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   2845篇
  免费   71篇
  国内免费   9篇
化学   1912篇
晶体学   45篇
力学   57篇
数学   448篇
物理学   463篇
  2023年   12篇
  2022年   50篇
  2021年   71篇
  2020年   64篇
  2019年   60篇
  2018年   46篇
  2017年   54篇
  2016年   85篇
  2015年   83篇
  2014年   95篇
  2013年   190篇
  2012年   155篇
  2011年   182篇
  2010年   148篇
  2009年   117篇
  2008年   174篇
  2007年   152篇
  2006年   127篇
  2005年   127篇
  2004年   109篇
  2003年   93篇
  2002年   83篇
  2001年   31篇
  2000年   37篇
  1999年   33篇
  1998年   28篇
  1997年   29篇
  1996年   27篇
  1995年   26篇
  1994年   23篇
  1993年   18篇
  1992年   25篇
  1991年   35篇
  1990年   28篇
  1989年   19篇
  1988年   21篇
  1987年   14篇
  1986年   16篇
  1985年   25篇
  1984年   25篇
  1983年   13篇
  1982年   17篇
  1981年   13篇
  1980年   21篇
  1979年   11篇
  1978年   16篇
  1977年   18篇
  1976年   16篇
  1975年   7篇
  1973年   7篇
排序方式: 共有2925条查询结果,搜索用时 31 毫秒
21.
Data on the mean multiplicity of - produced in minimum bias proton-proton, proton-neutron and proton-nucleus interactions as well as central nucleus-nucleus collisions at momenta of 1.4–400 GeV/c per nucleon have been compiled and studied. The results for neutron-neutron and nucleon-nucleon interactions were then constructed. The dependence of the mean pion multiplicity in proton-nucleus interactions and central collisions of identical nuclei are studied as a function of the collision energy and the nucleus mass number. The number of produced pions per participant nucleon in central collisions of identical nuclei is found to be independent of the number of participants at a fixed incident momentum per nucleon. The mean multiplicity of negatively charged hadrons per participant nucleon for central nucleus-nucleus collisions is lower by about 0.12 than the corresponding multiplicity for nucleon-nucleon interactions atp LAB 15 A·GeV/c, whereas the result at 200 A·GeV/c is above the corresponding nucleon-nucleon multiplicity. This may indicate change of the collision dynamics at high energy.  相似文献   
22.
23.
24.
Summary The asymptotic behaviour of random dynamical systems in Polish spaces is considered. Under the assumption of existence of a random compact absorbing set, assumption supposed to hold path by path, a candidate pathwise attractorA() is defined. The goal of the paper is to show that, in the case of stationary dynamical systems,A() attracts bounded sets, is measurable with respect to the -algebra of invariant sets, and is independent of when the system is ergodic. An application to a general class of Navier-Stokes type equations perturbed by a multiplicative ergodic real noise is discussed in detail.  相似文献   
25.
The palladium catalysed cross-coupling reaction of aryl iodides and bromides with pinacolborane in 1,3-dialkylimidazolium tetrafluoroborates and hexafluorophosphates producing arylboronates is described.  相似文献   
26.
A flow-through microdispenser has been coupled to a micro HPLC separation system and used as a solvent elimination interface for Fourier transform infrared (FTIR) and Raman spectroscopic detection of the separated compounds. Using the microdispenser picoliter sized droplets can be generated and deposited on an appropriate target placed on a computerized x, y-stage. Evaporation of volatile solvent and buffer is rapid and allows analysis of the obtained dry deposits by various techniques. Due to the destruction free character of Raman and FTIR spectroscopy they can be applied sequentially to interrogate the same deposit. In the reported application five phenolic acids typically present in wine have been separated on a C-18 column technique using a mixture of water, methanol and acetic acid as mobile phase. For spectrum acquisition infrared and Raman microscopes have been used. The spectra recorded from the dried deposits of the separated compounds agreed well with the reference spectra of corresponding components.  相似文献   
27.
The effect of NH3 and NH3/Ar plasma on ultrafiltration polysulfone membranes have been studied. Results of contact angle, FTIR-ATR and X-ray photoelectron spectroscopy experiments clearly showed that both plasmas introduced hydrophilic, nitrogen- and oxygen-containing moieties on the polymer surface and that NH3/Ar plasma was more efficient. That plasma was also more aggressive--signs of strong etching could be seen on the SEM pictures. Redeposition of etched material seemed to take place inside the pores. On the contrary, ammonia plasma was soft and caused cleaning the surface and pores enlargement. Performance of ammonia plasma modified membranes was greatly improved and independent on solution pH. The last observation proved amphoteric character of the surface. NH3/Ar plasma treatment gave membranes of acidic surface and filtration indices not so good as for ammonia plasma.  相似文献   
28.
Two newly identified supramolecular structures arise from self-assembly of the macrocyclic 1,5,9,18,22,26- hexaaza[11.11]-p-cyclophane salts with o-nitrophenol (C28H50N6)4+·4(C6H4NO2O) (1) and with HCl (C28H52N6)6+·6Cl-·4H2O (2). In both cases two-dimensional supramolecular sheets are formed.  相似文献   
29.
The crystal and molecular structure of nitrobenzene was determined at 103 K by X-ray diffraction, yieldingR=0.034 and a highly precise geometry of the molecule (esds of bond lengths 0.001 Å and bond angles 0.1°). The bond angles in the ring agree very well with additive scheme based on angular substituent parameters. X-X electron density maps support the view that the C-N bond does not exhibit-character, and, hence, the nitro group interacts with the ring mostly by inductive effects.  相似文献   
30.
An original computer-controlled solid-state photometer has been developed and its potential for simultaneous multicomponent flow-injection analysis of binary and ternary mixtures is demonstrated. The device is simple in construction. Its principle of operation is based on rapid sequential measurements of the absorbance of the complexes formed by the analytes with chromogenic reagents at the wavelengths corresponding to the emission maxima of three light emitting diodes (563, 580 and 638 nm).  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