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The study of D(?)-ribose complexing with calcium in aqueous solutions less than 1.64 × 10?1M by potentiometric measurements with a calcium selective electrode afforded the value of K1 = 1.70 liters × mole?1 (SD = 1.05 × 10?3). Numerical analysis indicated that complex species with 1:1 and 1:2 calcium to D(-)-ribose ratios are present simultaneously: k1 = 1.13 liters × mole?1 and K2 = 8.47 liters × mole?1 (SD = 0.95 × 10?3).In methanolic medium 1.24 × 10?2M with regard to calcium chloride both stoichiometric proportions were evidenced. A large error accompanying the stability constant K1 = 28 kg × mole?1 (RSD = 82%) renders unreasonable the K2 value obtained from the product K1 × K2 = 96.5 kg2 × mole?2.The results are discussed with respect to the data published for more concentrated (1.27 M) aqueous solutions obtained on the basis of 1H-NMR spectroscopic investigations. 相似文献
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Zvjezdana Lazarević Jasna Vorkapić-Furač Jasenka Mühl 《Monatshefte für Chemie / Chemical Monthly》1992,123(12):1175-1179
Summary Stable enolic isomers of 2-aroyl-4-aracyl-1,3-cyclopentanediones such as3 and4 were prepared by condensation of aryl methyl ketones and diethyl maleate using an excess of sodium ethoxide (Aryl=C6H5, 4-C6H4CH3, 4-C6H4Br and 4-C6H4Cl).
-Tricarbonyl Verbindungen. I. 2,4-Disubstituierte 1,3-Cyclopentandione
Zusammenfassung Stabile Enol-Isomere von 2-Aroyl-4-aracyl-1,3-cyclopentandionen wie3 und4 wurden durch Kondensation von Arylmethylketonen und Diethylmaleat mit einem Überschuß von Natriumethoxid dargestellt (Aryl=C6H5, 4-C6H4CH3, 4-C6H4Br und 4-C6H4Cl).相似文献
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The fluorescence characteristics of the Schiff bases 2-(3-pyridylmethyliminornethyl)phenol (1), 2-(2 pyridyliminomethyl)phenol (2), N.N-bis(salicylidene)-2,3-pyridinediamine (3), N,N'-bis(salicylidene)-2,6-pyridinediamine (4) and 2-(2-amino-4-methoxymethyl-6-methyl-3-pyridylmethyliminomethyl)phenol (5) were studied in various solvents at different pH values. Corresponding quantum efficiencies were determined. Compound 1, which showed a tendency towards tautomeric mterconversion to ketoamine in polar protic solvents, was not fluorescent at pH < 8. The fluorescence of other compounds was very sensitive to solvent polarity and the pH of the medium. Compounds 2-4, preferably present as enolimines in all solvents, were not fluorescent in non-polar and moderately polar solvents, whereas weak emission was observed in polar solvents, like methanol, dimethylformamide and dioxane/water 1/1 (0.001 < Q < 0.072). A significant increase in Stokes shifts and in quantum efficiencies was noted as a result of increasing polarity of dioxane/water mixtures, indicating specific interactions with polar water molecules. The emission was promoted at acidic pH values where a pyridinium cation was formed (0.061 < Q < 0.519, in dioxane/water 1/1 at pH 3.4). Compound 5, which was a tautomeric mixture of enoiimine and cyclic diamine in all solvents, was fluorescent in polar as well as in non-polar media. The quantum efficiency varied dependent on the solvent and pH (0.023 <Q< 0.435). The cyclic diamine, i. e. the more rigid structure was supposed to be responsible for the fluorescence in non-polar and aprotic solvents as well as at neutral, and weakly basic pH values. 相似文献
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The authors have elaborated an exact micro-volumetric method for the determination of lead with thionalide. The method has been successfully applied to the determination of lead in tin-base and lead-base alloys, following the isolation of lead as lead sulphate and its redissolution in ammonium acetate. 相似文献
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The protonation equilibria of 2-amino-3-aminomethyl-4,6-disubstituted pyridines were studied by potentiometric titrations and by UV and 13C NMR spectrometry. Protonation constants log K1 and log K2 potentiometrically determined for 4-methoxymethyl-6-methyl (8.959 and 5.778), 6-methoxymethyl-4-methyl (8.964 and 5.407), and 4,6-dimethyl derivative (9.141 and 6.604), were compared with the values obtained by the spectrometric methods. Complex formation of these compounds with Cu(II), Ni(II), Zn(II) and Co(II) was investigated in solution whereby the outstanding effect of the pH value was established and the presence of the species with 1 : 1 and 2 : 1 ligand to metal ratios confirmed. Stability constants obtained by potentiometric titrations show a decrease of the complex stability in the order Cu > Ni > Zn with respective log β1 values of 5.85, 3.56 and 2.93. Series of complexes isolated in the crude state were characterized by elemental analyses and spectrometric data, the latter serving also as the basis for making an attempt at the discernment of the coordination mode and sites. 相似文献