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101.
P. CsöRGő A. Drápal 《Abhandlungen aus dem Mathematischen Seminar der Universit?t Hamburg》2006,76(1):17-34
A loopQ is said to be left conjugacy closed (LCC) if the left translations form a set of permutations that is closed under conjugation. This papers investigates those LCC loops where the group generated by left translations is normal in the group generated by both left and right translations. 相似文献
102.
J.E.G. Lipson S. T. Milner 《The European Physical Journal B - Condensed Matter and Complex Systems》2009,72(1):133-137
Recent observations using fluorophore probes of local dynamics in polymer films
have provided new insight into the glass transition.
Using a percolation model, we predict the local Tg in a polymer film,
as a function of distance from a substrate or a free surface.
Our predictions are in good agreement
with the observed elevation of Tg near a substrate,
whereas the observed reduction of Tg near a free surface
is too strong to be accounted for by percolation effects. 相似文献
103.
We present results for step‐strain experiments and the resulting damping functions of polyethylene blends of different structures, including solutions of linear, star and comb polymers. Remarkably, an entangled melt of combs exhibits a damping function close to that for entangled linear chains. Diluting the combs with faster‐relaxing material leads to a more nearly constant damping function. We find similar behavior for blends of commercial low density polyethylene LDPE. Our results suggest a simple picture: on timescales relevant to typical damping‐function experiments, the rheologically active portions of our PE combs as well as commercial LDPE are essentially chain backbones. When strongly entangled, these exhibit the Doi‐Edwards damping function; when diluted, the damping function tends toward the result for unentangled chains described by the Rouse model – namely, no damping. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 3117–3136, 2007 相似文献
104.
Low-energy collision induced dissociation has been used to investigate the structure and stability of microsolvated clusters of the prototypical, aprotic multiply charged anion, Pt(CN)(4)(2-), i.e. Pt(CN)(4)(2-)·(H(2)O)(n) n = 1-4, Pt(CN)(4)(2-)·(MeCN)(m) m =1, 2, and Pt(CN)(4)(2-)·(H(2)O)(3)·MeCN. For all of the systems studied, the lowest energy fragmentation pathway was found to correspond to decay of the cluster with loss of the entire solvent ensemble. No sequential solvent evaporation was observed. These observations suggest that the Pt(CN)(4)(2-) solvent clusters studied here form hydrogen-bonded "surface solvated" structures. Electronic structure calculations are presented to support the experimental results. In addition, the detailed fragmentation patterns observed are interpreted with reference to the differential solvation of the ionic fragmentation and electron detachment potential energy surfaces of the core Pt(CN)(4)(2-) dianion. The results described represent some of the first experiments to probe the microsolvation of this important class of multiply charged anions. 相似文献
105.
Normal alkanes display multiple ordered phases, including an orthorhombic crystal (X) and two partially ordered rotator phases (RI and RII). The rotator phase transitions X-RI and RI-RII are of interest because they are weakly first-order, and because experiments suggest that crystalline polyethylene may nucleate via a metastable rotator phase. We have performed heating and cooling scans of all-atom NσT (isothermal, isostress) simulations of a pure C(23) solid. We find a sequence of phases, transition temperatures, structural and thermodynamic properties, all reasonably consistent with experiment, except that a monoclinic crystal is more stable in our simulations than the experimental orthorhombic structure. We find that the RI phase is well described as an orthorhombic crystal disordered by random ±90° rotations of molecules about their stem axis, and the RII phase can be represented as a loose hexagonal packing of parallel chain stems, which tend to orient with the in-plane projection of C-C bonds pointing between neighbors. To measure local orthorhombic, RI, or RII order, we define Potts- and Ising-like order parameters, from which global order parameters and correlation functions can be computed. We observe modest pretransitional fluctuations of local RI order in the RII phase near T(RI-RII), characteristic of this weakly first-order transition. 相似文献
106.
Andrea R. Milner PhD 《School science and mathematics》2012,112(5):267-269
107.
108.
109.
Polarization-sensitive optical coherence tomography (PS-OCT) was used to characterize completely the polarization state of light backscattered from turbid media. Using a low-coherence light source, one can determine the Stokes parameters of backscattered light as a function of optical path in turbid media. To demonstrate the application of this technique we determined the birefringence and the optical axis in fibrous tissue (rodent muscle) and in vivo rodent skin. PS-OCT has potentially useful applications in biomedical optics by imaging simultaneously the structural properties of turbid biological materials and their effects on the polarization state of backscattered light. This method may also find applications in material science for investigation of polarization properties (e.g., birefringence) in opaque media such as ceramics and crystals. 相似文献
110.
We describe a method for en face phase-contrast imaging of cells with a fiber-based differential phase-contrast optical coherence microscopy system. Recorded en face images are quantitative phase-contrast maps of cells due to spatial variation of the refractive index and (or) thickness of various cellular components. Quantitative phase-contrast images of human epithelial cheek cells obtained with the fiber-based differential phase-contrast optical coherence microscopy system are presented. 相似文献