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131.
Borsacchi S Geppi M Veracini CA Lazzeri A Di Cuia F Geloni C 《Magnetic resonance in chemistry : MRC》2008,46(1):52-57
Silica-coated BaSO4 submicronic particles, modified on the surface by treatment with stearic acid, have been characterized by means of 29Si, 13C, and 1H magic-angle-spinning (MAS) high-resolution techniques, and low-resolution 1H-FID analysis. Two types of adsorbed water were identified; adsorbed either inside or on the surface of BaSO4, most of the latter being removed by the silica coating. Evidences of silica-stearic acid interactions were found involving either carboxylic acid or carboxylate functional groups, and occurring by means of hydrogen and/or covalent bonds. Stearic acid was present as monolayer only, its chain being mostly rigid, even though a small fraction was subjected to fast inter-conformational motions. 相似文献
132.
Effect of formulation of silica‐based solution on corrosion resistance of silicate coating on hot‐dip galvanized steel 下载免费PDF全文
Shuang‐hong Zhang Gang Kong Zi‐wen Sun Chun‐shan Che Jin‐tang Lu 《Surface and interface analysis : SIA》2016,48(3):132-138
Several silica‐based solutions with 50 g/l of SiO2 were prepared from sodium silicate solutions and silica sol; the silicate conversion coatings were obtained by immersing hot‐dip galvanized steel sheets in these solutions. These solutions were characterized using high‐resolution transmission electron microscopy and 29Si nuclear magnetic resonance; the morphology of the coatings was observed by SEM and atomic force microscopy while the corrosion resistance was evaluated by electrochemical measurements as well as neutral salt spray tests. The results show that the coatings obtained from the single silica sol solution had poor adhesion and the coating obtained from the sodium silicate solution with low SiO2/Na2O molar ratio was uneven. By adding the silica sol to the silicate solution with low molar ratio, uniform coatings with better protection property were obtained. According to the results of 29Si nuclear magnetic resonance spectra, the effects of the distribution of silicate anions with various polymerization degrees in the silica‐based solutions on the microstructure and corrosion resistance of the silicate coatings are discussed. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
133.
NMR studies on the reaction of bis[bis(tri-tert-butoxysilanethiolato)cadmium(II)] with 3,5-dimethylpyridine in benzene-d(6) and toluene-d(8) solutions provide clear evidence for the equilibrium character of formation of mixed S,N-ligand cadmium complex. 相似文献
134.
Let Ed(x) denote the “Euler polynomial” x2+x+(1−d)/4 if and x2−d if . Set Ω(n) to be the number of prime factors (counting multiplicity) of the positive integer n. The Ono invariantOnod of is defined to be except when d=−1,−3 in which case Onod is defined to be 1. Finally, let hd=hk denote the class number of K. In 2002 J. Cohen and J. Sonn conjectured that hd=3⇔Onod=3 and is a prime. They verified that the conjecture is true for p<1.5×107. Moreover, they proved that the conjecture holds for p>1017 assuming the extended Riemann Hypothesis. In this paper, we show that the conjecture holds for p?2.5×1013 by the aid of computer. And using a result of Bach, we also proved that the conjecture holds for p>2.5×1013 assuming the extended Riemann Hypothesis. In conclusion, we proved the conjecture is true assuming the extended Riemann Hypothesis. 相似文献
135.
A phosphorus-containing tri-ethoxysilane (dopo-icteos) reacting from the nucleophilic addition reaction of 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (dopo) and 3-(trieoxysilyl) isocyanate (icteos) was synthesized. The structure of dopo-icteos was confirmed by 1H, 13C, 31P NMR and IR spectra. A triethylamine catalyzed mechanism for the dopo-icteos synthesis was proposed and verified by NMR spectra. The phosphorus-containing epoxy/SiO2 and polyimide/SiO2 nanocomposites were prepared from the in-situ curing of diglycidyl ether of bisphenol A (DGEBA)/4,4-diaminodiphenylmethane(DDM)/dopo-icteos, and imidization of poly(amic acid) of pyromellitic dianhydride (PMDA)/4,4′-oxydianiline (ODA)/dopo-icteos, respectively. The microstructure and morphology were investigated by 29Si NMR, scanning electron microscope (SEM), EDS (Si and P mapping) analysis and atomic force microscope (AFM). The thermal properties, flame retardancy and dielectric properties of the organic-inorganic hybrids were investigated by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), limiting oxygen index (LOI), thermal gravimetric analysis (TGA) and dielectric analyzer (DEA). 相似文献
136.
The crystal structure of Nb22O54 is reported for the first time, and the structure of orthorhombic Nb12O29 is reexamined, resolving previous ambiguities. Single crystal X-ray and electron diffraction were employed. These compounds were found to crystallize in the space groups P2/m (, , , β=102.029(3)°) and Cmcm (, , ), respectively and share a common structural unit, a 4×3 block of corner sharing NbO6 octahedra. Despite different constraints imposed by symmetry these blocks are very similar in both compounds. Within a block, it is found that the niobium atoms are not located in the centers of the oxygen octahedra, but rather are displaced inward toward the center of the block forming an apparent antiferroelectric state. Bond valence sums and bond lengths do not show the presence of charge ordering, suggesting that all 4d electrons are delocalized in these compounds at the temperature studied, T=200 K. 相似文献
137.
Studies of interactions between silane coupling agents and cellulose fibers with liquid and solid-state NMR 总被引:1,自引:0,他引:1
Salon MC Gerbaud G Abdelmouleh M Bruzzese C Boufi S Belgacem MN 《Magnetic resonance in chemistry : MRC》2007,45(6):473-483
The hydrolysis of three alkoxy-silane coupling agents, gamma-methacryloxypropyl trimethoxy silane (MPS), gamma-aminopropyl triethoxy silane (APS), and gamma-diethylenetriaminopropyl trimethoxy silane (TAS), was carried out in ethanol/water solutions (80/20 w/w) at different pH values and followed by 1H, 13C and 29Si NMR spectroscopy. Acidic media were found to stabilize the hydrolyzed forms. As expected, the formation of silanol groups was followed by their self-condensation to generate oligomeric structures, yielding, ultimately, solid homopolycondensated structures, as analyzed by 29Si and 13C high-resolution solid-state NMR. Hydrolyzed MPS in acidic media was then successfully adsorbed onto a cellulose surface and the ensuing substrates submitted to thermal treatment at 110-120 degrees C under reduced pressure, in order to create covalent bonds between cellulose and the coupling agent. 相似文献
138.
在TMEDA(四甲基乙基二胺)-Na2O-SiO2-Al2O3-H2O体系(I),Na2O-K2O-Al2O3-SiO2-H2O-HCO3^--CO3^2^-体系(II)及Py(吡啶)-PrNH2(正丙胺)-HF-SiO2-H2O体系(III)中, 分别合成了纯相FER沸石及FER硅沸石。用粉末XRD, FT-IR, 29Si MAS NMR及TG/DTA等表征其结构性质, 并用超微量电子真空吸附天平测定这些沸石样品对正己烷, 甲醇和水的吸附等温线。结果表明: 各体系合成的样品虽然结晶度高, 呈现出FER沸石的典型结构特征, 但由于它们的组成和晶格微结构不同, 热稳定性与吸附性质有明显的差异。在(I)体系中合成的FER沸石层错缺陷少, 晶格完美, 正己烷与甲醇的吸附量可达到理论值, 结构破坏温度为1190℃。红外精细谱及29Si MAS NMR高分辨谱证明FER硅沸石具有十分完美的骨架结构。由于晶胞收缩, 它对正己烷与甲醇吸附量略低于理论值, 并呈现出高度的疏水性。它的结构破坏温度高于1300℃。在(II)体系中合成的FER型沸石结构缺陷多, 沸石孔中的钾离子不易被质子完全交换。它的正己烷与甲醇吸附量均较低, 而水的吸附量相对较高。吸附现象表明, 正己烷和甲醇都被吸附于FER沸石的十元环主孔道中, 分压较高时, 甲醇可通过八元环进入小笼, 而水的吸附性质则主要与各样品的Si-OH缺陷及骨架中的阳离子含量有关。 相似文献
139.
Patrick Cancouët Elodie Daudet Grard Hlary Michel Moreau Georges Sauvet 《Journal of polymer science. Part A, Polymer chemistry》2000,38(5):826-836
Poly(hydrogenmethylsiloxane‐co‐dimethylsiloxane)s of various compositions have been prepared by cationic ring‐opening polymerization of octamethylcyclotetrasiloxane (D4) and 1,3,5,7‐tetramethylcyclotetrasiloxane (D) in the presence of hexamethyldisiloxane as end‐blocker or by rearrangement of poly(hydrogenmethylsiloxane) in the presence of D4. These copolymers were examined by high resolution 1H NMR (500.13 MHz) and 29Si NMR (99.37 MHz) spectroscopies. Triad effects were observed by 1H and up to heptad effects by 29Si NMR. The chemical shifts were assigned for these stereosequences. The intensities of the triad signals were used to calculate the quantitative parameters describing the microstructure of the copolymer chains: number‐average block length (L̄) and persistence ratio (η). The values of these parameters for copolymers prepared in various experimental conditions show that the time necessary for redistribution reactions (backbiting) is much larger than the time required to establish the equilibrium between linear polymer and cyclic oligomers. However, redistribution is fast enough to prevent the formation of block copolymers even in the case of the rearrangement of poly(hydrogenmethylsiloxane) in the presence of D4. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 826–836, 2000 相似文献
140.
Lucyna Herczynska Julian Chojnowski Liliane Lacombe Laurence Lestel Stefan Polowinski Sylvie Boileau 《Journal of polymer science. Part A, Polymer chemistry》1998,36(1):137-145
Nonequilibrium anionic ring-opening copolymerization of 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane (V4) with hexamethylcyclotrisiloxane (D3) was examined as a route to methylvinyl–dimethylsiloxane microsequential copolymers. The copolymerization was carried out in toluene and was initiated with Me3SiCH2Li using DMSO as the promoter. Distribution of siloxane units obtained from kinetic analysis based on first-order Markovian statistics was compared with that found from analysis by 29Si NMR spectroscopy. Results showed that although chain transfer and back-biting play some role in this system, the kinetics of copolymerization may be described to a reasonable approximation by the first-order Markov model. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 137–145, 1998 相似文献