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   1049篇
  免费   20篇
  国内免费   1篇
化学   636篇
晶体学   20篇
力学   82篇
数学   136篇
物理学   196篇
  2022年   10篇
  2021年   10篇
  2020年   12篇
  2019年   15篇
  2018年   8篇
  2017年   18篇
  2016年   20篇
  2015年   11篇
  2014年   33篇
  2013年   71篇
  2012年   67篇
  2011年   56篇
  2010年   37篇
  2009年   21篇
  2008年   40篇
  2007年   38篇
  2006年   43篇
  2005年   37篇
  2004年   27篇
  2003年   34篇
  2002年   35篇
  2001年   10篇
  2000年   10篇
  1998年   9篇
  1997年   17篇
  1996年   14篇
  1995年   17篇
  1994年   15篇
  1993年   11篇
  1992年   9篇
  1991年   16篇
  1990年   11篇
  1989年   15篇
  1988年   7篇
  1987年   7篇
  1986年   12篇
  1985年   16篇
  1983年   14篇
  1982年   13篇
  1981年   12篇
  1980年   12篇
  1979年   14篇
  1978年   13篇
  1977年   11篇
  1976年   11篇
  1975年   9篇
  1974年   9篇
  1973年   16篇
  1941年   11篇
  1936年   9篇
排序方式: 共有1070条查询结果,搜索用时 781 毫秒
1.
2.
NaBH4 reduction of a cage dione proceeds in a stereospecific fashion to give theendo,endo-diol. This reactivity is related to the crystal structure.  相似文献   
3.
4.
In this paper, we examine the orthogonal Latin squares (OLS) problem from an integer programming perspective. The OLS problem has a long history and its significance arises from both theoretical aspects and practical applications. The problem is formulated as a four-index assignment problem whose solutions correspond to OLS. This relationship is exploited by various routines (preliminary variable fixing, branching, etc) of the Branch & Cut algorithm we present. Clique, odd-hole and antiweb inequalities implement the ‘Cut’ component of the algorithm. For each cut type a polynomial-time separation algorithm is implemented. Extensive computational analysis examines multiple aspects concerning the design of our algorithm. The results illustrate clearly the improvement achieved over simple Branch & Bound.  相似文献   
5.
Studies conducted by Atomic Minerals Directorate of Exploration and Research (AMD) of Hyderabad, India had established the presence of higher concentrations of uranium in Lambapur and Peddagattu areas of Nalgonda district, AP, India and it was estimated that it could be a viable source for commercial extraction. The envisaged extraction process involves dispersion of radioactive particulate matter into atmosphere. Environmental radioactive studies in and around proposed mining areas at this point of time will be extremely useful for establishing base line data before a large scale uranium extraction process comes into existence. To this end, Solid State Nuclear Track Detectors were installed to evaluate indoor radon and thoron concentration levels in the dwellings of the area. The geometric means of radon and thoron concentration levels were found to be (7.1±0.2)×101 and (6.7±0.3)×101 Bq/m3, respectively. Simultaneously, natural background radiation measurements were also made and these levels are found to vary from 770 to 3995 μGy/y in the spatial distribution.  相似文献   
6.
7.
A mild and efficient oxidation of alcohols with o-iodoxybenzoic acid (IBX) catalyzed by beta-cyclodextrin in a water/acetone mixture (86:14) has been developed. A series of alcohols were oxidized at room temperature in excellent yields.  相似文献   
8.
[reaction: see text] A systematic investigation on a broad set of aldehydes reveals that the lifetimes of (Z)-photoenols can be modulated by variation of the substituents. We have found that the lifetimes of (Z)-enols (in benzene) can be varied by more than 1 order of magnitude with a judicious choice of the substituents that exert mesomeric and inductive effects as, for example, in the case of pentamethylbenzaldehyde (tau = 35 ns) and dicyanomesitaldehyde (tau = 760 ns). This study thus points to the fact that the electronic factors in conjunction with hydrogen bonding stabilization can considerably broaden the uni- as well as bimolecular chemistry based on photoenolization. Further, we have shown that the photoenols exhibit dramatic shifts in their absorption properties with variation of the substituents; although the photoenols have long been considered to be colored, their absorption properties have not been heretofore comprehensively examined.  相似文献   
9.
2‐Acetyl thiophenethiocynate (ATT) was synthesized and its characterization study was carried out using elemental analysis, IR and NMR techniques. The new reagent was proposed as an extractant for the development of the extractive spectrophotometric method for determination of Pt(IV) metal. The reagent complexes with the metal to produce a yellow colored complex which was then extracted into ethyl acetate at pH 11.2–11.6 having an absorption maxima at 400 nm. The thermal study showed that the extraction reactions are exothermic in nature with the reagent, and the stoichiometric ratio of Pt(IV) to 2‐acetyl thiophenethiocynate in the organic phase was 1:2. The method permits separation and determination of platinum from real and binary mixtures. The separation of Pt(IV) from bivalent metal ions has been also studied.  相似文献   
10.
The photocyclization to benzocyclobutenols of o-alkyl aromatic aldehydes that are predestined for gamma-hydrogen abstraction is found to occur efficiently in the solid state; in contrast, solution-phase photolysis is known to afford a mixture of several products. It is shown that mesitaldehyde, which is a liquid, also undergoes efficient cyclization when subjected to photolysis as a solid inclusion complex. The marginal energy differences in the relative energies of the E-enols and the corresponding cyclobutenols in the case of cyano-substituted mesitaldehydes has permitted direct observation, for the first time, of the E-enols en route to benzocyclobutenols. The AM1 calculations suggest that the cyano-substitution causes intrinsic stabilization of the E-enols relative to the corresponding cyclobutenols, while the bromo groups do the opposite. The lack of observation of the red color in bromo- and formyl-substituted aldehydes is attributed to rapid cyclization of the E-enols to the their respective cyclobutenols even at low temperatures.  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