全文获取类型
收费全文 | 12832篇 |
免费 | 1509篇 |
国内免费 | 4234篇 |
专业分类
化学 | 16499篇 |
晶体学 | 105篇 |
力学 | 221篇 |
综合类 | 154篇 |
数学 | 316篇 |
物理学 | 1280篇 |
出版年
2024年 | 25篇 |
2023年 | 169篇 |
2022年 | 339篇 |
2021年 | 439篇 |
2020年 | 641篇 |
2019年 | 615篇 |
2018年 | 533篇 |
2017年 | 534篇 |
2016年 | 652篇 |
2015年 | 637篇 |
2014年 | 810篇 |
2013年 | 1242篇 |
2012年 | 863篇 |
2011年 | 865篇 |
2010年 | 714篇 |
2009年 | 675篇 |
2008年 | 852篇 |
2007年 | 780篇 |
2006年 | 742篇 |
2005年 | 719篇 |
2004年 | 708篇 |
2003年 | 656篇 |
2002年 | 765篇 |
2001年 | 470篇 |
2000年 | 445篇 |
1999年 | 355篇 |
1998年 | 342篇 |
1997年 | 334篇 |
1996年 | 290篇 |
1995年 | 284篇 |
1994年 | 198篇 |
1993年 | 233篇 |
1992年 | 180篇 |
1991年 | 106篇 |
1990年 | 90篇 |
1989年 | 69篇 |
1988年 | 51篇 |
1987年 | 30篇 |
1986年 | 17篇 |
1985年 | 17篇 |
1984年 | 22篇 |
1983年 | 10篇 |
1982年 | 12篇 |
1981年 | 8篇 |
1980年 | 6篇 |
1979年 | 6篇 |
1977年 | 6篇 |
1976年 | 4篇 |
1974年 | 4篇 |
1973年 | 4篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
51.
Takanori Shiba 《Tetrahedron letters》2004,45(16):3211-3213
Rhodium-catalyzed carbonylation of 2-alkynylbenzylamines under water-gas shift reaction conditions gives a seven-membered heterocyclic product, 2,4-disubstituted-1,4-dihydrobenz[c]azepin-3-ones, in a good yield. 相似文献
52.
Andrea Grosso Marco Locatelli Fabio Schoen 《Computational Optimization and Applications》2007,38(3):351-370
In this paper we perform a computational analysis of a population based approach for global optimization, Population Basin
Hopping (PBH), which was proven to be very efficient on very challenging global optimization problems by the authors (see
). The experimental analysis aims at understanding more deeply how the approach works and why it is successful on challenging
problems. 相似文献
53.
Pedro lvarez‐Boo Jos Sergio Casas Alfonso Castieiras María Delfina Couce Eduardo Freijanes Eva Novoa Jos Sordo 《应用有机金属化学》2003,17(9):725-729
Reaction of dichloro‐ and dibromodimethyltin(IV) with 2‐(pyrazol‐1‐ylmethyl)pyridine (PMP) afforded [SnMe2Cl2(PMP)] and [SnMe2Br2(PMP)] respectively. The new complexes were characterized by elemental analysis and mass spectrometry and by IR, Raman and NMR (1H, 13C) spectroscopies. Structural studies by X‐ray diffraction techniques show that the compounds consist of discrete units with the tin atom octahedrally coordinated to the carbon atoms of the two methyl groups in a trans disposition (Sn? C = 2.097(5), 2.120(5) Å and 2.110(6), 2.121(6) Å in the chloro and in the bromo compounds respectively), two cis halogen atoms (Sn? Cl = 2.4908(16), 2.5447(17) Å; Sn? Br = 2.6875(11), 2.7464(9) Å) and the two donor atoms of the ligand (Sn? N = 2.407(4), 2.471(4) Å and 2.360(5), 2.455(5) Å). In both cases, the Sn? N(pyridine) bond length is markedly longer than the Sn? N(pyrazole) distance. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
54.
V. V. AntiĆ M. P. AntiĆ M. N. Govedarica P. R. DvorniĆ 《Journal of polymer science. Part A, Polymer chemistry》2007,45(11):2246-2258
The kinetics of the formation of poly(carbosiloxane), as well as of alkyl-substituted poly(siloxane), by Karstedt's catalyst catalyzed hydrosilylation were investigated. Linear poly(carbosiloxane), poly[(1,1,3,3-tetramethyldisiloxanyl)ethylene], (PTMDSE), was obtained by hydrosilylation of 1,3-divinyltetramethyldisiloxane (DVTMDS) and 1,1,3,3-tetramethyldisiloxane (TMDS), while alkyl-substituted poly(siloxane), poly(methyldecylsiloxane), (PMDS), was synthesized by hydrosilylation of poly(methylhydrosiloxane) (PMHS) and 1-decene. To investigate the kinetics of PTMDSE formation, two series of experiments were performed at reaction temperatures ranging from 25 to 56 °C and with catalyst concentrations ranging from 7.0 × 10−6 to 3.1 × 10−5 mol Pt/mol CHCH2. A series of experiments was performed at reaction temperatures ranging from 28 to 48 °C, with catalyst concentrations of 7.0 ×10−6 mol of Pt per mol of CHCH2, when kinetics of PMDS formation was investigated. All reactions were carried out in bulk, with equimolar amounts of the reacting Si H and CHCH2 groups. The course of the reactions was monitored by following the disappearance of the Si H bands using quantitative infrared spectroscopy. The results obtained showed typical first order kinetics for the PTMDSE formation, consistent with the proposed reaction mechanism. In the case of PMDS an induction period occurred at lower reaction temperatures, but disappeared at 44 °C and the rate of Si H conversion also started to follow the first-order kinetics. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 2246–2258, 2007 相似文献
55.
MTL代数的特征定理 总被引:3,自引:1,他引:2
对于逻辑系统代数结构的研究,是一个十分重要的研究课题.近期提出的BL代数,R_0代数,MTL代数就是这个方向具有代表性的研究成果.本文讨论MTL代数的性质与结构,给出这种代数的几个特征定理,澄清这种代数与其它代数结构的关系.鉴于单位区间中由左连续t-范数诱导的剩余蕴涵与MTL代数的紧密联系,本文还考察了这种模糊蕴涵的特征性质. 相似文献
56.
HU Qiao-Sheng HU Chang-MingLaboratory of Organofluorine Chemistry Shanghai Institute of Organic Chemistry Chinese Academy of Sciences Shanghai China 《中国化学》1997,15(3):286-288
Initiated by CrCl3/Fe redox couple, per(poly)fluoroalkyl iodides added to methyl a-acetylamino acrylate, giving B-per(poly)fluoroalkyl a-amino acid derivatives in good yields. 相似文献
57.
58.
Friedel-Crafts alkylation of indoles with epoxides to afford 3-alkyl indole derivatives at room temperature with moderate to good yields and high regioselectivity using nanocrystalline titanium(IV) oxide catalyst is described. 相似文献
59.
F. M. Tukhtaboeva K. S. Davronov I. Zh. Kurbonbaev K. K. Kuchkarov 《Chemistry of Natural Compounds》2006,42(4):477-478
The protein composition of seeds treated with a suspension of ultradisperse iron was studied using electrophoresis on PAAG.
Changes were noted in the fractions with relative electrophoretic mobility (REM) 0.11 of water-soluble and REM 0.37 of buffer-soluble
An-9 cotton seed proteins.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 384–385, July–August, 2006. 相似文献
60.
Recently, we have developed a new tight-binding quantum chemical molecular dynamics program “Colors” for combinatorial computational chemistry approach. This methodology is based on our original tight-binding approximation and realized over 5000 times acceleration compared to the conventional first-principles molecular dynamics method. In the present study, we applied our new program to the simulations on various realistic large-scale models of the automotive three-way catalysts, ultrafine Pt particle/CeO2(111) support. Significant electron transfer from the Pt particle to the CeO2(111) surface was observed and it was found to strongly depend on the size of the Pt particle. Furthermore, our simulation results suggest that the reduction of the Ce atom due to the electron transfer from the Pt particle to the CeO2 surface is a main reason for the strong interaction of the Pt particle and CeO2(111) support. 相似文献