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   25628篇
  免费   2287篇
  国内免费   3009篇
化学   8920篇
晶体学   154篇
力学   2065篇
综合类   230篇
数学   5899篇
物理学   2658篇
综合类   10998篇
  2024年   102篇
  2023年   329篇
  2022年   621篇
  2021年   724篇
  2020年   800篇
  2019年   679篇
  2018年   693篇
  2017年   819篇
  2016年   965篇
  2015年   794篇
  2014年   1216篇
  2013年   1774篇
  2012年   1542篇
  2011年   1434篇
  2010年   1170篇
  2009年   1462篇
  2008年   1467篇
  2007年   1722篇
  2006年   1463篇
  2005年   1269篇
  2004年   1180篇
  2003年   1028篇
  2002年   1020篇
  2001年   825篇
  2000年   741篇
  1999年   759篇
  1998年   608篇
  1997年   542篇
  1996年   445篇
  1995年   452篇
  1994年   396篇
  1993年   356篇
  1992年   278篇
  1991年   264篇
  1990年   210篇
  1989年   181篇
  1988年   146篇
  1987年   120篇
  1986年   75篇
  1985年   51篇
  1984年   39篇
  1983年   23篇
  1982年   29篇
  1981年   23篇
  1980年   23篇
  1979年   22篇
  1978年   8篇
  1977年   15篇
  1976年   7篇
  1957年   5篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
1.
2.
研究了离散型二维竞争系统的渐近稳定性,得到了这类竞争系统中各类平衡点的坐标及其性质,获得了系统在边界上的平衡点处渐近稳定的一系列充分条件.这些条件等价于该系统中的某个群体在竞争过程中消亡或被淘汰的相应条件.  相似文献   
3.
The resistance of metal–organic frameworks towards water is a very critical issue concerning their practical use. Recently, it was shown for microporous MOFs that the water stability could be increased by introducing hydrophobic pendant groups. Here, we demonstrate a remarkable stabilisation of the mesoporous MOF Al‐MIL‐101‐NH2 by postsynthetic modification with phenyl isocyanate. In this process 86 % of the amino groups were converted into phenylurea units. As a consequence, the long‐term stability of Al‐MIL‐101‐URPh in liquid water could be extended beyond a week. In water saturated atmospheres Al‐MIL‐101‐URPh decomposed at least 12‐times slower than the unfunctionalised analogue. To study the underlying processes both materials were characterised by Ar, N2 and H2O sorption measurements, powder X‐ray diffraction, thermogravimetric and chemical analysis as well as solid‐state NMR and IR spectroscopy. Postsynthetic modification decreased the BET equivalent surface area from 3363 to 1555 m2 g?1 for Al‐MIL‐101‐URPh and reduced the mean diameters of the mesopores by 0.6 nm without degrading the structure significantly and reducing thermal stability. In spite of similar water uptake capacities, the relative humidity‐dependent uptake of Al‐MIL‐101‐URPh is slowed and occurs at higher relative humidity values. In combination with 1H‐27Al D ‐HMQC NMR spectroscopy experiments this favours a shielding mechanism of the Al clusters by the pendant phenyl groups and rules out pore blocking.  相似文献   
4.
In view of immense importance of silylenes and the fact that their properties undergo significant changes on substitution with halogens, here, we have used B3LYP/6-311++G** level of theory to access the effects of 1–4 halogens (X = F, Cl, Br, and I) on four unprecedented sets of cyclopentasilylene-2,4-dienes; with the following formulas: SiC4H3X ( 1 X ), SiC4H2X2 ( 2 X ), SiC4HX3 ( 3 X ), and SiC4X4 ( 4 X ). In going down from F to I, the singlet (s)-triplet (t) energy gap (ΔEs-t, a possible indication of stability), and band gap (ΔEH-L) decrease while nucleophilicity (N), chemical potential (μ), and proton affinity (PA) increase. The overall order of N, μ, and PA for each X is 2 X > 1 X > 3 X > 4 X . Precedence of 2 X over 1 X is attributed to the symmetric cross conjugation in the former. The highest and lowest N are shown by 2 I and 4 F . The trend of divalent angle () for each X is 4 X > 1 X > 3 X > 2 X . The results show that in going from electron withdrawing groups (EWGs) to electron donating groups (EDGs), the ΔEs-t and ΔEH-L decrease while N, μ, and PA increase. Also, rather high N of our scrutinized silylenes may suggest new promising ligands in organometallic chemistry.  相似文献   
5.
We report a strong dependence of the thermal stability of Nafion® perfluorosulfonate ionomer on the nature of the counterion associated with the fixed sulfonate site. These results were obtained using thermal gravimetric analysis on a series of alkali metal and alkyl ammonium cation-exchanged Nafion films. We have found that the temperature of decomposition of Nafion is inversely dependent on the size of the exchanged cation; i.e., Nafion films show improved thermal stability as the size of the counter cation decreases. We attribute this inverse relationship of thermal stability with counterion size to an initial decomposition reaction which is strongly influenced by the strength of the sulfonate-coun-terion interaction. © 1993 John Wiley & Sons, Inc.  相似文献   
6.
We investigate the influence of slip boundary conditions on the onset of Bénard convection in an infinite fluid layer. It is shown that the critical Rayleigh number is a decreasing function of the slip length, and therefore boundary slip is seen to have a destabilizing effect. Chebyshev‐tau and compound matrix formulations for solving the eigenvalue problem are presented. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   
7.
This paper analyzes the extent to which standard dynamic renewable resource models possess refutable implications. Both the steady state comparative static and local comparative dynamic properties of the standard model are studied. A unified framework is developed which enables one to analyze the qualitative properties of any standard renewable resource model. This is achieved by explicitly linking the local stability, steady state comparative static, and local comparative dynamic properties of the model.  相似文献   
8.
水轮机水力稳定性的分析   总被引:2,自引:0,他引:2  
根据收集国内外水轮机水力稳定性资料 ,分析了引起水轮机水力不稳定性的因素 ,并结合实例分析可能引起的危害 ,最后提出了解决问题的方法和建议  相似文献   
9.
考虑一个具有时滞的非自治的捕食——食饵生态系统。该系统是由一个捕食,二个食饵种群所构成我们给出了系统的周期解是全局稳定的充分条件。  相似文献   
10.
This primer provides a self-contained exposition of the case where spatial birth-and-death processes are used for perfect simulation of locally stable point processes. Particularly, a simple dominating coupling from the past (CFTP) algorithm and the CFTP algorithms introduced in [13], [14], and [5] are studied. Some empirical results for the algorithms are discussed. Received: 30 June 2002  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