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   5123篇
  免费   1282篇
  国内免费   690篇
化学   2558篇
晶体学   83篇
力学   20篇
综合类   24篇
数学   19篇
物理学   1880篇
无线电   2511篇
  2024年   33篇
  2023年   78篇
  2022年   148篇
  2021年   173篇
  2020年   160篇
  2019年   139篇
  2018年   137篇
  2017年   202篇
  2016年   237篇
  2015年   230篇
  2014年   377篇
  2013年   694篇
  2012年   454篇
  2011年   449篇
  2010年   348篇
  2009年   313篇
  2008年   333篇
  2007年   377篇
  2006年   352篇
  2005年   329篇
  2004年   271篇
  2003年   258篇
  2002年   242篇
  2001年   126篇
  2000年   120篇
  1999年   103篇
  1998年   58篇
  1997年   55篇
  1996年   52篇
  1995年   50篇
  1994年   50篇
  1993年   31篇
  1992年   27篇
  1991年   18篇
  1990年   8篇
  1989年   13篇
  1988年   3篇
  1987年   6篇
  1986年   5篇
  1985年   4篇
  1984年   3篇
  1983年   2篇
  1982年   8篇
  1981年   6篇
  1980年   6篇
  1979年   2篇
  1977年   2篇
  1976年   1篇
  1974年   2篇
排序方式: 共有7095条查询结果,搜索用时 0 毫秒
31.
微波促进下N,N-二甲基甲酰胺中的Knoevenagel反应   总被引:2,自引:0,他引:2  
程力惠  李毅群 《合成化学》2002,10(6):504-505,509
在微波促进下,芳醛与丙二腈或氰基乙酸乙酯在DMF中进行Knoevenagel缩合反应,以77%~98%的产率生成相应E-式烯烃。  相似文献   
32.
在微波辐射下,不用任何有机溶剂和无机载体,苯亚磺酸钠和卤代烃能迅速发生反应生成相应的S-烃基化产物。  相似文献   
33.
The reaction of electron‐deficient alkenes with alkoxyalkynyl Fischer carbene complexes (FCCs) represents a straightforward route to a new type of captodative (donor–acceptor) alkynylcyclopropanes, which have been prepared in moderate to high yields and in a diastereoselective manner. Some studies regarding the employment of additives to facilitate the recovery of the metal moiety after the reaction are also described. Finally, the first example of a cyclopropanation reaction through employing Fischer carbene complexes under microwave irradiation is presented; this method proved to be an advantageous alternative to the thermal reaction.  相似文献   
34.
The phosphorescence spectrum of p-dichlorobenzene has been calculated using multiconfiguration self-consistent-field wave functions and the quadratic response technique. Attention has been paid to the intensity distribution of the singlet–triplet (3B1u1Ag) transition through a number of vibronic subbands. The second order spin–orbit coupling (SOC) contribution to the spin splitting of the 3B1u (3*) state is found to be almost negligible, and the calculations therefore provide a good estimate for the zero-field splitting (ZFS) parameters based only on the electron spin–spin coupling expectation values. Nuclear quadrupole resonance constants for the different Cl isotopes are also calculated to accomplish the ZFS assignment. The electric dipole activity of the spin sublevels in the triplet–singlet transitions to the ground-state vibrational levels is estimated by calculations of derivatives using distorted geometries which are shifted from the equilibrium position along different vibrational modes. A vibrational analysis of the phosphorescence spectrum, based on the SOC-induced mixing of the singlet and triplet states calculated along different vibrational modes, provides reasonable agreement with experimental data.Acknowledgment O. R.-P. would like to thank the European MOLPROP network for support. The authors thank Alexander Baev for fruitful discussions. This work was supported by the Swedish Royal Academy of Science (KVA).  相似文献   
35.
标题化合物C24H29NO4?1/2C2H5OH稨2O)由香兰素、5,5-二甲基-1,3-环己二酮、醋酸铵在微波辐射下干反应并经95%乙醇重结晶而得C24H29NO4穀2(C2H5OH稨2O)晶体。结构通过单晶X-射线衍射法确定,其晶体属单斜晶系,空间群P21/n, a = 9.810(2), b = 14.516(3), c = 17.008(3) ? b = 101.03(2), V = 2377.2(8) ?, Z = 4, Mr = 427.52, Dc = 1.195 g/cm3 , m(MoKa) = 0.082 mm-1, F(000) = 920。晶体结构用直接法解出,经全矩阵最小二乘法对原子参数进行修正,最终的偏离因子为R = 0.0406, wR = 0.0892。X-射线衍射分析结果表明,吡啶环和与之稠合的2个六员环均为信封式构象。  相似文献   
36.
The microwave-mediated reaction of 4-aryl-4-oxobutanoic acids with benzylamines furnished 1-arylmethyl-3-[(E)-1-arylmethylidene]-5-phenyl-2,3-dihydro-1H-pyrrolones. This result is in contract to the earlier report on this reaction conducted under neat conditions. Structures for the products were assigned on the basis of spectral data and confirmed by independent synthesis. __________ Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 368–373, March, 2007.  相似文献   
37.
The surface wave produced plasma belongs to a class of RF and microwave induced plasmas. It results from the propagation of an electromagnetic wave which uses the plasma column it sustains and the plasma tube as its sole propagating media. This type of plasma offers several advantages compared to the positive column plasma of dc discharges or to other RF and microwave produced plasmas. Surface wave plasmas require no internal electrodes, and they can be applied over an extremely broad range of wave frequencies (27 MHz to 10 GHz demonstrated) and gas pressures (about 10–4 Torr to a few times the atmospheric pressures). Using the surface wave plasma technique, a large variety of plasma column diameters have been created (0.5–150 mm demonstrated) and no limitation on plasma column length (column up to 6 m long demonstrated) has been found. The surface wave produced plasma is used in elemental analysis and to sustain emission in lasing media. This article is intended as a guide for potential users of surface wave plasmas in the field of plasma processing and plasma chemistry.  相似文献   
38.
Electron temperature and ion density are measured in an air microwave-induced plasma (2450 MHz) by means of a floating double probe. A 'cinetic scheme for ion formation and decay is set up, and a relationship between atomic oxygen and ion densities is obtained. From this relationship an order-of-magnitude of atomic oxygen concentration in the discharge is derived and compared with results obtained by optical actinometry in another work.  相似文献   
39.
在微波促进无溶剂条件下, 由N-甲基-2-甲基吡啶碘盐与取代芳香醛在哌啶作用下合成了一系列2-取代的吡啶半菁染料, 产物结构由元素分析, 1H NMR, MS, IR, UV得到确认. 该方法操作简便, 收率高. 在此基础上, 对N-甲 基-2-(p-N,N-二甲氨基-苯乙烯基)吡啶半菁染料的光谱性质进行了理论计算.  相似文献   
40.
手性芳酰胺类分子钳的设计与微波合成   总被引:3,自引:0,他引:3  
以间苯二甲酸为隔离基, 酰胺键桥联L-氨基酸甲酯构成手臂, 在微波辐射下合成了具有不同手性中心和裂穴的新型手性芳酰胺类分子钳. 结构均经1H NMR, IR及元素分析确证, 并考察了其对芳香胺类化合物和D/L-氨基酸甲酯的识别性能. 初步研究表明, 这类分子钳受体不仅对中性小分子具有优良的识别性能, 其结合常数(Ka)可达2.66×103 L•mol-1, 而且对D/L-氨基酸甲酯亦具有良好的手性识别能力.  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