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   4599篇
  免费   72篇
  国内免费   13篇
化学   3111篇
晶体学   12篇
力学   46篇
数学   719篇
物理学   796篇
  2016年   61篇
  2015年   52篇
  2014年   71篇
  2013年   122篇
  2012年   94篇
  2011年   122篇
  2010年   92篇
  2009年   65篇
  2008年   105篇
  2007年   139篇
  2006年   91篇
  2005年   124篇
  2004年   122篇
  2003年   85篇
  2002年   81篇
  2001年   69篇
  2000年   78篇
  1999年   62篇
  1998年   40篇
  1996年   52篇
  1995年   43篇
  1994年   63篇
  1993年   47篇
  1992年   51篇
  1991年   47篇
  1989年   41篇
  1988年   41篇
  1987年   52篇
  1986年   62篇
  1985年   63篇
  1984年   50篇
  1983年   43篇
  1982年   62篇
  1981年   75篇
  1980年   61篇
  1979年   44篇
  1978年   64篇
  1977年   53篇
  1976年   48篇
  1974年   49篇
  1972年   44篇
  1971年   40篇
  1967年   40篇
  1965年   55篇
  1964年   107篇
  1963年   133篇
  1962年   176篇
  1961年   158篇
  1960年   150篇
  1958年   54篇
排序方式: 共有4684条查询结果,搜索用时 15 毫秒
1.
2.
3.
We study conditions on the matrix mask of a vector subdivision scheme ensuring that certain polynomial input vectors yield polynomial output again. The conditions are in terms of a recurrence formula for the vectors which determine the structure of polynomial input with this property. From this recurrence, we obtain an algorithm to determine polynomial input of maximal degree. The algorithm can be used in the design of masks to achieve a high order of polynomial reproduction.  相似文献   
4.
Employing a cleavable carbohydrate–peptide linker, a new strategy for single-bead analysis of multivalent cyclic neoglycopeptides based on Edman degradation is described. Edman degradation of glycopeptides is hampered by the acid lability of the glycosidic bond and potential incompatibilities of phenylthiohydantoin (PTH) derivatives of glycosylated amino acids with PTH derivatives of the proteinogenic amino acids. To overcome this problem, carbohydrates are detached from the cyclopeptide templates before single-bead analysis, allowing for micro sequencing under routine conditions. With this strategy, application of multivalent cyclic neoglycopeptides in split-mix libraries with a subsequent screening process becomes possible for the first time.  相似文献   
5.
In spherically symmetric systems, in spite of Birkhoff's Theorem, the rates of clocks in vacuum regions on either side of moving mass shells must be continually readjusted to stay in synchrony. This shows up as time-dependence of the metric in terms of the globally meaningful time coordinate.  相似文献   
6.
The residual polarization of negative muons in crystal silicon samples with phosphorus (P: 1.6×1013 cm−3) and antimony (Sb: 2×1018 cm−3) impurities is investigated. The measurements are made in a 1000 G magnetic field oriented in a direction transverse to the muon spin in the temperature range 4–300 K. The relaxation rate and shift of the precession frequency in the silicon sample with the phosphorus impurity are measured more accurately than previously. It is found that in antimony-doped silicon the acceptor center μ A1 at temperatures below 30 K can be in both ionized and neutral states. The experimental data are interpreted on the basis of spin-lattice relaxation of the magnetic moment of an acceptor center, formation of acceptor-donor pairs, and recombination of charge carriers at the acceptor. Preliminary measurements showed a nonzero residual polarization of negative muons in germanium. Pis’ma Zh. éksp. Teor. Fiz. 68, No. 1, 61–66 (10 July 1998)  相似文献   
7.
In an earlier paper, Raphaël Rouquier and the author introduced the group of self-equivalences of a derived category. In the case of a Brauer tree algebra, we determined a nontrivial homomorphism of the Artin braid group to this group of self-equivalences. The class of Brauer tree algebras include blocks of finite group rings over a large enough field with cyclic defect groups. In the present paper we give an integral version of this homomorphism. Moreover, we identify some interesting arithmetic subgroups with natural groups of self-equivalences of the derived category.  相似文献   
8.
The synthesis of a specific isotopomer, C6D4H(ortho)-H(ortho)D4C6 of biphenyl is reported. The intramolecular dipolar coupling of the protons leads to a well-resolved single-crystal proton nuclear magnetic resonance (NMR) spectrum and allows one to study the dynamics of the phenyl rings in a unique way. At room temperature and above, the most conspicuous dynamical mode consists of 180° ring flips. The present data together with previous measurements of the total flip rate allow us to conclude that the rings flip almost exclusively independently of each other. Between the incommensurate (IC) phase transition of biphenyl at 38 K andT=250 K, the prominent namical mode consists of oscillatory twists ϕ(t) of the two rings. The data allow us to infer the mean square, (φ2), of these twists. (φ2) is found to grow linearly withT for 50<T<200 K. From the slope of (φ2) vs.T the frequency (the wave number[(v)\tilde]\tilde v) is derived. The result is[(v)\tilde] = 20\tilde v = 20 cm−1. ForT<38 K, the spectra give direct evidence of the IC phase transition and its nature (stripelike rather than quiltlike). The temperature dependence of the magnitude of the order parameter of the IC phase is obtained.  相似文献   
9.
10.
A systematic μSR study of the local magnetic field distribution in a series of oxygen deficient YBa2Cu3O x samples with 6.5⩽x⩽7.0 is reported. Special attention was given to perform the experiments under the same conditions, so that the oxygen content of the measured samples was the only parameter varied. The behavior of the depolarization rate σ as a function of the oxygen contentx was found to have strong similarities with the behavior of the critical temperatureT c as a function ofx. In particular, two step-like increases of σ were observed abovex=6.7 and 6.9. The temperature dependence of the normalized depolarization rate σ(T)/σ(0) is well described by the two-fluid model forx⩾6.781(1) and clearly deviates from this behavior forx⩽6.704(1). Our results are compared to those obtained by other groups.  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