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42.
43.
Natalia P. Kuzmina Dmitry M. Tsymbarenko Igor E. Korsakov Zoya A. Starikova Kostantin A. Lysenko Olga V. Boytsova Andrey V. Mironov Irina P. Malkerova Andrey S. Alikhanyan 《Polyhedron》2008
The novel mixed ligand complexes [Ca(hfa)2(diglyme)(H2O)] (I), [Sr(hfa)2(diglyme)(H2O)] (II) and [Ba(hfa)2(diglyme)2] (III) (Hhfa = 1,1,1,5,5,5-hexafluoropentane-2,4-dione, diglyme = 2,5,8-trioxanonane) were synthesized by the reactions of the alkaline earth element (AEE) carbonates in n-hexane with a mixture of Hhfa and diglyme, and they were characterized by elemental analysis, 1H and 13C NMR, and FTIR spectroscopy. The crystal structures of I–III, consisting of mononuclear isolated molecules, have been determined. The thermal behavior and composition of the vapor phase have been studied for I–III by thermal analysis at low pressure and mass spectrometry using a Knudsen cell. The stability of the mixed ligand complexes [M(hfa)2(diglyme)n] to the removal of diglyme molecules under heating decreases in the row I > II ≈ III, and only I evaporates as the mixed ligand complex after water removal. 相似文献
44.
Here, we report dielectric behaviour of lanthanum substituted Ba0.80Pb0.20Ti0.90Zr0.10O3 (BPZT) ceramics. The material series with compositional formula Ba0.80−xLaxPb0.20Ti0.90Zr0.10O3 (BLPZT) with x varying from 0 to 0.01 in the steps of 0.0025 was chosen for investigations. The material was synthesized by solid state reaction method. Reacted powder compacted in form of circular discs were sintered at 1325 °C. All the samples were subjected to X-ray diffraction (XRD) analysis and found to be single phase. Dielectric behaviour was studied as a function of frequency and temperature and Curie temperature (Tc) was determined. Tc was found to decrease with increasing x. The details are discussed and presented in this paper. 相似文献
45.
The calcium-substituted barium titanate ceramics were prepared by solid state reaction technique. High-energy ball-milling was used for processing the powder. The microstructure of Ba1−xCaxTiO3 ceramics was investigated by SEM techniques. The microstructure of Ba1−xCaxTiO3 ceramics shows dense and uniform micrograph in all samples and the grain size is large. In this study the quantitative analysis of the ceramographs is shown and the variation of the different parameters with various doping concentration is discussed. Compositional analysis is ascribed to the occupancy of some Ca2+ to the Ti4+ sites. 相似文献
46.
A previously proposed model describing the trapping site of the interstitial atomic hydrogen in borate glasses is analyzed. In this model the atomic hydrogen is stabilized at the centers of oxygen polygons belonging to B–O ring structures in the glass network by van der Waals forces. The previously reported atomic hydrogen isothermal decay experimental data are discussed in the light of this microscopic model. A coupled differential equation system of the observed decay kinetics was solved numerically using the Runge Kutta method. The experimental untrapping activation energy of 0.7×10−19 J is in good agreement with the calculated results of dispersion interaction between the stabilized atomic hydrogen and the neighboring oxygen atoms at the vertices of hexagonal ring structures. 相似文献
47.
48.
Coplanar Phase Shifters Based on Ferroelectric Thin Films 总被引:2,自引:0,他引:2
Chunlin Fu Fusheng Pan Hongwei Chen Shucheng Feng Wei Cai Chuanren Yang 《International Journal of Infrared and Millimeter Waves》2007,28(3):229-235
Barium strontium titanate (Ba0.6Sr0.4TiO3, short for BST) thin films were prepared by RF-magnetron sputtering. The dielectric tunability, loss tangent, remanent polarization
(2Pr) and coercive electric field (Ec) of the BST films are respectively 29.5%, 0.013, 2.29 μC/cm2 and 22.27 kV/cm at 1 kHz and 20 V. The designed coplanar waveguide (CPW) phase shifter consists of 56 same sections. It is
shown that the fabricated lines of electrodes are smooth and the widths at the tip of bottom electrodes are about 5 μm. At
the central frequency of 28 GHz and a bias voltage of 20 V, the figure of merit is approximately 13°/dB. 相似文献
49.
50.
The specificity of the exchange between divalent (Di2+ = Ca2+ or Ba2+) and monovalent (M+ = Li+, Na+ or K+) ions onto a polyacrylic chain is examined using conductometric and microcalorimetric techniques. Assuming the formation
of a bidentate complex between the Di2+ and the carboxylate groups, the conductometric data give the exchange ratio (Di2+/M+) and the speciation of the acrylic groups. No significant difference is observed between the three alkali-metal ions for
a given Di2+ ion. Comparisons between Ca2+ and Ba2+ show a stronger hydrophobicity of the former as it precipitates at a complexation ratio r = 0.33 versus r = 0.45 for the Ba2+ salt. Microcalorimetric data show that all Di2+/M+ exchange energies are positive and depend significantly on the type of cations. The largest displacement energy (the more
positive) is found for the binding of Ca2+ with sodium polyacrylate (8.13 kJ · mol−1) and the smallest for Ba2+ with lithium polyacrylate (1.88 kJ · mol−1). The interpretation of the data leads to the conclusion that specificity of the Di2+ binding originates in the dehydration phenomenon and specificity between the three alkali-metal ions is due to the decrease
in the electrostatic bond strength with an increase in the ionic radii. The Di2+/M+ exchange is entropically driven.
Received: 28 January 1999 Accepted in revised form: 7 April 1999 相似文献