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991.
F U Erko? S Ozsar B Güven G Kalkandelen E U?rar 《Journal of chromatographic science》1989,27(2):86-90
In the present work, a practical, rapid, reliable and isocratic reversed-phase high-performance liquid chromatographic (HPLC) method is described for the qualitative and quantitative analysis of estriol, estradiol-17 beta, estrone, testosterone, and progesterone. Chromatographic separation is complete in 16 min using a mobile phase of 50% acetonitrile (v/v) in water. The order of elution is estriol, testosterone, estradiol-17 beta, estrone, and progesterone; retention times are 2.5, 5.5, 5.6, 6.9, 16.3 min, respectively. Absorbance maxima of individual steroids is the limiting factor in quantitative determination. The recommended wavelengths for UV monitoring are E3 214, E2 280, T 254, E1 214, and P4 254 nm. 相似文献
992.
The addition of possible oxidation and/or isomerization products (butadiene, water, isomeric n-butenes) resulted in neither promotion nor inhibition in the oxidative dehydrogenation of n-butenes over tin-antimony mixed oxide catalysts. On the basis of these and other information on the influence of products an interpretation has been given to complete the reaction mechanism more realistic than those based on previous experimental results.
(, ) ( -) , . , , .相似文献
993.
Topological indices are graph invariants used in computational chemistry to encode molecules. A frequent problem when performing structure-activity studies is that topological indices are inter-correlated. We consider a simple topological index and show asymptotic independence for a random tree model. This continues previous work on the correlation among topological indices. These findings suggest that a size-dependence in a certain class of distance-based topological indices can be eliminated.AMS subject classification: 05C80, 60E10, 92E10 相似文献
994.
The equilibrium distribution of species formed between Cu(II) and N-acetylneuraminic (sialic) acid (I, LH) at 298 K has been determined using a two-dimensional (2D) simulation analysis of electron paramagnetic resonance (EPR) spectra. In acidic solutions (pH values < 4), the major species present are Cu(2+), [CuL]+ [logbeta = 1.64(4)], and [CuL2] [logbeta = 2.77(5)]. At intermediate pH values (4.0 < pH < 7.5), [CuL2H-1]- [logbeta = -2.72(7)] and two isomers of [CuLH-1] [logbeta (overall) = -3.37(2)] are present. At alkaline pH values (7.5 < pH < 11), the major species present is [CuL2H-2]2-, modeled as three isomers with unique giso and Aiso values [logbeta (overall) = -8.68(3)]. Two further species ([CuLH-3]2- and [CuL2H-3]3-) appear at pH values > 11. It is proposed that [CuL]+ most likely features I coordinated via the deprotonated carboxylic acid group (O1) and the endocyclic oxygen atom (OR) forming a five-membered chelate ring. Select Cu(II)-I species of the form [CuLH-1] may feature I acting as a dianionic tridentate chelate, via oxygen atoms derived from O1, OR, and one deprotonated hydroxy group (O7 or O8) from the glycerol tail. Alternatively, I may coordinate Cu(II) in a bidentate fashion as the tert-2-hydroxycarboxylato (O1,O2) dianion. Spectra predicted for Cu(II)-I complexes in which I is coordinated in either a O1,OR {I1-} or O1,O2 {I2-} bidentate fashion {e.g., [CuL]+ (O1,O R), [CuL2] (bis-O1,O R), [CuLH-1] (isomer: O1, O2), [CuL2H-1]- (O1, O R; O1, O2), and [CuL2H-2]2- (isomer: bis-O1, O2)} have "irregular" EPR spectra that are ascribed to the existence of Cu(II)-I(monomer) <==> Cu(II)-I(polymer) equilibria. The formation of polymeric Cu(II)-I species will be favored in these complexes because the glycerol-derived hydroxyl groups at the complex periphery (O, 7O, 8O9) are available for further Cu(II) binding. The presence of polymeric Cu(II)-I species is supported by EPR spectral data from solutions of Cu(II) and the homopolymer of I, colominic acid (Ipoly). Conversely, spectra predicted for Cu(II)-I complexes where I is coordinated in a {I2-} tridentate {e.g., [CuLH-1] (isomer: O1, O R, O7, or O8) and [CuL2H-2]2- (isomer: bis-O1,O R,O7, or O8)} or tetradentate fashion {I3-} {e.g., [CuLH-3]2- (O1, O R, O, 8O9)} are typical for mononuclear tetragonally elongated Cu(II) octahedra. In this latter series of complexes, the tendency toward the formation of polymeric Cu(II)-I analogues is small because the polydentate I effectively wraps up the mononuclear Cu(II) center. This work shows that Cu(II) could potentially mediate the chemistry of sialoglycoconjugate-containing proteins in human biology, such as the sialylated amyloid precursor protein of relevance to Alzheimer's disease. 相似文献
995.
García-Raso A Fiol JJ Tasada A Albertí FM Molins E Basallote MG Máñez MA Fernández-Trujillo MJ Sánchez D 《Dalton transactions (Cambridge, England : 2003)》2005,(23):3763-3772
Alkylidene-bis(2-aminopyrimidines) (pyr2Cx, x = 2-5) are useful ligands to interact with Ag(I) yielding discrete metallocycles. Crystal structures of the [(pyr2C2)Ag(NO3)]2 and [(H-pyr2C4)Ag(NO3)2]2 have been isolated where each macrocyclic moiety interacts with their surroundings through weak interactions, yielding 3D discrete structures, On the other hand, the solution study shows that the equilibrium constants for the formation of Ag(pyr2Cx)+ complexes are higher than the literature values for Ag(I) complexes with single pyrimidines, although the differences could be explained by invoking the solid-state structures of the Ag(I)-pyr2Cx complexes. 相似文献
996.
Montserrat Barquín María J. Gonzlez Garmendia Liher Larrínaga Elena Pinilla María R. Torres 《无机化学与普通化学杂志》2005,631(11):2210-2214
The complexes of copper formato with pyrazine and dimethylpyrazines: Cu(HCOO)2(pyrz) ( 1 ), Cu2(HCOO)4(pyrz) ( 2 ), Cu2(HCOO)4(2,3‐Me2pyrz) ( 3 ), Cu2(HCOO)4(2,5‐Me2pyrz) ( 4 ), and Cu2(HCOO)4(2,6‐Me2pyrz)2 ( 5 ) have been synthesized and characterized by chemical analysis and IR and electronic spectro scopies. The three‐dimensional structure of compound 1 consists of –Cu–pyrz–Cu–pyrz– chains joined by bridging formate groups coordinated, in configuration syn‐anti, to two copper atoms. The coordination around the copper atom is orthorhombic with two Cu–O distances of 2.374(1) Å, two Cu–O of 1.952 Å and two Cu–N of 2.080 Å. Compound 5 is formed by molecular dimers with the [Cu2(μ‐HCOO)4] unit, two copper atoms and four syn‐syn fomate groups, and two ligands coordinated to the copper atoms in the axial positions. In compounds 2 and 3 chains of [Cu2(μ‐HCOO)4] dimers with pyrz or 2,3‐Me2pyrz as bridging ligands are formed. The EPR signal of 1 is orthorhombic (g = 2.23, 2.20 and 2.06). In the EPR spectra of 2 – 5 compounds the triplet (S = 1) signals are observed. The g?, g∥ and D values are been calculated. 相似文献
997.
C. Sánchez-Pedreño M.Hernández Córdoba P.Viñas López-Pelegrín 《Microchemical Journal》1985,32(2):242-248
A kinetic method for the silver determination based on the catalytic effect of Ag(I) on the oxidation of o-dianisidine by persulfate at pH = 4.5 in the presence of 1,10-phenanthroline is proposed. Ag(I) can be determined by measuring the absorbance of the reaction product at 450 nm, using the fixed time method. Co(II) does not have a catalytic effect in the reaction, but in the simultaneous presence of silver and cobalt the reaction shows an induction period the length of which is related to the Ag/Co molar ratio. As a consequence, two new methods for the determination of cobalt and silver using the induction period method are proposed. The two methods for silver are applied to the determination of silver in lead. 相似文献
998.
Summary An atomic absorption method has been developed for the determination of iron and calcium impurities in magnesium oxide. The effect of the magnesium matrix has been eliminated by the addition of hydroiodic acid and hydrogen peroxide to generate iodinein situ. The relative standard deviations were 0.5% for iron and between 0.5 and 1.5% for calcium.
Die Bestimmung von Eisen- und Calcium-Verunreinigungen in Magnesiumoxid mit Hilfe der Atomabsorption
Zusammenfassung Zur Bestimmung der Eisen- und Calcium-Verunreinigungen in Magnesiumoxid wurde die Atomabsorptionsspektroskopie herangezogen. Der Einfluß der Magnesiummatrix wurde durch Zugabe von Jodwasserstoffsäure und Wasserstoffperoxid, d. h. durch Freisetzung von Jod in situ beseitigt. Die rel. Standardabweichung für Eisen betrug 0,5%, für Calcium 0,5–1,5%.相似文献
999.
N. Batbaryar D. Batsurén A. A. Semenov M. N. Sultankhodzhaev 《Chemistry of Natural Compounds》1993,29(5):658-661
In the course of a further study of the alkaloids of the epigeal part of Aconitum turczaninowiia new alkaloid has been isolated, which has been named turpelline. A structure for turpelline has been proposed on the basis of a study of its IR, mass, PMR, 13 C NMR, and 2D COSY spectra. 相似文献
1000.
V. Spěváček 《Tetrahedron》1973,29(15):2285-2291
Reaction mechanism of halogen exchange between arylhalogenide and halogenide anion is studied in a case when the aromatic core is inactivated with respect to the SNAr substitution by other substituents. The exchange of iodine between o-iodobenzoic acid and 131I labelled NaI serves as a modelling reaction. The reaction was found to proceed heterogeneously on a glass surface. In the case of a rapid course of the surface reaction the reaction mechanism is more complicated and the equation derived by McKay cannot be applied for expressing the time dependence of the degree of isotopic exchange. Reaction mechanism was proposed for this reaction and compared with experimental data. 相似文献