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   98753篇
  免费   5714篇
  国内免费   4652篇
化学   56238篇
晶体学   1331篇
力学   5582篇
综合类   322篇
数学   11837篇
物理学   33809篇
  2023年   750篇
  2022年   1710篇
  2021年   2053篇
  2020年   2310篇
  2019年   2506篇
  2018年   2892篇
  2017年   2823篇
  2016年   3486篇
  2015年   2410篇
  2014年   3478篇
  2013年   4917篇
  2012年   5060篇
  2011年   5360篇
  2010年   4254篇
  2009年   4259篇
  2008年   4455篇
  2007年   4181篇
  2006年   3809篇
  2005年   3378篇
  2004年   3036篇
  2003年   2713篇
  2002年   2831篇
  2001年   2549篇
  2000年   1989篇
  1999年   1602篇
  1998年   1534篇
  1997年   1330篇
  1996年   1294篇
  1995年   1078篇
  1994年   1156篇
  1993年   1097篇
  1992年   1062篇
  1991年   1124篇
  1990年   1118篇
  1989年   1039篇
  1988年   917篇
  1987年   915篇
  1986年   881篇
  1985年   921篇
  1984年   915篇
  1983年   822篇
  1982年   800篇
  1979年   801篇
  1978年   814篇
  1977年   806篇
  1976年   919篇
  1975年   812篇
  1974年   844篇
  1973年   847篇
  1972年   752篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
The crystal structures of 2-amino-4-phenyl-9H-pyrimido[4,5-b]indole and its nitrate were determined by XRD analysis. 13C NMR, XRD, and quantum-chemical data indicate that the acid proton is predominantly localized at the N(3) atom of the pyrimidine ring in both isolated nitrate molecules and in molecules in crystal and solution.  相似文献   
992.
It was found experimentally that stacking defects formed in the mechanochemical activation of zinc ferrite enhanced the specific catalytic activity in the reaction of CO oxidation. The specific rate of CO oxidation was a linear function of defect concentration, which was determined using Mössbauer spectroscopy and X-ray diffraction. A conclusion was drawn that the same centers are responsible for an increase in the catalytic activity, the sorption capacity for hydrogen sulfide, and the reactivity of zinc ferrite in the interaction with hydrochloric acid. It was assumed that analogous factors caused an increase in the catalytic activity and reactivity of magnesium ferrite.  相似文献   
993.
The results of a kinetic study of model reactions between substituted phenols and bromobenzene in the presence of potassium carbonate and the copper(I) chloride–8-hydroxyquinoline catalytic complex in N,N-dimethylformamide are presented. The reactions were found to obey a first-order rate law. Both orbital and charge interactions should be taken into account in a consideration of the effect of the structural characteristics of reactants on the rate of reaction. The kinetics of substitution of the phenoxide anion for an aromatically bound halogen atom in activated and nonactivated systems with the formation of practically valuable aryl ethers were comparatively studied. The results presented provide an opportunity to distinguish the common features and regularities of activated and nonactivated aromatic substitution in the test systems.  相似文献   
994.
He J  Yu B 《The Analyst》1998,123(10):2197-2200
An indirect laser photoacoustic technique is described. The basic principle, the experimental set-up and the influencing factors are discussed in detail. This method was used to quantify phenylamine, arginine and methylene blue on membranes. The linear ranges of the calibration curve are up to two orders of magnitude. With 1 microliter of sample solution, the detection limits are 0.25, 1.52 and 0.14 pmol for phenylamine, arginine and methylene blue, respectively.  相似文献   
995.
The thermodynamic characteristics of adsorption of several organic compounds on the carbon adsorbent Carbopack B before and after its modification by a monomolecular layer of cholesteryl-n-pentyl oxybenzoate were determined by gas chromatography. The initial adsorbent was close in its properties to graphitized carbon black. Modification weakened adsorbate-adsorbent attraction and increased the mobility of adsorbed molecules, to a greater extent for nonpolar adsorbents and to a lesser extent for compounds capable of specifically interacting with modifier molecules.  相似文献   
996.
997.
998.
999.
1000.
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