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41.
General transformations from multiplicative noise to additive noise are obtained for systems whose dynamical evolution is given by multidimensional Langevin equations. 相似文献
42.
Chafa A Tatischeff V Aguer P Barhoumi S Coc A Garrido F Hernanz M José J Kiener J Lefebvre-Schuhl A Ouichaoui S de Séréville N Thibaud JP 《Physical review letters》2005,95(3):031101
We report on the observation of a previously unknown resonance at E(lab)(R)=194.1+/-0.6 keV in the 17O(p,alpha)14N reaction, with a measured resonance strength omegagamma(palpha)=1.6 +/- 0.2 meV. We studied in the same experiment the 17O(p,gamma)18F reaction by an activation method and the resonance-strength ratio was found to be omegagamma(palpha)/omegagamma(pgamma) = 470 +/- 50. The corresponding excitation energy in the 18F compound nucleus was determined to be 5789.8 +/- 0.3 keV by gamma-ray measurements using the 14N(alpha, gamma)18F reaction. These new resonance properties have important consequences for 17O nucleosynthesis and gamma-ray astronomy of classical novae. 相似文献
43.
Using computer simulations, we investigate the time evolution of the (Boltzmann) entropy of a dense fluid not in local equilibrium. The macrovariables M describing the system are the (empirical) particle density f=[f(x,v)] and the total energy E. We find that S(f(t),E) is a monotone increasing in time even when its kinetic part is decreasing. We argue that for isolated Hamiltonian systems monotonicity of S(M(t))=S(M(X(t))) should hold generally for "typical" (the overwhelming majority of) initial microstates (phase points) X0 belonging to the initial macrostate M0, satisfying M(X0)=M(0). This is a consequence of Liouville's theorem when M(t) evolves according to an autonomous deterministic law. 相似文献
44.
We describe a reaction mechanism which is consistent with all available experimental information of high energy three-body breakup processes. The dominating channels are removal of one of the three halo particles leaving the other two either undisturbed or absorbed. We compare with the commonly used deceptive assumption of a decay through two-body resonance states. Our predictions can be tested by measuring neutron-neutron invariant mass spectra. 相似文献
45.
Supershell structure in alkali metal nanowires 总被引:1,自引:0,他引:1
Nanowires are formed by indenting and subsequently retracting two pieces of sodium metal. Their cross section gradually reduces upon retraction and the diameters can be obtained from the conductance. In previous work we have demonstrated that when one constructs a histogram of diameters from large numbers of indentation-retraction cycles such histograms show a periodic pattern of stable nanowire diameters due to shell structure in the conductance modes. Here, we report the observation of a modulation of this periodic pattern, in agreement with predictions of a supershell structure. 相似文献
46.
R. Álvarez-Rodrıguez E. Garrido A. S. Jensen D. V. Fedorov H. O. U. Fynbo 《The European Physical Journal A - Hadrons and Nuclei》2007,31(3):303-317
The hyperspherical adiabatic expansion is combined with complex scaling and used to calculate low-lying nuclear resonances
of 12C in the 3α model. We use Ali-Bodmer potentials and compare results for other potentials α-α with similar 8Be properties. A three-body potential is used to adjust the 12C resonance positions to desired values extending the applicability of the method to many-body systems decaying into three
α-particles. For natural choices of three-body potentials we find 14 resonances below the proton separation threshold, i.e. two 0+, three 2+, two 4+, one of each of 1±, 2-, 3±, 4-, and 6+. The partial-wave decomposition of each resonance is calculated as a function of the hyperradius. Strong variation is found
from small to large distance. The connection to previous experimental and theoretical results is discussed and agreements
as well as disagreements are emphasized. 相似文献
47.
Sandra Medel Jos Manuel García Leoncio Garrido Isabel Quijada‐Garrido Rodrigo París 《Journal of polymer science. Part A, Polymer chemistry》2011,49(3):690-700
A series of gradient and block copolymers, based on 2‐(2‐methoxyethoxy)ethyl methacrylate (MEO2MA) and tert‐butyl acrylate (tBA), were synthesized by atom transfer radical polymerization (ATRP) in a first step. The MEO2MA monomer leads to the production of thermosensitive polymers, exhibiting lower critical solution temperature (LCST) at around room temperature, which could be adjusted by changing the proportion of tBA in the copolymer. In a second step, the tert‐butyl groups of tBA were hydrolyzed with trifluoroacetic acid to form the corresponding block and gradient copolymers of MEO2MA and acrylic acid (AA), which exhibited both temperature and pH‐responsive behavior. These copolymers showed LCST values strongly dependent on the pH. At acid pH, a slightly decrease of LCST with an increase of AA in the copolymer was observed. However, at neutral or basic conditions, ionization of acid groups increases the hydrophilic balance considerably raising the LCST values, which even become not observable over the temperature range under study. In the last step, these carboxylic functionalized copolymers were covalently bound to biocompatible and biodegradable films of poly(3‐hydroxybutyrate‐co‐3‐hydroxyhexanoate) [P(HB‐co‐HHx)] obtained by casting and, previously treated with ethylenediamine (ED) to render their surfaces with amino groups. Thereby, thermosensitive surfaces of modified P(HB‐co‐HHx) could be obtained. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
48.
49.
Shan She Weimin Xuan Nicola L. Bell Robert Pow Eduard Garrido Ribo Zoe Sinclair De-Liang Long Leroy Cronin 《Chemical science》2021,12(7):2427
The precise control over the formation of complex nanostructures, e.g. polyoxometalates (POMs), at the sub-nanoscale is challenging but critical if non-covalent architectures are to be designed. Combining biologically-evolved systems with inorganic nanostructures could lead to sequence-mediated assembly. Herein, we exploit oligopeptides as multidentate structure-directing ligands via metal-coordination and hydrogen bonded interactions to modulate the self-assembly of POM superstructures. Six oligopeptides (GH, AH, SH, G2H, G4H and G5H) are incorporated into the cavities of Molybdenum Blue (MB) POM nanowheels. It is found that the helicity of the nanowheel can be readily switched (Δ to Λ) by simply altering the N-terminal amino acid on the peptide chain rather than their overall stereochemistry. We also reveal a delicate balance between the Mo-coordination and the hydrogen bonds found within the internal cavity of the inorganic nanowheels which results in the sequence mediated formation of two unprecedented asymmetrical nanowheel frameworks: {Mo122Ce5} and {Mo126Ce4}.Peptide sequence can be used to control the self-assembly and structures of nanoscale molybdenum blue polyoxometalate (POM) wheel-shaped clusters. 相似文献
50.
Hoeb M Auernhammer M Schoell SJ Brandt MS Garrido JA Stutzmann M Sharp ID 《Langmuir : the ACS journal of surfaces and colloids》2010,26(24):18862-18867
We present an approach for the thermally activated formation of alkene-derived self-assembled monolayers on oxygen-terminated single and polycrystalline diamond surfaces. Chemical modification of the oxygen and hydrogen plasma-treated samples was achieved by heating in 1-octadecene. The resulting layers were characterized using X-ray photoelectron spectroscopy, thermal desorption spectroscopy, atomic force microscopy, Fourier transform infrared spectroscopy, and water contact angle measurements. This investigation reveals that alkenes selectively attach to the oxygen-terminated sites via covalent C-O-C bonds. The hydrophilic oxygen-terminated diamond is rendered strongly hydrophobic following this reaction. The nature of the process limits the organic layer growth to a single monolayer, and FTIR measurements reveal that such monolayers are dense and well ordered. In contrast, hydrogen-terminated diamond sites remain unaffected by this process. This method is thus complementary to the UV-initiated reaction of alkenes with diamond, which exhibits the opposite reactivity contrast. Thermal alkylation increases the range of available diamond functionalization strategies and provides a means of straightforwardly forming single organic layers in order to engineer the surface properties of diamond. 相似文献