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31.
Jakub Opršal 《Order》2018,35(3):433-460
We provide a partial result on Taylor’s modularity conjecture, and several related problems. Namely, we show that the interpretability join of two idempotent varieties that are not congruence modular is not congruence modular either, and we prove an analog for idempotent varieties with a cube term. Also, similar results are proved for linear varieties and the properties of congruence modularity, having a cube term, congruence n-permutability for a fixed n, and satisfying a non-trivial congruence identity. 相似文献
32.
Jakub Przybyło 《Random Structures and Algorithms》2015,47(4):776-791
Consider a simple graph G = (V,E) and its proper edge colouring c with the elements of the set {1,2,…,k}. The colouring c is said to be neighbour sum distinguishing if for every pair of vertices u, v adjacent in G, the sum of colours of the edges incident with u is distinct from the corresponding sum for v. The smallest integer k for which such colouring exists is known as the neighbour sum distinguishing index of a graph and denoted by . The definition of this parameter, which makes sense for graphs containing no isolated edges, immediately implies that , where Δ is the maximum degree of G. On the other hand, it was conjectured by Flandrin et al. that for all those graphs, except for C5. We prove this bound to be asymptotically correct by showing that . The main idea of our argument relays on a random assignment of the colours, where the choice for every edge is biased by so called attractors, randomly assigned to the vertices. © 2014 Wiley Periodicals, Inc. Random Struct. Alg., 47, 776–791, 2015 相似文献
33.
Consider a simple graph and its proper edge coloring c with the elements of the set . We say that c is neighbor set distinguishing (or adjacent strong) if for every edge , the set of colors incident with u is distinct from the set of colors incident with v. Let us then consider a stronger requirement and suppose we wish to distinguishing adjacent vertices by sums of their incident colors. In both problems the challenging conjectures presume that such colorings exist for any graph G containing no isolated edges if only . We prove that in both problems is sufficient. The proof is based on the Combinatorial Nullstellensatz, applied in the “sum environment.” In fact the identical bound also holds if we use any set of k real numbers instead of as edge colors, and the same is true in list versions of the both concepts. In particular, we therefore obtain that lists of length ( in fact) are sufficient for planar graphs. 相似文献
34.
Consider a graph of minimum degree δ and order n. Its total vertex irregularity strength is the smallest integer k for which one can find a weighting such that for every pair of vertices of G. We prove that the total vertex irregularity strength of graphs with is bounded from above by . One of the cornerstones of the proof is a random ordering of the vertices generated by order statistics. 相似文献
35.
Marlena Pięta Jacek Kędzia Dorota Kowalczyk Jakub Wojciechowski Wojciech M. Wolf Tomasz Janecki 《Tetrahedron》2019,75(17):2495-2505
An efficient, versatile, enantioselective synthesis of 1,3-disubstituted and 1,3,6-trisubstituted 5-methylidenedihydrouracils applying Horner-Wadsworth Emmons methodology was developed. Starting 1,3-disubstituted 5-diethoxyphosphoryluracils were subjected to reduction of the double bond or addition of various Grignard reagents and obtained Horner-Wadsworth Emmons reagents were used for the olefination of formaldehyde. Enantioselective synthesis of 1,3,6-trisubstituted 5-methylidenedihydrouracils was accomplished by introducing (R,R)- or (S,S)-di(1-phenylethylamino)phosphoryl groups as chiral auxiliary. Additions of Grignard reagents in the presence of these groups were highly and complimentary diastereoselective (de?~?80%). Further separation of the diastereomeric mixtures by column chromatography enabled synthesis of (R)- and (S)-1,3,6-trisubstituted-5-methylidenedihydrouracils with ee?≥?98%. Furthermore, absolute configuration of the adducts and final products was established using single crystal X-ray analysis. Stereochemical course of the addition reactions is also discussed. 相似文献
36.
Krystyna Maslowska-Jarzyna Maria L. Korczak Jakub A. Wagner Micha J. Chmielewski 《Molecules (Basel, Switzerland)》2021,26(11)
Owing to their strong carbazole chromophore and fluorophore, as well as to their powerful and convergent hydrogen bond donors, 1,8-diaminocarbazoles are amongst the most attractive and synthetically versatile building blocks for the construction of anion receptors, sensors, and transporters. Aiming to develop carbazole-based colorimetric anion sensors, herein we describe the synthesis of 1,8-diaminocarbazoles substituted with strongly electron-withdrawing substituents, i.e., 3,6-dicyano and 3,6-dinitro. Both of these precursors were subsequently converted into model diamide receptors. Anion binding studies revealed that the new receptors exhibited significantly enhanced anion affinities, but also significantly increased acidities. We also found that rear substitution of 1,8-diamidocarbazole with two nitro groups shifted its absorption spectrum into the visible region and converted the receptor into a colorimetric anion sensor. The new sensor displayed vivid color and fluorescence changes upon addition of basic anions in wet dimethyl sulfoxide, but it was poorly selective; because of its enhanced acidity, the dominant receptor-anion interaction for most anions was proton transfer and, accordingly, similar changes in color were observed for all basic anions. The highly acidic and strongly binding receptors developed in this study may be applicable in organocatalysis or in pH-switchable anion transport through lipophilic membranes. 相似文献
37.
Dr. Santiago Alonso-Gil Dr. Kamil Parkan Dr. Jakub Kaminský Dr. Radek Pohl Dr. Takatsugu Miyazaki 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(14):e202200148
The conformational changes in a sugar moiety along the hydrolytic pathway are key to understand the mechanism of glycoside hydrolases (GHs) and to design new inhibitors. The two predominant itineraries for mannosidases go via OS2→B2,5→1S5 and 3S1→3H4→1C4. For the CAZy family 92, the conformational itinerary was unknown. Published complexes of Bacteroides thetaiotaomicron GH92 catalyst with a S-glycoside and mannoimidazole indicate a 4C1→4H5/1S5→1S5 mechanism. However, as observed with the GH125 family, S-glycosides may not act always as good mimics of GH's natural substrate. Here we present a cooperative study between computations and experiments where our results predict the E5→B2,5/1S5→1S5 pathway for GH92 enzymes. Furthermore, we demonstrate the Michaelis complex mimicry of a new kind of C-disaccharides, whose biochemical applicability was still a chimera. 相似文献
38.
39.
Timo Fuchs Valentín Briega-Martos Jakub Drnec Natalie Stubb Isaac Martens Federico Calle-Vallejo Prof. David A. Harrington Serhiy Cherevko Prof. Olaf M. Magnussen 《Angewandte Chemie (International ed. in English)》2023,62(34):e202304293
The degradation of Pt-containing oxygen reduction catalysts for fuel cell applications is strongly linked to the electrochemical surface oxidation and reduction of Pt. Here, we study the surface restructuring and Pt dissolution mechanisms during oxidation/reduction for the case of Pt(100) in 0.1 M HClO4 by combining operando high-energy surface X-ray diffraction, online mass spectrometry, and density functional theory. Our atomic-scale structural studies reveal that anodic dissolution, detected during oxidation, and cathodic dissolution, observed during the subsequent reduction, are linked to two different oxide phases. Anodic dissolution occurs predominantly during nucleation and growth of the first, stripe-like oxide. Cathodic dissolution is linked to a second, amorphous Pt oxide phase that resembles bulk PtO2 and starts to grow when the coverage of the stripe-like oxide saturates. In addition, we find the amount of surface restructuring after an oxidation/reduction cycle to be potential-independent after the stripe-like oxide has reached its saturation coverage. 相似文献
40.
Jakub Koza Margitta Uhlemann Annett Gebert Ludwig Schultz 《Journal of Solid State Electrochemistry》2008,12(2):181-192
The effect of a uniform magnetic field with flux density up to 1 T on the electrodeposition of Fe from sulphate electrolyte
has been investigated under different field configurations relative to the electrode surface. Voltammetric and chronoamperometric
experiments have been carried out coupled with an electrochemical quartz crystal microbalance for in situ mass change measurements.
The structure and morphology of the deposited films were determined by scanning electron microscopy, atomic force microscopy
and X-ray diffraction measurements. Results show that, when the magnetic field is applied parallel to the electrode surface,
the limiting current density and the deposition rate are increased due to the magnetohydrodynamic effect. The nucleation process
is also affected in parallel configuration; the current density of the maximum on the chronoamperograms is decreased, and
an additional nucleation step might be observed. This effect is attributed to the hydrodynamic response of the electrochemical
system. No significant influence on the electrochemical reaction was observed when a magnetic field was applied perpendicular
to the electrode. But in this configuration, the morphology of deposited layers is changed by the magnetic field. The morphology
changes are discussed. No effect of the magnetic field on the crystallographic structure was observed. 相似文献