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41.
O. Kindel F. J. Herrmann L. Schmidt 《Journal of Radioanalytical and Nuclear Chemistry》1994,183(2):219-224
By simulation experiments with a 10–5 mol/l solution of iodododecane labeled with131I in n-dodecane the influence of various materials and conditions, which are possible in nuclear fuel reprocessing, has been investigated. The formation of decomposition products was detected via HPLC with a radioactivity monitor. By means of252Cf plasma-desorption mass spectrometry (PDMS) the decomposition products were identified. It was found that a temperature of 100°C favored the formation of iodoalkanes with chain lengths of C1 to C11. The presence of TBP(tri-n-butyl-phosphate) accelerated the decomposition of iodododecane. In pure TBP only iodobutane was formed as a decomposition product. 相似文献
42.
Steven Schmidt Gü nter Lattermann Ralf Kleppinger Joachim H. Wendorff 《Liquid crystals》1994,16(4):693-702
Liquid crystalline complexes with chromium, molybdenum and with tungsten as metallic centres are reported. 1,4,7-Trisubstituted 1,4,7-triazacyclononane and three carbonyl groups are coordinated in an octahedral geometry. The observed mesophases are characterized as disordered rectangular columnar of a pyramidic type. 相似文献
43.
44.
B. Blank J. -J. Gaimard H. Geissel K. -H. Schmidt H. Stelzer K. Sümmerer D. Bazin R. Del Moral J. P. Dufour A. Fleury F. Hubert H. -G. Clerc M. Steiner 《Zeitschrift für Physik A Hadrons and Nuclei》1992,343(4):375-379
Total charge-changing cross sections have been measured for8Li on C and Pb targets, for9Li on C, Al, Cu, Sn and Pb targets, as well as for11Li on C, Sn and Pb targets at about 80 MeV/nucleon. These data are compared to measured total reaction cross sections and Glauber-type calculations using Hartree-Fock density distributions. These comparisons allow to draw conclusions on the proton density distribution of the neutronrich lithium isotopes. The results show that even for the most exotic nucleus11Li the proton distribution is only very weakly influenced by the long tail in the neutron density distribution already established in several experiments. 相似文献
45.
Nathalie Charton Achim Feldermann Alexander Theis Martina H. Stenzel Thomas P. Davis Christopher Barner‐Kowollik 《Journal of polymer science. Part A, Polymer chemistry》2004,42(21):5559-5559
The original article to which this Erratum refers was published in J Polym Sci Part A: Polym Chem (2004) 42(20) 5170–5179. No abstract. 相似文献
46.
P. K. Kashkarov B. V. Kamenev M. G. Lisachenko O. A. Shalygina V. Yu. Timoshenk M. Schmidt J. Heitmann M. Zacharias 《Physics of the Solid State》2004,46(1):104-108
The photoluminescence spectra and kinetics of both erbium-doped and undoped multilayer structures of quasi-ordered silicon
nanocrystals in a silicon dioxide matrix were studied. It was shown that the optical excitation energy of silicon nanocrystals
2–3 nm in size can be practically completely transferred to Er3+ ions in the oxide surrounding the nanocrystals, with its subsequent radiation at 1.5 μm. Possible reasons for the high excitation
efficiency of the Er3+ ions are discussed, and the conclusion is drawn that the F?rster mechanism is dominant in the energy transfer processes occurring
in these structures.
__________
Translated from Fizika Tverdogo Tela, Vol. 46, No. 1, 2004, pp. 105–109.
Original Russian Text Copyright ? 2004 by Kashkarov, Kamenev, Lisachenko, Shalygina, Timoshenko, Schmidt, Heitmann, Zacharias. 相似文献
47.
Oriňák Andrej Arlinghaus Heinrich Frank Vering Guido Justinová Martina Oriňáková Renáta Turčániová L’udmila Halama Maroš 《平面色谱法杂志一现代薄层色谱法》2003,16(1):23-27
JPC – Journal of Planar Chromatography – Modern TLC - Two interfaces have been tested for coupling thin-layer chromatography (TLC) with time-of-flight secondary-ion mass spectrometry... 相似文献
48.
Armin C. Schneider Christoph Pasel Michael Luckas Klaus Gerhard Schmidt Jan-Dirk Herbell 《Journal of solution chemistry》2004,33(3):257-273
The single ion activity coefficients of hydrogen and chloride ions in aqueous HCl solutions have been estimated at 25°C at concentrations up to 1 mol-kg–1, using potentiometric measurements with ion-selective electrodes and appropriate calibration procedures. Two methods are described for an internal calibration of the electrodes in the extended Debye–Hückel concentration range. The results are compared to the conventional pH calibration with external buffer solutions. Since the latter calibration method does not account for the liquid junction potential E
J which arises at the reference electrode, the resulting activity coefficients are quite different in HCl solutions of higher concentration. These differences between internal and external calibration decrease significantly, when a correction for E
J is introduced into the conventional pH calibration. Hence, in solutions of higher ionic strength the accuracy of the conventional pH electrode calibration using buffer solutions is very limited, when exact H+ activities are required. The consistency of the results indicates that the liquid junction potentials in the examined systems calculated by the Henderson/Bates approximation are of reasonable precision. 相似文献
49.
50.