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111.
112.
Ricardo ABREU-BLAYA Juan BORY-REYES Fred BRACKX Hennie DE SCHEPPER Frank SOMMEN 《数学学报(英文版)》2012,(11)
A Hilbert transform for Hlder continuous circulant (2 × 2) matrix functions, on the d-summable (or fractal) boundary Γ of a Jordan domain Ω in R2n , has recently been introduced within the framework of Hermitean Clifford analysis. The main goal of the present paper is to estimate the Hlder norm of this Hermitean Hilbert transform. The expression for the upper bound of this norm is given in terms of the Hlder exponents, the diameter of Γ and a specific d-sum (d d) of the Whitney decomposition of Ω. The result is shown to include the case of a more standard Hilbert transform for domains with left Ahlfors-David regular boundary. 相似文献
113.
Miguel A. Harvey María E. Díaz de Vivar Ricardo Baggio Sergio Baggio 《Journal of chemical crystallography》2011,41(11):1717-1721
Abstract
The title compound is monomeric with a Zn(II) hexacoordinated center. The coordination sphere is formed by four nitrogens from two phenanthroline molecules, one oxygen from a monodentate peroxodisulfate ion, and one oxygen from a water molecule. A non-coordinated water molecule completes the formula with an important role in the stabilization of the structure through the formation of two OHW–H···Opds bridges (acting as a donor) and one OCW–H···OHW bridge where it is an acceptor group (HW: hydration water; pds: peroxodisulfato; CW: coordinated water). The compound is triclinic, space group P-1 with a = 8.763 (3) ?, b = 9.068 (3) ?, c = 17.531 (6) ?, α = 96.48 (2)°, β = 103.94 (3)°, γ = 104.57 (3)°, V = 1286.0 (7) ?3 and Z = 2. The structure was solved by direct methods with a conventional R (on F) = 0.050 for 4534 reflections with Fo > 4σ(Fo). The compound is isomorphous with the Cd analogue (in Harvey et al. Aust J Chem 54:307, 2001). An eventual dependence of conformation and coordination mode of the peroxodisulfate anion on the ancillary organic ligand taking part in the coordination compounds analyzed is discussed. 相似文献114.
One of the most common environmental impacts of road transportation is the traffic noise. Linked to this, Start/Stop is a technology which has demonstrated to save fuel by powering off the engine when the vehicle is stopped, such as in front of a traffic light, and restarting the engine instantly when the driver pushes back the pedal brake to proceed. The technology helps also to reduce the CO2 emission, playing a key role in a way to accomplish stringent emission norms for vehicle manufacturer. However, we are not sure whether it reduces the noise emission and how much? Thus, the main aim of this work is to assess the engine noise emissions of a vehicle incorporating a Start/Stop system in urban traffic, and compare it with those radiated by the mean traffic stream. Experimental results demonstrate that there are no contributions of the Start/Stop system to reduce meaningfully the engine noise in urban traffic. 相似文献
115.
116.
Heloisa Beraldo Ricardo F. F. da Costa Rejane Lima Geraldo M. de Lima Ivana S. Lula Bernard Mahieu 《Phosphorus, sulfur, and silicon and the related elements》2013,188(10):2455-2463
The reaction of tin(IV) tetrachloride with 3-formylpyridine semicarbazone and different 3-formylpyridine thiosemicarbazones produces [Sn(HL)CL 3 ][SnCl 5 ] where HL stands for the neutral ligand. The tin(IV) complexes were characterized using a variety of spectroscopic techniques. Coordination through the pyridine nitrogen occurs in all cases. Solvation studies in DMSO indicated that dissociation of the ligands and their complete replacement by solvent molecules occurs. 相似文献
117.
Ray L. Frost Yunfei Xi Ricardo Scholz Andrés López Fernanda M. Belotti Mário L. S. C. Chaves 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):1526-1534
Abstract The metal lithium is very important in industry, including lithium batteries. An important source of lithium besides continental brines is granitic pegmatites as in Australia. Lithiophilite is a lithium and manganese phosphate with chemical formula LiMnPO4 and forms a solid solution with triphylite, its Fe analog, and belongs to the triphylite group that includes karenwebberite, natrophilite, and sicklerite. The mineral lithiophilite was characterized by chemical analysis and spectroscopic techniques. The chemical is: Li1.01(Mn0.60, Fe0.41, Mg0.01, Ca0.01)(PO4)0.99 and corresponds to an intermediate member of the triphylite-lithiophilite series, with predominance of the lithiophilite member. The mineral lithiophilite is readily characterized by Raman and infrared spectroscopy. 相似文献
118.
Luis Alvarez Thon Carlos Bustos Fernando Diaz‐Marín Maria Teresa Garland Ricardo Baggio 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(1):101-104
The title compound, C17H10F5N5O2, is described and compared with its 4‐nitrophenyl isomer [Bustos, Sánchez, Schott, Alvarez‐Thon & Fuentealba (2007). Acta Cryst. E 63 , o1138–o1139]. The title molecule presents its nitro group split into two rotationally disordered components, which in conjunction with the rotation of the `unclamped' rings constitute the main molecular differences. Packing is directed by a head‐to‐tail type `I' C—F...F—C interaction, generating double‐chain strips running along [100]. These substructures are interlinked by a variety of weak F...F, O...F, F...π and O...π interactions. 相似文献
119.
Luis Alvarez‐Thon Carlos Bustos Katherina Espinoza‐Santibaez Maria Teresa Garland Ricardo Baggio 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(10):1200-1204
The title compound, C17H11F5N4O, is described and compared with two closely related analogues in the literature. There are two independent molecules in the asymmetric unit, linked by N—H...O hydrogen bonds and π–π interactions into dimeric entities, presenting a noticeable noncrystallographic C2 symmetry. These dimers are in turn linked by a medium‐strength type‐I C—F...F—C interaction into elongated tetramers. Much weaker C—H...F contacts link the tetramers into broad two‐dimensional substructures parallel to (101). 相似文献
120.
The self-assembly and bioactivity of the peptide–polymer conjugate DGRFFF–PEG3000 containing the RGD cell adhesion motif has been examined, in aqueous solution. The conjugate is designed to be amphiphilic by incorporation of three hydrophobic phenylalanine residues as well as the RGD unit and a short poly(ethylene glycol) (PEG) chain of molar mass 3000 kg mol−1. Above a critical aggregation concentration, determined by fluorescence measurements, signals of β-sheet structure are revealed by spectroscopic measurements, as well as X-ray diffraction. At high concentration, a self-assembled fibril nanostructure is revealed by electron microscopy. The fibrils are observed despite PEG crystallization which occurs on drying. This suggests that DGRFFF has an aggregation tendency that is sufficiently strong not to be prevented by PEG crystallization. The adhesion, viability and proliferation of human corneal fibroblasts was examined for films of the conjugate on tissue culture plates (TCPs) as well as low attachment plates. On TCP, DGRFFF–PEG3000 films prepared at sufficiently low concentration are viable, and cell proliferation is observed. However, on low attachment surfaces, neither cell adhesion nor proliferation was observed, indicating that the RGD motif was not available to enhance cell adhesion. This was ascribed to the core–shell architecture of the self-assembled fibrils with a peptide core surrounded by a PEG shell which hinders access to the RGD unit. 相似文献