Reaction of nitriles under acidic conditions. Part VII. Study on the reaction of o-aminonitriles with cyanamides to synthesize 2,4-diaminothieno[2,3-d]pyrimidines

The reaction of N-arylcyanamides with thiophene o-aminonitriles under the influence of dry hydrogen chloride gas yields a mixture of two products. The major product has been identified as 2-amino-3-aryl-4-iminothieno[2,3-d]pyrimidine and the minor as 2-amino-3-arylthieno[2,3-H]pyrimidin-4(3H)-one.     

Reverse isotope dilution alpha spectrometry using plutionium-239 spike for determining plutonium concentration in high burn-up fuel samples without purification from americium-241 and a bulk of other impurities

A reverse isotope dilution alpha spectrometric /R-IDAS/ method using²³⁹Pu as a spike is described for the determination of plutonium concentration in high burn-up fuel samples wth²³⁸Pu/(²³⁹Pu+²⁴⁰Pu) alpha activity ratio >0.5, without resorting to any purification from²⁴¹Am and a bulk of other impurities. It involves the addition of a pre-clibrated spike solution to a known aliquot of the plutonium sample solution followed by source preparation using TEG as a spreading agent. The results obtained on a number of plutonium samples containing 20–80% of²⁴¹Am /alpha activity wise/ using this method are compared with those achieved by R-IDAS using purification with TTA, with respect to precision and accuracy. Precision and accuracy of 0.5% are demonstrated. This method eliminates the need of any separation and purification of plutonium from²⁴¹Am and a bulk of other impurities like uranium.     

Activities of Hydrolases and Oxidases as Influenced by the Application of Monocrotophos in Sandy Loam Soil of Rajasthan

Continuous and repeated use of pesticides affects soil microbial flora and fauna and hence indirectly affects the activity of diverse microbial enzymes present within it. The present study investigates the interaction effect of different concentrations of monocrotophos on diverse hydrolases and oxidases, viz., protease, alkaline phosphatase, acid phosphatase, cellulase, amylase, invertase, arginine deaminase, and dehydrogenase, present in sandy loam soil of Rajasthan under in vitro conditions for 30 days. Soil sample was inoculated with three different concentrations of monocrotophos, viz., 50, 100, and 150 μg kg^-1, and incubated in dark at room temperature. At regular interval of 5 days, sample was withdrawn and enzyme activity was calculated and compared with that of control. Application of various concentrations of monocrotophos enhanced the activity of diverse enzymes present in soil. Therefore, the study revealed synergistic or additive effect of monocrotophos on all the tested microbial enzyme entities. Increasing concentration of the pesticide, however, poses an antagonistic interaction on the increment of different enzymes activities. Therefore, it can be concluded from the study that monocrotophos impose a positive effect at low concentration of pesticide, whereas high concentration poses negative effect on the activity of different enzymes present in soil.     

Synthesis,characterization, molecular docking and biological activity of 5,6-bis-(4-fluoro-phenyl)-3,4,7,8-tetraaza-bicyclo[8.3.1]tetradeca-1(13),4,6,10(14),11-pentaene-2,9-dione and its transition metal complexes

Macrocyclic Schiff base ligand through the condensation of 1,3-dicarbonyl-phenyl-dihydrazide with 4,4′-difluorobenzil and its Co(II), Ni(II), Cu(II) and Zn(II) metal complexes have been synthesized. The ligand and metal complexes were characterized by analytical and physicochemical methods. An octahedral geometry arising from coordination of N2O2 donor atoms from the macrocyclic framework has been proposed for all metal complexes. Synthesized ligand and metal complexes were investigated for in vitro antibacterial and antioxidant activity. Complex [Ni(C₂₂H₁₄N₄F₂O₂)(OCOCH₃)₂] has shown remarkable antibacterial activity (Minimum inhibitory concentration 8–16?μg/ml) comparable to commercial antibiotic Ciprofloxacin. Anticancer activity of synthesized compounds against Squamous Cell Carcinoma (SCC4), head and neck cancer cell line has also been studied at different concentrations and at different time points. Complexes [Co(C₂₂H₁₄N₄F₂O₂)(NO₃)₂] and [Cu(C₂₂H₁₄N₄F₂O₂)(OCOCH₃)₂] have shown remarkable anticancer results (IC₅₀ 31.1 and 43.1?μM) against the tested cell line in concentration dependent manner. Molecular docking studies were carried out to find the binding mode of the synthesized macrocyclic Schiff base ligand to Epidermal Growth Factor Receptor (EGFR) Kinase (PDB ID: 1M17).     

Comparable Ionicity of the Solutions of Aprotic and Protic Ionic Liquids by Anion Substitution

Temperature dependent molar conductances and fluidities of bisulfate and ethyl sulfate anion-based ionic liquids were measured. The extent of dissociation of the ionic liquids was estimated from the Walden plot in term of ionicity. The ionicity mainly depends on the magnitude of Coulombic forces, altered by the anion’s Lewis basicity. Aqueous solutions of aprotic ionic liquids, in general, possesses ionicity in the range of ≈70–99%. This article reveals that the substitution of the anion by bisulfate and ethylsulfate reduces the ionicity of aqueous solution of these ionic liquids to the range of 10–37%. This is very close to that exhibited by some of the protic ionic liquids and phosphonium based ionic liquids with sweetner anions. The concentration dependent molar conductance of these ionic liquids has been fitted to Mahiuddin and Ismail’s equation. To our surprise, the molar conductances of bisulfate-based aprotic ionic liquids are remarkably high, even though these ionic liquids possess lower ionicity.     

Thermodynamics and kinetics of hydrogen absorption–desorption of vanadium synthesized by aluminothermy

This paper studies the addition (0–40% w/w) of natural zeolite (NZ, 84% clinoptilolite) in blended cements made with Portland cement (PC) with low and medium C₃A content. The isothermal calorimetry was used to understand the effect of NZ on the early cement hydration. For low C₃A cement, the addition of NZ produces mainly a dilution effect and then the heat released curve is similar to plain cement with lower intensity. For medium C₃A cement, the curve shows the C₃S peak in advance and a high intensity of third peak attributed to C₃A hydration. The high cation fixed of NZ reduces the ions concentration (especially alkalis) in the mixing water stimulating the PC hydration. The flowability decreases when the NZ replacement level increases. Results of Fratini’s test show that NZ with both PCs used presents slow pozzolanic activity. At early age, XRD and FTIR analyses confirm that hydration products are the same as that of the corresponding PC and the CH is progressively reduced after 28 days and some AFm phases (hemi- and monocarboaluminate) appear depending on the NZ percentage and the PC used. For low replacement levels, the compressive strength is higher than the corresponding PC from 2 to 28 days. For high replacement levels, the early compressive strength is lower than that of corresponding plain PC and the pozzolanic reaction improves the later compressive strength of blended cements.     

Oxidative degradation of levofloxacin by water-soluble manganese dioxide in aqueous acidic medium: a kinetic study

Pharmaceuticals, especially fluoroquinolone antibiotics, have received increasing global concern, due to their intensive use in the environment and potential harm to ecological system as well as human health. Degradation of antibiotics, such as oxidative degradation by metal oxides, often plays an important role in the elimination of antibiotics from the environment. The kinetics of oxidation of levofloxacin by water-soluble manganese dioxide has been studied in aqueous acidic medium at 25 °C temperature. The stoichiometry for the reaction indicates that the oxidation of 1 mol of levofloxacin requires 1 mol of manganese dioxide. The reaction is second order, that is first order with respect to manganese dioxide and levofloxacin. The rate of reaction increases with the increasing [H⁺] ion concentration. A probable reaction mechanism, in agreement with the observed kinetic results, has been proposed and discussed. The energy and enthalpy of activation have been calculated to be 30.54 and 28.07 kJ mol^?1, respectively.     

Gravimetric determination of molybdenum and tungsten using pyridoin as a reagent

Summary Pyridoin has been used as a reagent for the gravimetric determination of molybdenum and tungsten. The reagent quantitatively precipitates molybdenum from ammonium molybdate solution at p_H 2.0–9.5 and tungsten from sodium tungstate solution at p_H 2.0–4.5. The precipitate in each case is ignited to the oxide and weighed.

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Zusammenfassung Zur gravimetrischen Bestimmung von Molybdän und Wolfram wird Pyridoin als Reagens empfohlen. Molybdän wurde aus Ammoniummolybdatlösung bei p_H 2,0–9,5 quantitativ ausgefällt, Wolfram aus Natriumwolframatlösung bei p_H 2,0–4,5. Die Niederschläge wurden jeweils zum Oxid verglüht und dieses ausgewogen.

     

Polarographische Untersuchungen von aus Cadmium(II) und Propylendiamin in wäßrigem Dimethylformamid entstandenen Komplexen

The reduction of Cd(II) in propylenediamine was found to be reversible and diffusion controlled. The complexes of Cd(II) with propylenediamine in 25%, 50%, and 75% dimethylformamide have been studied polarographically using theDeFord andHume's treatment as extended byIrving. Increase in the stability constants was observed with increase in dimethylformamide percentage. The percentage composition of the various complexed and uncomplexed species in 25% and 50% dimethylformamide are presented.     

Diphenic acid as a selective reagent for the amperometric determination of thorium(IV)

Th(IV) has been titrated amperometrically at an applied e.m.f of −1.0 V (dropping mercury electrode vs. SCE) with diphenic acid (neutralized with sodium hydroxide). Th(IV) in the range 8.0–60.0 mg/100ml can be determined with an error of ±0.5%. A number of foreign ions including Ce(IV), Zr(IV), La(III), U(IV), U(VI) do not interfere even if present in excess but traces of Ti(IV) do. The method is rapid and selective and has been used for the determination of Th(IV) in monazite sand.