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   51588篇
  免费   4162篇
  国内免费   3799篇
化学   20619篇
晶体学   159篇
力学   2303篇
综合类   1113篇
数学   21416篇
物理学   13939篇
  2023年   364篇
  2022年   571篇
  2021年   1488篇
  2020年   1020篇
  2019年   1148篇
  2018年   942篇
  2017年   1090篇
  2016年   1333篇
  2015年   1280篇
  2014年   1996篇
  2013年   3171篇
  2012年   2195篇
  2011年   2643篇
  2010年   2431篇
  2009年   3115篇
  2008年   3229篇
  2007年   3428篇
  2006年   2794篇
  2005年   2129篇
  2004年   1866篇
  2003年   1882篇
  2002年   4255篇
  2001年   1613篇
  2000年   1266篇
  1999年   1062篇
  1998年   992篇
  1997年   836篇
  1996年   780篇
  1995年   664篇
  1994年   638篇
  1993年   618篇
  1992年   583篇
  1991年   417篇
  1990年   373篇
  1989年   281篇
  1988年   308篇
  1987年   267篇
  1986年   273篇
  1985年   393篇
  1984年   297篇
  1983年   186篇
  1982年   350篇
  1981年   526篇
  1980年   466篇
  1979年   502篇
  1978年   403篇
  1977年   309篇
  1976年   268篇
  1974年   87篇
  1973年   170篇
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
991.
Some new inequalities of Hermite-Hadamard's integration are established.As for as inequalities about the righthand side of the classical Hermite-Hadamard's integral inequality refined by S Qaisar in [3],a new upper bound is given.Under special conditions,the bound is smaller than that in [3].  相似文献   
992.
993.
In this study, we examine the feasibility and limitations of describing the motional behavior of three‐domain proteins in which the domains are linearly connected. In addition to attempting the determination of the internal and overall reorientational correlation times, we investigate the existence of correlations in the motions between the three domains. Since in linearly arranged three‐domain proteins, there are typically no experimental data that can directly report on motional correlation between the first and the third domain, we address this question by dynamics simulations. Two limiting cases occur: (1) for weak repulsive potentials and (2) when strong repulsive potentials are applied between sequential domains. The motions of the terminal domains become correlated in the case of strong interdomain repulsive potentials when these potentials do not allow the angle between the sequential domains to be smaller than about 60°. Using the model‐free (MF) and extended MF formalisms of Lipari and Szabo, we find that the motional behavior can be separated into two components; the first component represents the concerted overall motion of the three domains, and the second describes the independent component of the motion of each individual domain. We find that this division of the motional behavior of the protein is maintained only when their timescales are distinct and can be made when the angles between sequential domains remain between 60° and 160°. In this work, we identify and quantify interdomain motional correlations. © 2013 Wiley Periodicals, Inc.  相似文献   
994.
In this paper we study the nonlinear Chern–Simons–Schrödinger systems with an external potential. We show the existence, non-existence, and multiplicity of standing waves to this problem with asymptotically linear nonlinearities, which do not hold the Ambrosetti–Rabinowitz condition.  相似文献   
995.
The concept of the quantum Pfaffian is rigorously examined and refurbished using the new method of quantum exterior algebras. We derive a complete family of Plücker relations for the quantum linear transformations, and then use them to give an optimal set of relations required for the quantum Pfaffian. We then give the formula between the quantum determinant and the quantum Pfaffian and prove that any quantum determinant can be expressed as a quantum Pfaffian. Finally the quantum hyper-Pfaffian is introduced, and we prove a similar result of expressing quantum determinants in terms of quantum hyper-Pfaffians at modular cases.  相似文献   
996.
997.
Polymerization‐based signal amplification, a technique developed for use in rapid diagnostic tests, hinges on the ability to localize initiators as a function of interfacial binding events. We report here a new DNA detection method in which polymer growth in redox‐polymerization is used as a means to amplify detection signals. The introduction of biotin‐labeled chitosan (biotin‐CS) with highly dense amino groups into the polymerization amplification as macromolecular reducing agent, beneficially simplifies amplification operation, as well as, provides a large amount of initiation points to improve the sensitivity of detection. DNA hybridization, SA and biotin binding reactions led to the attachment of CS on a solid surface where specific DNA sequences were located. With the addition of the mixture containing monomer AM, crosslinker PEGDA and oxidant CAN onto the CS location, the growth of polymer films was triggered to render the corresponding spots readily distinguishable to the naked eye. Direct visualization of 0.21 fmol target DNA molecules of interest was demonstrated. Non‐small cell lung cancer p53 sequence was further selected as a proof‐of‐principle to detect DNA point mutation. The proposed method exhibited an efficient amplification performance for molecule detection, and paved a new way for visual diagnosis of biomolecules. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 1929–1937  相似文献   
998.
999.
We investigate the behavior of optical absorption of boron–nitride nanotubes (6,0) in the context of Hubbard model at the paramagnetic sector. GW approximation has been implemented in order to make self-energy matrix of electronic system. Afterwards, the real and imaginary parts of transverse dielectric functions have been obtained using linear response theory. The results show that the frequency gap in the optical absorption decreases with Coulomb repulsion strength. Moreover the results show that the local Coulomb interaction leads to the appearance of the excitonic effects in the optical spectrum. Finally the effects of electronic concentration on the frequency behavior of imaginary part of dielectric function have been investigated.  相似文献   
1000.
New metal-free phthalocyanine (7) fused symmetrically in peripheral positions with four dithiatetraoxa macrocycles, has been synthesized by cyclotetramerization of the isoindolinediimine derivative of macrocyclic 6. Metallophthalocyanine (8) was synthesized by reaction of phthalonitrile derivative (5) with anhydrous nickel(II) chloride. The new compounds were characterized by elemental analysis, 1H and 13C-NMR, IR UV–Vis and mass spectroscopies.  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