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   3948篇
  免费   649篇
  国内免费   404篇
化学   1557篇
晶体学   47篇
力学   76篇
综合类   66篇
数学   569篇
物理学   2686篇
  2024年   2篇
  2023年   32篇
  2022年   66篇
  2021年   114篇
  2020年   103篇
  2019年   116篇
  2018年   95篇
  2017年   118篇
  2016年   128篇
  2015年   118篇
  2014年   225篇
  2013年   262篇
  2012年   207篇
  2011年   219篇
  2010年   236篇
  2009年   355篇
  2008年   283篇
  2007年   298篇
  2006年   290篇
  2005年   210篇
  2004年   214篇
  2003年   182篇
  2002年   161篇
  2001年   114篇
  2000年   131篇
  1999年   100篇
  1998年   107篇
  1997年   77篇
  1996年   68篇
  1995年   59篇
  1994年   54篇
  1993年   35篇
  1992年   42篇
  1991年   33篇
  1990年   23篇
  1989年   28篇
  1988年   21篇
  1987年   10篇
  1986年   10篇
  1985年   15篇
  1984年   12篇
  1983年   4篇
  1982年   4篇
  1981年   3篇
  1980年   3篇
  1979年   2篇
  1975年   3篇
  1974年   3篇
  1973年   2篇
  1959年   1篇
排序方式: 共有5001条查询结果,搜索用时 294 毫秒
101.
Reported here are two novel quasi-racemic (bis)indole alkaloids, cycloaplysinopsin A (5) and cycloaplysinopsin B (6), isolated from tropical Indo-Pacific (Comoros, Philippines) scleractinian corals of the family Dendrophylliidae. Although their structures suggest a Diels-Alder cycloaddition origin from aplysinopsin-type precursors, neither experiments, nor theory allowed us to clearly distinguish an enzymatic process with scarce enantioselection from the intrusion of an adventitious catalyst in the coral extracts, where the chiral environment caused a slight asymmetric induction.  相似文献   
102.
用BOCMP方法及MonteCarlo模拟技术,对H2S导致Cu基催化剂失活的原因进行了计算分析。研究结果表明,当原料气中存在H2S时,WGS反应的活化能明显高于无H2S时的活化能,随着表面H2S浓度的增大(θ=0,0.10,0.25),反应的活化能也逐渐变大(其大小比为1∶1.34∶3.3),究其原因可归结为H2S的存在使得反应物分子的吸附热减小,从而使H2O的解离吸附(WGS反应的速控步骤)活化能增大。  相似文献   
103.
本文应用取代基效应(SCS)方法研究了乙烯-乙烯醇(EVA)共聚物,得到了羟基(-OH)在两种不同溶剂中的SCS参数:在苯酚+重水(80/20W/W)中参数为S_1=42.77±0.08ppm,S_2=7.155±0.06ppm,S_3(s)=-4.08±0.02ppm,S_3(t)=-3.09±0.02ppm,S_4=0.48±0.03ppm,S_5=0.26±0.05ppm,在以邻二氯苯为溶剂时参数为S_1=44.97±0.61ppm,S_2=7.40±0.00ppm,S_3(s)=-4.51±0.17ppm,S_3(t)=-3.13±0.00ppm,S_4=0.63±0.04ppm,S_5=0.36±0.00ppm,同时利用所得到的SCS参数对该共聚物的~(13)C NMR谱进行了归属。  相似文献   
104.
定义了烷烃分子中碳原子的离子性指数(INI),用离子性指数(INI)、极化效应指数(PEI)及N^i~H(i=αβΥ)结构信息参数研究了烷烃的^13CNMR化学位移模型,结果表明,烷烃^13CNMR化学位移(CS)可用下式来定量描述:CS=194.6156-37.7394(INI)+98.6505(ΣPEI)+27.1630(INI/ΣPEI)-652.9106(ΣPEI/INI)+0.7735N^α~H+2.2468N^β~H-0.1742N^γ~H。用上式估算了304个碳原子的化学位移,平均绝对误差仅为0.77δ,标准差0.9860δ,预测值与实验值非常吻合。  相似文献   
105.
106.
本文将迄今为止国内外文献报道的200余种达玛烷型皂甙类化合物的~(13)C化学位移按其结构特征分类整理,以原人参二(三)醇等为模型化合物,讨论了皂甙元结构变化引起的位移变化(Δδ_C)规律。  相似文献   
107.
High density and well surface-distributed oxygen microwave plasma with an extensible antenna-coupling design was utilized to modify a densely weaved and large-surface-area Nylon-6 fabric within a short treatment time. Plasma pretreatment and subsequent acrylic acid (AAc) or 2-hydroxyethyl methacrylate (HEMA) grafting process were studied and optimized at the stage after dyed and finished procedure. The monomer-grafted dyed Nylon-6 fabrics evolved lasting hydrophilic properties and thereafter created or improved surface properties such as water diffusion, drainage, moisture regain and water absorbency, in different degrees. The pHEMA-grafted sample exhibited minor effect in color perception, which was also much hydrophilic than the pAAc-grafted one. Based upon surface analyses and wetting assessment, the penetration of HEMA monomer into the plasma-treated fabric matrix contributed to the facilitation of wetting properties. This work accordingly ensures such plasma-induced system to incorporate with the pattern of hydrophilic properties on the analogous textiles without interrupting their finishing process.  相似文献   
108.
提出了控制电位电解和恒电流电解两类电解沉积的压电频移分析法测定的理论公式,用实验结果验证了它的正确性.  相似文献   
109.
The effect of thermal treatment on the structural incorporation of Cr2O3 in xCr2O3·(100 – x)SiO2 and 5R n xCr2O3·(95 – x)SiO2 (where x=0.01–1 mol.% and R=Li, Na and Ca) gel glasses was studied by optical absorption spectrophotometry, DTA-TG, XRD and electron microscopy.Samples heat treated at 60°C have green color due to the presence of Cr3+ in octahedral coordination. The optical transmission, and color (yellow, orange or ambar), of the samples heat treated between 200 and 700°C prove that Cr3+ (octahedrally coordinated) and Cr6+ (tetrahedrally coordinated) are both present. Segregation of Cr2O3 take place at temperatures above 800°C.In reducing conditions the gel glasses were green due to the presence of a high content of Cr3+ ions. Samples containing Li or Na show crystalline phases at temperatures below 850°C.  相似文献   
110.
Preparation, 19F NMR Spectroscopic Evidence and Study of the Formation of Metal-Mixed Cluster Anions [(Mo6?nWnCl )F ]2?, n = 0?6 The complete system of metal-mixed octahedral cluster ions [(Mo6?nWnCl)F]2?, n = 0?6, is prepared by tempering Mo powder with WCl6 at 600°C. A mixture containing inclusively the geometric isomers (n = 2, 3, 4) all ten possible species is transferred into the tetra-n-butylammonium salts (TBA)2[(Mo6?nWnCl)F]. In the 19F nmr spectrum the 24 expected signals are observed, assigned on the basis of their chemical shifts, multiplicities and intensities, and confirmed by a 2D-19F-19F COSY spectrum. From the integrated intensities the distribution of the different components is derived revealing a non-statistical formation, in that isomers with Mo…?Mo or W…?W atoms in trans-positions in comparision to those with mixed Mo…?W axes are favoured, and that especially the homoleptic compounds Mo6 and W6 are present to an over-average extent. Evaluation of 19F chemical shifts reveals that F bound to W which is in antipodal position to Mo resonates at higher field compared to F bound to W in a W…?W arrangement, caused by an increased shielding, which is synonymous to a positive antipodal-effect by Mo. Vice versa F bound to Mo with an antipodal W resonates at lower field compared with F bound to Mo in an Mo…?Mo arrangement caused by an increased deshielding and synonymous a negative antipodal-effect by W. The chemical shifts, resulting from antipodal-effects, are different for the compounds within the [(Mo6?nWnCl)F]2? - system. The difference of the antipodal effect of successive substitution products results in characteristic values designated as antipodal shift constants, depending on the kind of substituents, which is valid for other cluster systems, too.  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