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   3574篇
  免费   106篇
  国内免费   18篇
化学   2182篇
晶体学   15篇
力学   199篇
数学   764篇
物理学   538篇
  2023年   17篇
  2022年   13篇
  2021年   99篇
  2020年   73篇
  2019年   53篇
  2018年   66篇
  2017年   59篇
  2016年   119篇
  2015年   107篇
  2014年   84篇
  2013年   189篇
  2012年   216篇
  2011年   251篇
  2010年   150篇
  2009年   128篇
  2008年   207篇
  2007年   223篇
  2006年   169篇
  2005年   156篇
  2004年   145篇
  2003年   119篇
  2002年   100篇
  2001年   44篇
  2000年   27篇
  1999年   38篇
  1998年   35篇
  1997年   35篇
  1996年   40篇
  1995年   26篇
  1994年   34篇
  1993年   47篇
  1992年   19篇
  1991年   29篇
  1990年   30篇
  1989年   20篇
  1988年   26篇
  1987年   23篇
  1986年   24篇
  1985年   48篇
  1984年   41篇
  1983年   20篇
  1982年   26篇
  1981年   29篇
  1980年   28篇
  1979年   24篇
  1978年   27篇
  1977年   24篇
  1976年   23篇
  1975年   15篇
  1974年   21篇
排序方式: 共有3698条查询结果,搜索用时 15 毫秒
991.
We are concerned with a control problem related to the vanishing viscosity approximation to scalar conservation laws. We investigate the Γ -convergence of the control cost functional, as the viscosity coefficient tends to zero. A first-order Γ -limit is established, which characterizes the measure-valued solutions to the conservation laws as the zeros of the Γ -limit. A second-order Γ -limit is then investigated, providing a characterization of entropic solutions to conservation laws as the zeros of the Γ -limit.  相似文献   
992.
Rhodium metal particles, isolated as supported or unsupported powder starting from mesitylene solvated rhodium atoms, catalyse the hydrosilylation of aromatic nitriles to N,N-disilylamines in high conversion at 100°C. Different hydrosilanes (HSiMe3, HSi(OEt)3) can be employed. In the case of cinnamonitrile, the chemoselectivity of the reaction to 2-trimethylsilyl-3-phenylpropionitrile and (E)- and (Z)-1-di(trimethylsilyl)amino-3-phenyl-1-propene is strongly dependent on the reaction temperature. The commercial rhodium on γ-Al2O3 catalyst is considerably less active and selective than the analogous catalyst prepared via Metal Vapour Synthesis (MVS) probably owing to the different dimension and distribution of the metal particles in the two samples as shown by HRTEM analysis.  相似文献   
993.
994.
We present an integrated system with automated sample fabrication for combinatorial investigations of solution-processed organic materials. To illustrate the applicability of the system, we give examples of typical experimental results with organic electronic devices. Organic light emitting diodes (OLEDs) based on a poly-(N-vinylcarbazole) matrix system with small molecule hole-transporter N,N′-Bis(3-methylphenyl)-N,N′-diphenyl-benzidine (TPD) and electron transporter 2-(4-tert-butylphenyl)-5-(4-biphenylyl)-1,3,4-oxadiazole (PBD) were optimized. In a single experimental run, the optimum range of TPD and PBD concentrations has been determined. Furthermore, we screened the influence of a gate dielectric modification with poly(methyl silsesquioxane) in organic field effect transistors and show that the choice of the material system, which constitutes the interface between the gate dielectric and the organic semiconductor, modulates the mobility of the field-effect device by more than two orders of magnitude. Finally, we present a combinatorial study of the influence of PEDOT-PSS and P3HT-PC61BM layer thickness variation in organic photo voltaic cells. To summarize, we describe the possibilities of a combinatorial tool for solution based multilayer devices comprising functional materials. The tool is applicable to a vast variety of such materials. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 1587–1593, 2010  相似文献   
995.
In this note we provide a large deviation principle for Poisson shot noise processes under heavy tail semi-exponential conditions on the total shot per arrival. As in the light tail case, our result shows an insensitivity property of the model.  相似文献   
996.
The chain transfer to monomer reactions promoted by primary and secondary growing chains in the propene polymerization promoted by ansa‐zirconocenes and postmetallocene precursors are studied by using DFT methods. From the theoretical results it comes out that the prevalence of propene insertion over β‐hydrogen transfer to the monomer decreases drastically in the presence of a secondary chain. Furthermore, we explained the reason why C2‐symmetric metallocene catalysts promote the selective formation of cis but‐2‐enyls end group after a 2,1 inserted unit whereas for octahedral bis(phenoxy‐imine)titanium‐based catalysts, chain release promotes exclusively the formation of allyl terminated chain end. These results might be useful to design ligand precursors able to obtain not only high Mn PP polymers but also tuned chain end groups to build new polymer architectures. Overall, a more general picture of the enantioselectivity of the chain transfer to monomer processes is reported. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 699–708, 2010  相似文献   
997.
998.
999.
This paper provides a generalization of the main lemma and a correct proof of an extended version of Theorem 2, in [G. Vidossich, Differential inequalities for evolution equations, Nonlinear Anal. TMA 25 (1995) 1063-1069].  相似文献   
1000.
Let be the framebundle over an oriented, Riemannian surface . Denote by the first nonzero eigenvalue of the Laplace operator acting on differential forms of degree 1. We prove that for all with canonical metrics of volume 1.

  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