Six new triazole compounds were synthesized. These compounds containing the substituted benzylidenamino group were obtained
by reaction of 3-(pyridine-4-yl)-5-p-tolyl-4-amino-4H-l,2,4-triazole 1 with the corresponding aldehyde. The reduced forms were prepared with NaBH4 in methanol. The structures of the compounds were determined by IR, 1H NMR, and 13C NMR spectral data, and their interaction with cations such as Li+, Na+, K+, Rb+, Cs+, Ba2+, Sr2+, Ca2+, Cu2+, Cr3+, Co2+, Ni2+, Zn2+, Cd2+, Pb2+ and Ag+ were investigated by using UV-visible spectrophotometry. Of the tested metal cations, Cu2+, Cr3+, Co2+, Ni2+, Zn2+, Cd2+, Pb2+ and Ag+ complexed with the ligands. The complex stability constants (log 10K) were measured in slightly acidic aqueous media at 25.0±0.1 °C. These stability constants were determined by measuring the
increase in solubility of the nearly insoluble ligand molecule due to complex formation with a soluble cation, and this method
is discussed. It was found that the position of chlorine atoms on the benzene ring strongly affects the complexation of Cu2+ ion with these ligands. 相似文献
1-Decyl-2,3-dimethylimidazolium bromide (ddmimBr) has been synthesized by the reaction of 1,2-dimethylimidazole and 1-bromodecane. Micellization of ddmimBr surfactant in water (W) and water-ethanolamine (W-EA) with the weight percent of EA changing within the range 0-39.79%, has been investigated at 298.15 K. Information about the influence of the added EA on the critical micelle concentration (CMC) was obtained through density and surface tension measurements. This last provides information about the dependence of the surface excess concentration, the minimum area per surfactant molecule and the surface pressure at the CMC on the added weight percentage of organic solvent. The effect of binary aqueous mixtures of W-EA on the apparent molar volume (phi V) of the ddmimBr has been investigated. The apparent molar volume upon aggregation (Delta phi V) shows a maximum at about 15 wt% of EA, this behavior is discussed in terms of the changes of the solvent structure. Partial specific volume data, obtained by density measurements, indicate that the fraction of solvent molecules interact with the surfactant remained roughly constant. 相似文献
A simple, rapid, and stability-indicating reversed-phase high-performance liquid chromatographic (LC) method for analysis for dutasteride has been successfully developed. Chromatography was performed on a 150 mm × 4.6 mm C18 column with acetonitrile–water 60:40 (v/v) as isocratic mobile phase at 1.0 mL min−1. Ultraviolet detection of dutasteride was at 210 nm. Its retention time was approximately 10 min and its peak was symmetrical. Response was a linear function of concentration over the range 0.2–1 μg mL−1 (R2 = 0.997) and the limits of detection and quantitation were was 0.05 and 0.10 μg mL−1, respectively. The method was validated for linearity, precision, repeatability, sensitivity, and selectivity. Selectivity was validated by subjecting dutasteride stock solution to photolytic, acidic, basic, oxidative, and thermal degradation. The peaks from the degradation products did not interfere with that from dutasteride. The method was used to quantify dutasteride in pharmaceutical preparations.
Given a non-compact, simply connected homogeneous three-manifold X and a sequence {Ωn}n of isoperimetric domains in X with volumes tending to infinity, we prove that, as n→∞:
Kirchberg asked in 2004 whether the commutant of L(H) in its (norm) ultrapower is trivial. Assuming the Continuum Hypothesis, we prove that the answer depends on the choice of the ultrafilter. 相似文献