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41.
Serge Mignani Francis Lahousse Robert Merényi Zdenek Janousek Heinz Gunter Viehe 《Tetrahedron letters》1985,26(38):4607-4608
Carbanions carrying captodative substitution are readily oxidized to their dimers. 相似文献
42.
Infrared and Raman spectra of gaseous cyclopropanecarboxylic acid (C3H5COOH and C3H5COOD) were measured from 250 to 4000 cm?1. The bands were assigned respectively to the monomer and to an associate. The depolarization ratio measurement, the vib—rot envelope study and the detailed analysis of the v(CO) and v(CH) regions enabled the symmetry and the conformation of the molecular entities in equilibrium to be determined. The monomer belongs to the Cs symmetry group and the conformation of its predominant fraction is trans/trans. The associate is a centrosymmetrical dimer (Ci symmetry) having (trans/cis)2 conformation. Some features of the geometry of the pseudocycle are discussed. 相似文献
43.
Abohachem Laguecir Serge Ulrich Jérôme Labille Nicolas Fatin-Rouge Serge Stoll Jacques Buffle 《European Polymer Journal》2006,42(5):1135-1144
Monte Carlo simulations, experimental titrations and fluorescence correlation spectroscopy experiments were used to investigate the conformational and electrical properties of polyacrylic acids (PAA). On the one hand, titration curves were calculated to get an insight into the role of pH on the degree of ionization and conformation of PAA chains. On the other hand, experimental potentiometric titrations of PAA were also achieved for different PAA molecular weights and compared to the calculated titration curves obtained by Monte Carlo coarse grained simulations. It was found that for a large range at intermediate PAA ionizations, a good correlation is obtained between experimental and simulations data thanks to the prominence of electrostatic interactions in this domain. The effect of ionic concentration and PAA molecular weight on the titration curves was also investigated. In order to get a better understanding of PAA conformational behavior, we also investigated PAA diffusion properties in aqueous solutions as a function of pH and ionic strength by fluorescence correlation spectroscopy (FCS), thanks to its high sensitivity to measure diffusion coefficients of tracer solutes. Good qualitative agreements were observed between experimental diffusivities and polymer properties calculated from MC simulations. It was shown that the high molecular weight PAA chains display more significant changes in diffusivity in agreement with the ionization degrees and conformational changes observed in the simulations. 相似文献
44.
Christophe Thurieau Christel Guyard Serge Simonet Tony J. Verbeuren Jean-Luc Fauchre 《Helvetica chimica acta》1994,77(3):679-684
The synthesis on solid phase of a new derivative of the anticoagulant protein hirudin is described (see Scheme and Fig.1, I ). The henicosapeptide is a bivalent conjugate of the C-terminus of hirudin and of the active-site-binding tetrapeptide D -Phe-Pro-Arg-Pro linked via a tetraglycine spacer. The peptide, for which the name hirufos was coined, incorporates a stable phosphono derivative of L -phenylalanine which, combined with the other structural modifications, leads to a potent anticoagulant agent. Synthesis was readily achieved by the (9H-fluoren-9-yl)-methoxycarbonyl (Fmoc) strategy followed by acidolytic cleavage from the resin and deprotection, including the liberation of the crucial phosphonic group on L -phenylalanine. 相似文献
45.
Gérald S. Remaud Virginie Silvestre Serge Akoka 《Accreditation and quality assurance》2005,10(8):415-420
The choice of the reference, either as internal or external is not straightforward in quantitative NMR. In this context ERETIC™
methodology appears as an universal referencing technique. An electronic signal, generated by the NMR spectrometer during
the acquisition time, operates as a virtual working standard. The processes for ensuring a traceability to primary standards
is illustrated on the official method devoted to (D/H)i ratios measurement on ethanol, using quantitative 2H-NMR. The ERETIC approach is shown to be equivalent to its official homologue, in terms of accuracy and precision. Finally,
its performance could be beneficial to other analytes, matrices and nuclei. 相似文献
46.
Serge Schubert Philippe Renaud Pierre-Alain Carrupt Kurt Schenk 《Helvetica chimica acta》1993,76(7):2473-2489
Radical addition to enamines using Bu3SnH as reducing agent are reported (Schemes 2 and 4). The diastereoselectivity of these reactions was examined in different systems (Tables 1 and 2). Enamines derived from cyclic ketones such as cyclohexanone were alkylated with high diastereoselectivity with preferential formation of the cis-disubstituted cycloalkanes. In acyclic systems such as enamines derived from propiophenone and diethyl ketone, moderate to high stereoselectivities were observed in the H-abstraction step. A model based principally on minimization of allylic 1,3-strain (A1,3 strain) was deduced from the experimental results and semi-empirical (AM1) calculations. 相似文献
47.
Reversed phase high performance liquid chromatography (RPLC) is currently the method of choice for the analysis of basic compounds. However, with traditional silica materials, secondary interactions between the analyte and residual silanols produce peak tailing which can negatively affect resolution, sensitivity, and reproducibility. In order to reduce these secondary interactions, which comprise ion exchange, hydrogen bonding, and London forces interactions, chromatographic analyses can be carried out at low or high pH values where silanol groups and basic compounds are mostly uncharged. The chromatographic behaviour of a particular bidentate stationary phase, Zorbax Extend C18, was studied with a set of basic and neutral compounds. Thanks to a higher chemical stability than traditional silica based supports, analyses were carried out with a high pH mobile phase, which represents a good alternative to the acidic mobile phases generally used to reduce ion exchange interactions. The performance of this bidentate stationary phase was also compared with that of other supports and it was proved that it is advantageous to work with high pH mobile phases when analyzing basic compounds. 相似文献
48.
The quantum groupsgl
andA
are constructed. The representation theory of these algebras is developed and the universalR-matrix is presented. 相似文献
49.
The color of a complex number is defined as the number of vertices of the convex hull of powers of that number. This induces a coloring of the unit disk. The structure of the set of points where the color changes is investigated here. It is observed that there is a connection between this fractal set and some family of trinomial equations. Three algorithms for coloring the unit disk are described, the last one (related to the Farey sequence) arising out of a conjecture. This conjecture is formulated and proved in this presentation. 相似文献
50.
In order to detect small variations in 13C isotopomers concentrations, high sensitivity, accuracy and precision have to be achieved. To assess such criteria, when using 13C NMR, 13C bi-labelled ethanol has been proposed as a molecular probe. Advantage has been taken of the pre-established structural relationship between the peak areas of the 13C NMR spectrum of this molecule, i.e. the ratio of signal areas is set to a fixed value. It is shown that the quality performance, required by quantitative 13C NMR spectroscopy, is not affected by a large reduction of the repetition delay using relaxation reagents. 相似文献