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1.
This study investigates a holographic recording effect of biphotonic polarization gratings (BPGs) written on dye-doped liquid crystal (DDLC) films. One linearly polarized green light (λG = 514.5 nm) and a polarization-modulated interference pattern formed by two mutually coherent orthogonal (±45° with respect to the polarization of the green light) polarized red lights simultaneously excite the DDLC films to generate a BPG. The formation of BPGs depends primarily on the dichroism of the dye molecules and a sequence of mechanisms: photoisomerization, anisotropic adsorption and inhibition of dye adsorption. The cis-isomer absorbance-modulated distribution associated with the red polarization-modulation pattern induces the dye adsorption-modulated pattern, in turn, yielding the permanent BPG which generates a modulated twisted nematic (TN) structure pattern in the sample. It is found that each BPG is verified to be electrically switchable and thermally erasable. The switching time is in the order of milliseconds. Additionally, the recording time to form a BPG decreases with increasing intensity of the green pump beam. 相似文献
2.
Summary. We examine the convergence characteristics of iterative methods based on a new preconditioning operator for solving the linear
systems arising from discretization and linearization of the steady-state Navier-Stokes equations. With a combination of analytic
and empirical results, we study the effects of fundamental parameters on convergence. We demonstrate that the preconditioned
problem has an eigenvalue distribution consisting of a tightly clustered set together with a small number of outliers. The
structure of these distributions is independent of the discretization mesh size, but the cardinality of the set of outliers
increases slowly as the viscosity becomes smaller. These characteristics are directly correlated with the convergence properties
of iterative solvers.
Received August 5, 2000 / Published online June 20, 2001 相似文献
3.
H. S. Dollar N. I. M. Gould W. H. A. Schilders A. J. Wathen 《Computational Optimization and Applications》2007,36(2-3):249-270
The problem of finding good preconditioners for the numerical solution of a certain important class of indefinite linear systems is considered. These systems are of a 2 by 2 block (KKT) structure in which the (2,2) block (denoted by -C) is assumed to be nonzero. In Constraint preconditioning for indefinite linear systems, SIAM J. Matrix Anal. Appl. 21 (2000), Keller, Gould and Wathen introduced the idea of using constraint preconditioners that have a specific 2 by 2 block structure for the case of C being zero. We shall give results concerning the spectrum and form of the eigenvectors when a preconditioner of the form considered by Keller, Gould and Wathen is used but the system we wish to solve may have C ≠0. In particular, the results presented here indicate clustering of eigenvalues and, hence, faster convergence of Krylov subspace iterative methods when the entries of C are small; such a situations arise naturally in interior point methods for optimization and we present results for such problems which validate our conclusions. 相似文献
4.
Ermann M Simkovsky NM Roberts SM Parry DM Baxter AD 《Journal of combinatorial chemistry》2002,4(4):352-358
A solid-phase synthesis of substituted cyclic urea derivatives as potential heterocyclic library scaffolds is described. 2-Amino-3-nitropyridine is attached to Wang resin via a carbamate linkage. Reduction of the nitro group was achieved with SnCl(2).2H(2)O. Reductive alkylation with a range of substituted benzaldehydes followed by cyclative cleavage afforded a small library of 3-substituted imidazo[4,5-b]pyridine-2-ones in 33-45% yield and 59-88% purity. Subsequently, this methodology was applied to the synthesis of 3-substituted imidazo[4,5-f]quinolin-2-ones. 相似文献
5.
Jin-Wan Huang Liang-Nian Ji An-Kong Hsich T. S. Andy Hor 《Transition Metal Chemistry》1992,17(4):280-282
Photolytic decarbonylation of Rh2(CO)4(TPP) (TPP=tetraphenylporphyrinato) with pyridine (Py) in benzene gives an unusual monomeric RhII radical complex Rh(TPP)(Py), which has been characterised by thermal and spectroscopic measurements and by vapour pressure
osmosis. 相似文献
6.
Tleugabulova D Duft AM Zhang Z Chen Y Brook MA Brennan JD 《Langmuir : the ACS journal of surfaces and colloids》2004,20(14):5924-5932
At present, there is no direct experimental evidence that primary silica particles, which exist only transiently for a few seconds during the St?ber silica synthesis, can be stable in aqueous solutions. In the present work, we show that primary silica particles are formed spontaneously after the dissolution of diglycerylsilane (DGS) in aqueous solutions and remain stable for prolonged periods of time. By using time-resolved fluorescence anisotropy (TRFA), we demonstrate that this unique property of DGS is ascribed to the slow kinetics of silica particle growth in diluted sols at pH approximately 9.0. The anisotropy decay of the cationic dye rhodamine 6G (R6G), which strongly adsorbs to silica oligomers and nanoparticles in DGS sols, could be fit to three components: a fast (picosecond) scale component associated with free R6G, a slower (nanosecond) rotational component associated with R6G bound to primary silica particles, and a residual (nondecaying) anisotropy component associated with R6G that was bound to secondary or larger particles that were unable to rotate on the time scale of the R6G emission lifetime (4 ns). The data show that, under conditions where fast hydrolysis is obtained, the initial size of the nuclei depends on the silica concentration, with larger nuclei being present in more concentrated sols, while the rate of growth of primary particles depends on both silica concentration and solution pH. At low silica concentrations and high pHs, it was possible to observe the growth of stable, nonaggregating primary silica particles by a mechanism involving rapid nucleation followed by monomer addition. The presence of stable primary particles was confirmed by atomic force microscopy (AFM) imaging. At higher silica concentrations and lower pHs, there was an increase in the initial size of the nuclei formed, which subsequently grew to a larger radius (> 4.5 nm) or aggregated with time, and in such cases, nucleation and aggregation occurred simultaneously in the early stage of silica formation. The data clearly show the power of time-resolved fluorescence anisotropy decay measurements for probing the growth of silica colloids and show that this method is useful for elucidating the mechanism of particle formation and growth in situ. 相似文献
7.
Thilo Berkenbusch Andy Ch. Laungani Reinhard Brückner Manfred Keller 《Tetrahedron letters》2004,45(52):9517-9520
4-tert-Butyl-2-cyclohexen-1-one dimerizes in THF solution via its kinetic enolate, leading to di-tert-butylditwistane 8 in up to 36% yield (−78 °C → room temp., protonolysis, flash chromatography). X-ray crystallography shows that 8 incorporates one R and one S enantiomer of the starting ketone; none of the diastereomeric ditwistanes epi-8, epi’-8 or iso-8 was isolated. This means that the formation of 8 proceeds with mutual kinetic resolution and 100% induced diastereoselectivity. 相似文献
8.
9.
The potential of Fe(CO)4(η1-dppf) (dppf = 1,1′-bis(diphenylphosphino)ferrocene) as a precursor for heterometallic species is fully expanded in the synthesis of (OC)4Fe(μ-dppf)Cr(CO)5, (OC)4Fe(μ-dppf)W(CO)5, and (OC)4Fe(μ-dppf)Mn2(CO)9, all of which have been characterized by IR, NMR (1H and 31P) and elemental analyses. The low energy requirement of TMNO (Me3NO · 2H2O)decarbonylation allows the formation of monosubstituted Mn2(CO)10 as the major product. This aspect is further substantiated by the isolation of Mn4(CO)18(μ-dppf) in which the single bridging of a diphosphine group between two Mn2(CO)9 moieties is unprecedented. 相似文献
10.
Ruthenium(II) complexes of monodonor ligands: efficient reagents for asymmetric ketone hydrogenation
Xu YA Clarkson GC Docherty G North CL Woodward G Wills M 《The Journal of organic chemistry》2005,70(20):8079-8087
[Chemical reaction: See text] A series of BINOL-derived ligands have been prepared and incorporated into ruthenium(II) complexes containing a diamine ligand. The complexes have proven to be excellent catalysts for the asymmetric hydrogenation of ketones, giving reduction products with enantiomeric excesses of up to 99%. 相似文献