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   1180篇
  免费   23篇
  国内免费   6篇
化学   936篇
晶体学   13篇
力学   2篇
数学   42篇
物理学   216篇
  2023年   8篇
  2020年   14篇
  2019年   10篇
  2018年   13篇
  2017年   14篇
  2016年   15篇
  2015年   13篇
  2014年   21篇
  2013年   80篇
  2012年   56篇
  2011年   57篇
  2010年   44篇
  2009年   40篇
  2008年   73篇
  2007年   73篇
  2006年   66篇
  2005年   52篇
  2004年   60篇
  2003年   54篇
  2002年   43篇
  2001年   20篇
  2000年   11篇
  1999年   15篇
  1998年   10篇
  1997年   9篇
  1996年   10篇
  1995年   8篇
  1994年   11篇
  1993年   11篇
  1992年   10篇
  1991年   14篇
  1990年   9篇
  1989年   14篇
  1988年   6篇
  1986年   14篇
  1985年   16篇
  1984年   21篇
  1983年   7篇
  1982年   13篇
  1981年   11篇
  1980年   19篇
  1979年   17篇
  1978年   18篇
  1977年   12篇
  1976年   12篇
  1975年   14篇
  1974年   13篇
  1973年   18篇
  1971年   5篇
  1968年   6篇
排序方式: 共有1209条查询结果,搜索用时 703 毫秒
51.
Abstract

New chiral dopants β-hydroxy ketones 1, 1,3-diols 2, 1,3-dioxanes 3 and 1,3-dioxan-2-ones 4 were designed and synthesized. Reaction of (R)-1,2-epoxyoctane with carbanions derived from 2-(4-substituted phenyl)-1,3-dithianes followed by hydrolysis of the resulting hydroxy dithianes afforded 1. Reduction of 1 gave the diols 2, which yielded 3 upon acetalization and 4 upon carbonation. The syn isomers of 2, 3, and 4 exhibited larger spontaneous polarizations, when applied as chiral dopants, than the anti isomers or hydroxy ketones 1.  相似文献   
52.
53.
A series of porphyrins fused with acenaphthylene, phenanthroline, and benzofluoranthene polycyclic aromatic rings were prepared by means of a 3+1 porphyrin synthesis approach and subsequent retro‐Diels–Alder reaction of bicyclo[2.2.2]octadiene‐fused precursors. Analysis of the magnetic circular dichroism spectra and the results of time‐dependent DFT calculations are used to identify the reasons for the trends observed in the wavelengths and relative intensities of the Q bands of the products. Michl's perimeter model is used as a conceptual framework to explain the changes in the relative energies of the frontier π‐molecular orbitals.  相似文献   
54.
By using a giant amoeboid cell of the Physarum plasmodium, changes in the intracellular distribution of chemical components are studied in relation to information processing in cell behavior. Various kinds of metabolites oscillate, and so the protoplasm should be a collection of chemical oscillators. Spatially, characteristic chemical patterns are self-organized for different cell shapes, and hence cell behavior. New phase waves propagate throughout the cell upon local stimulation, their direction being opposite for attraction and repulsion. Locomotion is inhibited when the coherence of the oscillators breaks. Thus, pattern dynamics is correlated with information processing in the amoeboid cell.  相似文献   
55.
56.
We study the QCD phase structure at high temperature and density adopting a histogram method. Because the quark determinant is complex at finite density, the Monte-Carlo method cannot be applied directly. We use a reweighting method and try to solve the problems which arise in the reweighting method, i.e. the sign problem and the overlap problem. We discuss the chemical potential dependence of the probability distribution function in the heavy quark mass region and examine the applicability of the approach in the light quark region.  相似文献   
57.
Calix[6]arene hexacarboxylic acid binds instantly and with low symmetry to Pb, Sr and Ba. Later a highly symmetric up-down alternating conformation emerges. The solution structures are identical to their p-tert-butylcalix[6]arene hexacarboxylic acid counterparts. With either receptor, an octahedral cage is formed around the metal. The transformation from low to high symmetry however proceeds at significantly faster rates for the de-t-butylated host.  相似文献   
58.
Aryl‐substituted 1,1,4,4‐tetracyano‐1,3‐butadienes (FcTCBDs) and bis(1,1,4,4‐tetracyanobutadiene)s (bis‐FcTCBDs), possessing a ferrocenyl group on each terminal, were prepared by the reaction of a variety of alkynes with tetracyanoethylene (TCNE) in a [2+2] cycloaddition reaction, followed by retro‐electrocyclization of the initially formed [2+2] cycloadducts (i.e., cyclobutene derivatives). The characteristic intramolecular charge transfer (ICT) between the donor (ferrocene) and acceptor (TCBD) moieties were investigated by using UV/Vis spectroscopy. The redox behaviors of FcTCBDs and bis‐FcTCBDs were examined by cyclic voltammetry (CV) and differential pulse voltammetry (DPV), which revealed their properties of multi‐electron transfer depending on the number of ferrocene and TCBD moieties. Moreover, significant color changes were observed by visible spectroscopy under the electrochemical reduction conditions.  相似文献   
59.
Several well-defined 3,4-thienylene-ethynylene oligomers with different chain lengths have been synthesized and characterized. X-Ray crystallographic analyses proved their unique, totally helical conformations.  相似文献   
60.
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