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201.
Zusammenfassung Der Verfasser gibt eine allgemeine Lösung für die Verteilung des Druckes zwischen einem axialsymmetrischen Stempel und einem transversal-isotropen Halbraum. Es wird gezeigt, dass die Verteilung des Druckes für den flachen Stempel mit allgemeiner Belastung unabhängig ist von den elastischen Eigenschaften des Halbraums und auch genau dieselbe, als ob der Halbraum isotrop wäre. 相似文献
202.
JET quasistationary internal-transport-barrier operation with active control of the pressure profile
Crisanti F Litaudon X Mailloux J Mazon D Barbato E Baranov Y Bécoulet A Bécoulet M Challis CD Conway GD Dux R Eriksson LG Esposito B Frigione D Hennequin P Giroud C Hawkes N Huysmans G Imbeaux F Joffrin E Lomas P Lotte P Maget P Mantsinen M Moreau D Rimini F Riva M Sarazin Y Tresset G Tuccillo AA Zastrow KD 《Physical review letters》2002,88(14):145004
Quasistationary operation has been achieved on the Joint European Torus tokamak in internal-transport-barrier (ITB) scenarios, with the discharge time limited only by plant constraints. Full current drive was obtained over all the high performance phase by using lower hybrid current drive. For the first time feedback control on the total pressure and on the electron temperature profile was implemented by using, respectively, the neutral beams and the ion-cyclotron waves. Although impurity accumulation could be a problem in steady state ITBs, these experiments bring some elements to answer to it. 相似文献
203.
LetG be a finite group generated by reflections. It is shown that the elements ofG can be arranged in a cycle (a Gray code) such that each element is obtained from the previous one by applying one of the generators. The case G =A
1
n
yields a conventional binary Gray code. These generalized Gray codes provide an efficient way to run through the elements of any finite reflection group. 相似文献
204.
John B. Conway 《Integral Equations and Operator Theory》1987,10(5):659-706
If G is any region in the complex plane and HP (G), 1p, denotes the Hardy space of analytic functions on G, then the principal aim of this paper is to present the spectral properties of the multiplication operators M defined on HP(G) by Mf=f, where is any bounded analytic function on G. In order to do this, the speccial case in which G is bounded and (z)=z is studied in detail. In addition an operator called the truncation operator that is not a multilication operator and acts on the Hardy spaces of regions of the form /K for a compact set K is studied.Dedicated to the memory of my brotherThis research was partially supported by National Science Foundation grant MCS 83-204-26. 相似文献
205.
Adsorption and electrosorption of Cr(VI), Mo(VI), W(VI), V(IV), and V(V) ions from water samples at low concentration were studied at high-area C-cloth electrodes. The concentrations of ions in the solution were monitored using in situ UV spectroscopy. All the investigated ions, except V(IV), showed better adsorption in acidic media. Positive polarization of the C-cloth caused increased adsorption of Cr(VI), Mo(VI), and V(V) ions. When previously adsorbed, Mo(VI) and V(V) ions were shown to be largely desorbable by negative polarization of the C-cloth. Since V(IV) does not become adsorbed significantly at the C-cloth in acidic media, the method provides an interesting means for separation of V(V) and V(IV) species in solution. 相似文献
206.
Louis P. Conway Appaso M. Jadhav Rick A. Homan Weichao Li Juanita Sanchez Rubiano Richard Hawkins R. Michael Lawrence Christopher G. Parker 《Chemical science》2021,12(22):7839
The use of photo-affinity reagents for the mapping of noncovalent small molecule–protein interactions has become widespread. Recently, several ‘fully-functionalized’ (FF) chemical tags have been developed wherein a photoactivatable capture group, an enrichment handle, and a functional group for synthetic conjugation to a molecule of interest are integrated into a single modular tag. Diazirine-based FF tags in particular are increasingly employed in chemical proteomic investigations; however, despite routine usage, their relative utility has not been established. Here, we systematically evaluate several diazirine-containing FF tags, including a terminal diazirine analog developed herein, for chemical proteomic investigations. Specifically, we compared the general reactivity of five diazirine tags and assessed their impact on the profiles of various small molecules, including fragments and known inhibitors revealing that such tags can have profound effects on the proteomic profiles of chemical probes. Our findings should be informative for chemical probe design, photo-affinity reagent development, and chemical proteomic investigations.The chemical proteomic properties of five diazirine-based, fully-functionalized photoaffinity tags, including a newly developed, minimal tag, were compared. This study provides guidance for the development of new photoaffinity probes. 相似文献
207.
The product 2 in the 1,3-dipolar cycloaddition of one equivalent of diazomethane to p-toluquinone (1) was determined by 250 MHz nmr spectra to be approximately 85% 6-methyl-1-H-indazole-4,7-dione (2b). X-ray crystallographic analysis was employed in the characterization of 1,6-dimethyl-1-H-indazole-4,7-dione (4a), which was the major 1-N-methyl regioisomer in the methylation of the cycloaddition mixture 2 with diazomethane. Methylation of the cycloaddition product 2 with diazomethane also provided a regioisomeric mixture of the 2-N-methyl derivatives 5. This mixture was synthesized for characterization by an independent method which utilized the cycloaddition of 3-methylsydnone (10) to toluquinone (1). 1,5,6-Trimethyl-1-H-ind-azole-4,7-dione (9) was found to be a minor product in the reaction of diazomethane with the cycloaddition product 2. 相似文献
208.
B.E. Conway 《Journal of Electroanalytical Chemistry》1981,123(1):81-94
Two-dimensional concentrations of adsorbed ions in double-layers at charged interfaces, especially when appreciable specific adsorption obtains, are equivalent to quite substantial (1–4 M) three-dimensional concentrations in regular electrolyte solutions. Under such conditions, ion-specific Gurney co-sphere overlap interactions give an important contribution to the non-ideal free energy of electrolytes in solution. It is proposed that similar interaction effects arise two-dimensionally in double-layers, giving rise to a contribution to the lateral interaction energy in monolayer arrays of ions. Three types of calculations are described by which these interaction effects can be evaluated. One is applied to some recent data on tetrapropylammonium ion adsorption at Hg, where hydrophobic interactions arise.Related problems concerned with solvent dipole orientation in the inner layer, when appreciable surface concentrations of hydrated ions are present, are referred to. The probable role of field-gradient/quadrupole interactions is noted. 相似文献
209.
B.E. Conway 《Journal of Electroanalytical Chemistry》1975,65(2):491-504
Negative adsorption of ions, commonly observed at air-water interfaces, is examined in terms of models of restricted polarization of the solvent by ions at the interface and the structure of the liquid interface. The Born and other models of ionic hydration are applied to evaluate the self-energy of the ion arising in the region of solvent near its interface and in the vacuum or vapour beyond. The adsorption energy of an ion varies substantially with distance from the liquid interface so that a distribution of ions arises as a function of distance from the interface. Integration of this distribution gives an expression, and results, for the ionic surface excess. The diffuse-layer potential, which an unequal distribution of cations and anions give rise to, gives a contribution to the surface potential of the electrolyte solution at finite concentrations.Structural aspects of the liquid interface at which ions are negatively adsorbed are discussed in terms of Stefan's ratio and the superficial excess entropies of various liquid surfaces. These entropies are related to the cohesive energy densities of the bulk liquids. Ion solvent-structure co-sphere interactions with structured interfaces will lead to specificity of negative adsorption of ions. 相似文献
210.
H. Angerstein-Kozlowska B.E. Conway J. Klinger 《Journal of Electroanalytical Chemistry》1978,87(3):301-320
The kinetic behaviour of a surface process involving the deposition of a two-dimensional surface film by a nucleation and growth mechanism is treated for the case of linear potential sweep control. Features which distinguish nucleation and growth in monolayer formation from random electrodeposition (Langmuir case) treated in previous papers are emphasized. Two main mechanisms are considered: one where the growth occurs from a fixed surface density of nuclei and the other where growth occurs from a potential-dependent density of nuclei. Computer simulations and some analytical derivations of the kinetic behaviour for these two cases are made and the characteristic kinetic features of the process are deduced, enabling the latter to be distinguished in terms of experimentally accessible criteria. The extent of reversibility of the processes can be usefully expressed in terms of a limiting sweep-rate parameter, s0, which is related to the rate constant for nucleation or the surface density of nuclei and the rate constant for growth. 相似文献