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排序方式: 共有276条查询结果,搜索用时 15 毫秒
1.
Nada F. Atta 《Talanta》2007,72(4):1438-1445
The effect of adding surface-active agents to electrolytes containing terazosin, an antihypertensive drug, on the voltammetric response of glassy carbon electrode was studied. The current signal due to the oxidation process was a function of the amount of terazosin, pH of the medium, type of surfactant, and accumulation time at the electrode surface. Two surfactants were used, an anionic type, sodium dodecyl sulfate (SDS) and a cationic type, cetyl trimethyl ammonium bromide (CTAB). Addition of SDS to the terazosin-containing electrolyte was found to enhance the oxidation current signal while CTAB showed an opposite effect. Beside the interfacial interaction of the surfactant with the electrode surface in reference to the bias applied potential and the charge of surfactant, terazosin-surfactant interaction in the electrolytic solution was found to be critical to the magnitude of current signal. Addition of SDS to terazosin-containing buffer solution resulted in a decrease in the drug absorption spectrum both in the ultra-violet and visible (UV-vis) regions. Moreover, NMR measurements showed considerable chemical shifts for the aromatic protons of the quinazolinyl moiety of the terazosin in presence of SDS. The affected aromatic protons are positioned next to the interacting protonated amino-group of the terazosin with the charged sulfonate-group of SDS. On the other hand, addition of CTAB did not cause noticeable changes both to the UV-vis and NMR spectra of the drug. The use of SDS in the electrochemical determination of terazosin using linear sweep voltammetry and differential pulse voltammetry at solid glassy carbon electrode enhanced the detection limit from 6.00 × 10−7 mol L−1 in absence of surfactant to 4.58 × 10−9 mol L−1 when present. The validity of using this method in the determination of drug active ingredient in urine samples and tablet formulations was also demonstrated. 相似文献
2.
3.
Djaković-Sekulić Tatjana Perišić-Janjić Nada Sârbu Costel Lozanov-Crvenković Zagorka 《平面色谱法杂志一现代薄层色谱法》2007,20(4):251-257
JPC – Journal of Planar Chromatography – Modern TLC - Reversed-phase (RP) HPTLC with aqueous ammonia-organic modifier (acetonitrile, dioxane, acetone) mobile phases has been used to... 相似文献
4.
Perišić-Janjić Nada U. Ž. Jovanović Bratislav Janjić Natasa J. Rajković Olga S. Antonović Dušan G. 《平面色谱法杂志一现代薄层色谱法》2003,16(6):425-432
JPC – Journal of Planar Chromatography – Modern TLC - The chromatographic behavior of nine newly synthesized s-tri-azines has been studied by thin-layer chromatography on C18/UV254... 相似文献
5.
Nada F. Atta 《European Polymer Journal》2005,41(12):3018-3025
Polymeric films derived from thioflavin S were electrosynthesized on mild steel and silver electrodes in sulfuric acid and lithium perchlorate-containing aqueous solutions. The introduction of thioflavin S in an acidic solution protected the surface of steel from corrosion. The electrochemical behavior of the steel coated with a layer of poly(thioflavin) was examined by electrochemical impedance spectroscopy. The films exhibited a capacitive behavior and were semi-conductive in nature. Infra red reflectance measurements of the polymer films at the steel surface showed that the polymer structure retained the aromatic structure of the benzene and thiazole rings with the distinction of a nitrogen quinone vibrational band. Surface morphology of the polymer film was examined with scanning electron microscopy. The films are yellow, compact and dense when electrochemically formed onto steel surfaces when compared to a blue rather porous when formed onto silver electrode. The mechanism of electropolymerization of thioflavin is given and found similar to that of aniline with the possibility of metal chelation with the sulfur and/or nitrogen in the thiazole ring. 相似文献
6.
Nada Majkić-Singh Milan Konjović Marina Stojanov Slavisa Spasić Ivan Berkeš 《Analytica chimica acta》1981,130(2):419-423
Hydrogen peroxide, the product of diamine oxidase-catalyzed putrescine or cadaverine oxidation, formed in proportion to the enzyme activity, is measured spectrophotometrically by using the above sulfonate (ABTS) and peroxidase. Only one reagent solution containing 3 mmol of putrescine or 10 mmol of cadaverine, 4 mmol of ABTS and 3000 U of peroxidase per litre of 0.2 mol l-1 Tris—0.1 mol l-1 HCl buffer pH 7.5 is needed. Absorbance changes are measured at 410 nm over the first 3 min of the reaction. This initial oxidation rate of the chromogen enables diamine oxidase activity up to 230 U l-1 to be determined. 相似文献
7.
D. Minić Nada Štrbac I. Mihajlović Ž. Živković 《Journal of Thermal Analysis and Calorimetry》2005,82(2):383-388
In this paper, the results of copper-lead matte investigations are presented. Investigated copper-lead matte is intermediate
product of the lead production in TREPCA-Zvečan. In the first part of the paper characterization of starting material is presented,
consisting of: chemical composition analysis (XRQ), scanning electron microscopy (SEM) and diffractometry (XRD). Thermal properties
of investigated matte were determined using differential thermal analysis (DTA) at characteristic temperatures. Using results
of induced analysis, mechanism of matte oxidation process was determined. In the second part of the paper kinetic parameters
describing oxidative roasting of copper-lead matte are presented. For activation energy calculations, non-isothermal methods
defined by Kissinger and Ozawa were used [1, 2]. Kinetic equation describing oxidation process was determined using Sharps
method of reduced half time of reaction [3]. 相似文献
8.
The method is based on the oxidation of ethanol in the presence of alcohol oxidase, followed by oxidation of 2,2'-azino-di(3-ethylbenzthiazoline-6-sulfonate) in the presence of peroxidase. 相似文献
9.
Branislav Dugovi
Lubor Fiera MichalK. Cyranski Christian Hametner Nada Prnayov Marin Obranec 《Helvetica chimica acta》2005,88(6):1432-1443
The regio‐ and stereoselectivity of cycloadditions of the nitrone 1a and the chiral, sugar‐derived nitrones 13a and 13b with 3‐(prop‐2‐enoyl)‐1,3‐oxazolidin‐2‐one ( 2 ) depends on the nature of the Lewis acid catalyst used. Addition of Lewis acid reverses the regioselectivity of the cycloaddition, and improves the anti‐diastereoselectivity in the case of chiral nitrones. The sterically favored isoxazolidin‐5‐yl‐substituted adducts 3, 4 , and 14 – 17 are produced as the major products in the absence of Lewis acid, while the electronically favored regioisomers with isoxazolidin‐4‐yl substituents ( 5, 6 , and 18 – 21 , respectively) are obtained as major products in the [Ti(OiPr)2Cl2] catalyzed reactions. The reactions of nitrone 13b with 2 in the presence of other Lewis acids such as ZnCl2, ZnBr2, ZnI2 and MgI2/I2 gave both regioisomeric pairs of the diastereoisomers, favoring the 4‐substituted congeners. The diastereoisomeric isoxazolidines 3a – 6a were reduced with NaBH4 in THF/H2O with subsequent desilylation to yield the separable diols 9 – 12 . Reduction of the diastereoisomeric isoxazolidines 19a and 18a afforded the chiral alcohols 23 and 22 , the latter of which was analyzed by X‐ray crystallography. 相似文献
10.
Summary On small columns filled with the inorganic cation-exchanger zirconium phosphate, Zn2+-Cd2+ were quantitatively and Ni2+-Co2+ partly separated. The exchanger was in the NH4+ form, and 0.5–4N NH4Cl served as eluent. With the exchanger in the H+ form, U02
2+ was separated from bivalent cations and ferric iron by stepwise elution with 0.1, 0.5 and 4N HCl solutions.
Zusammenfassung An kleinen Säulen des anorganischen Kationenaustauschers Zirkoniumphosphat wurden Zn2+ und Cd2+ quantitativ, Ni2+ und Co2+ teilweise getrennt. Der Austauscher lag in der NH4+-Form vor, 0,5-bis 4-n Ammoniumchlorid diente als Eluent. Mit der H+-Form des Austauschers wurde UO2 2+ von zweiwertigen Kationen und von Fe3+ durch schrittweise Elution mit 0,1-, 0,5- und 4-n Salzsäure getrennt.
Résumé On a séparé Zn2+-Cd2+ quantitativement et Ni2+-Co2+ partiellement sur de petites colonnes remplies de phosphate de zirconium comme échangeur minéral cationique. L'échangeur se trouvait sous forme NH4+ et l'on a pris NH4Cl 0,5-4N comme éluant. Avec l'échangeur sous forme H+, on a séparé UO2 2+ des cations bivalents et de l'ion ferrique par élution graduelle avec des solutions chlorhydriques 0,1, 0,5 et 4N.相似文献