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51.
Petiot P Charnay C Martinez J Puttergill L Galindo F Lamaty F Colacino E 《Chemical communications (Cambridge, England)》2010,46(46):8842-8844
The synthesis of a new hydrophilic ammonium-based poly(ethylene glycol)-ionic liquid (PEG-IL) is reported; the structure was assigned by NMR ((1)H, (13)C) and MALDI mass spectrometry. The viscosity and thermal stability were also studied, as well as its polarity. Its application as an alternative solvent in the synthesis of dipeptides under microwave irradiation is also described. 相似文献
52.
Hurth C Smith SD Nordquist AR Lenigk R Duane B Nguyen D Surve A Hopwood AJ Estes MD Yang J Cai Z Chen X Lee-Edghill JG Moran N Elliott K Tully G Zenhausern F 《Electrophoresis》2010,31(21):3510-3517
The microfluidic integration of an entire DNA analysis workflow on a fully integrated miniaturized instrument is reported using lab‐on‐a‐chip automation to perform DNA fingerprinting compatible with CODIS standard relevant to the forensic community. The instrument aims to improve the cost, duration, and ease of use to perform a “sample‐to‐profile” analysis with no need for human intervention. The present publication describes the operation of the three major components of the system: the electronic control components, the microfluidic cartridge and CE microchip, and the optical excitation/detection module. Experimental details are given to characterize the level of performance, stability, reliability, accuracy, and sensitivity of the prototype system. A typical temperature profile from a PCR amplification process and an electropherogram of a commercial size standard (GeneScan 500?, Applied Biosystems) separation are shown to assess the relevance of the instrument to forensic applications. Finally, we present a profile from an automated integrated run where lysed cells from a buccal swab were introduced in the system and no further human intervention was required to complete the analysis. 相似文献
53.
Xi X Cegla FB Lowe M Thiemann A Nowak T Mettin R Holsteyns F Lippert A 《Ultrasonics》2011,51(8):1014-1025
The use of bubbles in applications such as surface chemistry, drug delivery, and ultrasonic cleaning etc. has been enormously popular in the past two decades. It has been recognized that acoustically-driven bubbles can be used to disturb the flow field near a boundary in order to accelerate physical or chemical reactions on the surface. The interactions between bubbles and a surface have been studied experimentally and analytically. However, most of the investigations focused on violently oscillating bubbles (also known as cavitation bubble), less attention has been given to understand the interactions between moderately oscillating bubbles and a boundary. Moreover, cavitation bubbles were normally generated in situ by a high intensity laser beam, little experimental work has been carried out to study the translational trajectory of a moderately oscillating bubble in an acoustic field and subsequent interactions with the surface. This paper describes the design of an ultrasonic test cell and explores the mechanism of bubble manipulation within the test cell. The test cell consists of a transducer, a liquid medium and a glass backing plate. The acoustic field within the multi-layered stack was designed in such a way that it was effectively one dimensional. This was then successfully simulated by a one dimensional network model. The model can accurately predict the impedance of the test cell as well as the mode shape (distribution of particle velocity and stress/pressure field) within the whole assembly. The mode shape of the stack was designed so that bubbles can be pushed from their injection point onto a backing glass plate. Bubble radial oscillation was simulated by a modified Keller–Miksis equation and bubble translational motion was derived from an equation obtained by applying Newton’s second law to a bubble in a liquid medium. Results indicated that the bubble trajectory depends on the acoustic pressure amplitude and initial bubble size: an increase of pressure amplitude or a decrease of bubble size forces bubbles larger than their resonant size to arrive at the target plate at lower heights, while the trajectories of smaller bubbles are less influenced by these factors. The test cell is also suitable for testing the effects of drag force on the bubble motion and for studying the bubble behavior near a surface. 相似文献
54.
Sandrine?Chaput Christian?CarrotEmail author Mickael?Castro Frederic?Prochazka 《Rheologica Acta》2004,43(5):417-426
The work focuses on the detection of the co-continuity window in immiscible polymer blends. The purpose of the paper is to describe how rheological techniques can help to evaluate the composition range of the co-continuous morphology through the study of a particular system: PEO/PVDF-HFP. First, the blends were characterized by selective dissolution experiments and SEM observations. Then the ability of dynamic mechanical spectroscopy to detect the co-continuity was investigated in the melt and in the solid state. The evolution of the storage modulus of molten blends with their composition at a constant low frequency gives information about the co-continuity interval, especially as far as the onset of the continuity of the PEO phase is concerned. Then the immiscibility of the polymers and the continuity of PVDF-HFP as a function of blend composition have been highlighted by means of dynamic mechanical spectrometry below the melting point of PVDF-HFP. Comparison with results from classical methods shows fair agreement.This paper was presented at the first Annual European Rheology Conference (AERC) held in Guimarães, Portugal, September 11-13, 2003. 相似文献
55.
A homogeneous, isotropic plate occupies the region 0x
1, |x
2|a, |x
3|h, where the ratio h/a is sufficiently small so that the classical theory of thin plate bending applies. The short end of the plate at x
1=0 is clamped while the long sides are free. This cantilever plate is now loaded at x
1=+ by an applied twisting moment, by a bending moment or by flexure. Despite the fundamental nature of these problems, and the long history of thin plate theory, no solutions are to be found in the existing literature that will determine (for instance) the important unknown resultants V
1, M
11 at the clamped end x
1=0. The main reason for this is that this combination of boundary conditions leads to severe oscillating singularities of the field in the corners (0, ±a). The fact that such singularities must exist is widely known, but we present here for the first time a method of solution that takes these singularities fully into account.Our numerical results show that the values of M
11, V
1 on x
1=0 bear little resemblance to those of the corresponding Saint-Venant solutions, which do not fully satisfy the boundary conditions at the clamped end. Indeed, significantly large values of these resultants were found at points far enough from the corners so as to be relevant in actual engineering applications. Also of interest are certain weighted integrals of M
11, V
1 which we calculate. These constants determine the effect of the clamping at large distances (greater than 4a, say) from the cla,ped end. At such distances, the effect of the clamping is merely to impose an additional rigid body deflection on the plate.Finally, we consider the plate of finite length. Provided that the aspect ratio is 2 or more, we give accurate approximate solutions for the torsion, bending or flexure of a finite plate clamped at both ends. 相似文献
56.
Marie‐Laure Louillat‐Habermeyer Rongwei Jin Prof. Dr. Frederic W. Patureau 《Angewandte Chemie (International ed. in English)》2015,54(13):4102-4104
A method was developed for the direct dehydrogenative construction of C? N bonds between unprotected phenols and a series of cyclic anilines without resorting to any kind of metal activation of either substrate and without the use of halides. The resulting process relies on the exclusively organic activation of molecular oxygen and the subsequent oxidation of the aniline substrate. This allows the coupling of ubiquitous phenols, thus furnishing aminophenols through an atom‐economical and most sustainable dehydrogenative amination method. This new reactivity, which relies on the intrinsic organic reactivity of cumene in what can be seen as a modified Hock activation process of oxygen, is expected to have a large impact on the formation of C? N bonds in organic synthesis. 相似文献
57.
58.
Poineau F Malliakas CD Weck PF Scott BL Johnstone EV Forster PM Kim E Kanatzidis MG Czerwinski KR Sattelberger AP 《Journal of the American Chemical Society》2011,133(23):8814-8817
Technetium dichloride has been discovered. It was synthesized from the elements and characterized by several physical techniques, including single crystal X-ray diffraction. In the solid state, technetium dichloride exhibits a new structure type consisting of infinite chains of face sharing [Tc(2)Cl(8)] rectangular prisms that are packed in a commensurate supercell. The metal-metal separation in the prisms is 2.127(2) ?, a distance consistent with the presence of a Tc≡Tc triple bond that is also supported by electronic structure calculations. 相似文献
59.
Abbotto A Sauvage F Barolo C De Angelis F Fantacci S Graetzel M Manfredi N Marinzi C Nazeeruddin MK 《Dalton transactions (Cambridge, England : 2003)》2011,40(1):234-242
The first example of a heteroarylvinylene π-conjugated quaterpyridine Ru(II) sensitizer (N1044) was synthesized and used in dye-sensitized solar cells; the dye has an effective panchromatic absorption band, covering the entire visible spectrum up to the NIR region, and superior electrochemical characteristics (HOMO/LUMO and bandgap energies) with respect to previous representative Ru(II) bi- and quaterpyridine sensitizers. A record IPCE curve ranging from 360 to 920 nm has been measured with a maximum of 65% at 646 nm and still 33% efficiency at 800 nm; this leads to substantially increased photocurrent (19.2 mA cm(-2)) when compared to the prototype N719 Ru(II) sensitizer. 相似文献
60.
A Rh catalyzed, no-chelate-assisted C-H activation/oxidative olefination reaction of bromoarenes has been discovered, in which the latter ones seem to act as a substrate, terminal oxidant, and catalyst modifier. 相似文献