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   4931篇
  免费   84篇
  国内免费   11篇
化学   2821篇
晶体学   9篇
力学   61篇
综合类   1篇
数学   506篇
物理学   1628篇
  2020年   51篇
  2019年   36篇
  2018年   38篇
  2016年   55篇
  2015年   53篇
  2014年   62篇
  2013年   106篇
  2012年   122篇
  2011年   161篇
  2010年   105篇
  2009年   77篇
  2008年   138篇
  2007年   176篇
  2006年   166篇
  2005年   157篇
  2004年   151篇
  2003年   133篇
  2002年   116篇
  2001年   114篇
  2000年   91篇
  1999年   84篇
  1998年   72篇
  1997年   68篇
  1996年   85篇
  1995年   89篇
  1994年   97篇
  1993年   93篇
  1992年   110篇
  1991年   73篇
  1990年   60篇
  1989年   53篇
  1988年   66篇
  1987年   68篇
  1986年   61篇
  1985年   64篇
  1984年   60篇
  1983年   50篇
  1982年   70篇
  1981年   59篇
  1980年   53篇
  1979年   52篇
  1978年   55篇
  1977年   51篇
  1976年   43篇
  1975年   51篇
  1974年   46篇
  1973年   64篇
  1972年   38篇
  1971年   42篇
  1956年   31篇
排序方式: 共有5026条查询结果,搜索用时 15 毫秒
181.
182.
The chromophore structures in the parent states Pr and Pfr as well as in the photocycle intermediate Lumi-R of oat phytochrome phyA are determined by comparison of the experimental resonance Raman spectra with calculated Raman spectra that have been obtained by density functional theory calculations (B3LYP) using scaled force fields. The spectra were calculated for various tetrapyrrole geometries including more than twenty different methine bridge isomers. For the parent states Pr and Pfr the best agreement in terms of vibrational frequencies, isotopic shifts, and Raman intensities was achieved with the ZZZasa and ZZEssa geometry, respectively. For the first intermediate Lumi-R, the chromophore geometry is concluded to be the ZZEasa configuration. These finding imply that the primary step of the photoactivation of phytochrome is the Z/E isomerization of the C-D methine bridge double bond, whereas the single bond remains in the anti conformation. The subsequent transition to the physiologically active state Pfr includes a (partial) single bond rotation of the A-B methine bridge.  相似文献   
183.
The polarized optical absorption and emission (spectra, decay times) of single crystals of [Pd(thpy)2] and [Pt(thpy)2] (thpy ≡ C(3′)-deprotonated form of 2-(2-thienyl)pyridine) at temperatures 1.9 K ? T ? 80 K are reported. The emission of [Pt(thpy)2] can be influenced strongly by applied magnetic fields (0 ? H ? 6 T). Depending on the central ions Pd and Pt, the lowest excited electronic states of the single complexes are ligand-centered (LC) states and metal-to-ligand charge transfer (MLCT) states, respectively. This difference leads to distinctly dissimilar properties of the emission of both compounds. The experimental data show that the emission of single crystals of [Pd(thpy)2] and [Pt(thpy)2] at T ? 30 K originates from several types of traps (defect states of symmetry 3B2?stabilized below the exciton band) with LC and MLCT character, respectively. In the Pt compound, the 3B2 is split by spin-orbit coupling into three states. The states B and A, which determine the emission properties, are separated by Δv ~ 13 cm?1. Both states can mix under the influence of an applied magnetic field yielding an increase of the emission intensity by a factor of ~ 1.5 at H = 6 T.  相似文献   
184.
The organometallic ions V+-(benzene) and V+-(benzene)2 are produced by laser vaporization in a pulsed nozzle source. They are trapped and mass selected in an ion-trap/time-of-flight mass spectrometer, and their infrared spectra are measured with resonance-enhanced multiphoton photodissociation (IR-REMPD) spectroscopy with a tunable free-electron laser. Vibrational bands in the 600-1800 cm-1 region are characteristic of the benzene molecular moiety perturbed by the metal cation bonding. Experimental data are compared to the IR spectra derived from density functional calculations. Vibrational patterns in V+-(C6H6) indicate that the metal is bound in an eta6 pi-bonding configuration, while V+-(C6H6)2 is a sandwich. Trapped-ion IR-REMPD is a general method to access the vibrational spectroscopy of organometallic ions and their clusters.  相似文献   
185.
The brain renin-angiotensin system enables the formation of different biological active forms of angiotensins within the brain. All enzymes and peptides necessary for the biosynthesis of these angiotensins have been recognized within the central nervous system. Since there are considerable mismatches concerning the localization of the different enzymes, this system is not fully understood. Moreover, since alternative pathways of the angiotensin biosynthesis exists, localization and generation, especially of the short forms of biologically active angiotensins, are largely enigmatic. The brain renin-angiotensin system mediates several classic physiological effects including body water balance, maintenance of blood pressure, sexual behaviors, and regulation of pituitary gland hormones. Beside these classic functions, the brain renin-angiotensin system has more subtle functions involving complex mechanisms such as learning and memory. The mechanisms of action seem to differ depending on the utilized different bioactive angiotensin fragments, which are formed by the action of a variety of enzymes. This phenomenon appears to represent an important mechanism for neuromodulation. Moreover, there is evidence to suggest that the renin-angiotensin system is involved in neurological disorders, as e.g. Alzheimer's or Parkinson's disease.  相似文献   
186.
Quadratically constrained least squares and quadratic problems   总被引:9,自引:0,他引:9  
Summary We consider the following problem: Compute a vectorx such that Ax–b2=min, subject to the constraint x2=. A new approach to this problem based on Gauss quadrature is given. The method is especially well suited when the dimensions ofA are large and the matrix is sparse.It is also possible to extend this technique to a constrained quadratic form: For a symmetric matrixA we consider the minimization ofx T A x–2b T x subject to the constraint x2=.Some numerical examples are given.This work was in part supported by the National Science Foundation under Grant DCR-8412314 and by the National Institute of Standards and Technology under Grant 60NANB9D0908.  相似文献   
187.
188.
189.
190.
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