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Martina Dotzler Astrid Schmidt Jochen Ellermann Falk A. Knoch Matthias Moll Walter Bauer 《Polyhedron》1996,15(24):4425-4433
BiBr3 or SbI3 react at 20°C with LiN(PPh2)2 (1) to give elementary Bi or Sb and the P---P coupled phosphazene ligand Ph2P---N=PPh2---PPh2=N---PPh2 (2). The reaction of AsI3 with 1 at room temperature formed yellow needles of the eight-membered heterocycle
(3), whereas AsI3 interacted at 80°C with 1 in the molar ratio of 1:3 to give elementary arsenic and 2. Treatment of AsI3 and 1 at 20°C in a 1:2 stoichiometry yielded the seven-membered, cyclic arsenium(I) salt I·4THF (5·4THF), which was characterized by elemental analysis, conductivity, mass, IR and NMR spectroscopy and single-crystal X-ray structural analysis. 相似文献
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45.
Matthias Deppner 《Journal of organometallic chemistry》2005,690(12):2861-2871
The synthesis is described of symmetric alkylidene bridged dinuclear zirconocene complexes. The influence of structural parameters and different cocatalysts such as methylaluminoxane (MAO), triphenyl tetrakis(pentafluorophenyl)borate- or tris(pentafluorophenyl)borane has been investigated for homogeneous propylene polymerization. The dinuclear catalysts show highest polymerization activities by activation with MAO. Activation with triphenyl tetrakis(pentafluorophenyl)borate results in polypropylenes with the highest degree of isotacticity. Compared to the mononuclear reference catalyst the dinuclear MAO activated complex achieved higher propylene polymerization activity and the polypropylene obtained from the dinuclear complex has a higher molecular weight than that one that was produced with the mononuclear complex. 相似文献
46.
The source of the effect of N-alkylation on the redox properties of Ni(II/I) and Cr(III/II) cyclam complexes has been investigated using DFT calculations. The structures of the anhydrous and hydrated complexes were optimized in the gas phase, and single point calculations were performed in a polarized continuum. The main results are the following: the decrease in outer sphere solvation upon N-alkylation is the major source of the relative stabilization of the lower oxidation state complexes by the tertiary amine ligands; tertiary amine nitrogen donors are stronger sigma-donors than the secondary amines, as predicted from the inductive effect of alkyls; steric strain elongates the metal-nitrogen bonds in the tertiary complexes and decreases the ligand strain energies; and the site of water binding to the complexes differs because of their different electronic structures (i.e., in the Ni complexes, the water molecules bind to the M[bond]N[bond]H sites, whereas in the Cr complexes they bind to the central metal cation). Outer sphere hydrogen bonding of water to the ligands in the coordination sphere lowers the ionization potentials by charge delocalization. 相似文献
47.
Annals of Global Analysis and Geometry - In the present paper, we consider star-shaped mean convex hypersurfaces of the real, complex and quaternionic hyperbolic space evolving by a class of... 相似文献
48.
Matthias Hoschneider 《Communications in Mathematical Physics》1994,160(3):457-473
In this paper we want to give a new definition of fractal dimensions as small scale behavior of theq-energy of wavelet transforms. This is a generalization of previous multi-fractal approaches. With this particular definition we will show that the 2-dimension (=correlation dimension) of the spectral measure determines the long time behavior of the time evolution generated by a bounded self-adjoint operator acting in some Hilbert space ?. It will be proved that for φ, ψ∈? we have $$\mathop {\lim \inf }\limits_{T \to \infty } \frac{{\log \int_0^T {d\omega \left| {\left\langle {\psi \left| {e^{ - iA\omega } } \right.\phi } \right\rangle } \right|^2 } }}{{\log T}} = - \kappa ^ + (2)$$ and that $$\mathop {\lim \sup }\limits_{T \to \infty } \frac{{\log \int_0^T {d\omega \left| {\left\langle {\psi \left| {e^{ - iA\omega } } \right.\phi } \right\rangle } \right|^2 } }}{{\log T}} = - \kappa ^ - (2),$$ wherek ±(2) are the upper and lower correlation dimensions of the spectral measure associated with ψ and ?. A quantitative version of the RAGE theorem shall also be given. 相似文献
49.
Michael Meyberg Elvezio Morenzoni Thomas Wutzke Uwe Zimmermann Franz Kottmann Klaus Jungmann Björn Matthias Thomas Prokscha 《Hyperfine Interactions》1994,87(1):1075-1081
At PSI we are investigating the technique of decelerating an existing very intense secondary beam of surface
+ (4 MeV) to an energy of 10 eV using appropriate moderators. These
+ can then be used as a source of a tertiary beam of low energy muons with tunable kinetic energy between 10 eV and 10 keV.With a 1000 A layer of solid Argon deposited on an Al substrate we obtain a moderation efficiency (with respect to the number of incoming surface
+) of the order of 10–4.Results of our investigations and the present status of the project are presented together with future plans and possibilities. 相似文献
50.
Morenzoni E. Birke M. Hofer A. Kottmann F. Litterst J. Matthias B. Meyberg M. Niedermayer Ch. Prokscha Th. Schatz G. Wutzke Th. 《Hyperfine Interactions》1996,97(1):395-406
During the last few decades, a variety of methods has been developed which makes use of polarized positive muons as a microscopic probe of the magnetic properties of condensed matter (muon spin rotation, relaxation, resonance,SR). Until now, available beams for SR studies have delivered 100% polarized muons with energies in the MeV range, resulting in a deep penetration of the muons into the sample material under investigation. This presently limits the applications of theSR technique to the study of the bulk characteristics of matter. To be able to control the implantation depth, a very low energy beam of polarized muons is being developed at the Paul Scherrer Institute. Very slow polarized muons (kinetic energy 10 eV, polarization 90%) are obtained from the moderation of a high energy muon beam in a thin film of an appropriate condensed gas. These muons can be used as a source for a beam of tunable energy between a few tens of eV and some tens of keV. Implantation depths in the range of few to a few hundreds of nanometers can thus be achieved by varying the energy. 相似文献