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101.
A theory of relativistic strings with non-vanishing mechanical mass is developed. The theory involves the usual massless strings, and the main features of the massless theory are retained so that the system is dual and ghost-free. Some new features appear especially in the mass spectrum of the pomeron sector. The mode with Neveu-Schwarz spin is also considered. 相似文献
102.
Makio Ishiguro 《Annals of the Institute of Statistical Mathematics》1978,30(1):479-498
A new scheme of adaptive control is proposed. This scheme does not require a priori knowledge of the structure of the plant
to be controlled. The principal part of the scheme is a procedure which decides the order of the model of the plant. A criterion
for the order determination is developed. Using this criterion, we can decide whether to keep the current controller or to
adopt a new controller based on the information gathered during the operation of the system. The effectiveness of the scheme
is illustrated by a numerical example.
The Institute of Statistical Mathematics 相似文献
103.
Yoshizawa M Miyagi S Kawano M Ishiguro K Fujita M 《Journal of the American Chemical Society》2004,126(30):9172-9173
The photoexcitation of a self-assembled M6L4-type coordination cage accommodating photochemically inert alkane guests (e.g., adamantane and cyclooctane) led to the regioselective oxidation of the guest within the cage. Under anaerobic conditions, the guest oxidation was accompanied by the stable radical formation as indicated by ESR spectrometry (g = 2.002) and change in solution color (from colorless to blue). These phenomena were shown to be characteristic of the self-assembled molecular systems: i.e., from the M6L4 supersetGn assembly, none of the components (M, L, or G) can be eliminated for the unusual oxidation and/or radical formation. 相似文献
104.
[structure: see text] Polyenyne macrocycles with pi-extended [9]- and [12]radialene frameworks have been synthesized. These radialenes exhibit restricted rotation of the aromatic rings, and the D3- and D4-symmetric structures in solutions have been determined by dynamic NMR. The macrocyclic radialenes bear small to medium inner cavities, and the small cavity of the pi-extended [9]radialene can incorporate a silver cation. 相似文献
105.
We present the first experimental analysis of drop coalescence in a case where the dynamics is not governed by viscous dissipation in the bulk nor by the inertia of the fluid flow, only by the geometry and mobility of surfaces. We found such a situation in the physics of 3He crystals near 0.32 K where the latent heat of crystallization vanishes. Two crystalline drops of 3He coalesce if their crystalline orientations are identical: a neck forms after the contact at time t=0, and the shape evolves towards that of one convex crystal by local growth and melting in a fraction of a second. We have found that the neck radius initially increases as t(1/3), as predicted by Maris. This behavior is also expected for superfluid drops. It is clearly distinguished from the logarithmic behavior and from the t(1/2) power law which have been predicted by Eggers et al. in more usual situations. 相似文献
106.
Mitsunori Asada Takao Fujimori Kenta Fujii Ryo Kanzaki Yasuhiro Umebayashi Shin‐ichi Ishiguro 《Journal of Raman spectroscopy : JRS》2007,38(4):417-426
The solvation structure of magnesium, zinc(II), and alkaline earth metal ions in N,N‐dimethylformamide (DMF) and N,N‐dimethylacetamide (DMA), and their mixtures has been studied by means of Raman spectroscopy and DFT calculations. The solvation number is revealed to be 6, 7, 8, and 8 for Mg2+, Ca2+, Sr2+, and Ba2+, respectively, in both DMF and DMA. The δ (O C N) vibration of DMF shifts to a higher wavenumber upon binding to the metal ions and the shift Δν(= νbound − νfree) becomes larger, when the ionic radius of the metal ion becomes smaller. The ν (N CH3) vibration of DMA also shifts to a higher wavenumber upon binding to the metal ions. However, the shift Δν saturates for small ions, as well as the transition‐metal (II) ions, implying that steric congestion among solvent molecules takes place in the coordination sphere. It is also indicated that, despite the magnesium ion having practically the same ionic radius as the zinc(II) ion of six‐coordination, their solvation numbers in DMA are significantly different. DFT calculations for these metalsolvate clusters of varying solvation numbers revealed that not only solvent–solvent interaction through space but also the bonding nature of the metal ion plays an essential role in the steric congestion. The individual solvation number and the Raman shift Δν in DMF–DMA mixtures indicate that steric congestion is significant for the magnesium ion, but not appreciable for calcium, strontium, and barium ions, despite the solvation number of these metal ions being large. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
107.
108.
Anoklase J.‐L. Ayitou Dr. Gaku Fukuhara Elango Kumarasamy Prof. Dr. Yoshihisa Inoue Prof. Dr. J. Sivaguru 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(13):4327-4334
Enantiospecific axial‐to‐point chiral transfer in light‐induced transformations was efficient under elevated pressure at high temperatures. Model photoreactions with atropisomeric compounds showed higher enantioselectivity in the photoproducts under elevated pressure. The ee values in the photoproducts were rationalized based on the increased stability of optically pure atropisomeric compounds at elevated pressure, even at high temperatures. 相似文献
109.
110.