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901.
It is shown that double-orthogonal sets (diamonds) in Minkowski space form an orthomodular complete lattice. Connection with empirical logic of Randall and Foulis is discussed. 相似文献
902.
Z. Šimša V. Roskovec F. Zounová P. Novotný W. Keilig 《Czechoslovak Journal of Physics》1977,27(1):88-98
An extended version of the noncollinear spin model bySawatzky et al. is developed to derive a dependence of the differential high field susceptibility on the degree of inversion of the ferrite MnFe2O4. Using the available data on the main molecular field coefficients it is shown that the present model imposes restrictions on values of. Determination of from the measurements of the field dependence of the saturated moments at low temperatures on samples with varying degrees of inversion reveals good quantitative agreement with the present model. 相似文献
903.
D. Šokčević Z. Lenac R. Brako M. Šunjić 《Zeitschrift für Physik B Condensed Matter》1977,28(4):273-281
We develop a theory of low energy electron loss spectroscopy of vibrational modes of molecules adsorbed on metal surfaces. Differential and total cross sections are calculated in the Distorted Wave Born Approximation, assuming i) strong elastic scattering on the metal surface, ii) direct electron-molecule interaction via the electric dipole field associated with the molecular vibration. The angular distributions are calculated and discussed for molecules adsorbed at various distances above the metal surface and for several electron energies and impact angles. The influence of electronic screening of dipolar oscillations is discussed and the consequences of the classical induced image dipoles are explored. It is shown that the metal surface selection rule known in IR spectroscopy is only approximately valid in electron scattering. Finally, we give numerical estimates of the inelastic scattering cross sections for the stretching vibrations of CO molecule adsorbed on transition metal surfaces, in reasonable agreement with experiments. 相似文献
904.
O. Yu. Ovsitser A. A. Davydov Z. G. Osipova V. D. Sokolovskii 《Reaction Kinetics and Catalysis Letters》1989,38(1):125-130
Rate constants for the aminolysis of o-(2,4-dinitrophenyl) cyclopentanone oxime with several primary alkylamines, C2H5NH2–C6H13NH2 and one secondary arylamine, purrolidine, in 11 water-acetonitrile are reported. With primary amines, base catalysis is absent, while with pyrrolidine saturation catalysis has been observed. Reduction in size of nonconjugated oxime moiety (leaving group), drastically decreases the rates. Thermodynamic parameters for these reactions have also been calculated.
O-(2,4-) (C2H5NH2–C6H13NH2) , , : =11. , . ( ) . .相似文献
905.
The decoloration yield of oxazine 720 in ethanolic solution was studied as a function of dose rate and concentration of the dye. Linear response for G values to a dose of 1.68 KGy was observed for various dye concentrations. The effect of various organic substances in the radiolysis of the dye was studied and the results were interpreted in terms of scavenging reactions. 相似文献
906.
S. V. Konovalikhin G. V. Shilov O. A. D'yachenko M. Z. Aldoshina R. N. Lyubovskaya R. B. Lyubovskii 《Russian Chemical Bulletin》1992,41(10):1819-1826
The compositions and structures of two new organic metals based on ET [where ET = bis(ethylenedithio)tetrathiafulvalene], viz., (ET)2[Hg(SCN)Cl2], with a metal-dielectric transition temperature (Tm-d) of 35°K, and (ET)2[Hg(SCN)2Br], with Tm-d = 140°K, were established by x-ray diffraction analysis. The crystal structures of the investigated compounds are similar to the structure of the previously studied organic metal (ET)2[Hg(SCN)2Cl] with Tm-d = 50°K. The principal crystallographic data for (ET)2[Hg(SCN)Cl2] are as follows: a = 36.64(1), b = 8.300(4), c = 11.798(1) Å, = 89.91(3)°, V = 3588.1(9) Å3, space group Cc, Z = 4, dcalc = 2.05 g/cm3. The principal crystallographic data for (ET)2[Hg(SCN)2Br] are as follows: a = 37.088(14), b = 8.338(3), c = 11.738(5) Å, = 89.71(3)°, V = 3629.6(8) Å3, space group C2/c, Z = 8, dcalc = 2.15 g/cm3. A characteristic feature of the crystal structure of the investigated compounds is alternation of the anion and cation layers along the a axis of the crystal. In the cation layer of the k type the ET are interconnected by shortened S...S intermolecular contacts (3.39–3.58 Å). The [Hg(SCN)3–nXn]– anions (X = Cl, Br; n = 1, 2) form polymeric chains with one or two bridged SCN groups. A tendency for a decrease in the metal-dielectric transition temperature with a decrease in the volume of the anion is detected in the (ET)2[Hg(SCN)3–nXn] salts, where X = Cl and Br, and n = 1 and 2.Institute of Chemical Physics, Russian Academy of Sciences, 142432 Chernogolovka. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 10, pp. 2323–2331, October, 1992. 相似文献
907.
A preparative method for 9a-hydroxylation of 5-3-hydroxysteroids using the fungi ofCircinella sp. 10Kh-1220 not capable of modifying theA ring has been developed. It is established that the yields of the main and the side products greatly depend on the transformation conditions, mycelium age, and the structure of the steroid substrate. Under the optimal transformation conditions novel 9-hydroxysubstituted derivatives of androstenolone, pregnenolone, 16-dehydro-16,17-epoxy-, and-16-methoxypregnenolone have been obtained in 36–80 % yields.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 737–743, April, 1994. 相似文献
908.
G. J. Balster W. van Huffelen H. W. Wilschut D. Chmielewska Z. Sujkowski 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1986,2(1):15-21
KX-ray production cross sections have been measured for beams of14N at 92, 103, 115 and 180 MeV and40Ar at 180 and 300 MeV on targets with atomic numbers ranging from 40 to 90. We find that the measured values can be well reproduced with a plane wave Born calculation, provided that corrections for the Coulomb deflection of the projectile, the increased binding energy of theK-shell electron and relativistic effects of theK-shell wave function are taken properly into account. 相似文献
909.
A novel chemiluminescence (CL) flow system has been developed for the sequential determination of Fe(II) and Fe(III) in water.
Fe(II) was detected by its catalytic effect on the CL reaction between luminol immobilized on an anion exchange resin column
and dissolved oxygen; Fe(III) was determined by difference measurement after on-line conversion to Fe(II) in a reducing mini-column
packed with Cu plated Zn granules. For both ions, the calibration graph was linear in the range 1 × 10–9 to 1 × 10–6 g/mL, and the detection limit was 4 × 10–10 g/mL. A complete analysis could be performed in 1.5 min with a relative standard deviation of less than 5%. The system could
be reused for over 200 times and has been applied successfully to the determination of Fe(II) and Fe(III) in natural water
samples.
Received: 13 March 1997 / Revised: 3 June 1997 / Accepted: 6 June 1997 相似文献
910.