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   92535篇
  免费   974篇
  国内免费   377篇
化学   32465篇
晶体学   828篇
力学   6984篇
数学   33854篇
物理学   19755篇
  2023年   144篇
  2021年   151篇
  2020年   226篇
  2019年   174篇
  2018年   10549篇
  2017年   10372篇
  2016年   6430篇
  2015年   1219篇
  2014年   646篇
  2013年   972篇
  2012年   4431篇
  2011年   11260篇
  2010年   5954篇
  2009年   6296篇
  2008年   7268篇
  2007年   9420篇
  2006年   907篇
  2005年   1879篇
  2004年   1966篇
  2003年   2372篇
  2002年   1378篇
  2001年   590篇
  2000年   565篇
  1999年   384篇
  1998年   387篇
  1997年   350篇
  1996年   400篇
  1995年   307篇
  1994年   248篇
  1993年   297篇
  1992年   255篇
  1991年   223篇
  1990年   187篇
  1989年   193篇
  1988年   181篇
  1987年   191篇
  1986年   205篇
  1985年   199篇
  1984年   224篇
  1983年   202篇
  1982年   214篇
  1981年   225篇
  1980年   213篇
  1979年   202篇
  1978年   205篇
  1977年   177篇
  1976年   165篇
  1975年   149篇
  1974年   135篇
  1973年   146篇
排序方式: 共有10000条查询结果,搜索用时 328 毫秒
1.
In the paper, the authors establish several integral representations for the generating functions of the large and little Schröder numbers and for the large and little Schröder numbers.  相似文献   
2.
Easily accessible benzylic esters of 3‐butynoic acids in a gold‐catalyzed cyclization/rearrangement cascade reaction provided 3‐propargyl γ‐butyrolactones with the alkene and the carbonyl group not being conjugated. Crossover experiments showed that the formation of the new C?C bond is an intermolecular process. Initially propargylic–benzylic esters were used, but alkyl‐substituted benzylic esters worked equally well. In the case of the propargylic–benzylic products, a simple treatment of the products with aluminum oxide initiated a twofold tautomerization to the allenyl‐substituted γ‐butyrolactones with conjugation of the carbonyl group, the olefin, and the allene. The synthetic sequence can be conducted stepwise or as a one‐pot cascade reaction with similar yields. Even in the presence of the gold catalyst the new allene remains intact.  相似文献   
3.
Mesoscopic modeling at the pore scale offers great promise in exploring the underlying structure transport performance of flow through porous media. The present work studies the fluid flow subjected to capillarity-induced resonance in porous media characterized by different porous structure and wettability. The effects of porosity and wettability on the displacement behavior of the fluid flow through porous media are discussed. The results are presented in the form of temporal evolution of percentage saturation and displacement of the fluid front through porous media. The present study reveals that the vibration in the form of acoustic excitation could be significant in the mobilization of fluid through the porous media. The dependence of displacement of the fluid on physicochemical parameters like wettability of the surface, frequency along with the porosity is analyzed. It was observed that the mean displacement of the fluid is more in the case of invading fluid with wetting phase where the driving force strength is not so dominant.  相似文献   
4.
5.
We prove that the group of diffeomorphisms of the interval [0, 1] contains surface groups whose action on (0, 1) has no global fix point and such that only countably many points of the interval (0, 1) have non-trivial stabiliser.  相似文献   
6.
7.
The development of novel, tumor-selective and boron-rich compounds as potential agents for use in boron neutron capture therapy (BNCT) represents a very important field in cancer treatment by radiation therapy. Here, we report the design and synthesis of two promising compounds that combine meta-carborane, a water-soluble monosaccharide and a linking unit, namely glycine or ethylenediamine, for facile coupling with various tumor-selective biomolecules bearing a free amino or carboxylic acid group. In this work, coupling experiments with two selected biomolecules, a coumarin derivative and folic acid, were included. The task of every component in this approach was carefully chosen: the carborane moiety supplies ten boron atoms, which is a tenfold increase in boron content compared to the l-boronophenylalanine (l-BPA) presently used in BNCT; the sugar moiety compensates for the hydrophobic character of the carborane; the linking unit, depending on the chosen biomolecule, acts as the connection between the tumor-selective component and the boron-rich moiety; and the respective tumor-selective biomolecule provides the necessary selectivity. This approach makes it possible to develop a modular and feasible strategy for the synthesis of readily obtainable boron-rich agents with optimized properties for potential applications in BNCT.  相似文献   
8.
9.
10.
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