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We study the structure of the complement of an F-bundle over a graph G when it can be expressed as an F-bundle over another graph G. In particular, we compute the characteristie polynomial of the complement of an F-bundle when its voltages lie in and abelian subgroup Г of Aut(F) which acts freely and transitively on the vertices of the fiber F Some applications to regular embeddings of graph bundles into Euclidean spaces are also discussed 相似文献
75.
This paper presents a new discrete-time sliding mode controller to alleviate undesirable chattering in vibration control of a flexible beam structure. A smart beam featuring a piezoelectric film is devised and its governing equation of motion is derived. A discrete-time sliding mode controller which consists of discontinuous part and equivalent part is then designed by considering the separation principle. By doing this, undesirable chattering of the beam structure can be attenuated in the settled phase. The proposed controller is experimentally realized, and both transient and forced vibration control responses are evaluated in time domain. 相似文献
76.
77.
We have designed and synthesised new anion receptors 1 and 2, both of their C–H groups were at the α positions to carbonyl groups and further polarised by the attached polarising substituents. This enabled us to study hydrogen bonding donor ability of C–H bonds. The polarising substituents are electron withdrawing cyano group for host 1, while charged pyridinium group for host 2. As expected from charge effects, host 2 shows roughly an order of magnitude higher binding constants against various anion guests than those of receptor 1. Since the magnitude of polarisation change should be greatest for C–H group among various hydrogen bonding groups, this indicates the importance of C–H hydrogen bonding. In contrast, the relative order of binding constants was the same for both host 1 and 2. The order of association constants was found to be (CH3)2POO? > CH3COO? > C6H5COO? > Cl? > Br?. DFT calculation results were in good agreement with experimental binding constants and confirmed the importance of charged group substitution. In addition, receptor 1 showed the highest association constant for dimethyl phosphinate, which is implicated in many metabolic diseases. 相似文献
78.
The main aim of this paper is to give some upper and lower bounds for the isoperimetric numbers of graph coverings or graph bundles, with exact values in some special cases. In addition, we show that the isoperimetric number of any covering graph is not greater than that of the base graph. Mohar's theorem for the isoperimetric number of the cartesian product of a graph and a complete graph can be extended to a more general case: The isoperimetric numberi(G × K
2n) of the cartesian product of any graphG and a complete graphK
2n on even vertices is the minimum of the isoperimetric numberi(G) andn, and it is also a sharp lower bound of the isoperimetric numbers of all graph bundles over the graphG with fiberK
2n. Furthermore, ifn 2i(G) then the isoperimetric number of any graph bundle overG with fibreK
n is equal to the isoperimetric numberi(G) ofG.
Partially supported by The Ministry of Education, Korea. 相似文献
79.
Sohn H Sailor MJ Magde D Trogler WC 《Journal of the American Chemical Society》2003,125(13):3821-3830
The synthesis, spectroscopic characterization, and fluorescence quenching efficiency of polymers and copolymers containing tetraphenylsilole or tetraphenylgermole with Si-Si, Ge-Ge, and Si-Ge backbones are reported. Poly(tetraphenyl)germole, 2, was synthesized from the reduction of dichloro(tetraphenyl)germole with 2 equivs of Li. Silole-germole alternating copolymer 3 was synthesized by coupling dilithium salts of tetraphenylsilole dianion with dichloro(tetraphenyl)germole. Other tetraphenylmetallole-silane copolymers, 4-12, were synthesized through the Wurtz-type coupling of the dilithium salts of the tetraphenylmetallole dianion and corresponding dichloro(dialkyl)silanes. The molecular weights (M(w)) of these metallole-silane copolymers are in the range of 4000 approximately 6000. Detection of nitroaromatic molecules, such as nitrobenzene (NB), 2,4-dinitrotoluene (DNT), 2,4,6-trinitrotoluene (TNT), and picric acid (PA), has been explored. A linear Stern-Volmer relationship was observed for the first three analytes, but not for picric acid. Fluorescence spectra of polymetalloles or metallole-silane copolymers obtained in either toluene solutions or thin polymer films displayed no shift in the maximum of the emission wavelength. This suggests that the polymetalloles or metallole-silanes exhibit neither pi-stacking of polymer chains nor excimer formation. Fluorescence lifetimes of polymetalloles and metallole-silanes were measured both in the presence and absence of TNT, and tau(o)/tau is invariant. This requires that photoluminescence quenching occurs by a static mechanism. 相似文献
80.
Joos TO Schrenk M Höpfl P Kröger K Chowdhury U Stoll D Schörner D Dürr M Herick K Rupp S Sohn K Hämmerle H 《Electrophoresis》2000,21(13):2641-2650
In order to quantify autoantibodies in the sera of patients with autoimmune disease, we have created a microarray-based immunoassay that allows the simultaneous analysis of 18 known autoantigens. The microarrays contain serial dilutions of the various antigens, thereby allowing accurate determination of autoantibody titer using minimal amounts of serum. The assay is very sensitive and highly specific: as little as 40 fg of a known protein standard can be detected with little or no cross-reactivity to nonspecific proteins. The signal intensities observed from serial dilutions of immobilized antigen correlate well with serial dilutions of autoimmune sera. Miniaturized and highly parallelized immunoassays like these will reduce costs by decreasing reagent consumption and improve efficiency by greatly increasing the number of assays that can be performed with a single serum sample. This system will significantly facilitate and accelerate the diagnostics of autoimmune diseases and can be adapted easily to any other kind of immunoassay. 相似文献