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   1367篇
  免费   13篇
  国内免费   5篇
化学   939篇
晶体学   10篇
力学   25篇
数学   203篇
物理学   208篇
  2023年   11篇
  2022年   32篇
  2021年   40篇
  2020年   36篇
  2019年   30篇
  2018年   37篇
  2017年   20篇
  2016年   52篇
  2015年   28篇
  2014年   45篇
  2013年   72篇
  2012年   59篇
  2011年   69篇
  2010年   43篇
  2009年   38篇
  2008年   65篇
  2007年   48篇
  2006年   42篇
  2005年   41篇
  2004年   35篇
  2003年   42篇
  2002年   36篇
  2001年   17篇
  2000年   12篇
  1999年   8篇
  1998年   12篇
  1997年   17篇
  1996年   17篇
  1995年   8篇
  1994年   7篇
  1993年   15篇
  1992年   10篇
  1991年   11篇
  1990年   7篇
  1987年   8篇
  1985年   7篇
  1984年   11篇
  1983年   8篇
  1981年   11篇
  1979年   8篇
  1976年   7篇
  1972年   6篇
  1918年   8篇
  1907年   6篇
  1905年   6篇
  1901年   11篇
  1895年   6篇
  1894年   6篇
  1888年   6篇
  1885年   9篇
排序方式: 共有1385条查询结果,搜索用时 15 毫秒
31.
32.
33.
34.
    
In the research of new compounds with multifunctional applications, heterobinuclear palladium (II) complexes based on organometallic dithiocarbazates (DTCZs) have been isolated. The organometallic DTCZ ligands of the general formula [{(η5-C5H4)-CH=NNHC(S)SCH3}]MLn [MLn = Re (CO)3 ( 2a ); Mn (CO)3 ( 2b ); FeCp ( 2c )] were prepared by the reaction between formyl organometallic precursors ( 1a−c ) with S-methyldithiocarbazate. Subsequently, a two-step reaction of 2a−c with: (i) K2[PdCl4] and (ii) PPh3 yielded heterobinuclear complexes [Pd{MLn(η5-C5H4)-CH=NNHC(S)SCH3}–(Cl)(PPh3)] [MLn = Re (CO)3 ( 3a ); Mn (CO)3 ( 3b ); FeCp ( 3c )]. All compounds were characterized by conventional spectroscopic techniques (infrared spectroscopy, nuclear magnetic resonance spectroscopy, mass spectrometry and elemental analysis). In addition, the molecular structures of 2a , 2c and 3c were determined by single-crystal X-ray diffraction. The new palladium (II) complexes ( 3a−c ) were evaluated as antiproliferative agents against non-small cell lung cancer cells (H1299 cells). Complexes 3a and 3b containing cyrhetrenyl- and cymantrenyl-DTCZ ligands, respectively, were more active than their ferrocenyl analogue 3c . The activity was associated with the electron-withdrawing properties of the (η5-C5H4)M (CO)3 moieties and their better lipophilicity than that of the ferrocenyl analogue. In addition, we studied the capacity of metalloligands ( 2a−c ) and palladium (II) complexes ( 3a−c ) to remove methylene blue in water under UV–visible light irradiation. The results established that the complexes showed moderate efficiency and were less active than their corresponding free ligands.  相似文献   
35.
The hydrostatic extrusion of polyethylene filled with hydroxyapatite has been studied. It is shown that the extrusion behavior is qualitatively similar to that of unfilled polymer. Extruded products with flexural moduli of at least 10 GPa and flexural strengths of 90 MPa have been produced, which can be considered as candidates for load-bearing bone substitute materials. © 1997 John Wiley & Sons, Ltd.  相似文献   
36.
    
Journal of Solid State Electrochemistry - A novel material was developed using sol-gel chemistry and an environmental-friendly grafting process of clay nanoparticles. In a previous work of our...  相似文献   
37.
38.
Tobacco-specific nitrosamines (TSNAs) are some of the most potent carcinogens in tobacco and cigarette smoke. Accurate quantification of these chemicals is needed to help assess public health risks. We developed and validated a specific and sensitive method to measure four TSNAs adsorbed to model surfaces and secondhand smoke (SHS) particles using gas chromatography–ion-trap tandem mass spectrometry. In an 18-m3 room-sized chamber, a smoking machine generated realistic concentrations of SHS that were actively sampled on Teflon-coated fiber glass (TCFG) filters, and passively sampled on cellulose substrates. A simple solid–liquid extraction protocol using methanol as solvent was successfully applied to both substrates with recoveries ranging from 85 to 115%. For each TSNA, tandem MS parameters were optimized and the major fragmentation pathways were elucidated. The method showed excellent performance, with a linear dynamic range from 2 to 1000 ng mL−1, low detection limits (S/N > 3) of 30–300 pg mL−1 and precision with experimental errors below 10% for all compounds. Moreover, no interfering peaks were observed, indicating a high selectivity of MS/MS without the need for a sample clean-up step. This method provides a suitable analytical tool to detect and quantify traces of TSNA in indoor environments polluted with SHS.  相似文献   
39.

An aqueous biphasic system has been used for selective extraction of U(VI) ions from Th(IV), Sm(III) and Ce(III). Role of different biomolecules like morin, catechin, hesperidin and 4-hydroxycoumarin have been studied. Morin serves as the best reagent when citrate ions are used as a masking agent. Citrate forms stronger complexes with the other metal ions than morin thereby restricting their extractions. Contrarily, U(VI) forms a stronger complex with morin than citrate and is selectively extracted under the same conditions. It was also observed that morin can act as a spectrophotometric reagent for ratiometric detection and analysis of U(VI) ions.

  相似文献   
40.
The fulvene complexes [(η6-C5Me4CH2)Re(CO)2(R)] (1a, RI; 1b, RC6F5) react at the exocyclic methylene carbon with a vinylmagnesium bromide solution to produce the anionic species [(η5-C5Me4CH2CHCH2)Re(CO)2(R)]. Protonation with HCl at 0 °C produces the hydride complexes [trans-5-C5Me4CH2CHCH2)Re(CO)2(R)(H)] (2a, RI; 2b, RC6F5). Thermolysis of an hexane solution of the iodo-hydride (2a) under a CO atmosphere yields the complex [(η5-C5Me4CH2CHCH2)Re(CO)3] (3) and [Re(CO)5I] as by-product. Thermolysis of 2b produced three new products, mainly the chelated complex [(η52-C5Me4CH2CHCH2)Re(CO)2] (4) and complex 3, with a non-coordinated olefin group, in moderated yield, and traces of [Re(CO)5(C6F5)]. Thermolysis of an hexane solution of 2 in presence of an excess of PMe3, afforded the phosphine derivative [(η5-C5Me4CH2CHCH2)Re(CO)2(PMe3)] (5). All the complexes were characterized by IR, 1H, 13C and 31P NMR spectroscopies and mass spectrometry. The molecular structure of 4 has also been determined. The molecule exhibits a formal three-legged piano-stool structure, with two CO groups, and the third position corresponding to the η2-coordination of the propenyl side arm of the η5-C5Me4 ring.  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