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51.
We propose to create ultracold ground state molecules in an atomic Bose-Einstein condensate by adiabatic crossing of an optical Feshbach resonance. We envision a scheme where the laser intensity and possibly also frequency are linearly ramped over the resonance. Our calculations for (87)Rb show that for sufficiently tight traps it is possible to avoid spontaneous emission while retaining adiabaticity, and conversion efficiencies of up to 50% can be expected. 相似文献
52.
Patrick Le Barz 《Comptes Rendus Mathematique》2005,340(10):743-746
We give a general new algorithm to find formulas for the number of k-secant d-planes to a smooth curve in , for any k, d, N. Partial results were given by Castelnuovo [Rend. Palermo 3 (1889) 27–37] and Tanturri [Ann. Mat. 4 (1900) 67–122]. See also E. Arbarello et al. [Geometry of Algebraic Curves, vol. 1, Grundlehren Math. Wiss., vol. 267, Springer-Verlag, 1985]. To cite this article: P. Le Barz, C. R. Acad. Sci. Paris, Ser. I 340 (2005). 相似文献
53.
Christiane Becker Michael Hodenius Gitta Blendinger Antonio Sechi Thomas Hieronymus Detlef Müller-Schulte Thomas Schmitz-Rode Martin Zenke 《Journal of magnetism and magnetic materials》2007
A challenge for future applications in nanotechnology is the functional integration of nano-sized materials into cellular structures. Here we investigated superparamagnetic Fe3O4 iron oxide nanoparticles coated with a lipid bilayer for uptake into cells and for targeting subcellular compartments. It was found that magnetic nanoparticles (MNPs) are effectively taken up into cells and make cells acquire magnetic activity. Biotin-conjugated MNPs were further functionalized by binding of the fluorescent tag streptavidin–fluorescein isothiocyanate (FITC) and, following uptake into cells, shown to confer magnetic activity and fluorescence labeling. Such FITC-MNPs were localized in the lysosomal compartment of cells which suggests a receptor-mediated uptake mechanism. 相似文献
54.
Prélot B Poinsignon C Thomas F Schouller E Villiéras F 《Journal of colloid and interface science》2003,257(1):77-84
Relationships between lattice parameters of manganese dioxides and their surface properties at the solid-aqueous solution interface were investigated. The studied series ranged from ramsdellite to pyrolusite and encompassed disordered MD samples. The structural model used takes into account structural defects: Pr (rate of pyrolusite intergrowth) and Tw (rate of microtwinning). Water adsorption isotherms showed that the cross sectional area of water molecules adsorbed in the first monolayer is positively correlated to Pr. Titration of the surface charge of the MD series evidenced a positive linear relationship between the PZC and Pr (Pr=0, Tw=0, PZC=1 for ramsdellite; Pr=1, Tw=0, PZC=7.3 for pyrolusite; gamma-MD with intermediate values of Pr (0.2 to 0.45) have increasing PZC values). The rate of microtwinning appeared as a secondary factor for the increase of the PZC. The above correlations are explained by the chemical defects at the origin of the structural disorder, respectively Mn(3+)/Mn4+ substitution for Pr and Mn vacancies for Tw, which result in proton affinity and thus in increased PZC. The experimental results are compared with data collected in the literature for manganese dioxides as well as for dioxides of transition elements with tetragonal structure. 相似文献
55.
Tournassat C Ferrage E Poinsignon C Charlet L 《Journal of colloid and interface science》2004,273(1):234-246
The potentiometric titration and CEC data presented in part I are modeled in this paper, part II. Two models are compared: the two pK, three complexation sites plus exchange sites nonelectrostatic model developed by Baeyens and Bradbury and a model based on the MUSIC approach developed by Hiemstra and Van Riemsdijk. Both morphological and structural information is used to develop this new model. Morphological information is taken from the literature, while structural information is taken from the literature and constrained by supporting FTIR experiments. The Baeyens and Bradbury model is found to reproduce the general tendency of the titration curve, whereas the model based on the Hiemstra and Van Riemsdijk MUSIC approach provides a better fit to the experimental data. The former uses only 3 edge reaction sites, whereas the latter uses at least 27 edge reaction sites. Five main reactive sites are sufficient to fit the MUSIC model curve, but the model allows us to derive the properties of 22 other reactive sites. Logically, the greater the number of sites, the better the fit. Nevertheless, fewer adjustable parameters are necessary for the Hiemstra and Van Riemsdijk MUSIC model than for the Baeyens and Bradbury model, thanks to structural and morphological constraints. The precision of the potentiometric titration curve is insufficient to verify that the properties of the 27 sites given by the MUSIC model are effective. Thus, we coupled some properties of clay minerals, such as dissolution, to the modeled acid-base properties of these sites to assess our model. We then questioned the ability of simplified models such as the Baeyens and Bradbury model to predict the interactions between clay minerals and solutions in natural environments. In addition, we derived the cation exchange selectivity coefficients for CaCl+ ionic pairs and H+ from our CEC data and gave an estimate for the CaOH+ selectivity coefficient. 相似文献
56.
Christiane Tretter 《Integral Equations and Operator Theory》1996,26(2):222-248
We study nonselfadjoint spectral problems for ordinary differential equationsN(y)–P(y)=0 with -linear boundary conditions where the orderp of the differential operatorP is less than the ordern ofN. The present paper addresses the question of the completeness of the eigenfunctions and associated functions in the Sobolev spacesW
2
k
(0,1) fork=0,1,...,n. To this end we associate a pencil
– of operators acting fromL
2(0,1) to the larger spaceL
2x(0,1)
n
with the given problem. We establish completeness results for normal problems in certain finite codimensional subspaces ofW
2
k
(0,1) which are characterized by means of Jordan chains in 0 of the adjoint of the compact operator
=
–1.Dedicated to Professor Heinz Langer on the occasion of his 60th birthday 相似文献
57.
Hofmann CC Lindner SM Ruppert M Hirsch A Haque SA Thelakkat M Köhler J 《Physical chemistry chemical physics : PCCP》2010,12(43):14485-14491
A flexible organic triad consisting of two perylene bisimide antennas covalently linked to a [60]fullerene by flexible spacers has been synthesized and studied by electrochemistry, steady-state and time-resolved spectroscopy. We found that π-π-stacking of the two antenna subunits has considerable impact on the photophysics of the system and leads to a reduction of the effective light-harvesting efficiency of the assembly. This finding is important for light harvesting in flexible materials based on the dye antenna-fullerene concept. 相似文献
58.
O'Dea AR Curtis AF Green NJ Timmel CR Hore PJ 《The journal of physical chemistry. A》2005,109(5):869-873
Monte Carlo simulations of the effects of weak magnetic fields on the recombination of interacting radical pairs undergoing free diffusion in solution have been performed, with the aim of determining the influence on the low field effect of the magnetic dipolar coupling between the radicals. The suppression of singlet-triplet interconversion in the radical pair by the dipolar interaction is found to be pronounced at magnetic field strengths comparable to the hyperfine interactions in the radicals, to the extent that the low field effect is completely abolished. The averaging of the dipolar coupling by the translational diffusion of the radicals around one another is relatively efficient in the presence of strong magnetic fields but becomes ineffective in weak applied fields where the strength of the dipolar interaction is independent of the orientation of the inter-radical vector. Low field effects are only likely to be observed if the motion of the radical pair is restricted in some way so as to increase the likelihood that, having separated to the large distance required for the dipolar interaction to have a negligible effect, the radicals subsequently encounter and have the opportunity to recombine. 相似文献
59.
Stefan Eibl Andrew Fitch Michela Brunelli Alexander Dominic Evans Philip Pattison Marie Plazanet Mark Robert Johnson Christiane Alba‐Simionesco Helmut Schober 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(6):o278-o280
The title compound, C10H18, a decalin stereoisomer, crystallizes with Z′ = 0.5 in the space group P21/n. The trans‐decalin molecule is located on an inversion centre with both rings in a chair conformation, making for a quasi‐flat overall shape. Despite the absence of hydrogen bonds, it crystallizes easily. In this work the unknown crystal structure of trans‐decalin has been solved and refined using X‐ray powder diffraction data. 相似文献
60.