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31.
Silvia Díez-González 《Journal of organometallic chemistry》2006,691(26):5531-5539
Various 2-methylidene-1-silacyclohexanes were prepared by straightforward syntheses from readily available polychloro- or polyfluorosilanes, magnesium and 2,6-dibromohex-1-ene using Barbier-type conditions or a previously synthesized Grignard reagent. Good yields were obtained considering the low stability of the products in the reaction conditions. 相似文献
32.
A new synthetic method for the manufacture of glutaric dialdehyde is investigated. Glutaric dialdehyde was prepared by the
addition-hydrolysis reaction of benzimidazolium salt with saturated dihalide as the di-Grignard reagent. The yield of glutaric
dialdehyde by this method can reach 73%. Both infrared spectra and melting point of the compound were consistent with those
reported earlier.
Translated from Journal of Northwest University (Natural Science Edition), 2005, 35(2) (in Chinese) 相似文献
33.
J.-Q. Shen H.-Y. Zhu P. Chen 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2003,23(2):305-313
There exist a number of typical and interesting systems and/or models, which possess three-generator Lie-algebraic structure,
in atomic physics, quantum optics, nuclear physics and laser physics. The well-known fact that all simple 3-generator algebras
are either isomorphic to the algebra sl (2, C) or to one of its real forms enables us to treat these time-dependent quantum systems in a unified way. By making use of
both the Lewis-Riesenfeld invariant theory and the invariant-related unitary transformation formulation, the present paper
obtains exact solutions of the time-dependent Schr?dinger equations governing various three-generator Lie-algebraic quantum
systems. For some quantum systems whose time-dependent Hamiltonians have no quasialgebraic structures, it is shown that the exact solutions can also be obtained by working in a
sub-Hilbert-space corresponding to a particular eigenvalue of the conserved generator (i.e., the time-independent invariant that commutes with the time-dependent Hamiltonian). The topological property of geometric phase factors and its adiabatic limit in time-dependent systems is briefly
discussed.
Received 6 July 2002 / Received in final form 21 October 2002 Published online 11 February 2003 相似文献
34.
Keigo Fugami Takashi Nishikata Masayuki Kameyama 《Journal of organometallic chemistry》2003,687(2):567-569
Palladium-catalyzed reaction between 1-alkenyltin trichlorides and norbornene resulted in stereoselective formation of 3-alkylidenepentacyclo[9.2.1.5,81.1,110.2,1004,9]pentadecane instead of an expected simple alkenylstannylation product. Generation of trichlorostannane and its decomposition product, tin(II) chloride, was confirmed by trapping it with methyl propiolate and norbornene and analysis of the reaction by 119Sn NMR, respectively. 相似文献
35.
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37.
基于厄米-双曲余弦高斯光束通过无光阑限制薄透镜聚焦的解析传输公式,研究了厄米-双曲余弦高斯光束聚焦区域的光强分布,并对光束的焦移进行了分析,讨论了偏心参数对光强主极大位置的影响。结果表明:TEM11模厄米-双曲余弦高斯光束的相对焦移(绝对值)随偏心参数和菲涅尔数的减小而增大,菲涅尔数较大时相对焦移趋于零。TEM22模光束在偏心参数小于0.54时,轴外与轴上光强极大值的比值大于1,此时光强主极大在轴外,偏心参数大于0.54时则相反;在偏心参数等于0.54时比值为1,此时光束有两个主极大,偏心参数愈大光强愈集中于轴上。使用LW法和GH法得到的TEM22模光束的相对焦移(绝对值)随偏心参数和菲涅尔数的变化规律与TEM11模光束一致,但相同参数下使用这两种方法得出的具体结果不同。 相似文献
38.
The use of reagent concentration has resulted in increased rates for all stages of the REM resin synthesis of tertiary amines. These increases in rate translate into faster reaction times, higher yields and lower reagent consumption. Of the methods examined, the most successful was the use of perfluorous solvents, either alone or with a small amount of organic co-solvent. 相似文献
39.
Historical perspectives for the chemistry of diene complexes of early transition metals developed at Osaka University in the period after 1970s were reviewed briefly and personally. Preparative chemistry of this field commenced from the magnesium-diene 1:1 compounds and quickly extended to almost all the early transition metals. By the studies operated together with other researchers, unique features of these diene complexes, especially their bonding and structure, selective reactions, and catalysis performances are described. 相似文献
40.
U.Deva Priyakumar 《Tetrahedron letters》2004,45(12):2495-2498
A novel preference for planar tetracoordination was observed over the conventional tetrahedral arrangement in a new series of C5H2, C5H4, C5H41+/2+ and related compounds. The stability of these molecules is assessed with the ring-opening barriers, HOMO-LUMO gap, singlet-triplet energy differences and nucleus independent chemical shift values. 相似文献