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281.
In Tucker3 analysis of three-way data array obtained from a chemical or biological system, it is sometimes possible to use a priori knowledge about the system to specify what is called a restricted Tucker3 model. Often, the restricted Tucker3 model is characterized by having some elements of the core forced to zero. As a simple example, an F-component PARAFAC model can be seen as a restricted (F, F, F) Tucker3 model in which only superdiagonal elements of the core are allowed to be nonzero. The core consistency diagnostic was previously introduced by Bro and Kiers for determining the proper number of components in PARAFAC analysis. In the current study, this diagnostic is extended to other restricted Tucker3 models to validate the appropriateness of the applied constraints. The new diagnostic is named Tucker core consistency (TuckCorCon). When the dimensionality and the pattern of the restricted core is valid, the simple core of restricted Tucker3 model and a corresponding unrestricted core will be similar and in this case the TuckCorCon will be close to maximum (100%). A simulated chemical equilibrium data set and two experimental data sets were used to evaluate the applicability of the TuckCorCon to decide about the appropriateness of dimensionality and pattern of the core nonzero elements in the restricted Tucker3 models.  相似文献   
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Determining the relative configuration or enantiomeric excess of a substance may be achieved using NMR spectroscopy by employing chiral shift reagents (CSRs). Such reagents interact noncovalently with the chiral solute, resulting in each chiral form experiencing different magnetic anisotropy; this is then reflected in their NMR spectra. The Keplerate polyoxometalate (POM) is a molybdenum-based, water-soluble, discrete inorganic structure with a pore-accessible inner cavity, decorated by differentiable ligands. Through ligand exchange from the self-assembled nanostructure, a set of chiral Keplerate host molecules has been synthesised. By exploiting the interactions of analyte molecules at the surface pores, the relative configuration of chiral amino alcohol guests (phenylalaninol and 2-amino-1-phenylethanol) in aqueous solvent was establish and their enantiomeric excess was determined by 1H NMR using shifts of ΔΔδ=0.06 ppm. The use of POMs as chiral shift reagents represents an application of a class that is yet to be well established and opens avenues into aqueous host-guest chemistry with self-assembled recognition agents.  相似文献   
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Two classes of aminomethyl polystyrene resin-bound linkers of p-acetoxybenzyl alcohol were subjected to reactions with 2-cyanoethyl N,N-diisopropylchlorophosphoramidite to produce the corresponding polymer-bound phosphitylating reagents. These were reacted with a number of unprotected nucleosides and carbohydrates in the presence of 1H-tetrazole. Oxidation with tert-butyl hydroperoxide followed by removal of the cyanoethoxy group with 1,8-diazabicyclo[5.4.0]undec-7-ene afforded the corresponding polymer-bound phosphate diesters. Acidic cleavage of the p-acetoxybenzyl alcohol linker yielded monophosphorylated products with high regioselectivity and trapped linkers on the resins that can be reused.  相似文献   
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This paper gives new sufficient conditions for the density ofthe set of norm attaining multilinear forms in the space ofall continuous multilinear forms on a Banach space. The symmetriccase is also discussed.  相似文献   
288.
State-of-the-art petawatt laser beams may be focused down to few-micron spot sizes and can produce violent electron acceleration as a result of the extremely intense and asymmetric fields. Classical fifth-order calculations in the diffraction angle show that electrons, injected sideways into the tightly focused laser beam, get captured and gain energy in the GeV regime. We point out the most favorable points of injection away from the focus, along with an efficient means of extracting the energetic electron with a static magnetic field.  相似文献   
289.
Within the context of Barut's self-field approach to quantum electrodynamics, we show that the exact relativistic expression for the Einstein A-coefficient of atomic spontaneous emission reduces, in the long wavelength approximation, to a form containing electric- and magnetic-like multipole contributions related to the transition charge and current distributions of the relativistic electron. A number of interesting features of the expressions involved are discussed, and their generalization to interacting composite systems is also pointed out.Dedicated to Prof. A. O. Barut, teacher and friend, on the occasion of his 65th birthday. I only hope it measures up to the man being honored.  相似文献   
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The electrocatalytic oxidation of glucose was investigated on a nickel-basedchemically modified electrode (Ni(II)-curcumin) prepared by electropolymerization of Ni-curcumin complex (curcumin=1,7-bis[4-hydroxy-3-methoxyphenyl]-1,6-heptadiene-3,5-dione) in alkaline solution. Reaction kinetic and mechanism were investigated by using cyclic voltammetry (CV) and chronoamperometry (CA) techniques and steady-state polarization measurements. Cyclic voltammetry studies indicated that in the presence of glucose the anodic peak current of surface redox mediator was increased, followed by decrease in the corresponding cathodic current. This indicates that glucose was oxidized at the surface of this modified electrode. The results were explained based on the concept of electrocatalytic reactions that occur in this chemically modified electrode. The diffusion coefficient of glucose and the rate constant of the catalytic oxidation of glucose were found to be 6.7×10−6 cm2 s−1 and 6.5×103 M−1 s−1, respectively. It has shown that by using the Ni-curcumin modified electrode, glucose can be determined with good response and low detection limit.  相似文献   
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