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121.
In this paper the nonlinear viscoelastic wave equation in canonical form with Dirichlet boundary condition is considered. By introducing a new functional and using the potential well method, we show that the damping induced by the viscoelastic term is enough to ensure global existence and uniform decay of solutions provided that the initial data are in some stable set. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   
122.
The first imine-bridged pyridyltetrathiafulvalene building block (TTF-CH=N-Py, 1) has been synthesized via the Schiff base condensation of formyltetrathiafulvalene and 2-aminopyridine. The preparation, X-ray crystal structure, electrochemical and magnetic characterization of a 1:1 copper complex [CuII(hfac)2(TTF-CH=N-Py)] (2) are reported. The crystal structure reveals that the imine N atom participates in chelation to the paramagnetic center, thus making this ligand an attractive precursor for the assembly of pi-d systems.  相似文献   
123.
Coordination compounds of MnII, CuII, FeIII and ZnII ions with 4-acetylpyridine nicotinoylhydrazone (4-APNH) were synthesized and characterized by elemental analyses, molar conductivity, magnetic moments, i.r., u.v./vis., m.s., 1H-n.m.r. and thermal analyses. I.r. spectra show that the ligand can act either in the enol form as monovalent bidentate or in the keto form as neutral bidentate depending on the metal salt used. Octahedral structures are proposed for Fe complex and square – planar for the Cu complex, while tetrahedral structures were suggested for Zn and Mn complexes on the basis of magnetic and spectral evidences. Semi-empirical calculations ZINDO/1 have been used to study the molecular geometry and the harmonic vibrational spectra with the purpose to assist the experimental assignment of the complexes. In memory of the late Professor Dr. Abdel Hamid M. Shallaby 2/5/2006  相似文献   
124.
Hydrazones 12a–c and ketazines 13a–c were prepared by the reaction of ketones 11a–c with hydrazine hydrate depending on the temperature and the reaction time. Some ketone (aryl)hydrazone derivatives 14a,c,e reacted with thionyl chloride to afford the chlorothiadiazoline derivatives 15a–c . Surprisingly, the chlorine atom in the latter compounds was found to undergo smooth nucleophilic substitution, and by boiling these compounds in absolute ethanol gave the corresponding ethoxythiadiazoline derivatives 16a–c . The structure of the ethoxythiadiazoline 16b was confirmed by single crystal X‐ray determination. © 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:223–228, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10125  相似文献   
125.
The industrial market depends intensely on wood-based composites for buildings, furniture, and construction, involving significant developments in wood glues since 80% of wood-based products use adhesives. Although biobased glues have been used for many years, notably proteins, they were replaced by synthetic ones at the beginning of the 20th century, mainly due to their better moisture resistance. Currently, most wood adhesives are based on petroleum-derived products, especially formaldehyde resins commonly used in the particleboard industry due to their high adhesive performance. However, formaldehyde has been subjected to strong regulation, and projections aim for further restrictions within wood-based panels from the European market, due to its harmful emissions. From this perspective, concerns about environmental footprint and the toxicity of these formulations have prompted researchers to re-investigate the utilization of biobased materials to formulate safer alternatives. In this regard, proteins have sparked a new and growing interest in the potential development of industrial adhesives for wood due to their advantages, such as lower toxicity, renewable sourcing, and reduced environmental footprint. This work presents the recent developments in the use of proteins to formulate new wood adhesives. Herein, it includes the historical development of wood adhesives, adhesion mechanism, and the current hotspots and recent progress of potential proteinaceous feedstock resources for adhesive preparation.  相似文献   
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In this article, the propagation of an intense laser pulse through underdense collisional plasma in the presence of planar magnetostatic wiggler is studied. It is shown that the electron density distribution, in the presence of planar wiggler with increasing of the normalized plasma length, increases initially and then reaches a peak for different values of wiggler amplitudes. In addition, it is found that the existence of wiggler field leads to an increase in the electron density distribution and subsequently enhancement of electric field. Moreover, it is observed that by increasing the wiggler field, as a result of the increase of the electron density distribution, the dielectric permittivity constant is reduced. It is seen that while wiggler magnetic field was applied appropriately, the total absorption coefficient in the underdense collisional isothermal magnetized plasma improves. In fact, increase of wiggler magnetic field causes the enhancement of the total absorption coefficient of plasma medium.  相似文献   
129.
Spectral dispersions of index of refraction \({n(\lambda )}\) and extinction coefficient \({\kappa (\lambda )}\) of undoped amorphous selenium (a-Se) films of three thicknesses (d?≈?0.5, 0.75, and 1.0 µm) were evaluated by analyzing experimental room-temperature normal-incidence transmittance-wavelength (\({{T_{{\text{exp}}}}(\lambda )} - \lambda\)) data (λ =?400–1100 µm) of their air-supported {a-Se film/thick glass slide}-stacks using Swanepoel’s transmission envelope theory of uniform films. Above a wavelength \({{\lambda _c}\,\, \approx \,\,640\;{\text{nm}}}\), as-measured \({{T_{{\text{exp}}}}(\lambda )}\,\, - \,\lambda\) spectra display well-resolved maxima and minima, with minor shrinkage in transparent and weak absorption regions (750–1100 nm). Below \({\lambda _{\text{c}}}\), a smeared sharp decline of \({{T_{{\text{exp}}}}(\lambda )}\) with decreasing λ, signifying strong absorption in a-Se films and existence of band-tail localized states. For λ > λ c, the \({n\,(\lambda )}\, - \,\lambda\) data retrieved from algebraic envelope procedures followed a Sellmeier-like dispersion relation, with the best-fit values of high-frequency dielectric constant \({{\varepsilon _\infty }\, \approx \,\,{\text{4.9}}}\), static index of refraction \({{n_{\text{0}}} = n\left( {E\, \to \,{\text{0}}} \right)\,\, \approx \,\,{\text{2.43}}}\), and resonance wavelength \({{\lambda _0}\, \approx \,490\,\,{\text{nm}}}\), which may be assigned to onset of photogeneration in a-Se. Urbach-like dependency of absorption coefficient \({\alpha (h{{\nu }})}\) of a-Se films on photon energy \({h{{\nu }}}\) was realized with an Urbach-tail breadth of 85 meV. All achieved optical parameters were found to be slightly dependent on film thickness. Findings of present algebraic analysis are consistent with reported literature results obtained on the basis of other optical analytical approaches.  相似文献   
130.
In this article we present an optimal Markov Decision‐based Call Admission Control (MD‐CAC) policy for the multimedia services that characterize the next generation of wireless cellular networks. A Markov decision process (MDP) is used to represent the CAC policy. The MD‐CAC is formulated as a linear programming problem with the objectives of maximizing the system utilization while ensuring class differentiation and providing quantitative fairness guarantees among different classes of users. Through simulation, we show that the MD‐CAC policy potentially achieves the optimal decisions. Hence our proposed MD‐CAC policy satisfies its design goals in terms of call‐class‐differentiation, fairness and system utilization. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   
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