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   193082篇
  免费   1439篇
  国内免费   265篇
化学   97255篇
晶体学   2676篇
力学   9641篇
综合类   7篇
数学   22780篇
物理学   62427篇
  2020年   2016篇
  2019年   2387篇
  2018年   3537篇
  2017年   3669篇
  2016年   4499篇
  2015年   2190篇
  2014年   3895篇
  2013年   7651篇
  2012年   6115篇
  2011年   7321篇
  2010年   5816篇
  2009年   5910篇
  2008年   7026篇
  2007年   6956篇
  2006年   6232篇
  2005年   5488篇
  2004年   5213篇
  2003年   4746篇
  2002年   4861篇
  2001年   5306篇
  2000年   3931篇
  1999年   3026篇
  1998年   2780篇
  1997年   2638篇
  1996年   2438篇
  1995年   2229篇
  1994年   2171篇
  1993年   2230篇
  1992年   2262篇
  1991年   2533篇
  1990年   2439篇
  1989年   2506篇
  1988年   2373篇
  1987年   2415篇
  1986年   2259篇
  1985年   2800篇
  1984年   2848篇
  1983年   2472篇
  1982年   2538篇
  1981年   2452篇
  1980年   2230篇
  1979年   2539篇
  1978年   2708篇
  1977年   2796篇
  1976年   2863篇
  1975年   2658篇
  1974年   2586篇
  1973年   2741篇
  1972年   2199篇
  1971年   2008篇
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
1.
2.
3.
4.
Easily accessible benzylic esters of 3‐butynoic acids in a gold‐catalyzed cyclization/rearrangement cascade reaction provided 3‐propargyl γ‐butyrolactones with the alkene and the carbonyl group not being conjugated. Crossover experiments showed that the formation of the new C?C bond is an intermolecular process. Initially propargylic–benzylic esters were used, but alkyl‐substituted benzylic esters worked equally well. In the case of the propargylic–benzylic products, a simple treatment of the products with aluminum oxide initiated a twofold tautomerization to the allenyl‐substituted γ‐butyrolactones with conjugation of the carbonyl group, the olefin, and the allene. The synthetic sequence can be conducted stepwise or as a one‐pot cascade reaction with similar yields. Even in the presence of the gold catalyst the new allene remains intact.  相似文献   
5.
6.
The aim of this work was to determine the parameters that have decisive roles in microwave-assisted reactions and to develop a model, using computational chemistry, to predict a priori the type of reactions that can be improved under microwaves. For this purpose, a computational study was carried out on a variety of reactions, which have been reported to be improved under microwave irradiation. This comprises six types of reactions. The outcomes obtained in this study indicate that the most influential parameters are activation energy, enthalpy, and the polarity of all the species that participate. In addition to this, in most cases, slower reacting systems observe a much greater improvement under microwave irradiation. Furthermore, for these reactions, the presence of a polar component in the reaction (solvent, reagent, susceptor, etc.) is necessary for strong coupling with the electromagnetic radiation. We also quantified that an activation energy of 20–30 kcal mol−1 and a polarity (μ) between 7–20 D of the species involved in the process is required to obtain significant improvements under microwave irradiation.  相似文献   
7.
This study was aimed at the development of a conductometric biosensor based on acetylcholinesterase considering the feasibility of its application for the inhibitory analysis of various toxicants. In this paper, the optimum conditions for enzyme immobilization on the transducer surface are selected as well as the optimum concentration of substrate for inhibitory analysis. Sensitivity of the developed biosensor to different classes of toxic compounds (organophosphorus pesticides, heavy metal ions, surfactants, aflatoxin, glycoalkaloids) was tested. It is shown that the developed biosensor can be successfully used for the analysis of pesticides and mycotoxins, as well as for determination of total toxicity of the samples. A new method of biosensor analysis of toxic substances of different classes in complex multicomponent aqueous samples is proposed.  相似文献   
8.
9.
10.
Russian Chemical Bulletin - Quantum chemical calculations and a comparative analysis of Raman spectra of 3,4,5-triphenyl-1-propyl-1,2-diphosphole (1),...  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