全文获取类型
收费全文 | 1119篇 |
免费 | 42篇 |
专业分类
化学 | 790篇 |
晶体学 | 9篇 |
力学 | 36篇 |
数学 | 85篇 |
物理学 | 241篇 |
出版年
2023年 | 7篇 |
2022年 | 25篇 |
2021年 | 22篇 |
2020年 | 15篇 |
2019年 | 23篇 |
2018年 | 5篇 |
2017年 | 7篇 |
2016年 | 20篇 |
2015年 | 26篇 |
2014年 | 46篇 |
2013年 | 46篇 |
2012年 | 69篇 |
2011年 | 88篇 |
2010年 | 53篇 |
2009年 | 72篇 |
2008年 | 87篇 |
2007年 | 70篇 |
2006年 | 67篇 |
2005年 | 46篇 |
2004年 | 31篇 |
2003年 | 27篇 |
2002年 | 28篇 |
2001年 | 19篇 |
2000年 | 15篇 |
1999年 | 18篇 |
1998年 | 14篇 |
1997年 | 19篇 |
1996年 | 15篇 |
1995年 | 11篇 |
1994年 | 16篇 |
1993年 | 13篇 |
1992年 | 15篇 |
1991年 | 8篇 |
1990年 | 8篇 |
1989年 | 6篇 |
1988年 | 6篇 |
1987年 | 4篇 |
1986年 | 8篇 |
1985年 | 8篇 |
1983年 | 3篇 |
1982年 | 5篇 |
1981年 | 6篇 |
1980年 | 8篇 |
1978年 | 5篇 |
1977年 | 3篇 |
1976年 | 8篇 |
1975年 | 5篇 |
1974年 | 12篇 |
1973年 | 12篇 |
1964年 | 2篇 |
排序方式: 共有1161条查询结果,搜索用时 15 毫秒
991.
Analysis of chitin oligosaccharides by capillary electrophoresis with laser-induced fluorescence 总被引:1,自引:0,他引:1
A method, using capillary electrophoresis (CE) with laser-induced fluorescence (LIF) detection for analyzing chitin oligosaccharides is described. Chitin oligosaccharides were derivatized with 9-aminopyrene-1,4,6-trisulfonate (APTS) via reductive amination at 37 degrees C for 16 h (optimized conditions). The APTS-chitin oligosaccharides were analyzed using either an acidic citric acid-phosphate buffer or an alkaline borate buffer. The effects of buffer types, buffer pH values, and buffer concentrations on the separation were examined. The analytes were successfully separated by using a pH 4.6 citric acid-phosphate within 19 min. The APTS-derivatized chitin monosaccharide (D-glucosamine) migrated first. The analytes were also completely separated by using a pH 9.0 borate buffer within 24 min. Moreover, the specificity of enzyme digestion on chitin polysaccharides using the optimized APTS labeling procedure and the CE-LIF method was demonstrated. 相似文献
992.
The impact of a plug of salts on the analysis of large volumes of dsDNA by capillary electrophoresis
A partially filling technique for the analysis of DNA markers and polymerase chain reaction (PCR) products by capillary electrophoresis in the presence of electroosmotic flow using polymer solutions is presented. Either after or prior to the sample injection, a plug of salts at high pH was hydrodynamically injected. During the separation, poly(ethylene oxide) (PEO) solution entered the capillary. We have found that the position, length, and composition of the plugs affect the sensitivity, resolution, and speed on the analysis of PhiX-174/HaeIII DNA restriction fragments or a DNA mixture (pBR 322/HaeIII digest, pBR 328/BglI digest and pBR 328/HinfI digest) with different degrees. Through careful evaluation of the impact of anions and cations on the analysis of DNA, we have suggested that the optimal condition is applying a plug consisting of 32 mM NaCl and 0.01 M NaOH at 30 cm height for 60 s after sample injection. In the presence of such a plug, PEO adsorption reduces, and thus the separation is faster, as well as the sensitivity improves. Using this condition, the analysis of a DNA mixture (injected at 30 cm for 360 s) containing ten different PCR products amplified after 17 cycles was complete in 25 min. About a 2000-fold improvement in the sensitivity was achieved when compared to that by a conventional method (10 s injection) without applying a plug. 相似文献
993.
The feasibility of combining the techniques of on-line concentration and capillary electrophoresis/low-temperature fluorescence spectroscopy (CE/LTFS) for the detection and identification of trans-resveratrol in red wine at 77 K is demonstrated for the first time. This technique, involving sweeping-micellar electrokinetic chromatography (sweeping-MEKC), was used for the initial on-line concentration and separation, after which a cryogenic molecular fluorescence experiment was performed at 77 K. In comparison with normal-MEKC mode, a approximately 1500-fold improvement in detection sensitivity could be obtained when the sweeping-MEKC was applied. The proposed method permits not only the separation and detection of trans-resveratrol from red wine extracts but also ensures that the on-line spectrum is readily distinguishable and can be unambiguously assigned at 77 K. 相似文献
994.
An approach is described with turbulent flow on-line extraction liquid chromatography/electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) for GLP quantitative bioanalysis of a drug candidate. Two systems were built in-house with standard laboratory parts and equipments. One system consisted of one gradient HPLC pump, one isocratic pump, one ten-port valve, two turbulent flow columns, one analytical column, one autosampler and one mass spectrometer. Using this system, an injection-to-injection cycle time of 0.8 min was achieved. By adding an additional valve, another analytical column and an isocratic pump, the injection-to-injection cycle time decreased to 0.4 min. Validation results from the two systems showed that precision and accuracy were acceptable for GLP quantitative analyses. The system was utilized to support sample bioanalysis of a drug candidate in a first-time in-human clinical trial. 相似文献
995.
Addition of trimethylsilyl trifluoroacetate to the carbanions of α‐fluorobenzyl‐phosphonate ( 3 ) or diisopropyl(fluorocarbethoxymethyl)phosphonate ( 9 ) formed the corresponding intermediates [CF3C(O)CFPh]?Li+ ( 10 ) and [CF3C(O)CFCO2Et]?Li+ ( 11 ), respectively. Subsequent protonation, alkylation or allylation of 10 and 11 afforded trifluoromethyl fluorobenzyl ketones 12 and ethyl 2,4,4,4‐tetra‐fluoroacetoacetates 13 . Based on the results obtained, a plausible mechanism was proposed. 相似文献
996.
997.
In this work, we propose a method to determine trace amounts of Cd in human whole blood samples by electrothermal atomic absorption spectrometry (ETAAS) with the combined chemical modifier including magnesium chloride and sodium hydroxide. Prior to the ETAAS analysis, dissolution of the blood samples is accomplished using a HNO3-HClO4double closed-vessel microwave digestion technique followed by drying of the dissolved blood samples by means of an infrared lamp. In using this approach, a MgCl2 chemical modifier is added to the digested samples, then they are injected into the graphite furnace for detecting the Cd level via atomic absorption spectrometer. Besides we used a NaOH chemical modifier, which removed the matrix major elements through prior ashing at 1200 ° C for 30 s, and the Cd is subsequently volatilized at 2200 °C and determined by AAS. However, the proposed method can be employed to determine the of Cd level in whole blood samples by the calibration technique and the standard-additions method. Its validity is confirmed with two certified reference whole blood materials (Seronorm Trace Elements Whole Blood Batch no. 205052 and Batch no. 203056). By using 10 μL injections, a detection limit of 0.052 ng mL?1 is achieved. 相似文献
998.
999.
1000.