全文获取类型
收费全文 | 10317篇 |
免费 | 183篇 |
国内免费 | 43篇 |
专业分类
化学 | 5901篇 |
晶体学 | 91篇 |
力学 | 364篇 |
数学 | 1708篇 |
物理学 | 2479篇 |
出版年
2022年 | 101篇 |
2021年 | 114篇 |
2020年 | 128篇 |
2019年 | 135篇 |
2018年 | 125篇 |
2017年 | 109篇 |
2016年 | 189篇 |
2015年 | 168篇 |
2014年 | 177篇 |
2013年 | 586篇 |
2012年 | 369篇 |
2011年 | 450篇 |
2010年 | 327篇 |
2009年 | 282篇 |
2008年 | 409篇 |
2007年 | 362篇 |
2006年 | 355篇 |
2005年 | 321篇 |
2004年 | 341篇 |
2003年 | 275篇 |
2002年 | 277篇 |
2001年 | 191篇 |
2000年 | 181篇 |
1999年 | 145篇 |
1998年 | 117篇 |
1997年 | 132篇 |
1996年 | 168篇 |
1995年 | 126篇 |
1994年 | 132篇 |
1993年 | 158篇 |
1992年 | 157篇 |
1991年 | 161篇 |
1990年 | 118篇 |
1989年 | 121篇 |
1988年 | 140篇 |
1987年 | 183篇 |
1986年 | 152篇 |
1985年 | 199篇 |
1984年 | 191篇 |
1983年 | 147篇 |
1982年 | 166篇 |
1981年 | 181篇 |
1980年 | 172篇 |
1979年 | 171篇 |
1978年 | 164篇 |
1977年 | 162篇 |
1976年 | 141篇 |
1975年 | 158篇 |
1974年 | 127篇 |
1973年 | 124篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
81.
Kaale E Leonard S Van Schepdael A Roets E Hoogmartens J 《Journal of chromatography. A》2000,895(1-2):67-79
A selective, sensitive, and rapid pre-capillary derivatization method for determination of the multicomponent aminoglycoside antibiotic gentamicin is described. The derivatization reagents 1,2-phthalic dicarboxaldehyde and mercaptoacetic acid were used and the thioisoindole derivative was UV detected at 330 nm. A central composite experimental design was performed to optimize selectivity and derivatization conditions. Baseline separation of gentamicin C1, C1a, C2, C2a, C2b, sisomicin and several minor components was achieved with a background electrolyte containing 30 mM sodium tetraborate, 7.5 mM beta-cyclodextrin and 12.5% (v/v) methanol at pH 10. Quantitative analysis was performed and illustrated the potential use of capillary electrophoresis for the identification and quantitation of gentamicin as an alternative to methods prescribed in the United States Pharmacopeia and European Pharmacopoeia. 相似文献
82.
83.
Accurate determinations of the platinum group elements (PGEs) and gold, known as the precious metals, have always been difficult tasks. The metals are often present at trace levels in sample types of complex composition. This situation has improved recently due to developments of instrumental methods and their applications to analyses of the precious metals in a variety of matrices. Attention has been given to determinations of traces of precious metals in biological, clinical and environmental samples. Foremost in importance is inductively coupled plasma mass spectrometry (ICP-MS) which has provided a sensitive means of simultaneous determination of traces of PGEs and gold. Important extensions and improvements in atomic absorption spectrometry (AAS), nuclear and electrochemical methods have been reported also. More research on sample treatments, especially fire assays, applied to PGEs has been carried out. Chlorination has proven to be a viable alternative to fire assays for preconcentration of PGEs and gold in analyses of geological materials. In addition, the recent availability of some additional reference materials will be of great assistance in research work on precious metals. 相似文献
84.
Differential pulse polarographic methods for determination of corticosteroids in multicomponent and complex pharmaceutical preparations are described. The influence of other reducible common components of such preparations and excipients on the height of the reduction peaks of corticosteroids and the accuracy of the results was investigated, as well as the interference of excipients by adsorption processes at the electrode or at solid particles of the preparations. In the procedures developed, variations in composition of the supporting electrolyte according to the lipophilicity of the preparation, and the use of standard additions, produce results quickly and reliably. Standard deviations vary from 0.8 to 2.8%. 相似文献
85.
86.
Qin W Baruah M Van der Auweraer M De Schryver FC Boens N 《The journal of physical chemistry. A》2005,109(33):7371-7384
The photophysical properties of seven new 8-(p-substituted)phenyl analogues of 4,4-difluoro-3,5-dimethyl-8-(aryl)-4-bora-3a,4a-diaza-s-indacene (derivatives of the well-known fluorophore BODIPY) in several solvents have been studied by means of absorption and steady-state and time-resolved fluorimetry. For each compound, the fluorescence quantum yield and lifetime are lower in solvents with higher polarity owing to an increase in the rate of nonradiative deactivation. Increasing the electron withdrawing strength of the p-substituent on the phenyl group in position 8 also leads to lower fluorescence quantum yields and lifetimes. When the p-substituent on the phenyl group in position 8 is a tertiary amine [8-(4-piperidinophenyl), 8-(4-N,N-dimethylaminophenyl), and 8-(4-morpholinophenyl)], the low quantum yields of these compounds in more polar solvents can be rationalized by the inversion of the energy levels of an apolar, highly fluorescent and a polar, nonfluorescent excited state, where charge transfer from the tertiary amine to the BODIPY unit occurs. These amine analogues can be protonated at low pH in aqueous solution. Fluorescence titrations yielded pK(a) values of their conjugate ammonium salts which are in agreement with the electron donating tendency of the amine group: piperidino (4.15) > dimethylamino (2.37) > morpholino (1.47), with the pK(a) values in parentheses. The rate constant of radiative deactivation (k(f)) is the same for all compounds in all solvents studied (k(f) = 1.4 x 10(8) s(-1)). 相似文献
87.
Huybrechts T Dewulf J Van Craeynest K Van Langenhove H 《Journal of chromatography. A》2001,922(1-2):207-218
A recently developed method for the sampling and analysis of volatile organic compounds in air has been evaluated. The system is based on the enrichment of analytes in tetraethylene glycol dimethyl ether or tetraglyme, a water-soluble organic liquid. The subsequent analysis consists of dispersion of a sample aliquot in water followed by purge-and-trap and gas chromatographic separation. Physico-chemical data were investigated for 10 volatile organic compounds, providing information on the possibilities and limitations of the tetraglyme method. The target analytes included chlorinated alkanes and alkenes, and monocyclic aromatic hydrocarbons. Air/tetraglyme partition coefficients Kat were determined over an environmental relevant temperature range of 2-25 degrees C to evaluate sorption efficiencies and estimate breakthrough volumes at the sampling stage. At 2 degrees C breakthrough volumes (allowing 5% of breakthrough) ranged from 5.8 (1,1-dichloroethane) to 312 l (1,1,2-trichloroethane) for 20 ml of tetraglyme. With regard to the desorption stage, the effect of tetraglyme on the air/water partition of organic compounds was investigated through the measurement of air/tetraglyme-water partition coefficients Kat-w for 2-31% (v/v) tetraglyme in water. Finally a clean-up procedure for tetraglyme was evaluated. Analysis of a blank tetraglyme-water (17:83, v:v) mixture by gas chromatography-flame ionization detection/mass spectrometry showed minor background signals. None of the target compounds were detected. 相似文献
88.
[reaction: see text] Since peroxidase-catalyzed dityrosine formation is inefficient for peptides, we have developed alternative conditions for intermolecular dityrosine formation using the Miyaura-Suzuki reaction. A one-pot reaction is effective for cross-linking short peptides, but longer peptides inhibit the Suzuki step, mandating a traditional two-step procedure using potassium acetate for the Miyaura reaction and potassium carbonate for the Suzuki coupling. These palladium-based methods are complementary to the well-established peroxidase-catalyzed oxidative phenolic coupling of full-length proteins. 相似文献
89.
90.
When a two-phase column consisting of paraffin oil and silicon oil is placed in an otherwise air-filled, horizontal glass capillary, the column starts moving spontaneously. Silicon oil displaces paraffin oil, which in its turn displaces air at atmospheric conditions; a stable film of silicon oil is left at the receding silicon oil/air meniscus. The driving force for the motion is the difference in capillary pressure at the free interfaces. However, the column moves considerably more slowly than predicted by the driving forces; it appears that the forces resisting the motion at the moving liquid/liquid/solid line are much larger than one would expect on the basis of the interfacial tension and the viscosities of the two phase system. Some considerations are made on the relationship of the theory of Fowkes to our system. Also, a method for measuring low interfacial tensions between immiscible liquids is proposed. 相似文献