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41.
Carmela Musella 《Rendiconti del Circolo Matematico di Palermo》2001,50(1):129-136
A subgroupH of a groupG is said to bealmost normal inG if it has only finitely many conjugates inG. The setan(G) of almost normal subgroups ofG is a sublattice of the lattice of all subgroups ofG. Isomorphisms between lattices of almost normal subgroups ofFC-soluble groups are considered in this paper. In particular, properties of images of normal subgroups under such an isomorphism
are investigated. 相似文献
42.
Costanza Aricò Marco Sinagra Tullio Tucciarelli 《Journal of computational physics》2012,231(4):1387-1425
A novel methodology is proposed for the solution of the flow equation in a variably saturated heterogeneous porous medium. The computational domain is descretized using triangular meshes and the governing PDEs are discretized using a lumped in the edge centres numerical technique. The dependent unknown variable of the problem is the piezometric head. A fractional time step methodology is applied for the solution of the original system, solving consecutively a prediction and a correction problem. A scalar potential of the flow field exists and in the prediction step a MArching in Space and Time (MAST) formulation is applied for the sequential solution of the Ordinary Differential Equation of the cells, ordered according to their potential value computed at the beginning of the time step. In the correction step, the solution of a large linear system with order equal to the number of edges is required. A semi-analytical procedure is also proposed for the solution of the prediction step. The computational performance, the order of convergence and the mass balance error have been estimated in several tests and compared with the results of other literature models. 相似文献
43.
A. M. Castro Luna A. Bonesi W. E. Triaca A. Di Blasi A. Stassi V. Baglio V. Antonucci A. S. Aricò 《Journal of nanoparticle research》2010,12(1):357-365
Three cathode catalysts (60% Pt/C, 30% Pt/C and 60% Pt–Fe/C), with a particle size of about 2–3 nm, were prepared to investigate
the effect of ethanol cross-over on cathode surfaces. All samples were studied in terms of structure and morphology by using
X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses. Their electrocatalytic behavior in terms of oxygen
reduction reaction (ORR) was investigated and compared using a rotating disk electrode (RDE). The tolerance of cathode catalysts
in the presence of ethanol was evaluated. The Pt–Fe/C catalyst showed both higher ORR activity and tolerance to ethanol cross-over
than Pt/C catalysts. Moreover, the more promising catalysts were tested in 5 cm2 DEFC single cells at 60 and 80 °C. An improvement in single cell performance was observed in the presence of the Pt–Fe catalyst,
due to an enhancement in the oxygen reduction kinetics. The maximum power density was 53 mW cm−2 at 2 bar rel. cathode pressure and 80 °C. 相似文献
44.
Incoronata Tritto Maria Carmela Sacchi Paolo Locatelli San Xi Li 《Macromolecular Symposia》1995,89(1):289-298
The reaction equilibria of Cp2Ti13CH3Cl and Cp2Ti(CH3)2 with AlMe3 (TMA) and/or methylaluminoxane (MAO) have been investigated by 13C NMR. Several adducts have been identified. A study of the 13C 90% enriched ethylene polymerization in an NMR tube in the presence of the above catalytic systems, in the most experimentally significant conditions, and a comparison of the NMR data with the catalytic activity have been made as well. It has been shown that: i) some species are side products, inactive for addition ethylene polymerization; ii) active cation-like species such as Cp2TiMe+Cl·[AlMeO]n- and Cp2TiMe+Me·[AlMeO]n- are formed in titanocene-MAO systems. Concerning the role of AlMe3, contained in MAO solutions, it has been shown that: a) AlMe3 is mainly bound to MAO; b) if some “free” AlMe3 exists in solution it is not the actual cocatalyst in the metallocene-MAO based catalytic systems; c) the amount of AlMe3 influences either active or inactive species. 相似文献
45.
Azzaroni O Mir M Alvarez M Tiefenauer L Knoll W 《Langmuir : the ACS journal of surfaces and colloids》2008,24(6):2878-2883
In the present work, we describe the properties of a bifunctional redox-labeled bioconjugate at electrode surfaces mediating the electron transfer across the electrode-electrolyte interface. We show that the assembly of ferrocene-labeled streptavidin on biotinylated electrodes results in a reproducible unidirectional current flow in the presence of electron donors in solution. Such rectifying films were built up by spontaneous binding of tetrameric streptavidin molecules to biotin centers immobilized on the electrode surface. Due to the high affinity of biotin to streptavidin, such bifunctional films completely bind any biotinylated compounds. The charge transport between donors in solution and the Au electrode is mediated by the ferrocene moieties, allowing us to develop a molecular rectifier. Our experimental results suggest that such redox-labeled proteins with a high binding capacity constitute a promising alternative to organic compounds used in molecular electronics. 相似文献
46.
Femoni C Iapalucci MC Longoni G Zacchini S 《Chemical communications (Cambridge, England)》2008,(27):3157-3159
Reaction of [Ni(6)(CO)(12)](2-) with CCl(4) in CH(2)Cl(2) gives the [HNi(25)(C(2))(4)(CO)(32)](3-) and [Ni(22)(C(2))(4)(CO)(28)Cl](3-) carbonyl clusters containing interstitial Ni(eta(2)-C(2))(4) and Ni(2)(micro-eta(2)-C(2))(4) acetylide moieties. 相似文献
47.
A study of the reduction of CuO in a ternary oxide system (Cu:Zn:Al, atomic ratio 62:14:24) demonstrated that at lower temperatures it occurred in two stages, whereas at higher temperatures it was no longer possible to display the formation of Cu2O. The rate of reduction of CuO was strongly reduced on decreasing the partial pressure of hydrogen, while the presence of CO2 stabilized the Cu2O, delaying the reduction to copper. On the basis of simpler systems it was possible to demonstrate the activating effect of Al2O3 and the delaying effect of ZnO on the reduction of CuO. 相似文献
48.
Dr. Christian Schmitz Prof. Walter Leitner Dr. Giancarlo Franciò 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(30):10696-10702
A library of α,α,α,α‐tetraaryl‐1,3‐dioxolane‐4,5‐dimethanol (TADDOL)‐based phosphoramidites has been synthesized and applied in the Ni‐catalyzed cycloisomerization of different dienes. Through the systematic variation of the three structural motifs of the lead structure, that is, the amine moiety, the protecting group, and the aryl substituents, the ligand features could be optimized for the asymmetric cycloisomerization of the model substrate diethyl diallylmalonate. The substrate scope of the new catalytic system was extended to other diallylic substrates, including unsymmetrical dienes. Overall remarkably high activities of up to approximately 13 500 h?1, very high selectivities toward five‐membered exo‐methylenecyclopentanes, and enantioselectivities of up to 92 % ee have been achieved. 相似文献
49.
Potential of prodendronic polyamines with modulated segmental charge density as novel coating for fast and efficient analysis of peptides and basic proteins by CE and CE‐MS 下载免费PDF全文
Tanize Acunha Clara Ibáñez María Isabel Pascual Reguera Mariagiovanna Sarò Rodrigo Navarro Juan Alfonso Redondo Helmut Reinecke Alberto Gallardo Carolina Simó Alejandro Cifuentes 《Electrophoresis》2015,36(14):1564-1571
In this work, the suitability of a new polymer family has been investigated as capillary coatings for the analysis of peptides and basic proteins by CE. This polymer family has been designed to minimize or completely prevent protein–capillary wall interactions and to modify the EOF. These coating materials are linear polymeric chains bearing as side cationizable moiety a dentronic triamine derived from N,N,N’,N’‐tetraethyldiethylenetriamine (TEDETA), which is linked to the backbone through a spacer (unit labeled as TEDETAMA). Four different polymers have been prepared and evaluated: a homopolymer which comprised only of those cationizable repetitive units of TEDETAMA, and three copolymers that randomly incorporate TEDETAMA together with neutral hydrosoluble units of N‐(2‐hydroxypropyl) methacrylamide (HPMA) at different molar percentages (25:75, 50:50 and 75:25). It has been demonstrated that the composition of the copolymers influences the EOF and therefore the separation of the investigated biopolymers. Among the novel polymers studied, poly‐(TEDETAMA‐co‐HPMA) 50:50 copolymer was successfully applied as coating material of the inner capillary surface in CE‐UV and CE‐MS, providing EOF reversing together with fast and efficient baseline separation of peptides and basic proteins. Finally, the feasibility of the polymer‐coated capillary was shown through the analysis of lysozyme in a cheese sample. 相似文献
50.
Hidalgo C Rios C Hidalgo M Salvadó V Sancho JV Hernández F 《Journal of chromatography. A》2004,1035(1):153-157
An existing method for the determination of glyphosate and its main metabolite aminomethylphosphonic acid (AMPA) in water has been improved. It is based on precolumn derivatization with the fluorescent reagent 9-fluorenylmethylcloroformate (FMOC) followed by large-volume injection in a coupled-column LC system using fluorescence detection (LC-LC-FD). The derivatization step was slightly modified by changing parameters such as volume and/or concentration of sample and reagents to decrease the limits of quantification (LOQ) of glyphosate and AMPA to 0.1 microg/l. Additionally, the use of Amberlite IRA-900 for preconcentration of glyphosate, prior to the derivatization step, was investigated; the LOQ of glyphosate was lowered to 0.02 microg/l. Drinking, surface and ground water spiked with glyphosate and AMPA at 0.1-10 microg/l concentrations were analysed by the improved LC-LC-FD method. Recoveries were 87-106% with relative standard deviations lower than 8%. Drinking and ground water spiked with glyphosate at 0.02 and 0.1 microg/l were analysed after preconcentration on the anion-exchange resin with satisfactory recoveries (94-105%) and precision (better than 8%). 相似文献