linked compound reduces, yet still remains larger than in the meta-linked polymer. We attribute the difference in exchange energy to the difference in wave function overlap between electron and hole in these compounds.