A novel series of 2,5-disubstituted 1,3,4-thiadiazoles as potential anticonvulsant agent

<正>In pursuit for better antiepileptic drug and the importance of semicarbazones and 2,5-disubstituted 1,3,4-thiadiazoles as anticonvulsant pharmacophore,a series of novel N-({5-[(6-methyl-1-benzofuran-3-y1)methyl]-1,3,4-thiadiazol-2-yl}carbamothioyl) -2/3/4-substitutedbenzamide were designed,synthesized and evaluated for their anticonvulsant activity.The findings of the present studies confirmed that the pharmacophore model with four binding sites is crucial for anticonvulsant activity. Structure-activity relationships among synthesized compounds were also established.     

A note on demand functions with uncertainty

Demand functions with “additive” and “multiplicative” uncertainty can fail to satisfy the “Slutsky symmetry” conditions required for demand to be based on utility maximization. This makes welfare analysis infeasible, which is important in many applications. Additive uncertainty can also generate negative demand realizations, and this can create non-trivial analytical problems.     

An efficient synthesis of benzyl bromides from aromatic aldehydes using polymethylhydrosiloxane and (bromodimethyl)sulfonium bromide or N-bromosuccinimide

Polymethylhydrosiloxane (PMHS) in combination with (bromodimethyl)sulfonium bromide or NBS has been utilized for the first time for reductive bromination of aromatic aldehydes at room temperature to afford the corresponding benzyl bromides in excellent yields.     

Transition metal chemistry of oxime containing ligands,VII

Complexes of pyridine-2-aldoxime (Hpox) with iron(II) and chromium(III) of type, [Fe(Hpox)₂ X ₂] (X=Cl, Br, I or NCS); [Cr(Hpox)₃]Cl₃·3 H₂O; [Cr(Hpox)₂ X ₂]ClO₄ (X=F, Cl or Br) and [Cr(Hpox)₂(H₂O)₂]Br₃·H₂O were prepared and characterized by analytical X-ray powder diffraction, magnetism, vibrational (conventional and far-infrared) and electronic spectroscopy techniques. X-ray and electronic spectral data indicate that all the complexes except [Cr(Hpox)₃]Cl₃·3 H₂O havetrans-pseudo-octahedral microsymmetry around the metal ion. Infrared spectral data indicate that the ligand, Hpox, behaves like a neutral ligand and coordinates to the metal ion through pyridine nitrogen atom and oxime nitrogen atom in all these complexes. The magnetic susceptibilities of chromium(III) complexes, measured over a temperature range 300–78 K, are independent of temperature whereas the magnetic moments of iron(II) complexes over a temperature range 300–20 K are dependent of temperature. The observed temperature dependence of magnetic moments of iron(II) complexes was used to evaluate the magnitude of orbital reduction factor,k, the low-symmetry distortion parameter, , and the extent of reduction in spin-orbital coupling, . In all these iron(II) complexes the magnetic results indicate the presence of an orbitally non-degenerate,⁵B_2g, ground state. Magnetically unperturbed and perturbedMössbauer spectra of iron(II) complexes at various temperatures have also been reported. Magnetically perturbedMössbauer spectra of iron(II) complexes at 4.2 K in an axial field of 60kGauss indicate that the principal component of electric field gradient tensor is positive and consistent with⁵B_2g ground electronic state in a tetragonal (D _4h) local site symmetry.

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Übergangsmetallkomplexe mit Oxim-enthaltenden Liganden, VII. Elektronische und strukturelle Eigenschaften vonFe(II)-undCr(III)-Komplexen mit Pyridin-2-aldoxim

Zusammenfassung Es wurden Komplexe von Pyridin-2-aldoxim (Hpox) mit Fe(II) und Cr(III) vom Typ [Fe(Hpox)₂ X ₂] (X=Cl, Br, I, NCS), [Cr(Hpox)₃]Cl₃·3 H₂O, [Cr(Hpox)₂ X ₂]ClO₄ (X=F, Cl, Br) und [Cr(Hpox)₂(H₂O)₂]Br₃·H₂O hergestellt. Charakterisierung und Diskussion von Geometrie und Bindungsverhalten in den Komplexen erfolgte auf Grund von analytischen Daten, Röntgen-Pulveraufnahmen, Elektronenanregungsspektroskopie, Infrarotspektroskopie, magnetischen Messungen undMössbauer-Spektroskopie.

     

PVC-based dicyclohexano-18-crown-6 sensor for La(III) ions

A new ion-selective electrode (ISE) based on dicyclohexano-18-crown-6 (DC18C6) as a neutral carrier is developed for lanthanum(III) ions. The electrode comprises of dicyclohexano-18-crown-6 (6%), PVC (33%), and ortho-nitrophenyl octyl ether (o-NPOE) (61%). The electrode shows a linear dynamic response in the concentration range of 10⁻⁶ to 10⁻¹ M with a Nernstian slope of 19 mV per decade and a detection limit as 5×10⁻⁷ M. It has a response time of <30 s and can be used for at least 5 months without any significant divergence in potentials. The selectivity coefficients for mono-, di-, and trivalent cations indicate good selectivity for La(III) ions over a large number of interfering cations. The sensor has been used as an indicator electrode in the potentiometric titrations of La(III) with EDTA. The membrane is successfully applied in partially non-aqueous medium. It can be used in the pH range 4-9.     

HPTLC-Aided Phytochemical Fingerprinting Analysis as a Tool for Evaluation of Herbal Drugs. A Case Study of Ushaq (Ammoniacum Gum)

JPC – Journal of Planar Chromatography – Modern TLC - The phytochemical fingerprint profile of ammoniacum gum (from Dorema ammoniacum) was defined by subjecting different extracts of...     

Characterization of the E1′ center in quartz: Role of aluminum hole centers and oxygen vacancies

The growth of E₁′ centers in a variety of natural and synthetic quartz crystals has been investigated by employing the electron spin resonance technique. It has been reported that the growth of E₁′ centers, formed by irradiation and subsequent annealing at 300 °C for 15 min, scale with the concentration of the aluminum hole center, [AlO₄]⁰, till a limit. Later, the E₁′ centers show saturation even when the [AlO₄]⁰-center continues to grow. For quartz with low efficiency of the formation of [AlO₄]⁰-center or irradiated with low accumulated doses, the intensity of E₁′ center was small where not all oxygen vacancies are converted to the E₁′ center. Thus, besides the availability of a number of oxygen vacancy sites, the number of holes released from the [AlO₄]⁰-center plays an important role in the formation of E₁′ centers in quartz.     

Retail replenishment models with display-space elastic demand

We study a single store multi-product inventory problem in which product sales are a composite function of shelf space. Since sales tend to deplete the amount of product on display, the effective shelf space assigned to the product diminishes with time unless replenishment occurs. We consider the problem of optimal replenishment times under these conditions. We assume a linear dependence of sales rate to effective shelf space in all our analysis. We present exact and approximate solutions for the single product and multi-product cases. For the single product case, we study the effect of space elasticity, cross elasticity and empty space elasticity on the optimal replenishment period. For the multi-product case we present a computationally attractive method using matrix exponentials and develop error bounds for this method.     

Structural,morphological and photoluminescence characteristics of sol-gel derived nano phase CeO<Subscript>2</Subscript> films deposited using citric acid

Homogenous nano structured CeO₂ films have been prepared by a sol-gel process using different mole ratios of citric acid as additive. XPS studies clearly illustrate an increase in Ce³⁺ proportion upon the use of higher citric acid content for the deposition of films. The crystallite sizes in the films lie in the nanorange. Photoluminescence emission in the films is attributed to various defects resulting from crystallization. Lowest transparency, high Ce³⁺ content and optimum sized crystallites in CeO₂ (1:1.5) films have led to its highest PL characteristics. Ce³⁺ chemical state is the major contributor to the PL activity of these films. The SEM micrographs show a reduced level of CeO₂ agglomeration in the films deposited using higher citric acid contents. A comparison of different properties of CeO₂ films deposited using citric acid and CeO₂–TiO₂ films has also been made.      

Organic reactions in water: an efficient one-pot synthesis of acyloxiranes from Baylis-Hillman adducts using hypervalent iodine

Treatment of Baylis-Hillman adducts with iodosobenzene (PhIO) in the presence of a catalytic amount of KBr in water at room temperature afforded the corresponding acyloxiranes in good yields.