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181.
Azzeddine Elmidaoui Said Belcadi Yves Houdus Thierry Cohen Claude Gavach 《Journal of polymer science. Part A, Polymer chemistry》1992,30(7):1407-1412
Using the preirradiation technique a kinetic study of the grafting of the 4-vinyl pyridine (V4P) and an aliphatic ammonium monomer (ALAM) onto the copolymer film of ethylene–tetrafluoroethylene (ETFE) has been performed. The influence of dose, temperature, and concentration of monomer, reticular agent, and inhibitor were investigated. The results are discussed on the basis of the interactions between monomer diffusibility and viscosity of the medium. The characteristics of some membranes were determined. Their applicability to the recovery of acid by dialysis is demonstrated. 相似文献
182.
183.
The many-to-many location-routing problem 总被引:1,自引:0,他引:1
In this paper the many to many location routing problem is introduced, and its relationship to various problems in distribution
management is emphasised. Useful mathematical formulations which can be easily extended to cater for other related problems
are produced. Techniques for tackling this complex distribution problem are also outlined. 相似文献
184.
A constant fixed cost of establishing a facility is introduced within the framework of minisum facility location in the continuous space. The solution method developed uses a multi-phase heuristic that first solves a discrete version of the problem by existing methods to obtain an estimate of the optimal number of facilities. Some results are presented for test problems taken from the literature and compared with best-known solutions of the multi-source Weber problem with the addition of the appropriate fixed costs. 相似文献
185.
186.
S Salhi 《The Journal of the Operational Research Society》1997,48(12):1233-1240
A constructive heuristic which has the flexibility of perturbing the solution while guiding the search toward a better solution is developed. Interesting findings are obtained when this heuristic is tested against reputable methods on a class of uncapacitated location problems. 相似文献
187.
It is shown that the relative intensity of the twisted intramolecular charge transfer (TICT) band of ester and benzonitrile
derivatives of dialkylaniline in polymethylmethacrylate polymer matrices of different molecular weights (MW) to increase with
increasing MW of the polymer. Our results emphasis the role of local free volumes (mobility in the matrix cage) and focus
attention on the role of the MW of the polymer on the fluorescence of various TICT probes. These observations are confirmed
by the red edge effect and fluorescence decay results. 相似文献
188.
Muhammad Akmal Kamarudin Ammar A. Khan Suhana Mohd Said Malik M. Qasim Timothy D. Wilkinson 《Liquid crystals》2018,45(1):112-121
The doping of polymer electrolytes (PEs) with liquid crystal (LC) materials has been shown to improve the performance of dye-sensitised solar cells (DSSCs). This is achieved by promoting ionic conduction and increasing optical path length through multiple-light scattering within the photovoltaic devices. In LCs, it is well known that the length of the alkyl chain plays an important role since the LC morphology and mesophase stabilisation depend strongly on the alkyl group. In this work, liquid crystal-polymer composite electrolytes (LC-PEs) are prepared using nematic LCs with different alkyl chain lengths. The morphology of the LC-PEs is investigated and correlated with their electrical properties. Subsequently, DSSCs are prepared using the LC-PEs as a direct example of its application. It is shown that increasing the alkyl chain length of the LCs reduces the efficiency of the solar devices. The longer alkyl chains are speculated to intertwine, thus trapping the mobile ions and reducing the bulk ionic conductivity. For the same reason, longer alkyl chain LCs are thought to be unable to passivate the TiO2 surface through the adsorption of cyanobiphenyl groups and hence the higher probability of back recombination reaction between the electrons in TiO2 and PE. 相似文献
189.
Structure and Bonding in CE5− (E=Al–Tl) Clusters: Planar Tetracoordinate Carbon versus Pentacoordinate Carbon
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Estefanía Ravell Said Jalife Jorge Barroso Mesías Orozco‐Ic Gerardo Hernández‐Juárez Dr. Filiberto Ortiz‐Chi Dr. Sudip Pan Dr. José Luis Cabellos Prof. Gabriel Merino 《化学:亚洲杂志》2018,13(11):1467-1473
The structure, bonding, and stability of clusters with the empirical formula CE5? (E=Al–Tl) have been analyzed by means of high‐level computations. The results indicate that, whereas aluminum and gallium clusters have C2v structures with a planar tetracoordinate carbon (ptC), their heavier homologues prefer three‐dimensional C4v forms with a pentacoordinate carbon center over the ptC one. The reason for such a preference is a delicate balance between the interaction energy of the fifth E atom with CE4 and the distortion energy. Moreover, bonding analysis shows that the ptC systems can be better described as CE4?, with 17‐valence electrons interacting with E. The ptC core in these systems exhibits double aromatic (both σ and π) behavior, but the σ contribution is dominating. 相似文献
190.
R. Trabelsi Shaik Babu H. Salhi N. Ouerfelli A. Toumi 《Physics and Chemistry of Liquids》2018,56(6):801-815
Excess molar volumes and refractive index, molar refraction deviations and isentropic compressibility changes in 1,4-dioxane + isobutyric acid binary mixtures (from 295.15 to 313.15) K. were calculated from experimental density, refractive index and sound velocity data presented in previous work. Here, these experimental values were used to test the applicability of the correlative reduced Redlich–Kister equation as well as their corresponding relative functions which are important to reduce the effect of temperature and, consequently, to reveal the effects of different types of interactions. The results of these observations have been interpreted in terms of structural effects of the solvents. The correlating equation recently proposed by Belda, has also been applied to the present system in order to assess the validity of this equation and to give thermodynamic limiting partial molar quantities interesting to evaluate solute–solvent interaction. 相似文献