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   207篇
  免费   8篇
化学   165篇
晶体学   7篇
力学   8篇
数学   2篇
物理学   33篇
  2023年   2篇
  2022年   2篇
  2021年   9篇
  2020年   10篇
  2019年   5篇
  2018年   7篇
  2017年   7篇
  2016年   12篇
  2015年   9篇
  2014年   2篇
  2013年   9篇
  2012年   11篇
  2011年   15篇
  2010年   6篇
  2009年   10篇
  2008年   12篇
  2007年   11篇
  2006年   8篇
  2005年   8篇
  2004年   5篇
  2003年   4篇
  2002年   10篇
  2001年   2篇
  2000年   9篇
  1999年   4篇
  1998年   4篇
  1997年   2篇
  1996年   3篇
  1995年   4篇
  1994年   1篇
  1992年   3篇
  1991年   1篇
  1990年   2篇
  1981年   5篇
  1979年   1篇
排序方式: 共有215条查询结果,搜索用时 15 毫秒
211.
The bulk single crystal of l-arginine 4-nitrophenolate 4-nitrophenol dihydrate (LAPP), an efficient organic NLO material of size 74 mm in length, 18 mm in diameter, was grown successfully by Sankaranarayanan–Ramasamy (SR) method. Single crystal X-ray diffraction study reveals that LAPP crystallizes into monoclinic system with the space group P21. The unidirectional growth along the plane (1 1 0) was confirmed from the powder XRD pattern with the sharp peak having maximum intensity. Optical absorption spectrum shows that LAPP has highly transparent in the entire visible and IR region with a wide band gap of 3.9 eV for large photon absorption. Vickers micro hardness measurement was performed to know the mechanical strength of the crystal. Dielectric profile of LAPP at room temperature brings forth low value of dielectric loss and dielectric constant at higher frequencies. Photoluminescence study reveals that LAPP exhibit green emission in the wavelength region 538 nm. The SHG efficiency of the crystal is measured by Kurtz's powder test using Nd:YAG Laser.  相似文献   
212.
A new series of 1,2,4-triazolo[4,3-a]-quinoline derivatives were designed and synthesized to meet the structural requirements essential for anticancer activity. N-1-(5-Methylisoxazol-4-yl/4-fluoro-2,3-dihydro-1H-inden-1-yl/aryl)-N’-3-(4,5-dihydro-1-methyl-[1,2,4]triazolo[4,3-a]quinolin-7-yl) urea derivatives were accomplished in good yields by the reaction of 4,5-dihydro-1-methyl-[1,2,4]triazolo[4,3-a]quinolin-7-amine with 3-(3-chloro-5-fluoro-2-methoxyphenyl)-5-methyl-isoxazole-4-carboxylic acid, 4-fluoro-2,3-dihydro-1H-indene-1-carboxylic acid, and various simple aromatic carboxylic acids in the presence of diphenyl phosphoryl azide (DPPA). All the newly synthesized title compounds were characterized by elemental and spectral data. Furthermore, anticancer activity was screened for the title compounds (12a–j) in vitro against human neuroblastoma cell lines (SK N SH) and human colon carcinoma cell lines (COLO 205) by using the MTT cell viability method. A few of them (12a and 12b) possess significant cytotoxicity, and some other compounds 12d-f and 12j displayed moderate cytotoxicity against both cell lines.  相似文献   
213.
In the present study, different transition metal forms of montmorillonite have been intercalated with mono-, di-, and triethanolammonium cations via d coordination mechanism to investigate their thermal behavior, structural characteristics, surface properties, and elemental composition using TG, XRD, BET, and CHNS techniques. Thermogravimetric analysis showed two thermal transition steps for transition metal-exchanged montmorillonites, which attributed to desorption of the physically adsorbed water and hydrated water, and dehydroxylation of the structural water; whereas for ammonium-montmorillonite complexes, the TG curves showed three thermal transition steps which attributed to desorption of the adsorbed water and dehydration, decomposition of the ammonium cations in the interlayer space of montmorillonite, and the dehydroxylation of the structural water. The thermal analysis of ammonium-montmorillonites affirmed that the molar mass of amine compounds used affects both desorption temperature (position) and the amount of the adsorbed water (intensity). XRD results revealed that the molar mass of amine used has linear relation with the basal spacings of the corresponding ammonium-montmorillonites, indicating structural changes. BET results showed that the molar mass of amines has an inverse effect on the surface area of the studied samples. CHNS analysis for the studied samples quantitatively confirmed the intercalation of ammonium cations into the interlayer space of montmorillonite.  相似文献   
214.
This paper describes the synthesis and photodynamic properties of six different chalcone derivatives. Using N,N-dimethyl-4-nitrosoaniline (RNO) bleaching assay, the singlet oxygen generating efficiencies of these chalcones are determined relative to rose bengal (RB). Superoxide dismutase (SOD) inhibitable cytochrome c reduction assay and electron magnetic resonance (EMR) spin trapping techniques are used to determine the superoxide anion radical (O?·?) yield upon photoirradiation. Photoinduced DNA scission studies show that O?·? is involved in the DNA strand break. In addition, antimicrobial activity of these chalcones is also investigated. Structure activity relationship accounts for the difference in the photogeneration of reactive oxygen species (ROS) by these sensitizers. Presence of electron releasing -OCH? groups enhances the photogeneration of ROS. Cyclic voltammetry studies indicate a correlation between enzymatic O?·? generation efficiency and redox potential of chalcones. Both O?·? (Type I) and 1O? (Type II) paths are involved in the photosensitization of chalcones. The LUMO energies obtained by molecular modeling correlate with the one-electron reduction potentials.  相似文献   
215.
We report a new sodium fast-ion conductor, Na3B5S9, that exhibits a high Na ion total conductivity of 0.80 mS cm−1 (sintered pellet; cold-pressed pellet=0.21 mS cm−1). The structure consists of corner-sharing B10S20 supertetrahedral clusters, which create a framework that supports 3D Na ion diffusion channels. The Na ions are well-distributed in the channels and form a disordered sublattice spanning five Na crystallographic sites. The combination of structural elucidation via single crystal X-ray diffraction and powder synchrotron X-ray diffraction at variable temperatures, solid-state nuclear magnetic resonance spectra and ab initio molecular dynamics simulations reveal high Na-ion mobility (predicted conductivity: 0.96 mS cm−1) and the nature of the 3D diffusion pathways. Notably, the Na ion sublattice orders at low temperatures, resulting in isolated Na polyhedra and thus much lower ionic conductivity. This highlights the importance of a disordered Na ion sublattice—and existence of well-connected Na ion migration pathways formed via face-sharing polyhedra—in dictating Na ion diffusion.  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