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21.
M. R. Setare 《International Journal of Theoretical Physics》2004,43(11):2237-2242
We compute particle creation for a real massive scalar field conformally coupled to a spatially closed Robertson–Walker space-time background, with time-dependent scale factor. This is a dynamical Casimir effect with moving boundaries. 相似文献
22.
Zh. D. Chaplanova Yu. K. Mikhailovskii V. E. Agabekov V. K. Ol’khovik N. A. Galinovskii E. A. Gracheva 《Journal of Applied Spectroscopy》2007,74(3):333-337
We have studied the spectral properties and morphology of thin films (TVD films) formed by thermal vacuum deposition of 4,4′-bis[(E)-1-(1,3-benzoxazol-2-yl)-2-ethenyl]-1,1′-biphenyl
and its substituted derivatives. We have shown that introducing bulky 2,2′-oxyhexyl substituents into the biphenyl units leads
to a shift of the fluorescence maximum for the TVD films toward shorter wavelengths, a decrease in their photostability, and
aggregation of the films during storage.
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Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 3, pp. 300–303, May–June, 2007. 相似文献
23.
In this paper, we discuss the detailed optical design of a beam line that is under construction on the synchrotron radiation source, Indus-1. Toroidal mirrors are used as pre-and post- focusing elements and a toroidal grating monochromator as a dispersing element. Using three interchangeable gratings, this monochromator will give, at a moderate resolution, a good throughput on the sample in the wavelength range 40 to 1000 Å. Effect of various parameters and their optimization on the resolution and throughput characteristics have been studied by ray tracing calculations, and presented. 相似文献
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采用某些特殊的放电和提取方法,如反向放电和甲苯高温高压提取等可以有效地提高稀土富勒烯的生成效率[‘,‘’,并已先后成功高效地合成了许多含稀土富勒烯「‘’.对其提纯、表征、衍生和应用也进行了研究[‘-’j.但对影响稀土富勒烯生成的因素研究较少.在石墨律中同时填入La,Y,Sc的稀土氧化物,对其稀土富勒烯生成效率的情况进行了研究,认为稀土元素的第一电离能是影响稀土富勒烯生成的主要因素‘’,’‘.Moro等采用激光和热解吸质谱对稀土富勒烯的研究结果表明,稀土元素的氧化态是影响稀土富勒烯生成的决定性因素”’.本… 相似文献
28.
A. Hollnder J. E. Klemberg-Sapieha M. R. Wertheimer 《Journal of polymer science. Part A, Polymer chemistry》1995,33(12):2013-2025
The emission from low-pressure microwave plasmas in the vacuum-ultraviolet (VUV) region (λ < 200 nm) was investigated in order to use these plasmas as light sources for the study of the VUV photochemistry of polyethylene (PE) and polypropylene (PP) as part of the study of plasma-polymer interaction. These polymers, immersed in low-presure oxygen, were exposed to radiation with wavelengths down to 112 nm, the cut off of magnesium fluoride used as a window to separate the polymer specimen from the plasma light source. Total oxygen incorporation in the surface [O], and the formation of hydroxyl, carbonyl, and carboxyl groups were measured using XPS in combination with chemical derivatizations, particularly their dependence upon the radiation spectrum and the oxygen pressure around the sample. In most experiments the surface oxygen concentration [O] attained a constant value that appears to be related to the initial oxidation rate; this suggests a competition between oxygen incorporation and chain scission reactions, followed by the removal of volatile oxidation products. PE is usually oxidized to a higher level than PP, the latter appearing to be more susceptible to reaction with atomic oxygen than PE. A general initiation mechanism for the VUV experiments is proposed that allows us to explain the observed differences in behavior between PE and PP, and the results obtained under different irradiation conditions. The nature of oxidation products is in both cases very similar to what is observed after direct plasma treatment of the polymers. We conclude that short wavelength radiation contributes very appreciably to the observed surface modification effects during plasma treatment of PE and PP. © 1995 John Wiley & Sons, Inc. 相似文献
29.
Flash vacuum pyrolysis (fvp) of some substituted [1,2,4]triazolo[3,4-c][1,2,4]benzotriazine derivatives (1a-d) has been studied between 450 and 600 °C. The only transformation observed up to 525 °C was the unexpected valence bond isomerization of the angularly fused starting compounds to the isomeric linearly fused [1,2,4]triazolo[4,3-b][1,2,4]benzotriazine derivatives (9a-d), whereas at higher temperatures fragmentation products such as aromatic nitriles were also formed. Kinetic measurements revealed negative entropies of activation in the isomerization process, which suggest a concerted ring closure reaction to an intermediate antiaromatic diazirine. Reversibiblity of the title isomerization reaction was also proved by FVP experiments. 相似文献
30.
Franco Cataldo 《Tetrahedron》2004,60(19):4265-4274
The products of the electric arc between graphite electrodes have been investigated by high performance liquid chromatography-diode-array detector (HPLC-DAD) analysis in various media: distilled water, liquid nitrogen, methanol, ethanol, n-hexane and benzene. In distilled water, hydrogen capped polyynes H-(CC)n-H were the unique products demonstrating that carbon is supplied by the graphite electrodes while hydrogen is supplied by the solvent plasmalysis (in this case water plasmalysis). Arcing graphite electrodes in liquid nitrogen produces cyanopolyynes: NC-(CC)n-CN demonstrating that in this case the end groups of the polyyne chains are supplied by molecular nitrogen plasmalysis caused by the electric arc. Graphite arcing in methanol and ethanol produces very clean solutions (by-products negligible or absent) of hydrogen-capped polyynes with C8H2 as the main product accounting for more than 70 mol percent of the total polyyne concentration. By replacing graphite electrodes with titanium electrodes in methanol or in ethanol, polyynes are not formed at all; only trace amounts of polycyclic aromatic hydrocarbons (PAHs) were detected. When arcing with graphite electrodes is conducted in n-hexane or in benzene, polyyne formation is accompanied by a significant production of PAH, especially in benzene. These results have been rationalized in terms of carbonization or coking tendency of a given solvent. The effect of using titanium electrodes in place of graphite electrodes has been investigated also in n-hexane and in benzene as well as the effects of very high electric current intensity employed to ignite and sustain the submerged electric arc. 相似文献