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41.
G. Kontrym-Sznajd H. Stachowiak 《Applied Physics A: Materials Science & Processing》1975,5(4):361-365
The purpose of this work is to understand Mogensen's and Petersen's positron annihilation curves for zinc. Mijnarends' approach
is used as an auxiliary method of localizing inhomogeneities of the electronic density in momentum space, as defined in the
paper.
Evidence is found for a new effect consisting of a strong enhancement of the annihilation probability in the lenses obtained
by the intersection of the Fermi surface with HMC surfaces. This effect, not the anisotropy of the Fermi surface, is the main
reason for the anisotropy of the annihilation curves.
Paper presented at 3rd Internat'l Conf. Positron Annihilation, Otaniemi, Finland (August 1973). 相似文献
42.
Becker-Szendy R Bratton CB Cady DR Casper D Claus R Crouch M Dye ST Gajewski W Goldhaber M Haines TJ Halverson PG Jones TW Kielczewska D Kropp WR Learned JG LoSecco JM McGrew C Matsuno S Mudan MS Price L Reines F Schultz J Sinclair D Sobel HW Stone JL Sulak LR Svoboda R Thornton G van der Velde JC 《Physical review D: Particles and fields》1990,42(9):2974-2976
43.
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45.
Dye ST Annis J Becker-Szendy R Bratton CB Casper D Claus R Crouch M Errede S Gajewski W Goldhaber M Haines TJ Jones TW Kielczewska D Kropp WR Learned JG LoSecco JM McGrew C Matthews J Mudan MS Price LR Reines F Schultz J Seidel S Sinclair D Sobel HW Stone JL Sulak LR Svoboda R Thornton G van der Velde JC 《Physical review letters》1989,62(18):2069-2072
46.
Grzegorz Stachowiak 《Order》1989,6(3):241-244
In this note, we prove that the comparability graph of a posetP has less edges than that of a posetQ on the same set of elements, thenP has more linear extensions thanQ. This solves a problem posed by Kelly [1].Research partially supported by the grant RP.I.09 from the Institute of Informatics, University of Warsaw. 相似文献
47.
Terence Davis Matthew C Dix Michal J Rokicki Amy JC Brook Caroline S Widdowson David Kipling Mark C Bagley 《Chemistry Central journal》2011,5(1):1-5
To develop more potent small molecules with enhanced free radical scavenger properties, a series of N-substituted isatin derivatives was synthesized, and the cytoprotective effect on the apoptosis of PC12 cells induced by H2O2 was screened. All these compounds were found to be active, and N-ethyl isatin was found with the most potent activity of 69.7% protective effect on PC12 cells. Structure-activity relationship analyses showed the bioactivity of N-alkyl isatins decline as the increasing of the chain of the alkyl group, furthermore odd-even effect was found in the activity, which is interesting for further investigation. 相似文献
48.
Hydrophilic surface modification of cyclic olefin copolymer microfluidic chips using sequential photografting 总被引:1,自引:0,他引:1
Stachowiak TB Mair DA Holden TG Lee LJ Svec F Fréchet JM 《Journal of separation science》2007,30(7):1088-1093
The plastic material known as cyclic olefin copolymer (COC) is a useful substrate material for fabricating microfluidic devices due to its low cost, ease of fabrication, excellent optical properties, and resistance to many solvents. However, the hydrophobicity of native COC limits its use in bioanalytical applications. To increase surface hydrophilicity and reduce protein adsorption, COC surfaces were photografted with poly(ethylene glycol) methacrylate (PEGMA) using a two-step sequential approach: covalently-bound surface initiators were formed in the first step and graft polymerization of PEGMA was then carried out from these sites in the second step. Contact angle measurements were used to monitor and quantify the changes in surface hydrophilicity as a function of grafting conditions. As water droplet contact angles decreased from 88 degrees for native COC to 45 degrees for PEGMA-grafted surfaces, protein adsorption was also reduced by 78% for the PEGMA-modified COC microchannels as determined by a fluorescence assay. This photografting technique should enable the use of COC microdevices in a variety of bioanalytical applications that require minimal nonspecific adsorption of biomolecules. 相似文献
49.
The relative rates of H-transfer between partners in ion-neutral complexes were compared with those in intramolecular rearrangements using results of first differential photoionization mass spectrometry measurements. Complex-mediated H-transfers are inferred to have rates of the same order as those for intramolecular hydrogen rearrangements, suggesting a similar range of motion of the reactive sites in both types of reactions. It is also concluded that at their fastest H-transfers take place between the partners in ion-neutral complexes within at most the time of several rotations of the partners in the complexes. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
50.