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71.
72.
A. El Kaddouri J. H’michane K. Bouras M. Moussa 《Complex Analysis and Operator Theory》2013,7(6):1889-1895
We characterize Banach lattices for which the class of order weakly compact operators (resp. b-weakly compact operators) between Banach lattices coincide with that of b-AM-compact operators. 相似文献
73.
74.
The Heyd-Scuseria-Ernzerhof (HSE) density functionals are popular for their ability to improve upon the accuracy of standard semilocal functionals such as Perdew-Burke-Ernzerhof (PBE), particularly for semiconductor band gaps. They also have a reduced computational cost compared to hybrid functionals, which results from the restriction of Fock exchange calculations to small inter-electron separations. These functionals are defined by an overall fraction of Fock exchange and a length scale for exchange screening. We systematically examine this two-parameter space to assess the performance of hybrid screened exchange (sX) functionals and to determine a balance between improving accuracy and reducing the screening length, which can further reduce computational costs. Three parameter choices emerge as useful: "sX-PBE" is an approximation to the sX-LDA screened exchange density functionals based on the local density approximation (LDA); "HSE12" minimizes the overall error over all tests performed; and "HSE12s" is a range-minimized functional that matches the overall accuracy of the existing HSE06 parameterization but reduces the Fock exchange length scale by half. Analysis of the error trends over parameter space produces useful guidance for future improvement of density functionals. 相似文献
75.
We propose a method to compute the entanglement degree of bipartite systems having dimension 2 × 2 and demonstrate that the partial transposition of density matrix, the Peres criterion, arise as a consequence of our method. Differently from other existing measures of entanglement, the one presented here makes possible the derivation of a criterion to verify if an arbitrary bipartite entanglement will suffers sudden death (SD) based only on the initial-state parameters. Our method also makes possible to characterize the SD as a dynamical quantum phase transition, with order parameter , having a universal critical exponent −1/2. 相似文献
76.
Jean-Pierre Bakhoum Olivier M. A. Mbaye Pape A. Diaw Moussa Mbaye Lamine Cisse Mame D. Gaye-Seye 《Analytical letters》2019,52(17):2782-2793
AbstractA new method was developed for determining trace amounts of pesticides, using an ultraviolet (UV) lamp to obtain photo-induced fluorescent (PIF) compounds, and then using laser excitation (LE) by a tunable source to excite and simultaneously characterize their fluorescence over a short acquisition time using an intensified charge-coupled device camera. This new UV-PIF-LE method was applied to determine isoproturon, oxadiazon, and fipronil in natural waters. This approach represents an improvement on the previously published direct laser photo-induced fluorescent (DL-PIF) approach that utilized the inclusion of a supplementary UV irradiation device in the experimental setup, permitting the separation of the formation and detection steps for the PIF analytes. This evolution improves the selectivity and increases the sensitivity while maintaining a short analysis time. The UV-PIF-LE method gave very good results with satisfactory analytical performance for the determination of the selected pesticides. This approach also demonstrated good reproducibility, with relative square deviation values between 3.3% and 6.3%, for spiked river water and seawater samples with detection limits in the ng mL?1 range. 相似文献
77.
Reactions of monooxidized thioyl and selenoyl bis(phosphanyl)amine ligands C10H7‐1‐N(P(E)Ph2)(PPh2) [E = S ( 1 ), Se ( 2 )] with Mo(CO)4(pip)2 and W(CO)4(cod) afforded the complexes [M(CO)4{ 1 ‐κ2P,S}] [M = Mo ( 3 ), W ( 4 )] and [M(CO)4{ 2 ‐κ2P,Se}] [M = Mo ( 5 ), W ( 6 )]. Complexes 3 – 6 were characterized by multinuclear NMR (1H, 13C, 31P, and 77Se NMR) and IR spectroscopy. Crystal‐structure determinations were carried out on 3 , 5 , and 6 , which represent the first examples of structurally characterized complexes of such ligands with group‐6 metal carbonyls. 相似文献
78.
Aggregation numbers of cationic oligomeric surfactants: a time-resolved fluorescence quenching study
Wattebled L Laschewsky A Moussa A Habib-Jiwan JL 《Langmuir : the ACS journal of surfaces and colloids》2006,22(6):2551-2557
The micelle aggregation numbers (N(agg)) of several series of cationic oligomeric surfactants were determined by time-resolved fluorescence quenching (TRFQ) experiments, using advantageously 9,10-dimethylanthracene as fluorophore. The study comprises six dimeric ("gemini"), three trimeric, and two tetrameric surfactants, which are quaternary ammonium chlorides, with medium length spacer groups (C(3)-C(6)) separating the individual surfactant fragments. Two standard cationic surfactants served as references. The number of hydrophobic chains making up a micellar core is relatively low for the oligomeric surfactants, the spacer length playing an important role. For the dimers, the number decreases from 32 to 21 with increasing spacer length. These numbers decrease further with increasing degree of oligomerization down to values of about 15. As for many conventional ionic surfactants, the micelles of all oligomers studied grow only slightly with the concentration, and they remain in the regime of small micelles up to concentrations of at least 3 wt %. 相似文献
79.
Mohamed E. M. Emam Magdy M. Bekheit Mahmoud N. H. Moussa Abd-El-Nasser A. El-Hendawy 《Transition Metal Chemistry》1994,19(1):117-118
Summary Metal complexes of general formula [M(DDE)·nH2O]· nH2O and [M(DDB)·nH2O] [where M = CoII, NiII, CuII, PdII and UO
2
2+
; n = 0–4; DDE and DDB are the anion of bis(1,2-diphenyl-1-hydroxyimino-2-ethylidine)-1,2-diaminoethane and bis(l,2-diphenyl-l-hydroxy-imino-2-ethylidine)-1,4-diaminobenzene, respectively] were prepared and characterized by i.r. electromagnetic and n.m.r. spectroscopy and magnetic measurements. 相似文献
80.
Bahia Abbas Moussa Hanaa M.A. Hashem Marianne Alphonse Mahrouse Sally Tarek Mahmoud 《Biomedical chromatography : BMC》2019,33(8)
Grapefruit juice inhibits esterase enzyme. Therefore, a possible interaction with ester prodrugs should be taken into consideration. In this study, the influence of grapefruit juice on sacubitril (SAC) rat liver S9 activation by esterase enzyme was evaluated. An RP‐HPLC method was developed and validated for estimation of SAC in rat liver S9 fraction using a C18 Cyano column as stationary phase and acetonitrile–sodium di‐hydrogen phosphate buffer (0.02 m , pH 4 adjusted by o‐phosphoric acid, 40:60, v/v), as mobile phase at a flow rate of 1 mL/min and UV detection at 254 nm. The method was successfully applied to an in vitro study in which SAC was incubated with rat liver S9 fraction prepared from rats that had previously ingested grapefruit juice for a week. The calculated SAC concentration after incubation was compared with that of SAC incubated with rat liver S9 fraction from the rat control group. The statistical significance between the results of test and control incubation sets was assessed. In conclusion, the current study demonstrated that grapefruit juice decreased SAC hydrolysis, hence delaying its activation to sacubitrilat (active form) in gut lumen. Based on this food–drug interaction, it may be required that grapefruit juice should be consumed with caution in patients receiving SAC. 相似文献