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31.
H. Hillig B. Cleff W. Mehlhorn W. Schmitz 《Zeitschrift für Physik A Hadrons and Nuclei》1974,268(2):225-233
TheK Auger spectrum of the free sodium atom, following electron impact ionization, was measured with 0.16% resolution using a sodium atomic beam as target. The absolute energies and relative intensities ofKLL, KLM and numerous satellite transitions have been determined. The absolute energies of theKLL transitions of the free sodium atom were found to be smaller by 13.1 eV than the corresponding energies found for sodium in Na2O (relative to the Fermi level) by Fahlmanet al. Also the relativeKLL intensities differed in two cases indicating solid state and/or chemical effects. The present relative intensities agree better with theoretical values calculated by McGuire, Walters and Bhalla, and Chen and Crasemann than those of Na2O. In an Appendix the natural line widths of theKLL andKM-LLM transitions of sodium have been calculated. 相似文献
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Based on the consideration that the energy transfer between two molecules is in close connection to the position of their absorption and fluorescence bands, the energy lowering of the first excited singlet state due to a geometrical relaxation has been estimated for 40 π-systems. A modified SCF-variable β*-technique given elsewhere1 has been used. The selection of the compounds treated has been carried out in view of their potential activity in the photo-Fries reaction to be donors or acceptors of energy. The results obtained are in good agreement with the absorption and fluorescence spectra even for compounds, which undergo a tautomerism in their excited states. 相似文献
34.
M. Thoma W. Weber W. Mehlhorn 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1994,31(1):53-54
From intensity of Auger transitions (1s2p)?1 1 P,3 P→2p ?3 2 P,2 D+e A ? relative to 1s ?1 2 S→2p ?2 1 D+e A ? measured at ?=54 and 90° relative to the primary electron beam we have determined the alignment of double vacancy states (1s 2p)?1 1 P and3 P of neon for electron impact ionization for the impact energies 1.5, 2.0, 2.5 and 4.0 keV. ForE 0=1.5, 2.0 and 2.5 keV the alignment is compatible with zero with an upper limit of , forE 0=4.0 keV a small negative value was found. 相似文献
35.
Dr. Violeta Simic‐Milosevic Dr. Michael Mehlhorn Prof. Dr. Karina Morgenstern 《Chemphyschem》2016,17(17):2679-2685
Dissociative adsorption of doubly substituted benzene molecules leads to formation of benzyne radicals. In this study, co‐adsorbed hydrogen molecules are used in scanning tunneling hydrogen microscopy to enhance the contrast of the meta‐ and the para‐isomers of these radicals on Cu(111) and Au(111). Up to three hydrogen molecules are attached to one radical. One hydrogen molecule reveals the orientation of the carbon ring and its adsorption site, allowing discrimination between the two radicals. Two hydrogen molecules reflect the bond picture of the carbon skeleton and reveals that adsorption on Cu(111) distorts the meta‐ isomer differently from its gas‐phase distortion. Three hydrogen molecules allow us to determine the bond picture of a minor species. 相似文献
36.
Study of three-dimensional structure in wire-array z pinches by controlled seeding of axial modulations in wire radius 总被引:1,自引:0,他引:1
Jones B Deeney C McKenney JL Garasi CJ Mehlhorn TA Robinson AC Wunsch SE Bland SN Lebedev SV Chittenden JP Bott SC Ampleford DJ Palmer JB Rapley J Hall GN Oliver BV 《Physical review letters》2005,95(22):225001
Three-dimensional perturbations have been seeded in wire-array z pinches by etching 15 microm diameter aluminum wires to introduce 20% modulations in radius with a controlled axial wavelength. These perturbations seed additional three-dimensional imploding structures that are studied experimentally and with magnetohydrodynamics calculations, highlighting the role of current path nonuniformity in perturbation-induced magnetic bubble formation. 相似文献
37.
Dirk Mehlhorn Daria Kondrashova Christian Küster Dirk Enke Thorsten Emmerich Armin Bunde Rustem Valiullin Jörg Kärger 《Adsorption》2016,22(7):879-890
The rate of mass transfer is among the key numbers determining the efficiency of nanoporous materials in their use for matter upgrading by heterogeneous catalysis or mass separation. Transport enhancement by pore space optimization is, correspondingly, among the main strategies of efficiency promotion. Any such activity involves probing and testing of the appropriate routes of material synthesis and post-synthesis modification just as the exploration of the transport characteristics of the generated material. Modelling and molecular simulation is known to serve as a most helpful tool for correlating these two types of activities and their results. The present paper reports about a concerted research activity comprising these three types of activities. Recent progress in producing pore space replicas enabled focusing, in these studies, on “complementary” pore spaces, i.e. on pairs of material, where the pore space of one sample did just coincide with the solid space of the other. We report about the correlations in mass transfer as observable, in this type of material, by pulsed field gradient NMR diffusion studies, with reference to the prediction as resulting from a quite general, theoretical treatment of mass transfer in complementary pore spaces. 相似文献
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Dirk Mehlhorn Alexandra Inayat Prof. Dr. Wilhelm Schwieger Dr. habil. Rustem Valiullin Prof. Dr. Jörg Kärger 《Chemphyschem》2014,15(8):1681-1686
Pulsed field gradient nuclear magnetic resonance (NMR) diffusion studies are performed by using cyclohexane to probe transport properties in a NaX‐type zeolite with a hierarchical pore structure (house‐of‐cards‐like assemblies of mesoporous nanosheets), which is compared with a purely microporous sample. With guest loadings chosen to ensure saturation of the micropores, and the meso‐ and macropores left essentially unoccupied, guest diffusion is shown to be enhanced by almost one order of magnitude, even at room temperature. Diffusivity enhancement is further increased with increasing temperature, which may, therefore, be unambiguously attributed to the contribution of mass transfer in the meso‐ and macropores. 相似文献