Crystal structure of monomethylammonium tribromocadmate(II)

CH₃NH₃CdBr₃ crystallizes in the space group Ccm2₁, a = 13.693(1) Å, b = 7.906(1) Å, c = 6.886(1) Å, V = 745.46(15) ų, Z = 4, D _x = 3.42 Mg m^–3. The structure of the title compound is one-dimensional consisting of infinite chains made of face sharing CdBr₆ octahedra. The methylammonium groups are situated in the space between chains. The cations and anions are joined by hydrogen bonding.     

Crystal structure of penthylenediammonium pentachlorothallate(III)

The penthylenediammonium pentachlorothallate(III) salt is orthorhombic with the following unit cell dimensions: a = 7.696(3) Å, b = 13.2890(17) Å, and c = 13.503(18) Å, space group P2₁2₁2₁ with Z = 4. The structure was solved by Patterson methods and refined to a final R value of 0.0387 for 1991 observed reflections. The structure consists of penthylenediammonium cations and polynuclear anions in which slightly distorted [TlCl₆]^3– octahedral sharing two vertices are interconnected into chains. These chains are themselves interconnected by means of the N–HCl bonds originating from the [NH₃(CH₂)₅NH₃]²⁺ entities forming a three-dimensional network.     

Activated bentonite (Maghnite-H+) as green catalyst for ring-opening polymerization of 1,3,5,7-tetravinyltetramethylcyclotetrasiloxane

Research on Chemical Intermediates - A new green technique to synthesize polysiloxane-type polymers is suggested based on use of chemically modified clay (Maghnite-H+) as heterogeneous,...     

Motion analysis of two-link nonholonomic swimmers

Nonlinear Dynamics - This paper presents a tool for analyzing the motion of two-link nonholonomic swimmers. We refer to these systems as Land-sharks, which are a generalization of the well known...     

Analysis of hydrodynamic and thermal dispersion in porous media by means of a local approach

A pore scale analysis is implemented in this numerical study to investigate the behavior of microscopic inertia and thermal dispersion in a porous medium with a periodic structure. The macroscopic characteristics of the transport phenomena are evaluated with an averaging technique of the controlling variables at a pore scale level in an elementary cell of the porous structure. The Darcy–Forchheimer model describes the fluid motion through the porous medium while the continuity and Navier–Stokes equations are applied within the unit cell. An average energy equation is employed for the thermal part of the porous medium. The macroscopic pressure loss is computed in order to evaluate the dominant microscopic inertial effects. Local fluctuations of velocity and temperature at the pore scale are instrumental in the quantification of the thermal dispersion through the total effective thermal diffusivity. The numerical results demonstrate that microscopic inertia contributes significantly to the magnitude of the macroscopic pressure loss, in some instances with as much as 70%. Depending on the nature of the porous medium, the thermal dispersion may have a marked bearing on the heat transfer, particularly in the streamwise direction for a highly conducting fluid and certain values of the Peclet number.     

Determination of Ciprofloxacin in Dried Blood Spots for Therapeutic Drug Monitoring

The use of blood spot collection cards is a simple way to obtain specimens for analysis of drugs for the purpose of therapeutic drug monitoring, assessing adherence to medications and preventing toxicity in certain groups of patients. We describe the development and validation of a microanalytical technique for the determination of ciprofloxacin from dried blood spots. The method is based on reversed phase liquid chromatography with fluorescence detection. Drug recovery in the developed method was found to be higher than 95%. The limits of detection and quantification were calculated to be to be 60 and 100 ng mL⁻¹, respectively. The intra- and inter-day precision (measured by CV%) was always less than 6% (13.07% at LOQ). The accuracy (measured by relative error, %) was always less than 8% (7.82% at LOQ). Stability analysis showed that ciprofloxacin is stable for at least 1 month when stored at −70 °C. The small volume of blood required (30 μL), combined with the simplicity of the analytical technique makes this method a potential procedure for monitoring ciprofloxacin concentrations in certain patient populations.

     

Synthesis,Crystal Structure,and Antibacterial Activity of 1,2,4‐Triazoles and 1,2,4‐Triazol‐3‐one

A straightforward method has been developed for the synthesis of 1,2,4‐triazol‐3‐one 3 and 1,2,4‐triazoles 6a , 6b , 6c , 6d starting from N¹‐substituted‐N¹‐tosylhydrazonates 2 and hydrazine monohydrate. This methodology affords a number of 1,2,4‐triazol‐3‐one 3 and 1,2,4‐triazoles 6a , 6b , 6c , 6d in reasonable yields. The structures of all new compounds were elucidated using infrared, ¹H and ¹³C NMR, high‐resolution mass spectrometry, elemental analysis, and the X‐ray crystallography (for compounds 3 and 6a ). Some of the newly synthesized compounds were screened for their antibacterial activity.     

Direct and indirect electrochemical oxidation of Indigo Carmine using PbO2 and TiRuSnO2

Journal of Solid State Electrochemistry - In this paper, the electrocatalytic properties of PbO2 and TiRuSnO2 anodes for direct and indirect electrochemical oxidation of a synthetic solution...     

Lipschitz conditions for the generalized discrete Fourier transform associated with the Jacobi operator on [0,π]

Our aim in this paper is to prove an analog of the classical Titchmarsh theorem on the image under the discrete Fourier–Jacobi transform of a set of functions satisfying a generalized Lipschitz condition in the space ${\mathbb{L}}_2^{(\alpha ,\beta )}$.     

Preparation and Reactions of 2‐Methyl‐7‐(3‐methyl‐5‐oxo‐1‐phenyl‐2‐pyrazolin‐4‐yl)‐5‐arylthiazolo[3,2‐a]‐pyrimido[4,5‐d]oxazin‐4(5H)‐one

Ethyl 7‐amino‐3‐(3‐methyl‐5‐oxo‐1‐phenyl‐2‐pyrazolin‐4‐yl)‐5‐aryl‐5H‐thiazolo[3,2‐a]pyrimidine‐6‐carboxylate was hydrolyzed with an ethanolic sodium hydroxide and the sodium salt thus formed underwent cyclization with acetic anhydride to afford 2‐methyl‐7‐(3‐methyl‐5‐oxo‐1‐phenyl‐2‐pyrazolin‐4‐yl)‐5‐arylthiazolo[3,2‐a]pyrimido[4,5‐d]oxazin‐4(5H)‐one. This compound was transformed to related heterocyclic systems via its reaction with various reagents. The biological activity of the prepared compounds was tested against Gram positive and Gram negative bacteria as well as yeast‐like and filamentous fungi. They revealed in some cases excellent biocidal properties.