首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   32649篇
  免费   215篇
  国内免费   292篇
化学   13672篇
晶体学   312篇
力学   1433篇
综合类   12篇
数学   9113篇
物理学   8614篇
  2021年   65篇
  2020年   84篇
  2019年   74篇
  2018年   1218篇
  2017年   1475篇
  2016年   773篇
  2015年   628篇
  2014年   561篇
  2013年   847篇
  2012年   3336篇
  2011年   2568篇
  2010年   1942篇
  2009年   1670篇
  2008年   850篇
  2007年   826篇
  2006年   877篇
  2005年   4670篇
  2004年   4115篇
  2003年   2492篇
  2002年   672篇
  2001年   336篇
  2000年   169篇
  1999年   223篇
  1998年   142篇
  1997年   108篇
  1996年   84篇
  1995年   81篇
  1994年   84篇
  1993年   63篇
  1992年   208篇
  1991年   181篇
  1990年   162篇
  1989年   128篇
  1988年   122篇
  1987年   83篇
  1986年   64篇
  1985年   75篇
  1984年   62篇
  1982年   46篇
  1981年   49篇
  1980年   44篇
  1979年   48篇
  1978年   47篇
  1976年   94篇
  1975年   57篇
  1974年   58篇
  1973年   59篇
  1972年   44篇
  1969年   41篇
  1968年   41篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
151.
A novel cage compound was obtained by irradiation of a quadruple-layered dithiacyclophane and showed thermally reverse reaction.  相似文献   
152.
153.
154.
The size of a glass sphere positioned in the center of a microdisk electrode is determined by using a simple electrochemical procedure and is confirmed, additionally, by a microscopical measurement of the sphere at the time of the electrochemical measurement. The cyclic voltammetric response of the naked electrode and of the electrode with the sphere positioned in its center is recorded over a wide range of scan rates (0.002-1.5 V s(-1)). The size of the sphere is then determined by comparison of the experimental voltammogram with simulations for each individual scan rate.  相似文献   
155.
Oligo(phenylene sulfide) (OPS) containing one disulfide bond at the end of the chain, which was obtained by the oxidative polymerization of diphenyl disulfide, had a relatively low Td10%(temperature for 10% weight loss) of 412 °C because of degradation of the disulfide bond. But this thermal cleavage of the disulfide bond promoted the curing reaction through thiophenoxy radical formation. OPS was allowed to react with diiodobenzene at 220 °C. The thermal stability of OPS was improved through the consumption of the disulfide bond and the coupling of the chain.  相似文献   
156.
Selenomethionine contents of NIST wheat reference materials   总被引:1,自引:0,他引:1  
Values of the total selenium and selenomethionine (Semet) content of four wheat-based reference materials have been obtained by gas chromatography-stable isotope dilution mass spectrometry methods. The total Se method is an established one, and the results obtained with it are consistent with previously-assigned values. The Semet method (previously reported by our laboratory) is based on reaction with CNBr. Our data indicate that the four wheat samples (wheat gluten, durum wheat, hard red spring wheat, and soft winter wheat), though having a 30-fold range in total Se content, all have about 45% of their total Se values in the form of selenomethionine. Investigation of the CNBr-based method suggests that additional experiments are needed to verify that all selenomethionine in the wheat samples is accounted for, but also indicates that the values obtained are within 15% of the true values. As the form in which Se occurs in foods and dietary supplements is important from a nutritional perspective, adding information about Se speciation to total Se values in appropriate reference materials makes these materials more valuable in relevant analytical work.  相似文献   
157.
158.
Two new silanols bearing very bulky silyl groups, (i-Pr3 Si)3SiOH and (t − BuMe2Si)3SiOH were prepared by peracidoxidation of their respective silanes. The X − ray crystallographic analysis revealed that (t − BuMe2Si)3 SiOH forms a dimeric structure with hydrogen bonding, while (i − Pr3 Si)3 SiOH exists as a monomer in the crystal. The effects of the size of the substituents as well as the reactivity of these silanols are discussed.  相似文献   
159.
160.
Yellow crystals of the title compound were obtained under solvothermal conditions reacting elemental Zn, Sb, and S in a solution of tris(2-aminoethyl)amine (=tren) and water. The compound crystallises in the monoclinic space group P21/c with a=13.0247(7), b=22.308(2), c=12.1776(6) Å, and =105.352(6)°. In the structure of [Zn(tren)]2Sb4S8·0.75 H2O two [Zn(tren)]2+ cations are bound to the [Sb4S8]4– anion via S atoms. The Zn2+ ions are in a trigonal bipyramidal environment of four N atoms of the tetradentate tren ligand and one S atom of the [Sb4S8]4– anion. The anion is formed by SbS3 and SbS4 units which share common corners and edges. The interconnection mode yields three different non-planar Sb2S2 heterorings. The shortest intermolecular Sb–S distance amounts to about 3.7Å, and taking this long separation into account undulated chains running along [001] are formed with the water molecules residing in the pocket-like cavities. Upon heating the compound decomposes in one step starting at about 240°C. The final decomposition product was identified as ZnS and Sb2S3 by X-ray powder diffractometry. Additionally, spectroscopic data as well as synthetic procedures for [Zn(tren)]2Sb4S8·0.75 H2O are reported.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号