全文获取类型
收费全文 | 3417篇 |
免费 | 161篇 |
国内免费 | 50篇 |
专业分类
化学 | 2603篇 |
晶体学 | 40篇 |
力学 | 102篇 |
综合类 | 3篇 |
数学 | 203篇 |
物理学 | 677篇 |
出版年
2024年 | 12篇 |
2023年 | 23篇 |
2022年 | 154篇 |
2021年 | 222篇 |
2020年 | 115篇 |
2019年 | 126篇 |
2018年 | 131篇 |
2017年 | 79篇 |
2016年 | 181篇 |
2015年 | 148篇 |
2014年 | 176篇 |
2013年 | 294篇 |
2012年 | 247篇 |
2011年 | 268篇 |
2010年 | 157篇 |
2009年 | 138篇 |
2008年 | 133篇 |
2007年 | 107篇 |
2006年 | 110篇 |
2005年 | 95篇 |
2004年 | 69篇 |
2003年 | 65篇 |
2002年 | 57篇 |
2001年 | 32篇 |
2000年 | 34篇 |
1999年 | 35篇 |
1998年 | 26篇 |
1997年 | 29篇 |
1996年 | 21篇 |
1995年 | 12篇 |
1994年 | 20篇 |
1993年 | 25篇 |
1992年 | 14篇 |
1991年 | 20篇 |
1990年 | 17篇 |
1989年 | 14篇 |
1988年 | 15篇 |
1987年 | 14篇 |
1986年 | 16篇 |
1985年 | 22篇 |
1984年 | 16篇 |
1983年 | 9篇 |
1982年 | 15篇 |
1981年 | 20篇 |
1980年 | 12篇 |
1978年 | 11篇 |
1977年 | 11篇 |
1976年 | 8篇 |
1975年 | 9篇 |
1959年 | 9篇 |
排序方式: 共有3628条查询结果,搜索用时 15 毫秒
1.
2.
3.
Eco‐friendly ionic liquid assisted capillary electrophoresis and α‐acid glycoprotein‐assisted liquid chromatography for simultaneous determination of anticancer drugs in human fluids
下载免费PDF全文
![点击此处可从《Biomedical chromatography : BMC》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Deia Abd El‐Hady Hassan M. Albishri Rajesh Rengarajan 《Biomedical chromatography : BMC》2015,29(6):925-934
In the current work, two eco‐friendly analytical methods based on capillary electrophoresis (CE) and reversed phase liquid chromatography (RPLC) were developed for simultaneous determination of the most commonly used anticancer drugs for Hodgkin's disease: methotrexate (MTX), vinblastine, chlorambucil and dacarbazine. A background electrolyte (BGE) of 12.5 mmol/L phosphate buffer at pH 7.4 and 0.1 µmol/L 1‐butyl‐3‐methyl imidazolium bromide (BMImBr) ionic liquid (IL) was used for CE measurements at 250 nm detection wavelength, 20 kV applied voltage and 25 °C. The rinsing protocol was significantly improved to reduce the adsorption of IL on the interior surface of capillary. Moreover, RPLC method was developed on α‐1‐acid glycoprotein (AGP) column. Mobile phase was 10 mmol/L phosphate buffer at pH 6.0 (100% v/v) and flow rate at 0.1 mL/min. As AGP is a chiral column, it was successfully separated l ‐MTX from its enantiomer impurity d ‐MTX. Good linearity of quantitative analysis was achieved with coefficients of determinations (r2) >0.995. The stability of drugs measurements was investigated with adequate recoveries up to 24 h storage time under ambient temperature. The limits of detection were <50 and 90 ng/mL by CE and RPLC, respectively. The using of short‐chain IL as an additive in BGE achieved 600‐fold sensitivity enhancement compared with conventional Capillary Zone Electrophoresis (CZE). Therefore, for the first time, the proposed methods were successfully applied to determine simultaneously the analytes in human plasma and urine samples at clinically relevant concentrations with fast and simple pretreatments. Developed IL‐assisted CE and RPLC methods were also applied to measure MTX levels in patients’ samples over time. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
4.
Umie F.M. Haziz Rosenani A. Haque Shun-Ze Zhan Hassan H. Abdallah Mohd R. Razali 《应用有机金属化学》2020,34(10):e5818
The synthesis and characterizations for a series of dinuclear gold (I)-di-NHC complexes, 1–8 through the trans-metalation method of their respective silver (I)-di-NHC complexes, i–viii are reported (where NHC = N-heterocyclic carbene). The successful complexation of a series of unusual non-symmetrical and symmetrical di-NHC ligands, 3,3'-(ethane-1,2-diyl)-1-alkylbenzimidazolium-1'-butylbenzimidazolium (with alkyl = methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, benzyl) with the gold (I) ions are suggested by elemental analysis, Fourier transform-infrared, 1H- and 13C-NMR data. The 13C-NMR spectra of 1–8 show a singlet sharp peak in the range of 190.00–192.00 ppm, indicating the presence of a carbene carbon that bonded to the gold (I) ion. From single crystal X-ray diffraction data, the structure of complex 6 with the formula of [di-NHC-Au (I)]2·2PF6 is obtained [where NHC = 3,3'-(ethane-1,2-diyl)-1-hexylbenzimidazolium-1'-butylbenzimidazolium]. The photophysical study in solid state of 6 displays an intense photoluminescence with a strong emission maxima, λem = 480 nm, upon excitation at 340 nm at room temperature. Interestingly, the emission maximum at 77 K shows a structural character with a strong peak at 410 nm, a medium at 433 nm and a weak at 387 nm, accompanied by a tail band to about 500 nm. 相似文献
5.
6.
H.S RagabA Shehap M.S Abo EllilW.H Osman F.H Abd El-Kader 《Journal of Physics and Chemistry of Solids》2002,63(10):1839-1847
Ternary-phase ceramic system of Li2O Al2O3 4SiO2 doped with CuO, FeO and TiO2 has been prepared and subjected to dc electrical conductivity and thermally stimulated depolarization current (TSDC) measurements as a function of temperature (30-250 °C) and field strength. The electrical conductivity results are explained by assuming both ionic and electronic conduction mechanisms coexist with different contributions over the whole temperature range of experiments. TSDC spectra have been found to be characterized by a broad intense relaxation peak, which can be attributed to an ionic charge polarization. The broad relaxation transitions are apparently a result of the nonuniform nature of this process. Activation energies are calculated for both dc electrical conductivity and TSDC according to Arrhenius equation and initial rise method, respectively. 相似文献
7.
B. M. Azizur Rahman A. K. M. Saiful Kabir Muttukrishnan Rajarajan Kenneth T. V. Grattan 《Optical and Quantum Electronics》2005,37(1-3):171-183
Modal solutions of planar photonic crystal waveguides with rectangular air-holes are presented by using a rigorous full-vectorial finite element-based approach. The effective indices, mode field profiles, spot-sizes, power confinements, modal hybridness, beat lengths and group velocity dispersions are shown for the fundamental and higher order modes of the quasi-TE and TM polarizations. 相似文献
8.
This paper deals with the development of a numerical method to study the non-linear wave-wave interactions in oceans. Based on works from Webb-Tracy-Resio, the Hasselmann’s non-linear mathematical model is reviewed numerically. With this theory and the selection of action density domain, a program to reduce time of computation has been developed. Results from new computation are displayed graphically and compared with previous program. This work augments our understanding better about the non-linear process of wave-wave interactions and it improves the numerical computations to obtain efficiency in operational forecast. 相似文献
9.
Pre—Separation Axioms in Fuzzifying Topology 总被引:1,自引:0,他引:1
K.M.AbdEl-Hakeim F.M.Zeyada 《模糊系统与数学》2003,17(1):28-36
1 IntroductionYing[5,6 ] introduced and elementally developed so called fuzzifying topology with the semanticmethod of continuous valued L ogic.Shen[7] introduced and studied T0 -,T1-,T2 (Hausdorff) -,T3(regularity) -,T4 (normality) -separation axioms in fuzzifying topology.In [3 ]the concepts of thefamily of fuzzifying pre-open sets,fuzzifying pre-neighbourhood structure of a point and fuzzifyingpre-closure are introduced and studied.It is worth to mention that pre-separation axioms are … 相似文献
10.
A simple procedure for the synthesis of an important standard, isotopically enriched methylmercury, which is not commercially available, has been established successfully. The isotopically enriched standard synthesized is utilized in conventional isotope dilution mass spectrometry (IDMS), as well as in speciated IDMS (SIDMS), for determination of the true concentration of methylmercury in environmental samples. The CH3201Hg+ standard has been synthesized from commercially available 201HgO and tetramethyltin. The synthesis time required is 1 h at 60°C. The product is highly pure, yielding more than 90% as 201Hg in CH3201Hg+. Hazardous dimethylmercury does not occur during this synthesis procedure. The product synthesized was analyzed using high‐performance liquid chromatography coupled with inductively coupled plasma mass spectrometry (ICP‐MS) and ICP‐MS alone in order to determine its concentration, isotopic composition and purity. The stability of the product was also evaluated for over 6 months and found to be stable at 4°C in the dark. The isotopically enriched methylmercury synthesized can be used in SIDMS and IDMS analyses as a standard. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献