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41.
Bourdolle A Allali M Mulatier JC Le Guennic B Zwier JM Baldeck PL Bünzli JC Andraud C Lamarque L Maury O 《Inorganic chemistry》2011,50(11):4987-4999
Two europium complexes with bis(bipyridine) azamacrocyclic ligands featuring pendant arms with or without π-conjugated donor groups are synthesized and fully characterized by theoretical calculations and NMR spectroscopy. Their photophysical properties, including two-photon absorption, are investigated in water and in various organic solvents. The nonfunctionalized ligand gives highly water-stable europium complexes featuring bright luminescence properties but poor two-photon absorption cross sections. On the other hand, the europium complex with an extended conjugated antenna ligand presents a two-photon absorption cross section of 45 GM at 720 nm but is poorly luminescent in water. A detailed solvent-dependent photophysical study indicates that this luminescence quenching is not due to the direct coordination of O-H vibrators to the metal center but to the increase of nonradiative processes in a protic solvent induced by an internal isomerization equilibrium. 相似文献
42.
Hossini I Harrad MA Ait Ali M El Firdoussi L Karim A Valerga P Puerta MC 《Molecules (Basel, Switzerland)》2011,16(7):5886-5895
Friedel-Craft acylation at 100 °C of 2,5,9,9-tetramethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene [ar-himachalene], a sesquiterpenic hydrocarbon obtained by catalytic dehydrogenation of α-, β- and γ-himachalenes, produces a mixture of two compounds: (3,5,5,9-tetramethyl-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-yl)-ethanone (2, in 69% yield), with a conserved reactant backbone, and 3, with a different skeleton, in 21% yield. The crystal structure of 3 reveals it to be 1-(8-ethyl-8-hydroperoxy-3,5,5-trimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-ethanone. In this compound O-H…O bonds form dimers. These hydrogen-bonds, in conjunction with weaker C-H…O interactions, form a more extended supramolecular arrangement in the crystal. 相似文献
43.
Harrad MA Valerga P Puerta MC Houssini I Ali MA El Firdoussi L Karim A 《Molecules (Basel, Switzerland)》2011,16(1):367-372
A recyclable catalyst, Ni(0)-CMC-Na, composed of nickel colloids dispersed in a water soluble bioorganic polymer, sodium carboxymethylcellulose (CMC-Na), was synthesized by a simple procedure from readily available reagents. The catalyst thus obtained is stable and highly active in alkene hydrogenations. 相似文献
44.
Nonlinear Dynamics - This paper examines periodic and quasi-periodic (QP) vibration-based energy harvesting (EH) in a nonlinear energy sink (NES) absorber that is coupled to an electric circuit... 相似文献
45.
Mustapha Aouchiche 《Discrete Mathematics》2007,307(2):262-265
A conjecture of Delorme, Favaron and Rautenbach [On the Randi? index, Discrete Math. 257 (2002) 29-38] about the Randi? index of a graph, in relation to its order and minimum degree, is refuted by the AutoGraphiX 2 system. Moreover, a modified conjecture is derived from presumably extremal graphs obtained with that system. 相似文献
46.
Mustapha Bahani Francoise Lauprêtre Lucien Monnerie 《Journal of Polymer Science.Polymer Physics》1995,33(2):167-178
Differential scanning calorimetry and torsional braid analysis investigations of the phase diagram of cis-1,4-polyisoprene/polybutadiene blends as a function of the polybutadiene microstructure were reported by several authors. Polybutadienes containing a high vinyl content were shown to be miscible with cis-1,4-polyisoprene on the DSC spatial scale, whereas polybutadienes containing a low vinyl content were immiscible. In this article, we used variable-temperature determinations of 1H NMR free induction decays and low-temperature, high-resolution solid-state 13C NMR measurements of proton spin-lattice relaxation times in the rotating frame to probe the phase behavior of the cis-1,4-polyisoprene/polybutadiene blends at the smaller spatial scale of the NMR technique. Blends of cis-1,4-polyisoprene with a polybutadiene having a large number of vinyl 1,2 linkages appeared to be miscible on the molecular scale, in spite of small regions in which the polybutadiene component is not uniformily dispersed in the other polymer. On the contrary, blends in which the polybutadiene has a low content of vinyl 1,2 sequences were phase separated over the whole temperature range considered and no intermixed regions could be detected. The limiting case was observed with the polybutadiene containing 33 wt % vinyl 1,2 units, for which miscibility on a molecular scale is highly dependent on the blend composition. © 1995 John Wiley & Sons, Inc. 相似文献
47.
Aromatization of cyclohexadienes by TEMPO electro-mediated oxidation: Kinetic and structural aspects
Cyclohexadienes are easily converted into the corresponding aromatics in excellent yield (>90%) in the presence of 2,2,6,6-tetramethyl-1-oxopiperidinium ion (TEMPO+). The TEMPO radical was used in catalytic amount and was electrochemically regenerated in the presence of 2,6-lutidine as a base in hydro-organic medium (AcCN/H2O 95/5). This work has been focused on the kinetic aspects. We have demonstrated that the reactivity of different cyclohexadienes is strongly dependent on the configuration of the double bonds and on the nature of the substituents. Competition between allylic functionalization and aromatization has been observed during the oxidation of 1,2-dihydro-4-phenylnaphthalene. 相似文献
48.
49.
Positivity - In this paper, we establish, in the setting of infinite dimensional Hilbert space, a new existence result for nonconvex sweeping process with right uniformly lower semicontinuous sets.... 相似文献
50.
Farida Benmouna Zohra Bouabdellah-Dembahri Mustapha Benmouna 《Journal of Macromolecular Science: Physics》2013,52(7):998-1008
The process of polymer synthesis based on polymerization-induced phase separation (PIPS) is revisited from the theoretical point of view. Cahn–Hilliard–Cook theories for spinodal decomposition are adapted to describe the kinetics of phase separation and deduce the time-resolved scattering function, while the double reaction model is used to describe the kinetics of polymerization. Coupling of these two kinetics is provided by the Carother's equation relating the fraction of reacted monomers to the degree of polymerization at time t, denoted N(t). It is argued that the approach to criticality is governed by a critical parameter, χc, that is different from the usual parameter for spinodal decomposition, χs, deduced from the second derivative of the free energy. While the latter parameter depends on the reciprocal degree of polymerization N?1(t), the former one depends on its time integral. This leads to significant consequences on the phase behavior developments during the PIPS process. Hydrodynamic interactions are found to speed up the emergence of instability modes. Although the qualitative trends remain similar to those of the Rouse dynamics, important quantitative changes are found due to the long-range viscous flow effects. 相似文献