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排序方式: 共有68条查询结果,搜索用时 437 毫秒
41.
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
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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
45.
Theoretical investigation of the halogen bonded complexes between carbonyl bases and molecular chlorine 下载免费PDF全文
Wiktor Zierkiewicz Dariusz C. Bieńko Danuta Michalska Thérèse Zeegers‐Huyskens 《Journal of computational chemistry》2015,36(11):821-832
The halogen bonded complexes between six carbonyl bases and molecular chlorine are investigated theoretically. The interaction energies calculated at the CCSD(T)/aug‐cc‐pVTZ level range between ?1.61 and ?3.50 kcal mol?1. These energies are related to the ionization potential, proton affinity, and also to the most negative values (Vs,min) on the electrostatic potential surface of the carbonyl bases. A symmetry adapted perturbation theory decomposition of the energies has been performed. The interaction results in an elongation of the Cl? Cl bond and a contraction of the CF and CH bonds accompanied by a blue shift of the ν(CH) vibrations. The properties of the Cl2 molecules are discussed as a function of the σ*(Cl? Cl) occupation, the hybridization, and the occupation of the Rydberg orbitals of the two chlorine atoms. Our calculations predict a large enhancement of the infrared and Raman intensities of the ν(Cl? Cl) vibration on going from isolated to complexed Cl2. © 2015 Wiley Periodicals, Inc. 相似文献
46.
Sinz DK Hanyak M Zeegers JC Darhuber AA 《Physical chemistry chemical physics : PCCP》2011,13(20):9768-9777
We conducted a combined experimental and numerical study of the spreading of insoluble surfactants on spatially confined thin liquid films. We found that the spreading dynamics can locally be represented by a power-law relation x~t(α). We determine the time evolution of the liquid film thickness and the corresponding spreading exponents α both from experiments using interference microscopy and numerical finite element simulations. The lateral confinement induces non-uniform height- and surface velocity profiles, which manifest themselves in a pronounced transition of the evolving rivulet morphology. Excellent agreement between experimental and simulation results has been achieved. 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.
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
49.
T. Wijchers H.A. Dijkerman P.J.Th. Zeegers C.Th.J. Alkemade 《Spectrochimica Acta Part B: Atomic Spectroscopy》1980,35(5):271-279
CW dye laser induced fluorescence emission and thermal emission spectra of YO-molecules in a 1 atm H2O2Ar flame of 2430 K were recorded simultaneously. Narrow band laser excitation was applied to four rotational lines in the (1, 1) Q-branch of the A2Π→X2Σ+ transition and broadband excitation was applied to several separate Q-branches of the A2Π,→X2Σ+ transitions. From the differences between the fluorescence emission spectra and thermal emission spectra, we conclude that collisional de-excitation of an excited vibronic level takes place by vibrational relaxation, decay to the electronic ground state and by intermultiplet transfer in order of increasing probability. 相似文献
50.
Hannu?TiitinenEmail author Anna?Mari?M?kel? Ville?M?kinen Patrick?JC?May Paavo?Alku 《BMC neuroscience》2005,6(1):62