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1.
We provide an approximate analysis of the transient sojourn time for a processor sharing queue with time varying arrival and
service rates, where the load can vary over time, including periods of overload. Using the same asymptotic technique as uniform
acceleration as demonstrated in [12] and [13], we obtain fluid and diffusion limits for the sojourn time of the Mt/Mt/1 processor-sharing queue. Our analysis is enabled by the introduction of a “virtual customer” which differs from the notion
of a “tagged customer” in that the former has no effect on the processing time of the other customers in the system. Our analysis
generalizes to non-exponential service and interarrival times, when the fluid and diffusion limits for the queueing process
are known. 相似文献
2.
A pair of coupled classical oscillators with a general potential and general form of coupling is investigated. For general
potentials, the single-frequency solution is shown to be stable for small excitations. For special potentials, such system
remains stable for an arbitrary excitation. In both cases, the stability does not depend on the form of coupling. Transition
to the instability regime follows from the way how nonlinear potential entrains the energy transfer between the oscillators.
Relation between the existence of multi-frequency quasi-periodic or periodic solutions and the instability of single-frequency
ones is discussed. 相似文献
3.
M. A. Morón C. Romero F. R. Ruiz del Portal 《Journal of Optimization Theory and Applications》1996,91(3):643-649
The purpose of this paper is to seek utility functions satisfying a weak condition which guarantees that the utility optimum always belongs to the compromise set. This set is a special subset of the attainable or feasible set, which is generated through the application of the well-known operational research approach called compromise programming. It is shown that there are large families of utility functions satisfying this condition, thus reinforcing the value of compromise programming as a good surrogate of the traditional utility optimum.Thanks are due to the reviewers for their helpful suggestions. The English editing by Ms. Christine Méndez is appreciated. The authors have been supported by the Comisión Interministerial de Ciencia y Tecnología (CICYT), Madrid, Spain. 相似文献
4.
5.
The direct potentiometric determination of sulphides in natural sea water with a sulphide-selective membrane electrode is proposed. The experimental evaluation of the “apparent mixed” dissociation constants and the thermodynamic activity coefficient in spiked sea water samples, by means of the electrode, permits direct calibration in terms of activity. Alternatively, it is possible to establish, for natural sea water, an experimental equation for the correction of the electrode potentials in terms of pH; this allows direct calibration of the electrodes in terms of total sulphide concentration. This criterion can be applied to any aqueous solution. 相似文献
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7.
Román LU Guerra-Ramírez D Morán G Martínez I Hernández JD Cerda-García-Rojas CM Torres-Valencia JM Joseph-Nathan P 《Organic letters》2004,6(2):173-176
[structure: see text] The triterpenes 8,14-seco-oleana-8(26),13-dien-3beta-ol (1) and its acetyl derivative 2 were isolated from Stevia viscida and Stevia eupatoria, respectively. Their structures were elucidated by 2D NMR, including carbon-carbon connectivity experiments, and confirmed by X-ray diffraction analysis of ketone 3. The absolute configuration was determined by NMR analysis of the Mosher esters of 1. The biogenetic implications of the new substances are discussed. 相似文献
8.
Summary The reactions of MCl4 (M = Ti or V) with R2P(S)P(S)R2 (R = Me or Et) yield hexacoordinate complexes MCl4 · R2P(S)P(S)R2 (M = Ti or V; R = Me or Et), whereas similar reactions with VOCl3 lead to reduction of vanadium and give rise to the vanadium(IV) pentacoordinated complexes: VOCl2-R2P(S)P(S)R2 (R = Me or Et). All the compounds have been characterized by elemental analyses, i.r., visible and e.p.r. spectra, which show thecis-chelate character of these ligands, although in the complexes containing Et4P2S2 the i.r. spectra indicates that thegauche conformation of the ligand is implicated in bonding to the metal. The occupation of the sixth coordination site in pentacoordinate complexes, VOCl2 · R2P(S)P(S)R2, by different donor solvents, has been studied by means of visible and e.p.r. spectra. 相似文献
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