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51.
Hidefumi Ohsugi 《Journal of Combinatorial Theory, Series A》2006,113(4):718-725
Athanasiadis [Ehrhart polynomials, simplicial polytopes, magic squares and a conjecture of Stanley, J. Reine Angew. Math., to appear.] studies an effective technique to show that Gorenstein sequences coming from compressed polytopes are unimodal. In the present paper we will use such the technique to find a rich class of Gorenstein toric rings with unimodal h-vectors arising from finite graphs. 相似文献
52.
We prove that the coinvariant ring of the irreducible Coxeter group of type H4 has the strong Lefschetz property. 相似文献
53.
本文讨论临界可压缩模类和结合环的弱Jacobson根.首先,我们证明了非平凡的临界可压缩模类是素模的特殊类.其次,我们引入结合环的弱Jacobson根.弱Jaonbson根是特殊根.最后,我们给出有关弱本原环,半弱本原环和弱Jacobson根环的某些性质. 相似文献
54.
In this paper, we give a construction of RDS in Galois ring by using some bent function, and obtain the equivalent relationship between RDS and a kind of bent function. At the same time, its existence is demonstrated. 相似文献
55.
本文把代数结构与分析体系结合起来,运用同调的方法,较系统地确定了A上C^*-模的部分理论,这里A为复数域C上的交换C^*-代数。即不仅定义了与C^*-模有关的某些新概念,而且还得到了有关C^*-模的若干结果。 相似文献
56.
von-Neumann正则环与左SF-环 总被引:6,自引:0,他引:6
环R称为左SF-环,如果每个单左R-模是平坦的.众所周知,Von-Neumann正则环是SF-环,但SF-环是否是正则环至今仍是公开问题,本文主要研究左SF-环是正则环的条件,证明了:如果R是左SF-环且R的每个极大左(右)理想是广义弱理想,那么R是强正则环.并且推广了Rege[3]中的相应结果. 相似文献
57.
P. Macko D. Romanini O.V. Naumenko A. Jenouvrier A. Campargue 《Journal of Molecular Spectroscopy》2004,227(1):90-108
The absorption spectrum of natural water vapour around 1.5 μm has been recorded with a typical sensitivity of 5 × 10−10 cm−1 by using a CW-cavity ring down spectroscopy set up based on fibred DFB lasers. A series of 31 DFB lasers has allowed a full coverage of the 6130.8-6748.5 cm−1 (1.63-1.48 μm) region corresponding to the H transparency band of the atmosphere. The line parameters (wavenumber and intensity) of a total of 5190 lines, including 4247 lines of water vapor, were derived by a one by one fit of the lines to a Voigt profile. Different isotopologues of water (H216O, H218O, H217O, and HD16O) present in natural abundance in the sample contribute to the spectrum. For the main isotopologue, H216O, 2130 lines were measured with line intensities as weak as 10−29 cm/molecule while only 926 lines (including a proportion of 30% inaccurate calculated lines) with a minimum intensity of 3 × 10−27 cm/molecule are provided by the HITRAN and GEISA databases. Our comparison in the whole 5750-7965 cm−1 region, has also evidenced that an error in the process of conversion of the intensity units from cm−2/atm to cm−1/(molecule × cm−2) at 296 K, has led to H216O line intensities values listed in the HITRAN-2000 database, systematically 8 % below the original FTS values. The rovibrational assignment was performed on the basis of the ab initio calculations by Schwenke and Partridge with a subsequent refinement and validation using the Ritz combination principle together with all previously measured water transitions relevant to this study. This procedure allowed determining 172, 139, 71, and 115 new energy levels for the H216O, H218O, H217O, and HD16O isotopologues, respectively. The results are compared with the available databases and discussed in regard of previous investigations by Fourier transform spectroscopy. The spectrum analysis has showed that most of the transitions which cannot be assigned to water are very weak and are due to impurities such as carbon dioxide and ammonia, leaving only about 3% of the observed transitions unassigned. The interest of a detailed knowledge of water absorption for trace detectors developed in the 1.5 μm range is underlined: for instance HDO contributes significantly to the considered spectrum while no HDO line parameters are provided by the HITRAN database. 相似文献
58.
讨论了Gpp环和Gp-内射模的一些性质;讨论了Gp-内射模和R-内射模的关系及Gp-内射模和Gpp环的若干联系.最后讨论了和Gpp环有关的有限生成模的投射盖问题. 相似文献
59.
Yoshitomo Ono Naoyuki Kawashima Hiroto Kudo Tadatomi Nishikubo Takabumi Nagai 《Journal of polymer science. Part A, Polymer chemistry》2007,45(14):2978-2988
The ring‐opening copolymerization of a glycidyl ester derivative having a benzophenone group and the donor–acceptor norbornadiene (D‐A NBD) dicarboxylic acid, 5‐(4‐methoxyphenyl)‐1,4,6,7,7‐pentamethyl‐2,5‐norbornadiene‐2,3‐dicarboxylic acid, monoglycidyl ester derivatives with D‐A NBD dicarboxylic anhydride using tetraphenylphosphonium bromide as a catalyst proceeded smoothly to give novel self‐photosensitizing NBD polymers in good yields. The molecular weight of these polyesters was about 4,000, and lower than that of analogous NBD polymers having no benzophenone group. All the synthesized NBD polymers isomerized smoothly to the corresponding quadricyclane (QC) polymers upon UV irradiation in tetrahydrofuran (THF) solution and in the film state. The rate of the photoisomerization of the D‐A NBD moieties in these polymers was higher than that of the D‐A NBD moieties in the polymer having no photosensitizing group. Furthermore, the rate of the photoisomerization of the D‐A NBD moieties in these polymers was also higher than that of the NBD polymer with low molecular weight photosensitizer in dilute solution. The photo‐irradiated polymers having QC moieties released thermal energies of 146–180 J/g. The D‐A NBD moieties contained in these NBD polymers possessed fair to good fatigue resistance. The degradation of the NBD moieties in these polymers was 15–30% after 50 repeated cycles of interconversion. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 2978–2988, 2007 相似文献
60.
Three different analytical solutions are presented for a potential vortex ring using three different streamfunctions. Verification studies confirm that all three approaches are valid. It is found that the solution obtained using the Biot–Savart law is the most efficient method due to its simplicity. It is shown that all analytical results are accurate to within machine accuracy and sample calculations are included. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献