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   4122篇
  免费   117篇
  国内免费   23篇
化学   3448篇
晶体学   46篇
力学   44篇
数学   184篇
物理学   540篇
  2023年   22篇
  2022年   30篇
  2021年   46篇
  2020年   62篇
  2019年   59篇
  2018年   34篇
  2017年   32篇
  2016年   69篇
  2015年   80篇
  2014年   94篇
  2013年   208篇
  2012年   221篇
  2011年   289篇
  2010年   151篇
  2009年   147篇
  2008年   313篇
  2007年   243篇
  2006年   298篇
  2005年   263篇
  2004年   241篇
  2003年   212篇
  2002年   200篇
  2001年   59篇
  2000年   70篇
  1999年   57篇
  1998年   36篇
  1997年   42篇
  1996年   49篇
  1995年   37篇
  1994年   39篇
  1993年   35篇
  1992年   39篇
  1991年   29篇
  1990年   22篇
  1989年   21篇
  1988年   27篇
  1987年   22篇
  1986年   22篇
  1985年   33篇
  1984年   39篇
  1983年   18篇
  1982年   28篇
  1981年   32篇
  1980年   30篇
  1979年   22篇
  1978年   19篇
  1977年   18篇
  1976年   19篇
  1975年   18篇
  1974年   14篇
排序方式: 共有4262条查询结果,搜索用时 62 毫秒
21.
We have developed a new magneto-optical measurement system using a rotational cavity system equipped with a millimeter vector network analyzer and a 14 T solenoid type super conducting magnet. The measurement can be performed in the transmission configuration down to 1.6 K. The results of the precise angular dependence measurement of quasi-one-dimensional organic conductor (DMET)2I3 using the new system are shown, and its Fermi surface will be discussed in connection with the previous reports.  相似文献   
22.
Total syntheses of the peptide enamide natural products terpeptin and aspergillamides A and B are reported. An oxidative decarboxylation-elimination protocol is employed to construct the indolic enamide moiety. Unambiguous stereochemical assignment of (−)-terpeptin is accomplished by synthesis of all possible stereochemical analogues. Select compounds have been evaluated in cell cycle inhibitor assays which show that the natural amino acid configuration of terpeptin has the most potent inhibitory activity.  相似文献   
23.
Pyridine-based, structurally isomeric two macrocyclic compounds displayed a remarkably different complexation nature. The cage-type compound has an ideal structure for spherical cations, especially for the NH4+ ion, but the reaction with some transition metals and Ln3+ produced its protonated species. On the other hand, its isomer formed complexes with alkali metals and lanthanides (1:1) and also with transition metals. Some structures of the complexes were clarified by crystallographic analyses.  相似文献   
24.
The kinetics and pathway of hydrothermal decomposition of aspartic acid were studied using a continuous‐flow tubular reactor. The reaction was carried out in the temperature range of 200–260°C and at a pressure of 20 MPa. Deamination was the primary reaction, indicated by the presence of significant amount of ammonia, fumaric acid, or maleic acid in the products. Other reaction products were pyruvic acid, malic acid, and traces of succinic and lactic acid. Traces of alanine were also detected, showing the possibility of decomposing high‐molecular weight amino acids to obtain simple amino acids such as glycine or alanine. Results on the effect of reaction parameters demonstrated that decomposition of aspartic acid is highly temperature dependent under hydrothermal conditions. For a slight temperature difference of 60°C (from 200 to 260°C), the first‐order reaction rate constants of 0.003 significantly increased to 0.231 s?1. The activation energy was 144 kJ/mol, as calculated by the Arrhenius equation. No significant effect was exhibited by other reaction parameters such as pH and pressure. The results are useful in controlling the hydrolysis of proteinaceous materials toward high yield of aspartic acid under hydrothermal conditions. © 2007 Wiley Periodicals, Inc. 39: 175–180, 2007  相似文献   
25.
26.
27.
According to the concept of the recognized visual space of illumination (RVSI) the lightness of an object surface is perceived in relation to its conceptualized size. To prove this proposition the lightness of gray test patches was judged when they were located at various positions inside an illuminated space composed of two rooms in the depth direction from a subject. No retinal image arrangement was changed in the test patch and its immediate surroundings, but the front room had walls, floors and furniture lower in lightness by the amount of N1.5 than the back room to make the RVSI of the former smaller despite the illuminance in the entire space being the same. The results showed that the apparent lightness of the patches was perceived higher by amount of about 13 in L units for the N4 test patch and about 20 for N6 when the patches were located in the front room, in accordance with the prediction. It was stressed that the experiment of lightness judgment should be conducted in a three dimensional space rather than two dimensional plane as done by several investigators.  相似文献   
28.
RIKEN Accelerator Research Facility data on the tensor analyzing power T 20 of the dd3Hen and dd3Hp reactions at zero angle for deuteron kinetic energies of 140, 200, and 270 MeV are reported. The observed positive sign of T 20 clearly demonstrates the sensitivity to the D/S-wave ratio in the 3He and 3H wave functions in the energy range of the experiment. Data on T 20 for the 3Hen channel are in agreement with those for the 3Hp channel within the experimental errors.  相似文献   
29.
30.
Two Kemp's acid diamides were synthesized and applied to chiral amine recognition using 1H NMR analysis. One derivative based on 1-(1-naphthyl)ethylamine had good chiral recognition of six amines and was useful to determine the optical purity for three amines, i.e., methylbenzylamine, 1-(1-naphthyl)ethylamine and 1- henylpropylamine,however, the cyclohexylethylamine derivative showed little discrimination for the amines studied. Together with the results for alkylamines, it was shown that aromatic structure was important for aromatic shielding anisotropy and –– interactions between host and guest. The structure of the 1-(1-naphthyl)ethylamine derivative in solution was also considered based on 1H NMR data and computer simulation.  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