全文获取类型
收费全文 | 689篇 |
免费 | 13篇 |
国内免费 | 6篇 |
专业分类
化学 | 330篇 |
晶体学 | 12篇 |
力学 | 20篇 |
数学 | 168篇 |
物理学 | 178篇 |
出版年
2022年 | 5篇 |
2021年 | 23篇 |
2020年 | 10篇 |
2019年 | 11篇 |
2018年 | 8篇 |
2017年 | 9篇 |
2016年 | 27篇 |
2015年 | 16篇 |
2014年 | 17篇 |
2013年 | 39篇 |
2012年 | 29篇 |
2011年 | 39篇 |
2010年 | 39篇 |
2009年 | 24篇 |
2008年 | 24篇 |
2007年 | 30篇 |
2006年 | 17篇 |
2005年 | 30篇 |
2004年 | 25篇 |
2003年 | 22篇 |
2002年 | 16篇 |
2001年 | 7篇 |
1999年 | 10篇 |
1998年 | 5篇 |
1997年 | 11篇 |
1996年 | 9篇 |
1995年 | 9篇 |
1994年 | 7篇 |
1993年 | 12篇 |
1992年 | 7篇 |
1991年 | 10篇 |
1989年 | 6篇 |
1988年 | 4篇 |
1987年 | 6篇 |
1986年 | 6篇 |
1985年 | 16篇 |
1984年 | 13篇 |
1983年 | 5篇 |
1982年 | 6篇 |
1981年 | 12篇 |
1979年 | 4篇 |
1978年 | 4篇 |
1973年 | 4篇 |
1936年 | 8篇 |
1935年 | 9篇 |
1934年 | 4篇 |
1930年 | 6篇 |
1929年 | 5篇 |
1928年 | 5篇 |
1924年 | 4篇 |
排序方式: 共有708条查询结果,搜索用时 15 毫秒
1.
The paper concerns several diagnostic techniques, which have been used in pulsed-power plasma experiments, i.e. Plasma-Focus and Z-Pinch devices, and which can be adapted to studies of Magnetic Confinement Fusion (MCF) facilities, e.g. Stellarators and Tokamaks. The application of Nuclear Track Detectors (NTDs) for time-integrated ion measurements in MCF experiments is described and the use of such detectors for time-resolved ion measurements is discussed. The application of special ?erenkov-type detectors for time resolved measurements of fast runaway electrons is considered. Also discussed is the use of selected nuclear reactions for measurements of fusion products, e.g. fast neutrons. 相似文献
2.
Piotr Bogusaw Mucha Witold Sadowski 《Mathematical Methods in the Applied Sciences》2005,28(15):1867-1880
The paper analyses long time behaviour of solutions of the Navier–Stokes equations in a two‐dimensional pipe‐like domain. The system is studied with perfect slip boundary conditions with arbitrary inflow conditions at infinity. The main results show the existence of global in time solutions and of an attractor for the dynamical system generated by the model. The paper also establishes an upper bound for the Hausdorff dimension of the attractor. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
3.
Witold Kuran Jerzy Borycki 《Journal of polymer science. Part A, Polymer chemistry》1981,19(5):1251-1259
Polymerization of acrylonitrile in the presence of systems that consisted of triphenylphosphine (PPh3) and a Lewis acid RmMXn (ZnCl2, Me3Al, Et3Al, Et2AlCl, EtAlCl2, AlCl3) was studied. The systems that contained Me3Al and Et3Al (i.e., Lewis acid of moderate acidity) were the most efficient catalysts. Conductometric measurements carried out in the polymerization systems showed the presence of ions. The presence of phosphonium cation in the polyacrylonitrile chain formed by the PPh3–RmMXn catalytic systems was determined by IR, 1H-NMR, and 31P-NMR spectroscopy. The average molecular weight measurements and kinetic chain lengths of polyacrylonitrile formed within the reaction time in the presence of PPh3–Et3Al showed that transfer reactions occur. According to the results obtained, the polymerization reaction of acrylonitrile by PPh3–RmMXn involved a zwitterion formed by the attack of PPh3 on acrylonitrile complexed by Lewis acid [Ph3P⊕? CH2? C?H? C?N → MRmXn] and the anion [CH2?C?? C?N] formed by the proton abstraction from the monomer. 相似文献
4.
5.
Summary The stability constants n of nitrato complexes of Pr, Nd, Sm, Ho, and Er were determined by UV/Vis spectroscopy. It was found that 1=0.87, 1.24, 1.94, 0.24, 0.11 forM (NO3)2+ (M=Pr, Nd, Sm, Ho, Er) and 2=0.06, 0.04 forM (NO3)
2
+
(M=Pr, Nd) at 25 °C. Detailed inspection of the lanthanide spectra shows that increasing nitrate concentration in the solution results in a bathochromic shift of the f-f bands for Nd and Sm which provides evidence for the formation of inner sphere nitrato complexes.
Spektroskopische Untersuchung von Lanthanidennitraten
Zusammenfassung Die Stabilitätskonstanten n der Nitratokomplexe von Pr, Nd, Sm, Ho und Er wurden UV/Vis-spektroskopisch bestimmt. Es ergaben sich Werte von 0.87, 1.24, 1.94, 0.24 und 0.11 für 1 (M(NO3)2+,M=Pr, Nd, Sm, Ho, Er) und 0.06 und 0.04 für 2 (M(NO3) 2 + ,M=Pr, Nd). Eine detaillierte Analyse der Lanthanidenspektren zeigt, daß steigende Nitratkonzentration in Lösung eine bathochrome Verschiebung der f-f-Banden von Nd und Sm bewirkt. Das weist auf die Bildung voninner sphere — Nitratokomplexen hin.相似文献
6.
Mangeney C Ferrage F Aujard I Marchi-Artzner V Jullien L Ouari O Rékaï el D Laschewsky A Vikholm I Sadowski JW 《Journal of the American Chemical Society》2002,124(20):5811-5821
Citrate-capped gold nanoparticles as well as planar gold surfaces can be efficiently grafted with a covalently attached polymer monolayer a few nanometers thick, by simple contact of the metal surface with dilute aqueous solutions of hydrophilic polymers that are end-capped with disulfide moieties, as shown by UV/vis absorption, dynamic light scattering, and surface plasmon resonance studies. The hydrophilic polymer-coated gold colloids can be freeze-dried and stored as powders that can be subsequently dissolved to yield stable aqueous dispersions, even at very large concentrations. They allow for applying filtrations, gel permeation chromatography, or centrifugation. They do not suffer from undesirable nonspecific adsorption of proteins while allowing the diffusion of small species within the hydrogel surface coating. In addition, specific properties of the original hydrophilic polymers are retained such as a lower critical solution temperature. The latter feature could be useful to enhance optical responses of functionalized gold surfaces toward interaction with various substrates. 相似文献
7.
The methods of analysis of the statistical ensembles of trapping sites, before and after electron localization, for electrons in disordered media are surveyed. The review covers the computer-search methods for pre-existing traps in polar matrices, random field theory of disordered polar matrices and the path integral simulations of solvated electron. The common picture provided by all these methods is emphasized: the solvated electron is a unique in chemistry statistical species characterized by statistical distributions of the structural parameters, energy states, reactivity, etc. The numerical examples are provided by the simulations of the trapping sites and the solvated electron in liquid methanol. 相似文献
8.
Jerzy Strzelbicki Witold A. Charewicz Yung Liu Richard A. Bartsch 《Journal of inclusion phenomena and macrocyclic chemistry》1989,7(3):349-361
Separation efficiencies and selectivities in solvent extraction of Co(II) and Ni(H) ammine cations from aqueous solutions into chloroform and toluene and in transport through bulk toluene membranes by proton-ionizable crown ethers have been determined. Six proton-ionizable crown ethers with differing lipophilicities, polyether cavity sizes and ionizable groups (carboxylic and sulfonic acid functions) were examined. Higher selectivity and efficiency for Co(II) ammine cation extraction was observed for the more lipophilic, proton-ionizable crown ethers. Highly lipophilic crown carboxylic acids provided effective and selective transport of Co(II) ammine cations through bulk toluene membranes.Presented in part at the 6th International Symposium on High Purity Materials in Science and Technology: Preparation, Characterization and Application of Well-Defined Materials, Dresden, GDR, May 1985, Poster D91, Poster Abstracts, pp. 144, 145.All extraction and transport experiments were conducted at this location. 相似文献
9.
Witold Danikiewicz Tadeusz Jaworski Stefan Kwiatkowski 《Monatshefte für Chemie / Chemical Monthly》1986,117(10):1177-1184
Starting from methyl 7-oxo-7-(1-cyclopentene)-heptanoate, a simple synthesis of the methyl esters of 7-oxo- and 7-hydroxy-9,11-dideoxy-PGF
1 as a model for 7-substituted prostaglandin analogues is described.
7-Substituierte Prostaglandin-Analoge — ein neuer Syntheseweg
Zusammenfassung Ausgehend von Methyl-7-oxo-7-(1-cyclopenten)-heptanoat wird eine einfache Synthese der Methylester von 7-Oxo- und 7-Hydroxy-9,11-dideoxy-PGF 1 als Modellverbindungen für 7-substituierte Prostaglandinanaloge beschrieben.相似文献
10.
Substituted benzoic acid anions undergo decarboxylation in the medium-pressure region of an electrospray ion source yielding in most cases the correspondingly substituted phenide anions in high yield. The location of the anionic center is specified by the position of the carboxylic group. The only exceptions are compounds with substituents containing acidic hydrogen atoms, like OH and NH(2) groups. For such compounds, either an intra- or an intermolecular (mediated by the molecules of methanol or water) proton transfer from the more acidic position to the benzene ring is observed. The generated anions can be selected using the first quadrupole for studying their ion-molecule chemistry in the second quadrupole of a triple quadrupole mass spectrometer. Their reactions with CO(2), O(2), CH(3)COCH(3) and CCl(4) may serve as typical examples. The general applicability of this method for the generation of phenide anions has been confirmed on three different mass spectrometers. Experiments performed using carboxylic acids other then benzoic acid and its derivatives show that this method is not limited to phenide anions and can be used for the generation of a much wider range of carbanions in the gas phase. 相似文献