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   2856篇
  免费   99篇
  国内免费   16篇
化学   2003篇
晶体学   20篇
力学   79篇
数学   281篇
物理学   588篇
  2023年   13篇
  2022年   45篇
  2021年   48篇
  2020年   43篇
  2019年   47篇
  2018年   36篇
  2017年   46篇
  2016年   100篇
  2015年   66篇
  2014年   87篇
  2013年   157篇
  2012年   173篇
  2011年   193篇
  2010年   100篇
  2009年   94篇
  2008年   172篇
  2007年   154篇
  2006年   132篇
  2005年   126篇
  2004年   133篇
  2003年   113篇
  2002年   103篇
  2001年   58篇
  2000年   63篇
  1999年   46篇
  1998年   17篇
  1997年   27篇
  1996年   45篇
  1995年   66篇
  1994年   52篇
  1993年   48篇
  1992年   53篇
  1991年   26篇
  1990年   30篇
  1989年   19篇
  1988年   19篇
  1987年   20篇
  1986年   23篇
  1985年   29篇
  1984年   26篇
  1983年   10篇
  1982年   23篇
  1981年   18篇
  1980年   12篇
  1979年   13篇
  1978年   7篇
  1977年   6篇
  1975年   6篇
  1974年   5篇
  1973年   7篇
排序方式: 共有2971条查询结果,搜索用时 211 毫秒
991.
Immobilization of small proteins designed to perform protein–protein assays can be a difficult task. Often, the modification of reactive residues necessary for the interaction between the immobilized protein and the matrix compromises the interaction between the protein and its target. In these cases, glutathione-S-transferase (GST) is a valuable tag providing a long arm that makes the bait protein accessible to the mobile flow phase of the chromatography. In the present report, we used a GST fusion version of the 8-kDa protein serine protease inhibitor Kazal-type 3 (SPINK3) as the bait to purify anti-SPINK3 antibodies from a rabbit crude serum. The protocol for immobilization of GST-SPINK3 to glutathione–agarose beads was modified from previously reported protocols by using an alternative bifunctional cross-linker (dithiobis(succinimidyl propionate)) in a very simple procedure and by using simple buffers under physiological conditions. We concluded that the immobilized protein remained bound to the column after elution with low pH, allowing the reuse of the column for alternative uses, such as screening for other protein–protein interactions using SPINK3 as the bait.
Figure
?  相似文献   
992.
[CoCl(μ‐Cl)(HpzPh)3]2 ( 1 ) and [CoCl2(HpzPh)4] ( 2 ) were obtained by reaction of CoCl2 with HC(pzPh)3 and HpzPh, respectively (HpzPh=3‐phenylpyrazole). The compounds were isolated as air‐stable solids and fully characterized by IR and far‐IR spectroscopy, MS(ESI+/?), elemental analysis, cyclic voltammetry (CV), controlled potential electrolysis, and single‐crystal X‐ray diffraction. Electrochemical studies showed that 1 and 2 undergo single‐electron irreversible CoII→CoIII oxidations and CoII→CoI reductions at potentials measured by CV, which also allowed, in the case of dinuclear complex 1 , the detection of electronic communication between the Co centers through the chloride bridging ligands. The electrochemical behavior of models of 1 and 2 were also investigated by density functional theory (DFT) methods, which indicated that the vertical oxidation of 1 and 2 (that before structural relaxation) affects mostly the chloride and pyrazolyl ligands, whereas adiabatic oxidation (that after the geometry relaxation) and reduction are mostly metal centered. Compounds 1 and 2 and, for comparative purposes, other related scorpionate and pyrazole cobalt complexes, exhibit catalytic activity for the peroxidative oxidation of cyclohexane to cyclohexanol and cyclohexanone under mild conditions (room temperature, aqueous H2O2). In situ X‐ray absorption spectroscopy studies indicated that the species derived from complexes 1 and 2 during the oxidation of cyclohexane (i.e., Ox‐ 1 and Ox‐ 2 , respectively) are analogous and contain a CoIII site. Complex 2 showed low in vitro cytotoxicity toward the HCT116 colorectal carcinoma and MCF7 breast adenocarcinoma cell lines.  相似文献   
993.
Phytochemical investigation of the aerial parts of Gymnema sylvestre has led to the isolation of seven new triterpenes, six oleane types ( 5, 7 – 11 ) and a new lupane type ( 12 ), and of the six known analogues 1 – 4, 6 , and 13 . The structures and relative configurations of these compounds were elucidated by spectroscopic analyses, including 1D‐ and 2D‐NMR spectroscopy and mass spectrometry, and by the comparison of their NMR data with those of related compounds.  相似文献   
994.
Castro  Mario H.  Massa  Eugenio  Peron  Ana Paula 《Positivity》2019,23(4):853-874
Positivity - In this paper we consider Positive Definite functions on products $$\Omega _{2q}\times \Omega _{2p}$$ of complex spheres, and we obtain a condition, in terms of the coefficients in...  相似文献   
995.
996.
The reactions of secondary alicyclic amines with the title substrate (PDTC) are subjected to a kinetic study in 44 wt.% aqueous ethanol, 25.0°C, ionic strength 0.2 M (KCl). Pseudo-first-order rate coefficients (kobs) are found under amine excess. Linear plots of [N]/kobs against 1/[N], where N is the free amine, are obtained for the reactions with piperidine, piperazine, 1-(2-hydroxyethyl)piperazine, and morpholine. The reaction with 1-formylpiperazine exhibits a linear plot of kobs against [N]2. These results are interpreted through a mechanism consisting of two tetrahedral intermediates: a zwitterionic ( T ±) and an anionic ( T ?), where the amine catalyzed proton transfer from T ± to T ? is partially rate determining for the four former reactions and is fully rate determining for the reaction of 1-formylpiperazine. The rate microcoefficients involved in the reaction scheme are either determined experimentally or estimated. Comparison with the corresponding microcoefficients reported for the same reactions in water reveals that the rate coefficient for formation of T ± from reactants (k1) is smaller and that for the reversal of this (k?1) is larger in aqueous ethanol compared to water, in agreement with the expected structure of the corresponding transition state. Bronsted-type plots are obtained for k1, k?1, and K1 (=k1/k?1) with slopes ca. 0.4, ?0.6, and 1.0, respectively. Comparison of the present stepwise reactions with the concerted ones found in the same aminolysis of O-ethyl 2,4,6,-(trinitrophenyl) dithiocarbonate indicates that T ± is so destabilized by the change of PhS by the 2,4,6-trinitrobenzenethio group that T ± no longer exists and becomes a transition state. © 1995 John Wiley & Sons, Inc.  相似文献   
997.
998.
Controlling the surface chemistry of oxide systems has emerged an effective tool to obtain desirable nanostructures and macro properties. A relatively simple way to achieve this is by using dopants that are prone to segregate to the surfaces of the powders. In this work, we delineate the effect of Mg and Fe on SnO2 nanopowders focusing on the surface modifications caused by surface segregation. The effects of increasing the temperature of calcinations are particularly addressed to evaluate the surface modifications at high temperatures. The powders were studied by infrared spectroscopy, zeta potential measurements, X-ray diffraction, and specific surface area measurements. Since sintering is a high-temperature process strongly dependent on surface characteristics, we drawn a relationship between the final densities after sintering and the surface chemistry of the doped powders. Doped SnO2 pellets were sintered to over 95% of the theoretical density within a few seconds (fast firing) when significant surface modifications were observed.  相似文献   
999.
 A spectrophotometric method for the determination of acetaldehyde in liquid, semi-solid and solid food samples, employing the coupling of a continuous flow configuration to a pervaporation unit, has been proposed. It is based on the reaction of the analyte with fuchsin in acidic medium and subsequent formation of a coloured product (alkylsulphonic acid chromophore) with sodium sulphite, which was monitored spectrophotometrically. Variable sensitivity was obtained by altering the pervaporation temperature and the thickness of the membrane. The detection limits went down to 4.2 μg/mL and the precision was between 1.2 and 3.6%. Received: 5 August 1996/Revised: 16 October 1996/Accepted: 18 October 1996  相似文献   
1000.
This work reports the role of alpha particles generated by Americium (241Am) stripes placed inside the discharge channel in providing a bias ionized background plasma before, during, and after the discharge of the N2 TE UV laser (337.1 nm) circuit. The enhancement in stimulated radiation output characteristics in terms of gas pressure, charging voltage, and pulse width, with and without alpha particles, are shown. The increased laser yield is interpreted qualitatively through plasma impedance in the discharge circuit. PACS 42.60.By; 42.60.Lh  相似文献   
[首页] « 上一页 [95] [96] [97] [98] [99] 100 下一页 » 末  页»
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