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951.
R. Selwin Joseyphus C. Justin Dhanaraj M. Sivasankaran Nair 《Transition Metal Chemistry》2006,31(6):699-702
The cobalt(II), nickel(II), copper(II) and zinc(II)-vanillidene-L(+)alanine complexes were synthesized and characterized by
elemental analysis, conductivity measurements, magnetic behavior, infrared, electronic spectral measurements, X-ray powder
diffraction and biological studies. The conductance measurements indicate that all the complexes are non-electrolytes. The
infrared spectra indicate the coordination of imino nitrogen, phenolic oxygen and carboxylato oxygen atoms. The electronic
spectral measurements demonstrate that cobalt(II) and nickel(II)-vanillidene-L(+)alanine complexes are tetrahedral, while
copper(II)-vanillidene-L(+)alanine complex has square planar geometry. The cobalt(II) complex is found to be ferromagnetic.
The powder XRD studies confirm the crystalline nature of the complexes. The ligand and complexes were less active against
PN, PA and BC, whereas copper complex shows moderate activity against AN. 相似文献
952.
P. R. Nair M. Xavier S. G. Marathe H. C. Jain 《Journal of Radioanalytical and Nuclear Chemistry》1991,152(2):519-523
A biamperometric method for the determination of sulfate has been developed. Its application to the determination of sulfate content in rubidium uranium trisulfate is discussed. Sulfate is determined by titration with lead nitrate in aqueous ethanolic medium using ferrocyanide-ferricyanide redox system as biamperometric indicator. Initially, the method has been tested for standard. K2SO4 solutions. In case of Rb2 U(SO4)3, since uranium interferes, it is precipitated as ammonium diuranate and excess ammonia is removed prior to the titration. Precision of better than 0.3% was achieved with no significant bias. 相似文献
953.
The electric dipole moment of 205Tl19F has been measured in its higher vibrational states up to ν = 7 by studying the Statk effect in the J = O → 1 rotational transitions. The variation of the electric dipole moment with vibrational states is discussed. The electric dipole moment can be written as lμνl = 4.1941 (15) + 0.0681(12) (ν + ) D. 相似文献
954.
At wavelengths near 1 mm six rotational transitions of GaCl have been observed. The analysis including previous measurements on the rotational transitionJ = 1 ← 0 resulted in extended sets of the Dunham parametersY 01,Y 11,Y 21,Y 31,Y 02,Y 12 andY 03 of the four isotopic species69Ga35Cl,71Ga35Cl,69Ga37Cl and71Ga37Cl. With these microwave data the constantsY 10 ≈ εe and —Y 20 ≈ ω e x e were determined. The parameters of the Dunham potentiala 0,a 1,a 2,a 3 andr e are given. The GaCl was produced by reaction of gaseous CCl4 with Ga evaporated at 1,500°C. 相似文献
955.
A potentiometric titration method and a conductometric titration method were standardized for the determination of nitrate in thorium, uranium and plutonium solutions in the range of 2–10 mg, and 15–30 mg, respectively, with a precision and accuracy of 2% in both cases. The results were compared with those of other methods like Devarda's alloy reduction method and volumetric titration method. The procedures standardized have been recommended for the determination of nitrate in heavy element solutions used for the preparation of oxide and mixed oxide microspheres by the sol-gel technique. 相似文献
956.
P. K. R. Nair A. Mittal S. V. Kadamne K. Srinivasulu 《Reaction Kinetics and Catalysis Letters》1982,19(1-2):201-205
Oscillatory behavior in the uncatalyzed aqueous acidic bromate oxidation of 3,4-dimethoxybenzaldehyde (veratraldehyde) is reported. The generally used H2SO4 can be substituted by HNO3, HClO4, CCl3 COOH and H3PO4 in this system. The length of the induction period is found to be dependent on the initial concentrations of the reagents and this effect is more prominent in the case of acidity. The precipitate accumulated in the reaction during oscillations has been identified. A plausible mechanism is also suggested. Experiments with allyl alcohol, a bromine scavenger, suggest that elemental bromine formed in the reaction has a role in the mechanism together with or besides bromide inons.
3,4- () . H2SO4 HNO3, HClO4, CCl3 COOH H3PO4 . . , , . . , , , , , .相似文献
957.
The kinetics and mechanism of the thermal decomposition of perchlorate, nitrate and iodide complexes of lanthanum with the
Schiff base 1,2-(diimino-4'-antipyrinyl)ethane (abbreviated as GA) have been studied by TG and DTG techniques. The kinetic
parameters like the activation energy, the pre-exponential factor and the entropy of activation were calculated for the major
decomposition stages (Stages I and II) using Coats-Redfern equation. The rate controlling process obey ‘Mampel model’ with
random nucleation with one nucleus on each particle. The kinetic parameters indicate that the ligands are loosely bound to
metal ion and the activated complex formed in the decomposition reaction is more ordered than the reactants.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
958.
The structure of the dimer ( 5 ) from 2-pyridyl isothiocyanate ( 1 ) has been confirmed by 13C nmr spectral studies. The cycloaddition of 2-pyridyl isothiocyanate with 1-azirines results in the formation of thiazoles ( 10 ). Thermal decomposition of the vinyl azide ( 14 ) gives the pyrrole ( 15 ) and the pyridazine ( 16 ) instead of 2-(2-pyridyl)-1-azirine ( 12 ). 相似文献
959.
C. V. Karekar Keshav Chander G. M. Nair P. R. Natarajan 《Journal of Radioanalytical and Nuclear Chemistry》1986,107(5):297-305
A potentiometric titration method was developed for the determination of plutonium and uranium in the same aliquot in nitric acid medium. Plutonium was first determined by oxidation to Pu/VI/ by fuming with conc. HClO4. Pu/VI/ formed was reduced to Pu/IV/ with known excess of Fe/II/ and the excess Fe/II/ was titrated with standard K2Cr2O7 to a potentiometric end point. Uranium in the same solution was determined by reduction to U/IV/ with Fe/II/ in conc. H3PO4 medium and titrating U/IV/ formed with standard K2Cr2O7 using the potentiometric end point detection technique. For the quantity of plutonium and uranium each in the range of 3–5 mg per aliquot a precision of ±0.2% and ±0.4%, respectively, was obtained. 相似文献
960.
K. Sudarshan A. G. C. Nair A. Goswami 《Journal of Radioanalytical and Nuclear Chemistry》2003,256(1):93-98
An internal mono-standard method has been proposed for multi element analysis. This method gives the relative concentration of the elements in a sample of non-standard shape and size. It utilizes an in-situ relative efficiency calibration and hence, does not need the cumbersome procedures, otherwise required to correct for -attenuation in the sample. To validate this method, the relative concentration of elements in IAEA RM's SL-3 and Soil-7 were analyzed with sample amounts ranging from a few milligrams to grams. The samples were counted in different non-specific geometries. The results are in good agreement with the recommended values, suggesting that this methodology could be applied for the analysis of samples of non-standard size and shape, and in principle, for the analysis of large samples. 相似文献