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   538篇
  免费   55篇
  国内免费   91篇
化学   563篇
晶体学   2篇
力学   8篇
综合类   5篇
数学   33篇
物理学   73篇
  2023年   2篇
  2022年   1篇
  2019年   1篇
  2017年   2篇
  2016年   4篇
  2015年   1篇
  2014年   32篇
  2013年   52篇
  2012年   45篇
  2011年   8篇
  2010年   2篇
  2009年   4篇
  2008年   23篇
  2007年   20篇
  2006年   16篇
  2005年   22篇
  2004年   31篇
  2003年   40篇
  2002年   89篇
  2001年   194篇
  2000年   31篇
  1999年   24篇
  1998年   13篇
  1997年   11篇
  1996年   3篇
  1995年   4篇
  1994年   4篇
  1993年   1篇
  1992年   1篇
  1991年   2篇
  1990年   1篇
排序方式: 共有684条查询结果,搜索用时 15 毫秒
51.
A new amperometric biosensor for hydrogen peroxide was developed based on adsorption of horseradish peroxidase at the glassy carbon electrode modified with zinc oxide nanoflowers produced by electrodeposition onto multi-walled carbon nanotubes (MWNTs) film. The morphology of the MWNTs/nano-ZnO electrode has been investigated by scanning electron microscopy (SEM), and the electrochemical performance of the electrode has also been studied by amperometric method. The resulting electrode offered an excellent detection for hydrogen peroxide at -0.11 V with a linear response range of 9.9×10^-7 to 2.9×10^-3 mol/L with a correlation coefficient of 0.991, and response time 〈5 s. The biosensor displays rapid response and expanded linear response range, and excellent stability.  相似文献   
52.
The similar electrochemical oxidation behaviors of hydroxypivalaldehyde in ionic liquids (ILs) medium, C4MIMPF6, C4MIMBF4 and CsMIMPF6, are investigated using classic electrochemical methods, respectively. Only the product, hydroxypivalic acid is detected by high performance liquid chromatography (HPLC). It can be conferred that the electrochemical oxidation of hydroxypivalaldehyde consists of two successive one-electron irreversible reactions at glass carbon (GC) electrode and the possible reaction mechanism in the ILs is proposed firstly. The diffusion coefficients of hydroxypivalaldehyde are obtained according to the electrochemical characteristics of hydroxypivalaldehyde in C4MIMPF6, C4MIMBF4 and CsMIMPF6.  相似文献   
53.
The eudesmane derivative, (-)-10-epi-α-cyperone 1, is widely used as a chiral starting material for the synthesis of other fused-ring sesquiterpenes1. The first synthetic work was reported by Howe and co-workers via condensation of (+)-dihydrocarvone 2 with 1-diethylaminopentan-3-one methiodide in 32% yield2. Previously, our group reported the synthesis of compound 1 by treating ketone 2 with ethyl vinyl ketone (EVK) directly under different conditions1a, but the yields were not satisfacto…  相似文献   
54.
In this paper,a compound-type inclusion interval of basic coneigenvalues of(com- plex)matrix is obtained.The corresponding boundary theorem and isolating theorem are given.  相似文献   
55.
Lappaconitine (Figure 1) is a diterpenoid alkaloid, naturally occurring in roots and rhizomes of Aconitum and delphinium1. Lap reveals bradycardic and hypotensive activity2. But its application is restrained owing to its poor water solubility, toxicity and side effects on humans. In a number of pharmaceutical studies, b-CD has been reported to interact with many drug molecules to form inclusion complexes for improving the water solubility of drugs, and reducing their toxicity3. We have p…  相似文献   
56.
研究了10K Ar基质中CF3I与O2经266nm脉冲激光辐照的光氧化反应,利用低温基质隔离技术和付里叶变换红外光谱法检测反应过程中产生的中间体有CF3OOI、CF3OO、CF3O和CF3OI。通过量子化学从头算,对CF3OOI的结构和振动频率进行计算,并对观察到的3个吸收峰进行了归属,首次确证CF3OOI为新的中间体,根据CF3OO、CF3OOI、CF3O、CF3OI随光照时间的生长和衰减,提出  相似文献   
57.
珠算穿梭式加减法,是珠算界学者、专家在总结传统加减算法的基础上,根据珠算自身的性质,而改进推出的一种新的珠算加减打法,它不仅改进了传统加减法中手指逆向(自右向左)空回的缺陷,也大大地提高了珠算加减法的运算速度。但是,经过几年的实践,广大珠算爱好者们发现,珠算穿梭式加减法在进行逆向加减运算时,  相似文献   
58.
IBONACCISEQUENCEANDCANTOR′STERNARYSETTONGJINGCHENGSAMONS,J.ManuscriptreceivedSeptember12,1994.RevisedDecember15,1996.Depar...  相似文献   
59.
CONSTRUCTIONOFSOLUTIONSTOM-DRIEMANNPROBLEMSFORA2×2QUASILINEARHYPERBOLICSYSTEMCHENSHUXINGManuscriptreceivedDecember26,1994....  相似文献   
60.
珠算是我国古代劳动人民发明创造的,具有悠久历史的宝贵文化遗产之一,作为传统的计算技术,它一直被广泛地应用在人们的经济生活中和金融财贸工作中。  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