全文获取类型
收费全文 | 4345篇 |
免费 | 197篇 |
国内免费 | 42篇 |
专业分类
化学 | 2867篇 |
晶体学 | 41篇 |
力学 | 144篇 |
数学 | 452篇 |
物理学 | 1080篇 |
出版年
2024年 | 19篇 |
2023年 | 44篇 |
2022年 | 235篇 |
2021年 | 224篇 |
2020年 | 170篇 |
2019年 | 169篇 |
2018年 | 170篇 |
2017年 | 136篇 |
2016年 | 210篇 |
2015年 | 148篇 |
2014年 | 219篇 |
2013年 | 386篇 |
2012年 | 311篇 |
2011年 | 304篇 |
2010年 | 245篇 |
2009年 | 194篇 |
2008年 | 218篇 |
2007年 | 184篇 |
2006年 | 143篇 |
2005年 | 74篇 |
2004年 | 99篇 |
2003年 | 56篇 |
2002年 | 56篇 |
2001年 | 32篇 |
2000年 | 28篇 |
1999年 | 31篇 |
1998年 | 20篇 |
1997年 | 29篇 |
1996年 | 26篇 |
1995年 | 12篇 |
1994年 | 27篇 |
1993年 | 20篇 |
1992年 | 19篇 |
1991年 | 11篇 |
1990年 | 20篇 |
1989年 | 13篇 |
1988年 | 15篇 |
1987年 | 16篇 |
1985年 | 23篇 |
1984年 | 23篇 |
1983年 | 15篇 |
1982年 | 20篇 |
1981年 | 13篇 |
1980年 | 38篇 |
1979年 | 11篇 |
1977年 | 15篇 |
1976年 | 11篇 |
1973年 | 11篇 |
1969年 | 9篇 |
1968年 | 8篇 |
排序方式: 共有4584条查询结果,搜索用时 31 毫秒
991.
Lauricella R Allouch A Roubaud V Bouteiller JC Tuccio B 《Organic & biomolecular chemistry》2004,2(9):1304-1309
A new kinetic approach to the evaluation of rate constants for the spin trapping of superoxide/hydroperoxyl radical by nitrones in buffered media is described. This method is based on a competition between the superoxide trapping by the nitrone and the spontaneous dismutation of this radical in aqueous media. EPR spectra are recorded as a function of time at various nitrone concentrations, and kinetic curves are obtained after treatment of these spectra using both singular value decomposition and pseudo-inverse deconvolution methods. Modelling these curves permits the determination of the rate constants k(T) and k(D) for the superoxide trapping and the adduct decay reactions, respectively. Kinetics parameters thus obtained with six nitrones, namely the 2-ethoxycarbonyl-2-methyl-3,4-dihydro-2H-pyrrole N-oxide (EMPO), the 5-diethoxyphosphoryl-5-methyl-3,4-dihydro-5H-pyrrole N-oxide (DEPMPO), the 5,5-dimethyl-3,4-dihydro-5H-pyrrole N-oxide (DMPO), the 1,3,5-tri[(N-(1-diethylphosphono)-1-methylethyl)-N-oxy-aldimine]benzene (TN), the N-benzylidene-1-ethoxycarbonyl-1-methylethylamine N-oxide (EPPN), and the N-[(1-oxidopyridin-1-ium-4-yl)methylidene]-1-ethoxycarbonyl-1-methylethylamine N-oxide (EPPyON), indicate that cyclic nitrones trapped superoxide faster than the linear ones. However, the low k(T) values obtained for compounds show that there is still a need for new molecules with better spin trapping capacities. 相似文献
992.
993.
Eid EE Abdul AB Rasedee A Suliman FE Sukari MA Fatah SA 《Journal of mass spectrometry : JMS》2011,46(8):772-781
A rapid, sensitive, specific and selective LC-MS/MS method for the determination of zerumbone (ZER) in human plasma using 2,4-diamino-6-(4-methoxyphenyl)-1,3,5-triazine (DMTZ) as an internal standard (IS) has been developed and validated. ZER was chromatographed on C8 column using a mobile phase of acetonitrile/water (80:20, v/v) at a flow rate of 0.25 ml min(-1) . Quantitation was achieved using ESI+ interface, employing multiple reaction monitoring (MRM) mode at m/z 219 > 81 and 218 > 134 for ZER and IS, respectively. The calibration standards were linear over a range of 5-3000 ng ml(-1) (r(2)=0.9994) with an LLOQ of 5 ng ml(-1) (RSD %; 11.4% and bias%; 9.5%). Intra- and inter-day precision of ZER assay ranged from 0.18 to 3.56% with accuracy (bias) that varied between -5.09 and 4.3%, demonstrating good precision and accuracy. Recoveries of ZER and the IS from human plasma were above 85%. The developed method was validated for the determination of ZER in rat plasma. Linearity, stability of ZER and the ME on rat plasma were discussed. The applicability of the developed method was demonstrated by measuring ZER in rat plasma samples following intravenous and intraperitoneal administration of ZER prepared in hydroxypropyl-β-cyclodextrin (HPβCD) and sodium carboxymethyl cellulose (CMC), respectively, in 20 mg kg(-1) and this study indicated a clear significant difference (p<0.05) in pharmacokinetic parameters of ZER in ZER/HPβCD complex compared with ZER in CMC preparation. 相似文献
994.
Khaldun M. Al Azzam Ahmad Makahleah Bahruddin Saad Sharif M. Mansor 《Journal of chromatography. A》2010,1217(23):3654-3659
A three-phase hollow fiber liquid-phase microextraction (HF-LPME) coupled either with capillary electrophoresis (CE) or high performance liquid chromatography (HPLC) with UV detection methods was successfully developed for the determination of trace levels of the anti-diabetic drug, rosiglitazone (ROSI) in biological fluids. The analyte was extracted into dihexyl ether that was immobilized in the wall pores of a porous hollow fiber from 10 mL of aqueous sample, pH 9.5 (donor phase), and was back extracted into the acceptor phase that contained 0.1 M HCl located in the lumen of the hollow fiber. Parameters affecting the extraction process such as type of extraction solvent, HCl concentration, donor phase pH, extraction time, stirring speed, and salt addition were studied and optimized. Under the optimized conditions (extraction solvent, dihexyl ether; donor phase pH, 9.5; acceptor phase, 0.1 M HCl; stirring speed, 600 rpm; extraction time, 30 min; without addition of salt), enrichment factor of 280 was obtained. Good linearity and correlation coefficients of the analyte was obtained over the concentration ranges of 1.0–500 and 5.0–500 ng mL−1 for the HPLC (r2 = 0.9988) and CE (r2 = 0.9967) methods, respectively. The limits of detection (LOD) and limits of quantitation (LOQ) for the HPLC and CE methods were (0.18, 2.83) and (0.56, 5.00) ng mL−1, respectively. The percent relative standard deviation (n = 6) for the extraction and determination of three concentration levels (10, 250, 500 ng mL−1) of ROSI using the HPLC and CE methods were less than 10.9% and 13.2%, respectively. The developed methods are simple, rapid, sensitive and are suitable for the determination of trace amounts of ROSI in biological fluids. 相似文献
995.
This paper is concerned with asymptotic stability of a system of reaction-diffusion equations which is expressed in terms of Volterra integrals, under homogeneous Dirichlet boundary conditions. The effect of diffusion and delays on the stability of the system are analyzed, and sufficient conditions are given for the existence of positive solutions of the corresponding steady-state problem. Their global attraction with respect to nonnegative solutions of the time-dependent system is discussed. The main tools are Lyapunov functionals, positive definite kernels, and Laplace transforms. 相似文献
996.
In the present article, we have revisited the electronic band gap nature of ZnOxS1?x (0 ≤ x ≤ 1) with the recently developed modified Becke and Johnson exchange potential and the calculated band gaps are found consistent with the experimental results. We expect that the band gap bowing parameter obtained in the present work will be close to the experimental one. As the optical properties of ZnOxS1?x (0 ≤ x ≤ 1) are very important, therefore different optical parameters like dielectric functions, refractive index and reflectivity are also calculated. The results are illustrated in terms of band structures, band gap energy as a function of oxygen composition, total and partial density of states. © 2012 Wiley Periodicals, Inc. 相似文献
997.
Ahmad AL-SALMAN 《Frontiers of Mathematics in China》2021,16(1):13-28
We introduce a class of singular integral operators on product domains along twisted surfaces.We prove that the operators are bounded on Lp provided that the kernels satisfy weak conditions. 相似文献
998.
Ahmad H. Alghamdi 《Journal of Saudi Chemical Society》2010,14(1):1-7
The adsorptive collection of zinc(II) complex with alizarin ligand, coupled with the square-wave voltammetric technique at the hanging mercury drop electrode, yields a very sensitive electroanalytical procedure for the determination of zinc. The optimized experimental conditions include: supporting electrolyte (carbonate buffer), pH (11), alizarin concentration (1 × 10?6 mol l?1), accumulation time (60 s), accumulation potential (?0.1 V), scan rate (700 mV s?1), pulse amplitude (0.06 V) and SW frequency (80 Hz). The monitored stripping voltammetric current was linear over the range of 5 × 10?8 – 4 × 10?7 mol l?1 and the detection limit was 1 × 10?8 mol l?1. The relative standard deviation was calculated as 1.3% (n = 10) for 1 × 10?8 mol l?1 Zn(II) and the obtained electrochemical signal was stabile for up to 60 min. Possible interferences by either co-existing metal ions or other chelating agents were also investigated. The applicability of the proposed SW-AdSV method to the analysis of foodstuff was assessed by the determination of zinc content in instant coffee samples. The accuracy of the obtained voltammetric analytical results was validated by comparing with that obtained by atomic absorption spectrometric method and conducting the necessary statistical evaluation. 相似文献
999.
1000.
Rika M. Y. A. Rahman M. M. Salleh A. A. Umar A. Ahmad 《Journal of Solid State Electrochemistry》2010,14(11):2089-2093
A nanoparticle TiO2 solid-state photoelectrochemical cell has been fabricated. The effect of ionic conductivity of a solid electrolyte of polyacrylonitrile
(PAN)–propylene carbonate (PC)–lithium perchlorate (LiClO4) on the performance of a photoelectrochemical cell of indium tin oxide (ITO)/TiO2/PAN–PC–LiClO4/graphite has been investigated. A nanoparticle TiO2 film was deposited onto ITO-covered glass substrate by controlled hydrolysis technique. A solid electrolyte of PAN–LiClO4 with PC plasticizer prepared by solution casting technique was used as a redox couple medium. The room temperature conductivity
of the electrolyte was determined by AC impedance spectroscopy technique. A graphite electrode was prepared onto a glass slide
by electron beam evaporation technique. The device shows a photovoltaic effect under illumination. The short-circuit current
density, J
sc, and open-circuit voltage, V
oc, vary with the conductivity of the electrolyte. The highest J
sc of 2.82 μA cm−2 and V
oc of 0.56 V were obtained at the conductivity of 4.2 × 10−4 Scm−1 and at the intensity of 100 mW cm−2. 相似文献