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101.
The eigenvalues of the weakly coupled T ? t Jahn‐Teller problem are known for several decades, and the same holds also true for the eigenstates. These, however, are only given in the traditional position representation, which proves inconvenient if one attempts to extend the weak‐coupling treatment into the region of stronger coupling. Here the solution of the T ? t eigenvalue problem at weak coupling is derived in terms of creation and annihilation operators. This reformulation of the problem is nontrivial, since the algebraic form of the oscillator eigenvectors, being simultaneous angular‐momentum eigenstates, has been worked out only recently and is probably still widely unknown. The electronic and oscillator eigenstates are then coupled to form eigenvectors of the total angular momentum. Finally, in preparation for an extension of the weak‐coupling treatment, the action of the boson creation and annihilation operators on the oscillator eigenvectors is calculated, thus completing the algebraic approach to the weakly coupled T ? t system.  相似文献   
102.
We present a plane parallel radiative transfer model for polarized light, that provides the intensity vector as well as the derivatives of the four Stokes parameters with respect to atmospheric trace gas profiles. These derivatives are essential for retrieval of height resolved trace gas information from satellite measurements of backscattered sunlight. The model uses the Gauss-Seidel iteration technique for solving the radiative transfer equation. For the first time, the forward-adjoint radiative perturbation theory is applied for the linearization of a radiative transfer model including polarization. The accuracy of the model is better than 0.025% for all four Stokes parameters and better than 0.03% for the derivatives.  相似文献   
103.
An analytic approach is proposed for the evaluation of weighting functions for remote sensing of a blackbody planetary atmosphere based on straightforward, general linearization. In the present paper, this approach is applied to the case of remote sensing with the nadir (down-looking) geometry. Expressions for weighting functions for various atmospheric parameters are derived. It is demonstrated that in a realistic case of temperature-dependent atmospheric absorption, an additional term appears in the expression for the temperature weighting function which contains the temperature derivative of the atmospheric absorption coefficient. The approach is applied to the case of a semi-infinite atmosphere and then, to the atmosphere of a finite optical depth with the underlying surface. In this, latter case, the expressions are also obtained for partial derivatives of observed radiances with respect to surface parameters: surface pressure, temperature and emissivity.  相似文献   
104.
HarmonicAnalysisontheCompactHomogeneousSpaces──aboutFourierMultiplierofH~P(M)Space¥DongDaozhen;ZhengXuean(HenanUniversity,Kai?..  相似文献   
105.
Dibutyltin-3-hydroxyflavone, Bu2Sn(of), is a new fluorescence probe inhibitor of F1F0-ATPase and oxidative phosphorylation which inhibits by titration of an unidentified component of F0. Its site of action is closely related to that of the trialkyltins and of venturicidin. This F0 component is part of a pool of this component which is present in the heart mitochondrial inner membrane at levels of 5–7 nmol (mg protein)?1 [18 ± 3 Bu2Sn(of) sites per mol F1F0-ATPase]. However, ATPase activity in submitochondrial particles is near maximally inhibited by titration of approx. three Bu2Sn(of) sites per mol F1F0-ATPase. Over 60% (60–80%) of the Bu2Sn(of) interaction sites can be lost during the purification of F1F0-ATPase from submitochondrial particles. The number of Bu2Sn(of) interaction sites in various F1F0-ATPase preparations is variable. The high numbers of Bu2Sn(of) sites per mol F1F0-ATPase for heart mitochondria (18–21) and submitochondrial particles (15–19.5) decline in ATP synthase (11–15) to the low values obtained in Complex V (7–10.5) and the minimal values observed in highly purified F1F0?ATPase (3.5–5.6), thus indicating a variable dissociable component or cofactor of ATP synthase. The Bu2Sn(of) interaction site, a component of ATP synthase, is responsive to the redox status of the respiratory chain and the interaction with Bu2Sn(of) is with the reduced form of this component. Fluorescence titration studies show that this component is in redox equilibrium with the ubiquinone pool of the respiratory chain. It is proposed that this redox component serves as an inhibitor titratable cofactor pool which cycles through an F0 interaction site (or sites) via a system which serves as an energy-transfer link between the respiratory chain and ATP synthase.  相似文献   
106.
Reactions of pentafluorobenzoylpyruvic acid with amines afford the respective enamines. The intramolecular cyclization of the latter results inN-substituted 4-quinolone-2-carboxylic acids. Ammonia and triethylamine favor the cyclization of pentafluorobenzoylpyruvic acid to 2-carboxychromone.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 299–302, February, 1994.  相似文献   
107.
108.
岑建苗 《数学研究》1995,28(4):79-82
本文讨论临界可压缩模类和结合环的弱Jacobson根.首先,我们证明了非平凡的临界可压缩模类是素模的特殊类.其次,我们引入结合环的弱Jacobson根.弱Jaonbson根是特殊根.最后,我们给出有关弱本原环,半弱本原环和弱Jacobson根环的某些性质.  相似文献   
109.
Coupling losses have been calculated for laser resonators with unequal apertures and extended Fresnel Numbers. This was done using both, diffraction theory and a simple linear model.A close form expression was derived to calculate coupling losses with reasonable accuracies for a limited range of paramters. This should help in the preliminary design of hole coupling laser resonators.  相似文献   
110.
Low‐molecular‐weight poly(acrylic acid) (PAA) was synthesized by reversible addition fragmentation chain transfer polymerization with a trithiocarbonate as chain‐transfer agent (CTA). With a combination of NMR spectroscopy and matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry, the PAA end‐groups of the polymer were analyzed before and after neutralization by sodium hydroxide. The polymer prior to neutralization is made up of the expected trithiocarbonate chain‐ends and of the H‐terminated chains issued from a reaction of transfer to solvent. After neutralization, the trithiocarbonates are transformed into thiols, disulfides, thiolactones, and additional H‐terminated chains. By quantifying the different end‐groups, it was possible to demonstrate that fragmentation is the rate limiting step in the transfer reaction. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5439–5462, 2004  相似文献   
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