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11.
Sergio Guerrero Oleg Yurievich Imanuvilov Jean-Pierre Puel 《Comptes Rendus Mathematique》2006,343(9):573-577
This Note deals with the two-dimensional Navier–Stokes system. In this context, we prove a result concerning its global approximate controllability by means of boundary controls. To cite this article: S. Guerrero et al., C. R. Acad. Sci. Paris, Ser. I 343 (2006). 相似文献
12.
Jean-Marc Kern Jean-Pierre Sauvage Gerard Bidan Bernadette Divisia-Blohorn 《Journal of polymer science. Part A, Polymer chemistry》2003,41(22):3470-3477
This article provides an overview of the fundamental principles of the synthesis of metallocatenanes and metallorotaxanes. It also describes the synthesis and properties of electronic conducting polymers—polypyrrole and polythiophene—built around metallocatenanes and metallorotaxanes. The particular properties of this new class of polymers, including the possibility of transmetallation reactions being performed with them and the observation of electronic coupling between the metal centers and the conducting matrix, are discussed. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3470–3477, 2003 相似文献
13.
Jean-Pierre Françoise 《Journal of Dynamics and Differential Equations》2008,20(4):777-786
This article is devoted to one-dimensional perturbative theory on R × S
1. There is a recursive formula for the successive obstructions to parametric center at any order of the perturbation parameter.
The first obstruction is studied by means of complex analysis techniques. This extends to the trigonometric case what was
done previously for the polynomial case (Israel J. Math. 142, 273–283, 2004).
This article is dedicated to Professor Zhang Zhi-Fen on the occasion of her 80th Birthday 相似文献
14.
Results of H. Cartan about holomorphic automorphisms on bounded domains are generalized to the case of hyperbolic manifolds in the sense of Kobayashi. In this setting, we give an identity theorem together with its topological version. We show also that a sequence of automorphisms which converges uniformly on some nonempty open set, has a limit on the whole space which is an automorphism. At the end of the paper, conditions are given for the sequence of iterates of a self holomorphic map in order to be an automorphism. 相似文献
15.
A series of photoreactive complexes of the type Ru(terpy*)(N-N)(L)(2+), where terpy* is 4'-(3,5-ditertiobutylphenyl)-2,2':6',2' '-terpyridine, N-N is the bidentate chelate phen or dmp (phen = 1,10-phenanthroline, dmp = 2,9-dimethyl-1,10-phenanthroline), and L is the monodentate ligand dms, MeBN, or MeOBN (dms = dimethyl sulfide, MeBN = 2,6-dimethyl benzonitrile, MeOBN = 2,6-dimethoxybenzonitrile), has been synthesized and fully characterized by proton NMR spectroscopy, electrospray mass spectrometry, and UV-vis spectroscopy. The X-ray structures of four complexes were also obtained. In neat pyridine, the quantum yields for the photosubsitution of L by pyridine were measured and showed dramatic variations depending on the steric interactions between the spectator bidentate ligand and the leaving monodentate ligand L. The use of dmp instead of phen multiplied the photosubstitution efficiency by a factor of 20-50, depending on L. This effect could be qualitatively correlated to the distortions observed in the X-ray structures of the corresponding complexes. The highly distorted structure of Ru(terpy)(dmp)(dms)(PF(6))(2) showed a very high photosubsitution quantum yield phi = 0.36 in neat pyridine. The high photoreactivity of some of the compounds makes them particularly promising as components of future light-driven molecular machines. 相似文献
16.
Ab initio pseudopotential SCF calculations were performed on tetrahedral X4 molecules using double-zeta basis sets with and without d functions. The inclusion of d orbitals shortens the bond lengths, stabilizes the X4 structures and intensifies the electron density inside the tetrahedron. The cubic X8 molecules, calculated without d AOs, are not predicted to be more stable than 2X4. Repulsions between parallel bonds in X8 may compensate the lack of ring strain. 相似文献
17.
Titration calorimetry was used to construct the solid-liquid equilibrium line in ternary systems containing the solute and an aqueous mixed solvent by measuring the heat of dissolution of the solid solute during successive additions of the liquid solvent. The plot of cumulated heats versus the mole ratio, nsolvent/nsolute, yields two (almost) linear increases of different slopes. These two lines represent successively the enthalpy of dissolution then the enthalpy of dilution of the medium; their intersection gives the solubility and the enthalpy of dissolution of the solute. Phase diagrams have been established over the whole concentration range for o-anisaldehyde, 1,3,5-trimethoxybenzene and vanillin, in water + methanol, +ethanol, or +n-propanol at 303, 313 and 318 K. 相似文献
18.
Leclerc E Buchmann W Taphanel MH Morizur JP 《Rapid communications in mass spectrometry : RCM》2002,16(7):686-695
Ion/molecule reactions between O=P(OCH(3))(2)(+) phosphonium ions and six aromatic hydrocarbons (benzene, toluene, 1,2,4-trimethylbenzene, naphthalene, acenaphthylene and fluorene) were performed in a quadrupole ion trap mass spectrometer. The O=P(OCH(3))(2)(+) phosphonium ions, formed by electron impact from neutral trimethyl phosphite, were found to react with aromatic hydrocarbons (ArHs) to give (i) an adduct [ArH, O=P(OCH(3))(2)](+) and (ii) for ArHs which have an ionization energy below or equal to 8.14 eV, a radical cation ArH(+ *) by charge transfer reaction. Collision-induced dissociation experiments, which produce fragment ions other than the O=P(OCH(3))(2)(+) ions, indicate that the adduct ions are covalent species. Isotope-labeled ArHs were used to elucidate fragmentation mechanisms. The charge transfer reactions were investigated using density functional theory at the B3LYP/6-311 + G(3df,2p)//B3LYP/6-31G(d,p) level of theory. The potential energy surface obtained from B3LYP/6-31G(d,p) calculations for the reaction between O=P(OCH(3))(2)(+) and benzene is described. 相似文献
19.
A free-radical cyclization process makes glycosidic orthoester structures readily available in a one-pot procedure. 相似文献
20.
The palladium catalysed condensation of Grignard reagents with silyl derivatives of 8-bromopurine nucleosides and 8-bromoadenosine-3′,5′ cyclic monophosphate is a convenient method for the preparation of free 8-alkylpurine nucleosides and 8-alkyladenosine-3′,5′ cyclic monophosphate. 相似文献