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31.
M. A. Ahmed El Sayed Yousef M. F. Abdel-Messih 《Journal of Sol-Gel Science and Technology》2011,60(1):58-65
Nanocomposite samples containing various molar compositions of tin and titanium oxides were synthesized by a sol–gel method
using octadecylamine as controlling template agent. The structural and the crystalline features of the samples were investigated
with Fourier Transformer Infra-red, X-ray diffraction, Transmission electron microscope (TEM) where the surface area was estimated
by BET analysis. The crystalline parameters and the particle size were estimated by Rietveld quantitative phase analysis.
It is interesting to mention that a reduction in the lattice parameters was detected upon introduction of various molar compositions
of titanium oxide revealing that a part of titania is incorporated into the SnO2 lattice forming Ti1−xSnxO2 solid solution. The quantitative analysis claims that part of titanium oxide is incorporated substitutionally in the crystal
lattice of SnO2, forming a solid solution and other parts are either segregated as separate rutile titania phase or dispersed as amorphous
phase on the grain boundary of SnO2. The results show a remarkable reduction in particle size from 42 to 5 nm and increasing in the specific surface area up
to 176 m2/g upon introduction of various content of titania implying the role of titania particles in preventing SnO2 crystallites from further growing up during the progress of calcination. TEM images show that pure tin oxide particles arranged
in large aggregation in wormhole like structure, while the existence of titanium oxide are successfully creates spherical
nanoparticles system organized in a definite structure. The optical absorbance spectra indicate a red shift and band gap narrowing
upon introduction of titania which increase with increasing in titania contents. 相似文献
32.
Bani-Jaber AK Alkawareek MY Al-Gousous JJ Abu Helwa AY 《Chemical & pharmaceutical bulletin》2011,59(2):155-160
The aim of this study was to evaluate the influence of Na-bicarbonate as an effervescent agent on the floating and sustained-release characteristics in 0.1 M HCl of tablets made of Eudragit E PO (EE) and/or Eudragit L-100-55 (EL) as matrix formers at different EE:EL weight ratios: 0:100, 25:75, 50:50, 75:25, and 100:0. The tablets were made by direct compression utilizing metronidazole as a model drug. Effervescent tablets with 50EE/50EL (w/w) showed the best floating and sustained drug release properties in the dissolution medium. The corresponding noneffervescent tablets were nonfloating and showed significantly faster drug release. Effervescent tablets with single polymers showed an immediate drug release pattern. These results were explained by Fourier-transform infrared spectroscopy and elemental analysis, which showed strong evidence of interpolyelectrolyte complexation between EE and EL when they were exposed to 0.1 M HCl as an effervescent hybrid matrix, but not as a noneffervescent hybrid matrix. The role of Na-bicarbonate in allowing EE-EL complexation during dissolution was explained as due to raising the pH around EL particles for sufficient polymer ionization and ionic-interaction with the ionized EE. 相似文献
33.
Seyyed Mojtaba Mousavi Seyyed Alireza Hashemi Masoomeh Yari Kalashgrani Ahmad Gholami Yousef Mazaheri Mohsen Riazi Darwin Kurniawan Mohammad Arjmand O. Madkhali Mahmood D. Aljabri Mohammed M. Rahman Wei-Hung Chiang 《Chemical record (New York, N.Y.)》2024,24(1):e202200266
The ever-growing demand of human society for clean and reliable energy sources spurred a substantial academic interest in exploring the potential of biological resources for developing energy generation and storage systems. As a result, alternative energy sources are needed in populous developing countries to compensate for energy deficits in an environmentally sustainable manner. This review aims to evaluate and summarize the recent progress in bio-based polymer composites (PCs) for energy generation and storage. The articulated review provides an overview of energy storage systems, e. g., supercapacitors and batteries, and discusses the future possibilities of various solar cells (SCs), using both past research progress and possible future developments as a basis for discussion. These studies examine systematic and sequential advances in different generations of SCs. Developing novel PCs that are efficient, stable, and cost-effective is of utmost importance. In addition, the current state of high-performance equipment for each of the technologies is evaluated in detail. We also discuss the prospects, future trends, and opportunities regarding using bioresources for energy generation and storage, as well as the development of low-cost and efficient PCs for SCs. 相似文献
34.
Rushdi I. Yousef Tobias Rüffer Harry Schmidt Dirk Steinborn 《Journal of organometallic chemistry》2005,690(5):1178-1191
MgMe2 (1) was found to react with 1,4-diazabicyclo[2.2.2]octane (dabco) in tetrahydrofuran (thf) yielding a binuclear complex [{MgMe2(thf)}2(μ-dabco)] (2). Furthermore, from reactions of MgMeBr with diglyme (diethylene glycol dimethyl ether), NEt3, and tmeda (N,N,N′,N′-tetramethylethylenediamine) in etheral solvents compounds MgMeBr(L), (L = diglyme (5); NEt3 (6); tmeda (7)) were obtained as highly air- and moisture-sensitive white powders. From a thf solution of 7 crystals of [MgMeBr(thf)(tmeda)] (8) were obtained. Reactions of MgMeBr with pmdta (N,N,N′,N″,N″-pentamethyldiethylenetriamine) in thf resulted in formation of [MgMeBr(pmdta)] (9) in nearly quantitative yield. On the other hand, the same reaction in diethyl ether gave MgMeBr(pmdta) · MgBr2(pmdta) (10) and [{MgMe2(pmdta)}7{MgMeBr(pmdta)}] (11) in 24% and 2% yield, respectively, as well as [MgMe2(pmdta)] (12) as colorless needle-like crystals in about 26% yield. The synthesized methylmagnesium compounds were characterized by microanalysis and 1H and 13C NMR spectroscopy. The coordination-induced shifts of the 1H and 13C nuclei of the ligands are small; the largest ones were found in the tmeda and pmdta complexes. Single-crystal X-ray diffraction analyses revealed in 2 a tetrahedral environment of the Mg atoms with a bridging dabco ligand and in 8 a trigonal-bipyramidal coordination of the Mg atom. The single-crystal X-ray diffraction analyses of [MgMe2(pmdta)] (12) and [MgBr2(pmdta)] (13) showed them to be monomeric with five-coordinate Mg atoms. The square-pyramidal coordination polyhedra are built up of three N and two C atoms in 12 and three N and two Br atoms in 13. The apical positions are occupied by methyl and bromo ligands, respectively. Temperature-dependent 1H NMR spectroscopic measurements (from 27 to −80 °C) of methylmagnesium bromide complexes MgMeBr(L) (L = thf (4); diglyme (5); NEt3 (6); tmeda (7)) in thf-d8 solutions indicated that the deeper the temperature the more the Schlenk equilibria are shifted to the dimethylmagnesium/dibromomagnesium species. Furthermore, at −80 °C the dimethylmagnesium compounds are predominant in the solutions of Grignard compounds 4-6 whereas in the case of the tmeda complex7 the equilibrium constant was roughly estimated to be 0.25. In contrast, [MgMeBr(pmdta)] (9) in thf-d8 revealed no dismutation into [MgMe2(pmdta)] (12) and [MgBr2(pmdta)] (13) even up to −100 °C. In accordance with this unexpected behavior, 1:1 mixtures of 12 and 13 were found to react in thf at room temperature yielding quantitatively the corresponding Grignard compound 9. Moreover, the structures of [MgMeBr(pmdta)] (9c), [MgMe2(pmdta)] (12c), and [MgBr2(pmdta)] (13c) were calculated on the DFT level of theory. The calculated structures 12c and 13c are in a good agreement with the experimentally observed structures 12 and 13. The equilibrium constant of the Schlenk equilibrium (2 9c ? 12c + 13c) was calculated to be Kgas = 2.0 × 10−3 (298 K) in the gas phase. Considering the solvent effects of both thf and diethyl ether using a polarized continuum model (PCM) the corresponding equilibrium constants were calculated to be Kthf = 1.2 × 10−3 and Kether = 3.2 × 10−3 (298 K), respectively. 相似文献
35.
36.
Polycrystalline ferrites with general formula Co0.5CdxFe2.5−xO4 (0.0?x?0.5) were prepared by sol-gel method. The dielectric properties ε′, ε″, loss tangent tan δ and ac conductivity σac have been studied as a function of frequency, temperature and composition. The experimental results indicate that ε′, ε″, tan δ and σac decrease as the frequency increases; whereas they increase as the temperature increases. These parameters are found to increase by increasing the concentration of Cd content up to x=0.2, after which they start to decrease with further increase in concentration of Cd ion. The dielectric properties and ac conductivity in studied samples have been explained on the basis of space charge polarization according to Maxwell and Wagner's two-layer model and the hoping between adjacent Fe2+ and Fe3+ as well as the hole hopping between Co3+and Co2+ ions at B-sites. The values of activation energies Ef for conduction process are determined from Arrhenius plots, and the variations in these activation energies as a function of Cd content are discussed. The complex impedance analysis is used to separate the grain and grain boundary of the system Co0.5CdxFe2.5−xO4. The variations of both grain boundary and grain resistances with temperature and composition are evaluated in the frequency range 42 Hz-5 MHz. 相似文献
37.
A total cover of a graph G is a subset of V(G)E(G) which covers all elements of V(G)E(G). The total covering number 2(G) of a graph G is the minimum cardinality of a total cover in G. In [1], it is proven that 2(G)[n/2] for a connected graph G of order n. Here we consider the extremal case and give some properties of connected graphs which have a total covering number [n/2]. We prove that such a graph with even order has a 1-factor and such a graph with odd order is factor-critical. 相似文献
38.
39.
Thomas Kappe Yousef Ravai Wolfgang Stadlbauer 《Monatshefte für Chemie / Chemical Monthly》1983,114(2):227-241
Tricyclic pyrimidine betaines2, which are obtained from the reaction of 2-anilino quinolines (4) and 2,4,6-trichlorophenyl malonates (3) rearrange at temperatures above 200°Cvia ketene intermediates. Formation of either the ketene11 or the acylketene16 depends upon the reaction medium (2,4,6-trichlorophenol or diphenyl ether as solvent). The structures of the resulting rearranged products6 or7, resp., were established in the case of the pyrimido[3,4-a]quinoline7 by an independent synthesis, and for the 4-hydroxy-2-quinolone6 by degradation to the quinazolone19. 相似文献
40.
Timberlake GT Yousef AL Chiles SR Moses RA Givens RS 《Photochemistry and photobiology》2005,81(5):1180-1185
Photoactivated bis-diazopyruvamide-N,N'-bis(3-diazopyruvoyl)-2,2'-(ethylenedioxy)bis-(ethylamine), (DPD)-was previously shown to bond materials containing type I collagen. However, tensile strength of bonded collagenous tissue ( approximately 78% water) was low compared with that of dehydrated collagenous gelatin ( approximately 14% water). Here we investigated the role of water in corneal tissue bond strength and in bonding corneal tissue to glass. Bonding corneal tissue to glass may be of value in surgically anchoring keratoprostheses to corneas to alleviate problems with extrusion. Bovine corneal samples were lyophilized for various times resulting in tissue hydrations of zero (no water content) to approximately 3.7 (normal water content). The lyophilized corneal tissue was bonded to solid gelatin sheets, to other corneal samples and to glass using 0.3M DPD in chloroform. Control runs used chloroform only. Samples were irradiated with 100 or 200 J of 320-500 nm light. Strong bonds formed with all three materials when corneal tissue hydration was =1. No bonds or extremely weak bonds formed when tissue hydration levels were >1. No bonding occurred with chloroform alone. Formation of strong bonds only occurs with hydration levels =1 because corneal collagen fibrils are tightly packed and close enough to cross-link with the 1.78 nm long DPD. 相似文献