全文获取类型
收费全文 | 8540篇 |
免费 | 358篇 |
国内免费 | 1023篇 |
专业分类
化学 | 8439篇 |
晶体学 | 98篇 |
力学 | 33篇 |
综合类 | 28篇 |
数学 | 250篇 |
物理学 | 1073篇 |
出版年
2024年 | 9篇 |
2023年 | 115篇 |
2022年 | 137篇 |
2021年 | 206篇 |
2020年 | 291篇 |
2019年 | 246篇 |
2018年 | 211篇 |
2017年 | 274篇 |
2016年 | 234篇 |
2015年 | 211篇 |
2014年 | 330篇 |
2013年 | 1022篇 |
2012年 | 371篇 |
2011年 | 350篇 |
2010年 | 324篇 |
2009年 | 436篇 |
2008年 | 524篇 |
2007年 | 511篇 |
2006年 | 497篇 |
2005年 | 526篇 |
2004年 | 467篇 |
2003年 | 376篇 |
2002年 | 246篇 |
2001年 | 243篇 |
2000年 | 233篇 |
1999年 | 237篇 |
1998年 | 209篇 |
1997年 | 102篇 |
1996年 | 108篇 |
1995年 | 118篇 |
1994年 | 154篇 |
1993年 | 106篇 |
1992年 | 98篇 |
1991年 | 64篇 |
1990年 | 36篇 |
1989年 | 43篇 |
1988年 | 35篇 |
1987年 | 29篇 |
1986年 | 21篇 |
1985年 | 17篇 |
1984年 | 29篇 |
1983年 | 8篇 |
1982年 | 23篇 |
1981年 | 19篇 |
1980年 | 12篇 |
1979年 | 19篇 |
1978年 | 12篇 |
1977年 | 9篇 |
1976年 | 8篇 |
1973年 | 7篇 |
排序方式: 共有9921条查询结果,搜索用时 15 毫秒
1.
Caesium carbonate supported on hydroxyapatite‐encapsulated Ni0.5Zn0.5Fe2O4 nanocrystallites as a novel magnetically basic catalyst for the one‐pot synthesis of pyrazolo[1,2‐b]phthalazine‐5,10‐diones
下载免费PDF全文
![点击此处可从《应用有机金属化学》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Behrooz Maleki Samaneh Barat Nam Chalaki Samaneh Sedigh Ashrafi Esmail Rezaee Seresht Farid Moeinpour Amir Khojastehnezhad Reza Tayebee 《应用有机金属化学》2015,29(5):290-295
A novel nanomagnetic basic catalyst of caesium carbonate supported on hydroxyapatite‐coated Ni0.5Zn0.5Fe2O4 magnetic nanoparticles (Ni0.5Zn0.5Fe2O4@HAP‐Cs2CO3) was prepared. This new catalyst was fully characterized using Fourier transform infrared spectroscopy, transmission and scanning electron microscopy, X‐ray diffraction and vibrating sample magnetometry techniques, and then the catalytic activity of this catalyst was investigated in the synthesis of 1H‐pyrazolo[1,2‐b]phthalazine‐5,10‐dione derivatives. Also, Ni0.5Zn0.5Fe2O4@HAP‐Cs2CO3 could be reused at least five times without significant loss of activity and could be recovered easily by applying an external magnet. Thus, the developed nanomagnetic catalyst is potentially useful for the green and economic production of organic compounds. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
2.
《Tetrahedron letters》2019,60(24):1582-1586
Rh(II)-catalyzed decomposition of certain cyclic α-diazocarbonyl compounds in the presence of cyclic ethers has been shown to give bicyclic ring expansion products. These are thought to arise from a [1,4]-alkyl shift toward the carbonyl oxygen atom and are in contrast with the recently observed spirocyclic products of a Stevens-type [1,2]-alkyl shift within the postulated oxonium ylide intermediate. Quantum chemical calculations performed at the B3LYP/6-31G* level of theory showed that the former reaction pathway (toward fused bicycles) is kinetically preferred. 相似文献
3.
Double Michael additions of lithium enolaie of 1,4-dioxaspiro[4.5]dec-6-en-8-one to four acrylates afforded bicyclo[2.2.2]octan-2-ones with high regio- and stereoselectivities in moderate yields. 相似文献
4.
5‐Amino‐4‐methyl‐2‐phenyl‐6‐substitutedfuro[2,3‐d]pyrimidines ( 2a‐c ) were reacted with 2,5‐dimethoxytetrahydrfuran to afford the pyrrolyl derivatives 3a‐c . Compound 3a was chosen as intermediate for the synthesis of poly fused heterocycles incorporated furopyrimidines moiety 4–11 . Some of the synthesized compounds were screened for their antibacterial and antifungal activities. 相似文献
5.
A practical access to alkyl- and aryl-substituted (E)-2-(azidomethyl)alkenoates and related azido compounds from the corresponding allylic bromides in aqueous acetone is described. An alternative method to obtain the starting bromides based on heterogeneous catalysis under mild conditions was also investigated. 相似文献
6.
Atsuo Nakazaki 《Tetrahedron》2006,62(26):6264-6271
The stereoselective total syntheses of (±)-α-vetispirene, (±)-hinesol, and (±)-β-vetivone were accomplished based on a Claisen rearrangement in an alkenyl bicyclic dihydropyran system. The most striking feature of this approach is that the Claisen rearrangement of bicyclic dihydropyran proceeds stereoselectively to provide a multi-functionalized spiro[4.5]decane, which is an efficient precursor for the synthesis of the vetivane sesquiterpenes. 相似文献
7.
非线性奇异边值问题的正解 总被引:1,自引:0,他引:1
路慧芹 《应用泛函分析学报》2002,4(3):217-221
利用锥映射的不动点指数定量,研究了一类非线性奇异边值问题多个正解的存在性问题。在构造的解的存在条件之下,证明了奇异边值问题至少有两个正解的存在性定理。 相似文献
8.
图G称为K1,n-free图,如果它不含K1,n作为其导出子图.对K1,n-free图具有给定性质的[a,b]-因子涉及到最小度条件进行了研究,得到一个充分条件. 相似文献
9.
Thin films of Ti1−xCoxO2 (x=0 and 0.03) have been prepared on sapphire substrates by spin-on technique starting from metalorganic precursors. When heat treated in air at 550 and 700 °C, respectively, these films present pure anatase and rutile structures as shown both by X-ray diffraction and Raman spectroscopy. Optical absorption indicate a high degree of transparency in the visible region. Such films show a very small magnetic moment at 300 K. However, when the anatase and the rutile films are annealed in a vacuum of 1×10−5 Torr at 500 and 600 °C, respectively, the magnetic moment, at 300 K, is strongly enhanced reaching 0.36μB/Co for the anatase sample and 0.68μB/Co for the rutile one. The ferromagnetic Curie temperature of these samples is above 350 K. 相似文献
10.
在程序升温条件下 ,用DSC研究了标题化合物的放热分解反应动力学 .用线性最小二乘法、迭代法以及二分法与最小二乘法相结合的方法 ,以积分方程、微分方程和放热速率方程拟合DSC数据 .在逻辑选择建立了微分和积分机理函数的最可几一般表达式后 ,用放热速率方程得到相应的表观活化能 (Ea)、指前因子 (A)和反应级数 (n)的值 .结果表明 :该反应的微分形式的经验动力学模式函数、Ea 和A值分别为 (1-α) 0 .44、2 30 .4kJ/mol和 10 18.16s-1.借助加热速率和所得动力学参数值 ,提出了标题化合物放热分解反应的动力学方程 .该化合物的热爆炸临界温度为 30 2 .6℃ .上述动力学参数对分析、评价标题化合物的稳定性和热变化规律十分有用 . 相似文献