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1.
R. U. Khafizov N. Severijns O. Zimmer H. -F. Wirth D. Rich S. V. Tolokonnikov V. A. Solovei M. R. Kolhidashvili 《JETP Letters》2006,83(1):5-9
The aim of this work is the experimental observation of and research into a rare neutron mode, the radiative beta decay, where
a new particle, the radiative gamma quantum, is formed along with the expected decay products: a beta electron, a recoil proton,
and an antineutrino. The discovery of this rare neutron decay mode was conducted through identification of triple-coincidence
events: simultaneous registration of a beta electron, a proton, and a radiative gamma quantum. The ordinary neutron decay
was registered by double coincidences of a beta electron and a recoil proton. The statistics collected allow one to deduce
the branching ratio (BR) BR = (3.2 ± 1.6) × 10−3 (90% C.L.) in the gamma energy region greater than 35 keV. This value of BR is consistent with standard electroweak theory.
The text was submitted by the authors in English.
An erratum to this article is available at . 相似文献
2.
Phenomena accompanying electrochemical doping of solid fullerene films with potassium were studied by sputter ion depth profiling
(XPS and SIMS). The potassium distribution was determined, and artifacts associated with possible damage of the layer composition
caused by ion impact were investigated and discussed. To compare the charge transfer while reductive doping is taking place
at fullerene/solution interface with doping from gas phase, model layers were prepared and doped by potassium under UHV conditions.
It was found that sputtering by Ar+ primary ions yields both accurate information on the alkaline metal distribution and on its concentration. Sputtering by
O+ ions led to an enrichment of potassium, apparently due to the reactivity of oxygen with the fullerene matrix. It is shown
that the reductive doping starts at the fullerene/solution interface. The concentration of potassium in the doped films was
found to be lower than expected from the charge transferred during the electrochemical reduction. Other phase transformations
such as hydrogenation are discussed.
Received March 4, 2002; accepted July 26, 2002 相似文献
3.
This author wants to express his thanks to the School of Information Engineering at Teesside Polytechnic, Middlesbrough, England, for its support and hospitality during a visiting appointment of 3 months in 1989, when this paper was written. 相似文献
4.
Oswald Claassen 《Fresenius' Journal of Analytical Chemistry》1913,52(3-4):233
Ohne Zusammenfassung 相似文献
5.
6.
7.
P. Oswald 《Liquid crystals》1991,10(5):709-714
We describe the dynamics of spreading of a smectic A liquid crystal deposited on a rotating disc. We show the existence of several regimes according to the film thickness. If it is thick enough, the thinning is controlled by bulk permeation; at intermediate thicknesses the surface dissipation dominates, whereas viscous effects begin to be felt only at very small thickness. 相似文献
8.
G. Rauprich H. J. Hähn M. Karus P. Nießen K. R. Nyga H. Oswald L. Sydow H. Paetz gen Schieck Y. Koike 《Few-Body Systems》1988,5(2):67-77
The
elastic scattering was investigated especially in the Coulomb sensitive scattering regions. Angular distributions of the differential cross section and of the analyzing powerA
y, with emphasis on small scattering angles, were measured at 10.0 and 14.1 MeV. For extreme backward angles up toJ
c.m.=179° the differential cross section was measured at 12.0, 14.1 and 16.5 MeV. The data have been compared with recent Faddeev calculations based on the realistic meson-exchange Paris potential and including an approximate Coulomb correction. There are discrepancies between the data and the calculations especially for the analyzing power. This indicates that the approximate treatment of Coulomb effects and possibly also the purely nuclear part of the calculations need to be improved. 相似文献
9.
Ohne Zusammenfassung 相似文献
10.
Hans Zimmer R. Palmer-Sungail Douglas Ho Adel Amer 《Journal of heterocyclic chemistry》1993,30(1):161-167
The reaction pathway towards formation of 4-aroyl-3-hydroxy-2(5H)-furanones 1 from the base catalyzed reaction between an acetophenone, diethyl oxalate and formaldehyde was investigated. If methoxide was used as base, a transesterification was found to occur in the first step, while a side reaction, namely the retro Claisen reaction, was in competition with the desired lactone formation in the second step. The nature of the solvent and the acidic character of 1 as well as the basicity of the aminoarylene were found to have a profound influence on the course of the reaction of 1 with aminoarylenes. 相似文献