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541.
Orthotropic bone remodeling: case of plane stresses 总被引:1,自引:0,他引:1
Cancellous bone is constituted by a porous solid matrix filled with fluid. Matrix microstructure gives bone most of its mechanical strength properties. In our macroscopic approach, bone is seen as a continuous medium with a local (at our scale) time-dependent linearly elastic orthotropic behavior. Remodeling consists, by matrix material apposition or resorption, in microstructure modifications in order to optimize its mechanical characteristics. The proposed model is built on a time iterative procedure where the compliance tensor evolves such that, depending on the applied stresses, principal strains tend to fall within an admissible domain. The suggested remodeling laws in this work modify the elasticity “constants” as well as the orthotropy directions. The first results presented here correspond to the plane stresses case. 相似文献
542.
The study of fluid flow in a duct requires characteristic parameters of the flow and dimensionless numbers to correlate and compare experimental results. For Newtonian fluids in simple configurations, the definition of the Reynolds number is quite standard, but for non-Newtonian fluid flows in ducts with arbitrary shape of cross section, the dependence of the apparent viscosity with the shear rate requires a generalization of this dimensionless number. This note proposes a general method valid for a large class of non-Newtonian fluids and for all duct shapes. An application is developed for a viscoelastic flow through a rectangular duct. Results obtained in the present investigation are in a good agreement with available correlations. To cite this article: M. Mahfoud et al., C. R. Mecanique 333 (2005). 相似文献
543.
Organophosphates have been widely used in agrochemistry, as reagents for organic synthesis, and in biochemistry. Phosphate mimics possessing four unique substituents, and thereby a chirality center, are useful in transition metal catalysis and as nucleotide therapeutics. The catalytic, stereocontrolled synthesis of phosphorus-stereogenic centers is challenging and traditionally depends on a resolution or use of stochiometric auxiliaries. Herein, enantioenriched phosphorus centers have been synthesized using chiral nucleophilic catalysis. Racemic H-phosphinate species were coupled with nucleophilic alcohols under halogenating conditions. Chiral phosphonate products were synthesized in acceptable yields (33–95%) and modest enantioselectivity (up to 62% ee) was observed after identification of an appropriate chiral catalyst and optimization of the solvent, base, and temperature. Nucleophilic catalysis has a tremendous potential to produce enantioenriched phosphate mimics that could be used as prodrugs or chemical biology probes. 相似文献
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545.
In this work we prove some existence and uniqueness results for pseudo-almost periodic and pseudo-almost automorphic solutions to a class of semi-linear differential equations in Hilbert spaces using theoretical measure theory. The main technique is based upon some appropriate composition theorems combined with the Banach contraction mapping principle and the method of the invariant subspaces for unbounded linear operators. A few illustrative examples will be discussed at the end of the paper. 相似文献
546.
Akila Benmachiche Saber‐Mustapha Zendaoui Salah‐Eddine Bouaoud Bachir Zouchoune 《International journal of quantum chemistry》2013,113(7):985-996
The geometric parameters, electronic structures, and haptotropic migration of a series of hypothetical compounds of general formula CpM(C13H9N) and (CO)3M(C13H9N) (M = fist row transition metal, Cp = C5H5, and C13H9N = phenanthridine ligand) are investigated by means of the density functional theory. The phenanthridine ligand can bind to the metal through η1 to η6 coordination mode, in agreement with the electron count and the nature of the metal, showing its capability to adapt itself to the electronic demand of the metal as well as to the polycyclic aromatic hydrocarbons. In the investigated species, the most favored closed‐shell count is 18‐electron except for the Ti and V models which are deficient open‐shell 16‐electron configuration. This study has shown the difference in coordination ability of this heteropolycyclic ligand: the coordination of the central C5N ring is less favored than the terminal C6 rings, in agreement with the π‐electron density localization. Most of the investigated complexes are expected to exhibit a rich fluxional behavior. This flexibility favors the possibility for the existence of several isomers as well as their interconversion through haptotropic shifts. © 2012 Wiley Periodicals, Inc. 相似文献
547.
Amin F. Fahmy Jürgen Sauer Mohamed Salah K.Youssef Mohamed Said AbdelHalim Mamdouh A. Hassan 《合成通讯》2013,43(15):2871-2886
N-Hydroxyquinolinimide 1 reacts with each of aromatic amines, hydrazine hydrate and aromatic hydrocarbons to give arylcarbamoyl pyridines 2, pyrrolopyridines 3, pyridopyridazines 4 and pyridooxazinones 5 and 6. The heterocycles 5 and 6 can be transformed to the condensed systems, triazolopyridopyridazines 14 and 15 through series of reactions. 相似文献
548.
An analytical method is described for the analysis of furosemide, [4-chloro-2-furfurylamino-5-sulfamoylbenzoic acid], using PMR. The procedure reported in this study is simple, rapid and gives accurate results 98.19 ± 1.34% and 99.23 ± 0.88% for furosemide ampoules and tablets respectively. Furthermore, the PMR spectrum obtained provides a mean for qualitative identification of the drug and checking its purity. 相似文献
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550.