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   259291篇
  免费   4312篇
  国内免费   1329篇
化学   146146篇
晶体学   3421篇
力学   9528篇
综合类   62篇
数学   32071篇
物理学   73704篇
  2020年   2339篇
  2019年   2423篇
  2018年   3315篇
  2017年   3295篇
  2016年   5118篇
  2015年   3610篇
  2014年   4694篇
  2013年   11431篇
  2012年   10101篇
  2011年   11673篇
  2010年   8119篇
  2009年   7663篇
  2008年   10821篇
  2007年   10727篇
  2006年   10049篇
  2005年   9385篇
  2004年   8284篇
  2003年   7243篇
  2002年   7023篇
  2001年   7414篇
  2000年   5805篇
  1999年   4197篇
  1998年   3462篇
  1997年   3350篇
  1996年   3472篇
  1995年   2960篇
  1994年   3111篇
  1993年   2950篇
  1992年   3241篇
  1991年   3217篇
  1990年   3071篇
  1989年   2910篇
  1988年   2845篇
  1987年   2763篇
  1986年   2780篇
  1985年   3656篇
  1984年   3688篇
  1983年   3062篇
  1982年   3290篇
  1981年   3089篇
  1980年   2823篇
  1979年   3014篇
  1978年   3209篇
  1977年   3244篇
  1976年   3288篇
  1975年   2985篇
  1974年   3116篇
  1973年   3176篇
  1972年   2436篇
  1971年   1940篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
101.
Nonlinear Dynamics - The main purpose of this paper is to study both the underdamped and the overdamped dynamics of the nonlinear Helmholtz oscillator with a fractional-order damping. For that...  相似文献   
102.
103.
The first examples of the catalytic asymmetric 1,3‐dipolar cycloaddition of azomethine ylides with acyclic activated 1,3‐dienes (and 1,3‐enynes) are described. Under copper catalysis, a selective cycloaddition at the terminal γ,δ‐C?C bond is observed. In addition, depending on the ligand used, either the exo or the endo adduct can be obtained with high selectivity. Under appropriate reaction conditions, the acyclic 1,6‐addition product is detected, suggesting a stepwise mechanism. The resulting C4‐alkenyl‐substituted pyrrolidines are suitable substrates for further access to polycyclic systems, as highlighted by the preparation of hexahydrochromeno[4,3‐b]pyrrole and the tetracyclic core of the alkaloid gracilamine.  相似文献   
104.
105.
106.
Journal of Structural Chemistry - An analysis is presented for the results obtained in the studies initiated by A. E. Shvelashivili, Corresponding Member, Academy of Sciences of Georgia, and...  相似文献   
107.
108.
Thin films (monolayer and bilayer) of cylinder forming polystyrene‐block‐polydimethylsiloxane (PS‐b‐PDMS) were shear aligned by the swelling and deswelling of a crosslinked PDMS pad that was physically adhered to the film during solvent vapor annealing. The nanostructures formed by self‐assembly were exposed to ultraviolet‐ozone to partially oxidize the PDMS, followed by calcination in air at 500 °C. In this process, the PS segments were fully decomposed, while the PDMS yielded silica nanostructures. The highly aligned PDMS cylinders were thus deposited as silica nanolines on the silicon substrate. Using a bilayer film, the center‐to‐center distance of these features were effectively halved from 38 to 19 nm. Similarly, by sequential shear‐alignment of two distinct layers, a rhombic array of silica nanolines was fabricated. This methodology provides a facile route to fabricating complex topographically patterned nanostructures. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1058–1064  相似文献   
109.
The natural product lupeol 1 was isolated from aerial parts of Vernonia scorpioides with satisfactory yield, which made it viable to be used as starting material in semisynthetic approach. Ten lupeol derivatives 2–11 were prepared by classical procedures. Including, five new esters derivatives 7–11, which were obtained by structural modifications in the isopropylidene fragment. All semisynthetic compounds and lupeol 1–11 were confirmed by 1H NMR, 13C NMR and HRMS. Their antiprotozoal activity was evaluated in vitro against L. amazonensis and T. cruzi. Derivative 6 showed the best antitrypanosomal activity (IC50 = 12.48 μg/mL) and the lowest cytotoxic derivative (CC50 = 161.50 μg/mL). The mechanism of action of the most active derivatives (4, 6 and 11) is not dependent from the enzyme trypanothione reductase.  相似文献   
110.
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