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   471篇
  免费   7篇
  国内免费   1篇
化学   291篇
晶体学   5篇
力学   10篇
数学   53篇
物理学   120篇
  2023年   4篇
  2020年   7篇
  2019年   3篇
  2018年   4篇
  2017年   5篇
  2016年   4篇
  2015年   3篇
  2014年   10篇
  2013年   11篇
  2012年   4篇
  2011年   13篇
  2010年   9篇
  2009年   11篇
  2008年   13篇
  2007年   13篇
  2006年   18篇
  2005年   22篇
  2004年   20篇
  2003年   23篇
  2002年   22篇
  2001年   15篇
  2000年   16篇
  1999年   9篇
  1998年   11篇
  1997年   12篇
  1996年   8篇
  1995年   10篇
  1994年   13篇
  1993年   16篇
  1992年   21篇
  1991年   12篇
  1990年   7篇
  1989年   6篇
  1988年   8篇
  1987年   4篇
  1986年   5篇
  1985年   7篇
  1982年   5篇
  1981年   6篇
  1980年   9篇
  1979年   10篇
  1978年   4篇
  1977年   7篇
  1976年   5篇
  1975年   6篇
  1973年   6篇
  1970年   5篇
  1967年   2篇
  1965年   3篇
  1931年   2篇
排序方式: 共有479条查询结果,搜索用时 171 毫秒
101.
102.
In 1953 Arrow, Barankin, and Blackwell proved that, ifR n is equipped with its natural ordering and ifF is a closed convex subset ofR n , then the set of points inF that can be supported by strictly positive linear functionals is dense in the set of all efficient (maximal) points ofF. Many generalizations of this density result to infinite-dimensional settings have been given. In this note, we consider the particular setting where the setF is contained in the topological dualY * of a partially ordered, nonreflexive normed spaceY, and the support functionals are restricted to be either nonnegative or strictly positive elements in the canonical embedding ofY inY *. Three alternative density results are obtained, two of which generalize a space-specific result due to Majumdar for the dual system (Y,Y *)=(L 1,L ).This research was supported in part by funds provided by the Provident Chair of Excellence in Applied Mathematics at the University of Tennessee, Chattanooga, Tennessee.  相似文献   
103.
104.
105.
106.
107.
Aryl- and heteroaryl-nitrenes can take part in intra-and intermolecular reactions in both of their possible electronic states (triplet and singlet). In this review we have endeavored to high-light recent synthetic uses of these reactive intermediates as well as draw attention to avenues open to further exploration in this field. Singlet arylnitrenes will interact with suitable ortho-positioned substituents to give a variety of fused azoles, some in excellent yield. In suitable solvents and in presence of amines and alcohols, phenylnitrenes undergo ring expansion to azepines which can also occur in nitrenes of certain fused bicyclic aromatics (naphthalene, quinoline, isoquinoline, benzo[b]thiophene). The latter nitrenes may also give rise to o-diamines which are useful starters for further heterocyclic synthesis. Triplet arylnitrenes (usually regarded as having only a nuisance effect in synthetic work) may also be utilized in practicable heterocyclic syntheses within a suitable molecular framework. Decomposition of aryl azides in a mixture of an organic and polyphosphoric acid leads to fused oxazoles. The mechanism is discussed for all the reactions considered.  相似文献   
108.
109.
110.
Electrospray ionization (ESI) mass spectra have been measured on a magnetic-sector double-focusing mass spectrometer for a number of proteins and peptides. It is pointed out how in theory raising the mass resolution of a mass spectrometer from 800–1000 to 2400–3000 significantly increases the precision with which the envelope of isotopic peaks of a protein ion (or other organic ion) can be defined, particularly at higher masses. Better definition of the isotopic envelope ought to lead to higher precision in the experimental determination of molecular mass, which has been demonstrated. It is shown how ESI mass spectra of high-mass molecules are significantly less congested at higher m/z values, so that for these molecules (RMM > 40 000) there is an advantage in being able to record peaks at higher m/z values (m/z > 2000) representing ions with fewer charges. Fragmentation of a small peptide in the ESI source has been found to provide sequence information.  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