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Raffaella Suriano Jasmin Hume Marco Cereda Marco De Fazio Marco Bianchessi Marinella Levi Stefano Turri 《Surface and interface analysis : SIA》2011,43(12):1498-1508
There is a great need to improve the biocompatibility of silicon‐based lab‐on‐chip substrate materials for reliable quantitative analysis of biological solutions. These advanced microdevice surfaces need not only be biocompatible but also have surfaces of defined wettability characteristics. The inhibition of biomolecular activity due to microdevice surface interaction is common and can result in inaccurate results or decreased reaction yields. In this work we investigate different techniques for the chemical functionalization of oxidized silicon (SiOx) surfaces in order to: (i) obtain defined hydrophobic/hydrophilic surfaces; and (ii) increase the efficiency of performing Real‐Time Polymerase Chain Reaction (PCR) on a silicon‐based lab‐on‐chip. Silicon oxide surfaces are functionalized by grafting alkylic chain silanes and poly(ethylene glycol) (PEG) chains to the surfaces, rendering them hydrophobic or hydrophilic. Functionalized surfaces are characterized through contact angle and atomic force microscopy (AFM) measurements, showing stable hydrophobic surfaces with contact angles of 69–78° and layer thicknesses of 11–15 Å and hydrophilic surfaces displaying contact angles of 5–6° and thicknesses of 22–52 Å. PCR experiments carried out directly on bare silicon oxide lab‐on‐chip surfaces show low yields of DNA amplification. Hydrophobic surfaces decrease the inhibition of PCR. Hydrophilic surfaces are a major improvement on the bare silicon oxide exhibiting the same maximum reaction yield as obtained with a standard thermocycler. We have found that the best results are associated with PEG modified surfaces, which prove very suitable for the fabrication of reliable PCR silicon lab‐on‐chips. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
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We report a concise, enantioselective total synthesis of (-)-taiwaniaquinone H and the first enantioselective total synthesis of (-)-taiwaniaquinol B by a route that includes asymmetric palladium-catalyzed α-arylation of a ketone with an aryl bromide that was generated by sterically controlled halogenation via iridium-catalyzed C-H borylation. This asymmetric α-arylation creates the benzylic quaternary stereogenic center present in the taiwaniaquinoids. The synthesis was completed efficiently by developing a Lewis acid-promoted cascade to construct the [6,5,6] tricyclic core of an intermediate common to the synthesis of a number of taiwaniaquinoids. Through the preparation of these compounds, we demonstrate the utility of constructing benzylic quaternary stereogenic centers, even those lacking a carbonyl group in the α-position, by asymmetric α-arylation. 相似文献
64.
A biased potential molecular dynamics simulation approach, accelerated molecular dynamics (AMD), has been implemented in the framework of ab initio molecular dynamics for the study of chemical reactions. Using two examples, the double proton transfer reaction in formic acid dimer and the hypothetical adiabatic ring opening and subsequent rearrangement reactions in methylenecyclopropane, it is demonstrated that ab initio AMD can be readily employed to efficiently explore the reactive potential energy surface, allowing the prediction of chemical reactions and the identification of metastable states. An adaptive variant of the AMD method is developed, which additionally affords an accurate representation of both the free-energy surface and the mechanism associated with the chemical reaction of interest and can also provide an estimate of the reaction rate. 相似文献
65.
Decio Levi Piergiulio Tempesta 《Journal of Mathematical Analysis and Applications》2011,376(1):247-258
We propose a new approach to the multiple-scale analysis of difference equations, in the context of the finite operator calculus. We derive the transformation formulae that map any given dynamical system, continuous or discrete, into a rescaled discrete system, by generalizing a classical result due to Jordan. Under suitable analytical hypotheses on the function space we consider, the rescaled equations are of finite order. Our results are applied to the study of multiple-scale reductions of dynamical systems, and in particular to the case of a discrete nonlinear harmonic oscillator. 相似文献
66.
D. Brunelli S. T. Levi P. Fragnoli A. Renzulli P. Santi E. Paganelli M. C. Martinelli 《Applied Physics A: Materials Science & Processing》2013,113(4):855-863
An integrated microchemical–petrographic approach is here proposed to discriminate the provenance of archaeological pottery artefacts from distinct production centres. Our study focuses on a statistically significant sampling (n=186) of volcanic temper-bearing potteries representative of the manufacturing and dispersion among the islands of the Aeolian Archipelago during the Bronze Age. The widespread establishment of new settlements and the abundant recovery of Aeolian-made ceramic in southern Italy attest for the increased vitality of the Archipelago during the Capo Graziano culture (Early Bronze Age–Middle Bronze Age 2; 2300–1430 BC). Potteries from three of the main known ancient communities (Lipari, Filicudi and Stromboli) have been studied integrating old collections and newly excavated material. Volcanic tempers have been first investigated through multivariate analyses of relative abundances of mineral and rock clasts along with petrographic characters. In addition, we performed in-situ mineral chemistry microanalyses by Electron Microprobe and Laser Ablation—Inductively Coupled Plasma Mass Spectrometry to assess major and trace element composition of the most common mineral phases. Four Temper Compositional Reference Units have been recognised based on compositional trends. Two units (AI and AX) are unequivocally distinct by their peculiar trace element enrichment and petrographic composition; they mostly contain samples from the sites of Lipari and Stromboli, respectively. Units AIV and AVIII, restricted to the sites of Filicudi and Stromboli, show distinct petrographic characters but overlapped geochemical fingerprints. 相似文献
67.
Most of TM6-cluster compounds (TM = transition metal) are soluble in polar solvents, in which the cluster units commonly remain intact, preserving the same atomic arrangement as in solids. Consequently, the redox potential is often used to characterize structural and electronic features of respective solids. Although a high lability and variety of ligands allow for tuning of redox potential and of the related spectroscopic properties in wide ranges, the mechanism of this tuning is still unclear. Crystal chemistry approach was applied for the first time to clarify this mechanism. It was shown that there are two factors affecting redox potential of a given metal couple: Lever’s electrochemical parameters of the ligands and the effective ionic charge of TM, which in cluster compounds differs effectively from the formal value due to the bond strains around TM atoms. Calculations of the effective ionic charge of TMs were performed in the framework of bond valence model, which relates the valence of a bond to its length by simple Pauling relationship. It was also shown that due to the bond strains the charge depends mainly on the atomic size of the inner ligands. 相似文献
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自从发现热电直接转换中的泽贝克效应(Seebeck effect,又称温差电效应,1821 年)、佩尔捷效应(Peltier effect, 1833 年) 和汤姆孙效应(Thomson effect,1855年),人们逐渐意识到了热电转换技术在量热、发电和制冷等方面的应用。近几十年来,随着全球能源短缺与环境恶化问题日益突出,可再生能源的利用受到广泛关注。具有小尺寸、高可靠性、无传动部件、无噪音、无污染等优点的热电转换技术成为材料科学研究热点之一。 相似文献