Synthesis, characterization, and electrochemical and electrochromic properties of sandwich dilutetium tetraphthalocyanine

A new sandwich-tpype dilutetium tetraphthalocyanine 4 has been synthesized by the reaction of dimeric lutetium(III) phthalocyanine 3 with two equiv. of dilithium octakishexylthiophthalocyanine in amyl alcohol. Compound 3 was prepared from 4',5',4",5"-tetraiminoisoindoline(1,4,7,10-tetrathia-12-crown-4) 1, 4,5-bis(hexylthio)-1,2-diiminoisoindoline and lutetium acetate in amyl alcohol. Compounds 3 and 4 were characterized by elemental analysis, UV/visible, IR, (1)H NMR and ESR spectroscopy. The electrochemical and electrochromic properties of 3 and 4 have been examined by cyclic voltammetry. Both 3 and 4 displayed well-defined electrochromic behavior.     

Auto-Bäcklund transformations and solitary wave solutions for the nonlinear evolution equation

In the present work, according to the concept of extended homogeneous balance method and with help of Maple, we get auto-Bäcklund transformations for a (2 + 1)-dimensional nonlinear evolution equation. Subsequently, by using these auto-Bäcklund transformation, exact explicit solutions of this equation are obtained.     

Furo- and thieno-fused 1,3-diazepine-4,6-diones

We report the first preparation of furo- and thieno-fused 1,3-diazepine-4,6-dione derivatives starting from ethyl 2-(2-methoxy-2-oxoethyl)-3-furancarboxylate and -thiophencarboxylate. The ester functionalities connected to the hetero-ring were converted regiospecifically into the desired amides. The ester groups attached to the methylene unit were converted into isocyanates via Curtius rearrangement. The ring-closure reaction was performed in the presence of lithium bis(trimethylsilyl)amide at room temperature to give furo- and thieno-fused diazepinone derivatives.     

Determination of radiological hazard parameters and radioactivity concentrations in bauxite samples: the case of the Sutlegen Mine Region (Antalya,Turkey)

Journal of Radioanalytical and Nuclear Chemistry - Iron phosphate glasses with melting temperatures of?~?1300 °C were developed to immobilize spent nuclear fuels. The...     

A comparative analysis of linear,nonlinear and improved nonlinear thermodynamic models of voltage-dependent ion channel kinetics

The linear, nonlinear and improved nonlinear thermodynamic models of the voltage-dependent ion channels were proposed to deduce the exact functional form of the rate constants. In this context, we present a comparative analysis of the linear, nonlinear and improved nonlinear thermodynamic models of voltage-dependent channel kinetics based on the sodium activation experimental data of Cav3.1 channel. We also provide some insight on the assumptions used to derive the thermodynamic models of the channels and show that the improved nonlinear thermodynamic model provides a simple and physically plausible approach to describe the behavior of the voltage-dependent ion channels.     

Determination of p<Emphasis Type="Italic">K</Emphasis><Subscript>a</Subscript> values of clinically important perfluorochemicals in nonaqueous media

Perfluorochemicals (PFCs) are clinically and biotechnologically important species. In this work, the potentiometric titration method in nonaqueous media is proposed for the determination of acidity constant values of six different perfluorinated compounds. The saturated and nonsaturated perfluoroacids, perfluorocarnosine, and perfluoroalkyl-β-alanine were potentiometrically titrated in acetonitrile, N,N-dimethylformamide, acetone, ethanol, methanol, and pyridine with tetrabutylammonium hydroxide. The half-neutralization potentials and acidity constants of PFCs have been calculated from the titration curves by using the computerized derivative method. Except for R_F-Carnosine, all of the potentiometric titration curves of the PFCs exhibited one stoichiometric and well-defined endpoints in all of the solvents employed. The reproducibility and sensitivity of the method were evaluated. The text was submitted by the authors in English.     

Lead Fractionation Analysis in Lipstick Samples by Inductively Coupled Plasma-Mass Spectrometry

A new analytical approach based on fractionation was introduced for lead in lipstick samples. Different separation techniques including n-hexane, glycerol extraction, and activated carbon adsorption were used to characterize the lipid fraction, polar and aromatic components of the samples. Additionally, artificial saliva and food stimulant extractions were used for the risk assessment studies. Trace metal levels in fractions were determined by inductively coupled plasma-mass spectrometry. Method validation parameters in the total element determinations were defined in terms of detection limits, accuracy, and precision. The limits of detection and quantification were 0.02 and 0.07 mg kg^?1 for Pb; whereas the repeatability and reproducibility of the results based on percent relative standard deviation were 3.0% and 7.2% for lead, respectively.     

Determination of some phthalate acid esters in artificial saliva by gas chromatography-mass spectrometry after activated carbon enrichment

The determination of six phthalate acid esters was achieved in artificial saliva using gas chromatography-mass spectrometry following activated carbon enrichment of samples. Central composite experimental design was applied to optimize method parameters, such as pH, adsorption time and amount of activated carbon. The best compromise of analytical conditions for the simultaneous determination of analytes from spiked artificial saliva were found to be: pH (3), adsorption time (30 min), activated carbon amount (1.8 g L⁻¹) and elution solvent (chloroform). These conditions were applied to study the migration of phthalate acid esters from different children's toys into saliva. A horizontal agitation method was applied to extract the analytes from plastic toys into saliva for 2 h at 37 °C. The detection limits of the method were in the range of 1.3-5.1 μg L⁻¹, while the relative standard deviation (%) values for the analysis of 100 μg L⁻¹ of the analytes were below 3.0% (n = 5). Di-2-ethylhexyl phthalate was the main analyte found in these samples.     

On differential inclusions with prescribed attainable sets

In this article, the inverse problem of the differential inclusion theory is studied. For a given ε>0 and a continuous set valued map t→W(t), t∈[t₀,θ], where W(t)⊂Rⁿ is compact and convex for every t∈[t₀,θ], it is required to define differential inclusion so that the Hausdorff distance between the attainable set of the differential inclusion at the time moment t with initial set (t₀,W(t₀)) and W(t) would be less than ε for every t∈[t₀,θ].