全文获取类型
收费全文 | 48145篇 |
免费 | 1553篇 |
国内免费 | 44篇 |
专业分类
化学 | 29418篇 |
晶体学 | 261篇 |
力学 | 786篇 |
综合类 | 1篇 |
数学 | 9052篇 |
物理学 | 10224篇 |
出版年
2023年 | 335篇 |
2022年 | 359篇 |
2021年 | 558篇 |
2020年 | 716篇 |
2019年 | 662篇 |
2018年 | 958篇 |
2017年 | 878篇 |
2016年 | 1722篇 |
2015年 | 1424篇 |
2014年 | 1399篇 |
2013年 | 3102篇 |
2012年 | 2956篇 |
2011年 | 2818篇 |
2010年 | 1888篇 |
2009年 | 1629篇 |
2008年 | 2454篇 |
2007年 | 2259篇 |
2006年 | 2015篇 |
2005年 | 2056篇 |
2004年 | 1775篇 |
2003年 | 1486篇 |
2002年 | 1294篇 |
2001年 | 1012篇 |
2000年 | 1004篇 |
1999年 | 697篇 |
1998年 | 543篇 |
1997年 | 449篇 |
1996年 | 613篇 |
1995年 | 431篇 |
1994年 | 507篇 |
1993年 | 452篇 |
1992年 | 478篇 |
1991年 | 415篇 |
1990年 | 466篇 |
1989年 | 376篇 |
1988年 | 382篇 |
1987年 | 340篇 |
1986年 | 326篇 |
1985年 | 454篇 |
1984年 | 424篇 |
1983年 | 338篇 |
1982年 | 335篇 |
1981年 | 353篇 |
1980年 | 281篇 |
1979年 | 275篇 |
1978年 | 271篇 |
1977年 | 263篇 |
1976年 | 277篇 |
1974年 | 253篇 |
1973年 | 264篇 |
排序方式: 共有10000条查询结果,搜索用时 8 毫秒
211.
212.
J. Balogh D. Kaptás L. F. Kiss T. Kemény L. Bujdosó I. Vincze 《Hyperfine Interactions》2006,169(1-3):1343-1347
Magnetic multilayers of 57Fe with nominal thickness, T
nom, between 0.4 and 1.0 nm separated by 3.0 nm Al spacer layers were prepared by alternate deposition of the constituents in
high vacuum. The samples were investigated at 4.2 K in external magnetic field. A fraction of Fe atoms corresponding to about
0.3 nm equivalent Fe-thickness was found to mix into the Al spacer. The extremely strong magnetic anisotropy observed for
T
nom < 0.8 nm is attributed to Fe layers of approximately two atomic planes thick. The anisotropy decreases considerably after
the building up of the third Fe atomic layer starts at T
nom = 0.8 nm, but full saturation was not achieved even for T
nom = 1 nm and 3 T magnetic field applied perpendicularly to the sample plane. 相似文献
213.
The stoichiometric reactions of trimethylaluminum with 2,6‐(MeOCH2)2C6H3OH (LH) revealed compounds L3Al ( 1 ) and L2AlMe ( 2 ). On the other hand reaction of 1 equiv. of LH with trimethylaluminum did not lead to the formation of complex LAlMe2 ( 3 ), rather 2 together with Me3Al were observed as a result of a disproportionation of 3 . Compounds 1 and 2 were characterized by elemental analysis, 1H and 13C NMR spectroscopy and in the case of 1 by X‐ray diffraction. Derivative 2 underwent transmetalation with Ph3SnOH, giving LSnPh3 ( 4 ) as the result of a migration of ligand L from the aluminum to the tin atom. The identity of 4 was established by elemental analysis, 1H, 13C and 119Sn NMR spectroscopy and 1H, 119Sn HMBC experiments. The system 2 and B(C6F5)3 in a 1:1 molar ratio was shown to be active in the polymerization of propylene oxide and ε‐caprolactone. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
214.
Abull is the (self-complementary) graph with verticesa, b, c, d, e and edgesab, ac, bc, bd, ce; a graphG is calledBerge if neitherG not its complement contains a chordless cycle whose length is odd and at least five. We prove that bull-free Berge graphs are perfect; a part of our argument relies on a new property of minimal imperfect graphs.This work was done while both authors were at the School of Computer Science, McGill University; support by NSERC is gratefully acknowledged. 相似文献
215.
The preparation of polyhydroxylated 6-oxa-nor-tropane glycomimetics structurally related to the glycosidase inhibitor family of the calystegines is reported. The synthetic strategy involves the furanose→piperidine rearrangement of 5-deoxy-5-ureido-l-idose precursors, followed by intramolecular glycosylation involving the primary hydroxyl group. Inversion of the configuration at C-3 in the resulting 6-oxa-(+)-calystegine B2 analogue allows accessing the elusive 3-epi-6-oxa-(+)-calystegine B2 skeleton. Acid-catalyzed opening of the nor-tropane bicycle was observed, however, which could be avoided by careful neutralization of the reaction mixture. The inhibition results suggest that (+)-calystegine B2 derivatives and the corresponding C-3 epimers can be seen as glucomimetics and galactomimetics, respectively, pointing to a 1-azasugar mode of action for this family of alkaloids. 相似文献
216.
Singularity patterns in a chemotaxis model 总被引:3,自引:0,他引:3
217.
Francisco-Javier Muñoz-Delgado Victoriano Ramirez-González Paul Sablonnière 《分析论及其应用》1995,11(1):62-71
In this work we study linear polynomial operators preserving some consecutive i-convexities and leaving invariant the polynomials
up to a certain degree. First, we study the existence of an incom patibility between the conservation of certain i-convexities
and the invariance of a space of polynomials. Interpolation properties are obtained and a theorem by Berens and DeVore about
the Bernstein's operator is extended. Finally, from these results a generalized Bernstein's operator is obtained.
This work was supported by Junta de Andalucia. Grupo de investigación: Matemática Aplicada. Código: 1107 相似文献
218.
Csaba Sándor 《Periodica Mathematica Hungarica》1996,33(2):121-134
219.
C. N. Carducci S. E. Lucangioli V. G. Rodríguez G. C. Fernndez Otero 《Journal of chromatography. A》1996,730(1-2):313-319
Sample preparation procedures using octadecyl (C18) extraction disks were developed to obtain accurate and reproducible results for determinations of clenbuterol (20 μg per dose) and levothyroxine (100 μg per dose) in dissolution media of solid oral dosage forms. Preconcentration of samples allowed final concentrations of 1.1 μg/ml of clenbuterol and 4.0 μg/ml of levothyroxine to be reached prior to CE analysis. The results obtained by CE were in good agreement with those of HPLC. The precision of the migration time, peak area, peak height and accuracy were determined in both intea-day (n = 6) and inter-day (n =18) assays. Linearity was demonstrated over the ranges 0.5–80.0 μg/ml of clenbuterol and 1.0–30.0 μg/ml of levothyroxine. The mean recoveries were higher than 94.0%, ranging from 50 to 125% levels with respect to dose potencies. The proposed methodology may be generally applied to determine drugs at ng/ml concentrations. 相似文献
220.
I. P. Romanova S. G. Fattakhov A. A. Nafikova I. I. Vandyukova R. R. Shagidullin N. M. Azancheev V. S. Reznik O. G. Sinyáshin 《Russian Chemical Bulletin》1998,47(9):1812-1819
The reactions of phosphine derivatives of diallyl isocyanurates with palladium(ii) dichloride lead to the formation of complexes, whose structure, composition, and stability depend on the length of the methylene
chain between the isocyanurate and diphenylphosphine fragments in the ligand. 1,3-Diallyl-5-[5′-(diphenylphosphino)pentyl
and 10′-(diphenyl-phosphino)decyl] isocyanurates with PdCl2 form monomeric L2PdCl2
trans-complexes in which P atoms of the ligands participate in coordination with the metal. 1,3-Diallyl-5-[2′-(diphenylphosphino)ethyl]
isocyanurate with PdCl2 forms a dimeric (LPdCl2)2 complex, which decomposes in a solution to the monomer including solvent molecule into the coordination sphere of the metal.
The reactions of 1,3-diallyl-5-[4′-(diphenylphosphino)butyl] isocyanurate and 1,3-diallyl-5-[6′-(diphenylphosphino)hexyl]
isocyanurate with PdCl2 give monomeric chelate LPdCl2 complexes in which one of the allyl groups of the isocyanurate cycle participates in coordination with the central ion along
with the phosphorus atom.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1859–1865, September, 1998. 相似文献