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41.
Lev?B.?Levitin Tom?ToffoliEmail author Zac?Walton 《International Journal of Theoretical Physics》2005,44(2):219-228
We consider a fixed quantum measurement performed over n identical copies of quantum states. Using a rigorous notion of distinguishability based on Shannon’s 12th theorem, we show that in the case of a single qubit, the number of distinguishable states is
, where (α1,α2) is the angle interval from which the states are chosen. In the general case of an N-dimensional Hilbert space and an area Ω of the domain on the unit sphere from which the states are chosen, the number of distinguishable states is
. The optimal distribution is uniform over the domain in Cartesian coordinates. 相似文献
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44.
This paper considers an aging multi‐state system, where the system failure rate varies with time. After any failure, maintenance is performed by an external repair team. Repair rate and cost of each repair are determined by a corresponding corrective maintenance contract with a repair team. The service market can provide different kinds of maintenance contracts to the system owner, which also can be changed after each specified time period. The owner of the system would like to determine a series of repair contracts during the system life cycle in order to minimize the total expected cost while satisfying the system availability. Operating cost, repair cost and penalty cost for system failures should be taken into account. The paper proposes a method for determining such optimal series of maintenance contracts. The method is based on the piecewise constant approximation for an increasing failure rate function in order to assess lower and upper bounds of the total expected cost and system availability by using Markov models. The genetic algorithm is used as the optimization technique. Numerical example is presented to illustrate the approach. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
45.
Ryzhkov LR 《The Journal of organic chemistry》1996,61(8):2801-2808
Thermal decomposition of a primary alkyl diacyl peroxide 2 is investigated. Dependence of product yields on temperature, viscosity, and solvent polarity is examined in a variety of media. The excess of the alkene disproportionation product 4 and the presence of ester 3 and acid 5 is argued to demonstrate the existence of a discrete acyloxy-alkyl geminate radical pair. Stereoselective deuterium labeling of 2 and subsequent (1)H-NMR analysis of the resulting isotopomers of 4 confirm the radical nature of detected decomposition products. 相似文献
46.
Lee Y Lee DH Sarjeant AA Zakharov LN Rheingold AL Karlin KD 《Inorganic chemistry》2006,45(25):10098-10107
To model thioether-copper coordination chemistry including oxidative reactivity, such as occurs in the copper monooxygenases peptidylglycine -hydroxylating monooxygenase (PHM) and dopamine beta-hydroxylase (DbetaH), we have synthesized new tridentate N2S ligands LSEP and LSBz [LSEP = methyl(2-phenethylsulfanylpropyl)(2-pyridin-2-ylethyl)amine; LSBz = (2-benzylsulfanylpropyl)methyl(2-pyridin-2-ylethyl)amine)]. Both copper(I) and copper(II) complexes have been prepared, and their respective O2 and H2O2 chemistry has been studied. Under mild conditions, oxygenation of [(LSEP)CuI]+ (1a) and [(LSBz)CuI]+ (2a) leads to ligand sulfoxidation, thus exhibiting copper monooxygenase activity. A copper(II) complex of this sulfoxide ligand product, [(LSOEP)CuII(CH3OH)(OClO3)2], has been structurally characterized, demonstrating Cu-Osulfoxide ligation. The X-ray structure of [(LSEP)CuII(H2O)(OClO3)]+ (1b) and its solution UV-visible spectral properties [S-CuII LMCT band at 365 nm (MeCN solvent); epsilon = 4285 M-1 cm-1] indicate the thioether sulfur atom is bound to the cupric ion in both the solid (CuII-S distance: 2.31 A) and solution states. Reaction of 1b with H2O2 leads to sulfonation via the sulfoxide; excess hydrogen peroxide gives mostly sulfone product. These results may provide some insight into recent reports concerning protein methionine oxidation, showing the potential importance of copper-mediated oxidation processes in certain biological settings. 相似文献
47.
Ignat'eva DV Goryunkov AA Tamm NB Ioffe IN Avdoshenko SM Sidorov LN Dimitrov A Kemnitz E Troyanov SI 《Chemical communications (Cambridge, England)》2006,(16):1778-1780
Two isomers of C70(CF3)12 have been isolated from a mixture obtained by trifluoromethylation of C70 with CF3I; their molecular structures determined by X-ray crystallography are in good agreement with the results of theoretical DFT calculations for the most stable C70(CF3)12 isomers. 相似文献
48.
The Incorporation of Titania into Modified Silicates for Solar Photodegradation of Aqueous Species 总被引:2,自引:0,他引:2
Lowell R. Matthews David Avnir Alexander D. Modestov Srinivasan Sampath Ovadia Lev 《Journal of Sol-Gel Science and Technology》1997,8(1-3):619-623
A new class of sol-gel-derived photocatalytic materials has been synthesized and used in solar-assisted photodegradation studies. The materials are comprised of a homogeneous dispersion of commercial TiO2 powder into silica and organically modified silicate (Ormosil) hosts. The efficiency of the photocatalytic properties of these TiO2-containing materials was determined by their relative performance in the solar photodecomposition of aqueous rhodamine B. The improved adsorption properties of the modified materials compared to commercial TiO2 increase the photodecomposition rate and the buoyancy properties, although excess hydrophobicity decreases the wetted section of the catalyst and its photocatalytic performance. These materials can be used as floatable catalysts for solar-assisted water purification. 相似文献
49.
In the two-photon visible dissociation of the iodobenzene cation, laser pulse shape is unimportant when collisional relaxation is slow compared to the time between pulses but becomes important when the relaxation rate is comparable to time between pulses. The dissociation can be simulated using an internal energy-governed computer model. 相似文献
50.
High resolution HF product time-of-flight spectra measured for the reactive scattering of F atoms from n-H2(p-H2) molecules at collision energies between 69 and 81 meV are compared with exact coupled-channel quantum mechanical calculations based on the Stark-Werner ab initio ground state potential energy surface. Excellent agreement between the experimental and computed rotational distributions is found for the HF product vibrational states v'=1 and v'=2. For the v'=3 vibrational state the agreement, however, is less satisfactory, especially for the reaction with p-H2. The results for v'=1 and v'=2 confirm that the reaction dynamics for these product states is accurately described by the ground electronic state 1 (2)A' potential energy surface. The deviations for HF(v'=3, j' > or =2) are attributed to an enhancement of the reaction resulting from the 25% fraction of excited ((2)P(12)) fluorine atoms in the reactant beam. 相似文献