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71.
Constant current chronopotentiometry is employed in conjunction with cyclic voltammetry and ac voltammetry to present in‐depth interfacial characterisations of the adsorption behaviour of a peptide affinity probe (Cys‐p53), of a thiolated hepta(ethylene glycol) (t‐OEG) and of mixed monolayers of these at mercury electrodes. The peptide sequence is derived from the interaction site of the protein p53 with the protein Mdm2. The adsorbed Cys‐p53 peptide is catalytically active towards the hydrogen evolution reaction, giving rise to very intense peaks in chronopotentiometry, whereas the oligo(ethylene glycol) is not. This difference enables one to monitor the presence of the peptide within mixed monolayers. It is shown that in the binary layers, the adsorption of t‐OEG is kinetically favoured while Cys‐p53 is thermodynamically more strongly adsorbed. 相似文献
72.
Claire Dubot Cyrille Allery Vincent Melot Claudine Bghein Mourad Oulghelou Clment Bonneau 《Entropy (Basel, Switzerland)》2021,23(10)
Predicting the void fraction of a two-phase flow outside of tubes is essential to evaluate the thermohydraulic behaviour in steam generators. Indeed, it determines two-phase mixture properties and affects two-phase mixture velocity, which enable evaluating the pressure drop of the system. The two-fluid model for the numerical simulation of two-phase flows requires interaction laws between phases which are not known and/or reliable for a flow within a tube bundle. Therefore, the mixture model, for which it is easier to implement suitable correlations for tube bundles, is used. Indeed, by expressing the relative velocity as a function of slip, the void fraction model of Feenstra et al. and Hibiki et al. developed for upward cross-flow through horizontal tube bundles is introduced and compared. With the method suggested in this paper, the physical phenomena that occur in tube bundles are taken into consideration. Moreover, the tube bundle is modelled using a porous media approach where the Darcy–Forchheimer term is usually defined by correlations found in the literature. However, for some tube bundle geometries, these correlations are not available. The second goal of the paper is to quickly compute, in quasi-real-time, this term by a non-intrusive parametric reduced model based on Proper Orthogonal Decomposition. This method, named Bi-CITSGM (Bi-Calibrated Interpolation on the Tangent Subspace of the Grassmann Manifold), consists in interpolating the spatial and temporal bases by ITSGM (Interpolation on the Tangent Subspace of the Grassmann Manifold) in order to define the solution for a new parameter. The two developed methods are validated based on the experimental results obtained by Dowlati et al. for a two-phase cross-flow through a horizontal tube bundle. 相似文献
73.
74.
Starting from a crude mixture of N-acetylmannosamine and N-acetylglucosamine, N-acetylneuraminic acid has been easily synthesized on 2.8 millimoles scale, with one immobilized enzyme. 相似文献
75.
Addition of an intercalating but nonaggregating porphyrin, AuT4, to a preformed adduct between DNA and a strongly aggregating porphyrin, t-H2Pagg, permits control of the extent of aggregation of the latter. The size and the intensity of the ICD and RLS signals depend linearly on the concentration of the intercalating dye and decrease markedly on increasing the concentration of the available binding sites on the biopolymer template. 相似文献
76.
Judith Polonsky Jacqueline Gallas Jeannette Varenne Thierry Prangé Claudine Pascard Henri Jacquemin Christian Moretti 《Tetrahedron letters》1982,23(8):869-872
Karinolide is a structurally novel C20 quassinoid isolated from the French Guyanan Simaroubaceae, Simaba multiflora A.Juss. whose structure was established by X-ray diffraction analysis. 6α-Senecioyloxychaparrin , the known 6α-senecioloyxychaparrinone and 9-methoxycanthin-6-one were also isolated ; their structure were determined by spectral means. 相似文献
77.
Weyer-Menkhoff J Devauchelle C Grossmann A Grünewald S 《Computational Biology and Chemistry》2005,29(3):662-203
The task of the quartet puzzling problem is to find a best-fitting binary X-tree for a finite n-set from confidence values for the 3n4 binary trees with exactly four leaves from X, its fitness being measured by the sum of the confidence values of all "induced" four-leaves subtrees. We describe a method for finding an exact solution of this problem by integer linear programming. Similar procedures can also be used for finding, e.g. best-fitting "circular" networks. A crucial problem in this context is, of course, how to obtain the input confidence values for the quartet trees. We propose to use inner products of rate-matrix diagonals calculated for pairs of taxa and present the trees resulting from applying our approach to two data sets of up to 36 mitochondrial sequences of mammals including an outgroup. 相似文献
78.
Daniel Taton Alain Le Borgne Nicolas Spassky Claude Friedrich Claudine Noël 《先进技术聚合物》1994,5(4):203-215
Racemic and chiral [(4-cyano-4′-biphenyl)oxy] and [(4-methoxy-4′-biphenyl)oxy]methyloxiranes were prepared from racemic epichlorohydrin or racemic and chiral glycidols and polymerized in dimethylsulfoxide (DMSO) with ButOK as the initiator system. Initial phase identifications were made by differential scanning calorimetry (DSC) and optical microscopy techniques and confirmed by X-ray diffraction measurements. Upon heating, all the monomers show only a crystal–isotropic phase transition. The racemic and chiral [(4-cyano-4′-biphenyl)oxy]methyloxiranes exhibit a nematic and a cholesteric monotropic phase, respectively. Methoxybiphenyl substituted polyethers are crystalline and insoluble in virtually all common solvents. Cyanobiphenyl substituted polyethers are soluble under the same experimental conditions and show enantiotropic liquid crystalline properties. The racemic polymer exhibits a nematic phase, while the optically active polymer forms a cholesteric phase. 相似文献
79.
Monteux C Llauro MF Baigl D Williams CE Anthony O Bergeron V 《Langmuir : the ACS journal of surfaces and colloids》2004,20(13):5358-5366
The synergistic adsorption and complexation of polystyrene sulfonate, PSS (a highly charged anionic polyelectrolyte), and dodecyltrimethylammonium bromide, C12TAB (a cationic surfactant), at the air-water interface can lead to interfacial gels that strongly influence foam-film drainage and stability. The formation and characteristics of these gels have been studied as a function of PSS molecular weight by combining surface tension, ellipsometry, and foam-film drainage experiments. Simultaneously the solution electromotive force has been measured to track the polymer-surfactant interactions in the bulk solution. It has been found that there is a critical molecular weight for surface gelation as well as for bulk precipitation and aggregation. Furthermore, we show that for the lowest molecular weights, PSS adsorbs with C12TAB in compact layers at the air-water interface. In particular, for mixtures of C12TAB with the monomer compound of the PSS repeat unit (e.g. Mw = 208), interfacial complexation is found to be similar to that of catanionic mixtures (mixtures of surfactants of opposite charge). 相似文献
80.
The sequential two-electron reduction of benzaldehyde to the radical anion and dianion species in 1-butyl-3-methylimidazolium triflimide and 1-butyl-1-methylpyrrolidinium triflimide is reported. In 1-butyl-1-methylpyrrolidinium triflimide, the heterogeneous electrochemistry and follow-up chemical reactivity are essentially equivalent to that in conventional molecular-solvent-based electrolytes where no interaction with the media is observed. In 1-butyl-3-methylimmidazolium triflimide, reduction occurs via the same two heterogeneous processes; however, the apparent heterogeneous rate constants are smaller by ca. 1 order of magnitude which leads to quasi-reversible electrochemical behavior. Since the bulk viscosities of the liquids are similar, the slower heterogeneous kinetics are attributed to local interfacial viscosity due to local ordering in the imidazolium-based medium. Also, a dramatic anodic shift in the reduction potentials is observed in 1-butyl-3-methylimidazolium triflimide media that is attributed to a stabilizing interaction of the radical anion and dianion species with the imidazolium cation. 相似文献