Synthesis,characterization and spectroscopic studies of pyrazinamide metal complexes

The present paper deals with the synthesis and characterization of Schiff base complexes of pyrazinamide an antitubercular drug. Metals selected for complexation are copper, silver, gold, zinc, mercury, iron and cobalt. The complexes have been suitably synthesized and isolated in pure powdered form. Analytical data agrees with the compositions M(L), M′(L)₂ and M″(L)₂·2H₂O, respectively where M = Ag, M′ = Cu, Au, Zn and Hg and M″ = Fe and Co, ligand metal ratios were also confirmed by monovariation method and Job’s method of continuous variation. Molar conductance values suggest the non ionic nature of the complexes. The tentative structure assigned to the complexes on the basis of stoichiometry and analytical data were further supported by spectral studies viz; IR, NMR, magnetic susceptibility and electronic spectra. A preliminary attempt has also been made to compare the potencies of metal complexes with parent drug. The Cu and Ag complexes are giving encouraging results. Particle size studies further suggest that the drug molecule undergoes reduction in size on complexation.     

New phosphoroamidate compounds: Synthesis,structural characterization and studies on ZnCl2 assisted hydrolysis of the P–N bond

A variety of phosphorodiamidate compounds were synthesized from the corresponding phosphorodichloridate intermediates and phosphorus oxychloride. These were completely characterized using different spectroscopic methods and single crystal X-ray diffraction studies on one of them. Studies revealed that water in the presence of a mild Lewis acid like ZnCl₂ was found to assist the hydrolysis of the P–N linkage. The proof of this concept was effectively realized through the hydrolysis of hexamethylphosphoramide.     

High temperature magnetic ordering in La2RuO5

Magnetic susceptibility, heat capacity and electrical resistivity measurements have been carried out on a new ruthenate, La₂RuO₅ (monoclinic, space group P2₁/c) which reveal that this compound is a magnetic semiconductor with a high magnetic ordering temperature of 170 K. The entropy associated with the magnetic transition is 8.3 J/mol K close to that expected for the low spin (S=1) state of Ru⁴⁺ ions. The low temperatures specific heat coefficient γ is found to be nearly zero consistent with the semiconducting nature of the compound. The magnetic ordering temperature of La₂RuO₅ is comparable to the highest known Curie temperature of another ruthenate, namely, metallic SrRuO₃, and in both these compounds the nominal charge state of Ru is 4+.     

AC susceptibility measurements in some RTiFe11-xCox (R = Dy, Ho, Er) compounds: Spin-reorientation behavior

The DyTiFe_{11 - x}Co_x (x = 0, 1, 3), HoTiFe_{11 - x}Co_x (x = 0, 3) and ErTiFe₁₁ compounds, all exhibiting the T hMn₁₂-type structure, were studied for their ac susceptibility in the temperature range 20–300 K. The Dy- and Ho-containing compounds exhibited spin reorientation from axial to cone to planar, or from axial to cone in the temperature range 250-50 K, as expected. In this structure Dy and Ho with negative second-order Stevens' coefficients (_J < 0) favor planar rare earth sublattice anisotropy, while Fe and Co sublattices favor uniaxial and planar anisotropies, respectively and would be in competition as a function of temperature. A spin-reorientation type of behavior was also observed in the ErTiFe₁₁ compound near 50 K. This observation appears to imply that, in this compound, the higher-order crystal-field terms are important. The magnetization data revealed that in these systems the rare earth and transition metal sublattices coupled antiparallel, as is normally the case in the heavy rare-earth-transition-metal compounds.     

On the solutions of the Wick-Cutkosky model in the instantaneous approximation

By reexamining the analysis of Basu and Biswas, based on the stereographic projection method of Fock and Levy, it is shown that the general solution of the Wick-Cutkosky model in the instantaneous approximation, hitherto unreported, involves only one quantum number; this is contrasted with the well-known solution which involves two quantum numbers, but for which the spectrum is degenerate with respect to one of them. The latter situation is shown to hold under a rather special circumstance.     

Effects of cationic head groups of ionic liquid on micellization in aqueous solution of PEO-PPO-PEO triblock copolymer

The interaction of ionic liquids (ILs) with non-ionic triblock copolymer, Pluronic® P123 in aqueous solutions has been investigated using DLS, surface tension, and viscosity measurements. The addition of ILs increased the Critical Micelle Concentration (CMC) of P123, which appears to be logistic. As the added IL enhances the solubility of PPO moiety (and PEO), which makes them to behave like a more hydrophilic block copolymer that would be micellized at high copolymer concentration. The DLS data is in good agreement to the results observed from surface tension measurements. Viscosity results show the propensity in micellar size reduction upon addition of ILs, and hence, intrinsic viscosity decreases as compared to pure P123 aqueous solution. The results are studied and discussed as a function of cationic head groups of N-octyl-pyridinium/imidazolium chloride based ILs.     

Enhancement of electrical conductivity,director relaxation frequency and slope of electro-optical characteristics in the composites of single-walled carbon nanotubes and a strongly polar nematic liquid crystal

In the present work, single-walled carbon nanotubes (SWCNTs) were dispersed in a room temperature nematic liquid crystal 4-pentyl-4′-cyanobiphenyl at the concentration of 0.02 and 0.05 wt%. Differential scanning calorimetry and temperature-dependent dielectric studies suggest decrease in clearing temperature of the composite materials as compared to the pure material. Ionic conductivity increases by two orders of magnitude due to the dispersion of such a low concentration (0.05 wt%) of SWCNTs. Dielectric studies also show that the presence of the SWCNTs decreases the effective longitudinal as well as transverse components of the dielectric permittivity. For homeotropic aligned samples, a relaxation mechanism has been detected in the lower MHz region both for the pure as well as dispersed samples. Presence of SWCNTs increases the relaxation frequency corresponding to flip-flop motion of molecules around their short axes. From frequency-dependent dielectric studies, important dielectric parameters such as relaxation frequency, dielectric strength and distribution parameters have been determined. Electro-optical experiments show that the threshold voltage decreases and the steepness of the transmission voltage curve improves due to the dispersion of SWCNTs.     

Synthesis and spectral study of biologically active macrocyclic complexes of divalent transition metal ions

The condensation reaction of succinyldihydrazide with glyoxal in the presence of divalent metal ions (1: 1: 1) results in the formation of the complexes of type [M(C₆H₈N₄O₂)X₂], where M = Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and X = Cl⁻, NO₃⁻, CH₃COO⁻. The complexes have been characterized with the aid of elemental analyses, conductance measurements and electronic, NMR, infrared spectral studies. On the basis of these studies, a six-coordinated distorted octahedral geometry in which two nitrogen and two carbonyl oxygen atoms are suitably placed for coordination toward metal ion, has been proposed for all the complexes. The complexes were tested for their in vitro antibacterial activity. Some of the complexes showed remarkable antibacterial activities against some selected bacterial strains.