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21.
Zusammenfassung Mit Hilfe von Gemischen wurden die formalen Redoxpotentials einiger einfacher Aminophenoxazone-(3) und 2-substituierter Gallocyaninmethylesterderivate (Prune) mit den Substituenten — NH-C6H4X [X = H, CH3, OCH3, OH, NH2, N(C2H5)2] in 50%iger Äthanollösung mit einer konstanten Ionenstärke in der Abhängigkeit vom pu bei 25° C gemessen.Die auf pH=0 extrapolierten Potentiale stehen mit den Hammetschen -Konstanten in guter Korrelation.
Wir danken Herrn Ing.Z. Stránský C. Sc. für wertvolle Erinnerungen bei der Interpretation der Ergebnisse. 相似文献
Summary With the aid of mixtures the formal redox potentials of several simple aminophenoxazones-(3) and 2-substituted gallocyaninmethylester derivates (Prunes) with the substituents -NH-C6H4X [X = H, CH3, OCH3, OH, NH2, N(C2H5)2] were measured in 50% ethanol solution with a constant ionic strength with respect to the dependence of pn at 25° C. The potentials extrapolated to pn = 0 are in good correlation with the Hammet -constants.
Wir danken Herrn Ing.Z. Stránský C. Sc. für wertvolle Erinnerungen bei der Interpretation der Ergebnisse. 相似文献
22.
Preconcentration was effected using a 50 mm × 2 mm i.d. minicolumn packed with a spherical cellulose sorbent with chemically bound quinolin-8-ol function groups (Ostorb Oxin). The column was connected to the nebulizer of the atomic absorption spectrometer and the sample solution and eluent (2 M hydrochloric acid) were sucked through it at a flow-rate of 2–3 ml min?1 by utilizing the negative pressure of the nebulizer. The experimental design was tested with the determination of traces of copper. Peak-area and peak-height measurements were compared. Owing to the simple calibration, the former method was used for quantification. The dynamic range was from 0.3 ng ml?1 (detection limit) to 5 μg ml?1 (breakthrough). The reproducibility in the concentration range 25 ng ml?1-5 μg ml?1 was better than 5%. Water-soluble inorganic salts, ammonia and sodium hydroxide were analysed. The accuracy of the results was checked by anodic-stripping voltammetry and by electrothermal AAS. 相似文献
23.
The reduction of Ni2+ ions at mercury electrodes in acidic perchlorate solutions, at perchlorate concentrations below 0.2 M, is characterized by absence of kinetic control in the preceding step, and by a complex reaction mechanism following the electron transfer. This reaction sequence is known to involve intermetallic compound formation between Ni and Hg and is best described, as shown here, by a parallel second and third order kinetic scheme. Apparent rate coefficients for this kinetic scheme were determined using cyclic chronopotentiometric data and fitting by digital simulation. A linearization test of computed kinetic rate coefficients versus the number of transitions permits quantitative tests of validity of assumptions made. 相似文献
24.
The electronic spectra of tetrathiotetracene (TTT) and of its mono- and dipositive ions have been calculated by the Pariser-Parr-Pople (PPP) method. Furthermore, the band polarizations of the first two bands of TTT have been measured. A reasonable band assignment is given using a new set of PPP parameters based on spectral data of a naphthalene derivative containing similar typical weak S-S bond. Other physical parameters as ionization potential, disproportionation energy, S-S bond length and net π-charges are discussed. 相似文献
25.
Summary The effect of pre-adsorbed benzene and ethanol on the adsorptive properties of natural zeolite (clinoptilolite) has been studied
by gas-solid chromatography. It has been shown that modification of the solid surface by volatile organics has a significant
influence on the adsorptive properties. The modification is of the same order as the more difficult modification by inorganics,
as illustrated here by clinoptilolite modification with Co2+. Energy distribution of surface adsorptive sites appears to be continuous and confirms previous finding that only a small
proportion of active sites is responsible for most adsorbate retention.
Part II reference [4] 相似文献
26.
Electrodes containing glucose oxidase or xanthine oxidase adsorbed on modified glassy carbon electrodes or on conductive complexes, accumulate charge in the presence of substrates, the discharge of which gives the chronoamperometric stripping current. This current is 15 times higher than the stationary current after preconcentration for 8 min. A ten-fold increase in sensitivity of the determination of glucose or hypoxanthine is observed. The stripping current of electrodes based on cytochrome b2 adsorbed on a graphite electrode is 25 times higher than the stationary current. The electrode is useful for lactate determinations for more than 7 days. 相似文献
27.
G. Čík J. Lesný F. Šeršeň L. Szabo 《Journal of Radioanalytical and Nuclear Chemistry》1994,186(2):175-182
The influence of -radiation on the electric properties of Langmuir-Blodgett (LB) films of partially iodine-doped poly-(3-hexadecylthiophene) and stearic acid in interaction with selected environment-polluting gases has been studied. CO2, CO and NO2 increase the LB films conductivity and NO has a tendency to decrease the electric conductivity. The influence of -radiation was expressive onyl in the case of CO2, whereas NO2 brought about degradation of the conductive polymer. 相似文献
28.
Dubravka Matković-Čalogović Zora Popović Branka Korpar-Čolig 《Journal of chemical crystallography》1995,25(8):453-458
[Hg(terpy)2](CF3SO3)2·0.5(CH3)2CO crystallizes in the triclinic
space group witha=14.631(6),b=15.258(4),c=18.785(7) Å, =69.66(2), =70.72(1), =88.55(1)°. The crystal structure consists of two independent [Hg(terpy)2]2+ cations, four trifluoromethanesulfonate anions and an acetone molecule in the asymmetric unit. Each mercury atom is coordinated by two tridentate terpyridine ligands forming an irregular six-coordination polyhedron. The Hg–N bond lengths range from 2.27(2) to 2.53(2) Å. 相似文献
29.
The electrical resistivity of as deposited polycrystalline copper thin films as a function of varying the process parameters has been investigated. Trying to minimize the resistivity of the copper thin films is important in the semiconductor industry, due to the fact that low resistivity copper can be employed to great advantage for new metallization schemes in advanced ultralarge scale integrated circuits. This paper presents the optimum choice of parameters that are necessary to achieve low resistivities of the thin films in reproducible experiments. All the depositions were performed using an unbalanced d.c. planar magnetron sputtering source (consisting of a circular copper target (98% purity, 0.01% Fe, 0.005% Ni, 0.005% Si) with a diameter of 100mm fitted with two electromagnets). The copper thin films were deposited onto glass substrates with argon being used as the sputtering gas. The resistivity was studied as a function of the pressure of the sputtering gas, the substrate bias, the substrate to target distance, the magnetron power, and the substrate temperature. It was found that depositions producing thin films with a resistivity of that approaching the bulk material (1.7×10–8m) were obtained if the sputtering gas pressure was below 0.2 Pa. The effect of the substrate bias was insignificant at these pressures. The crystallographic structure of the copper thin films, determined by X-ray diffraction, is also reported.The authors would like to thank Dr. Soukup for his support during this research. We would also like to express our gratitude to Mr. A. Rajský for improving the design of the sputtering device. This work was partially financed by a grant from the Grant Agency of the Czech Republic No. 202/93/0508. 相似文献
30.