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141.
Fractal analysis of hydroxyapatite from nitrogen isotherms 总被引:10,自引:0,他引:10
Samples of calcium hydroxyapatite, CaHap, were prepared via a wet method and subjected to thermal treatment in air in the temperature range 100-900 degrees C. Nitrogen adsorption-desorption isotherms were obtained on different samples, and their data points were used to analyze the fractal properties of the obtained solids. Both FHH and Neimark's equations were used for such purpose, and the agreement or disagreements between obtained results on using both equations are discussed. Considering the appropriate values of the obtained surface fractal dimensions D, it was concluded that an appreciable defractalization of the prepared hydroxyapatite is only noted upon calcinations at 900 degrees C. Below this temperature the loss in surface area and pore volume result from simultaneous bulk and surface mass transport, which conserve the initial surface roughness and average pore radius. Calcination at 900 degrees C caused sintering to proceed via bulk mass transport, with a consequent pore widening and a decrease in surface roughness. 相似文献
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143.
Bin Du Adam Langlois Daniel Fortin Christine Stern Pierre D. Harvey 《Journal of Cluster Science》2012,23(3):737-751
The title cluster is luminescent at 77?K and exhibits an unsaturated site for binding anions when the counter ion is PF6 ?. A series of five non-luminescent metalloporphyrins exhibiting carboxylate anchoring groups were synthesized and characterized. These are the sodium salts of the 5-carboxyphenyl-tri-10,15,20-tolyl-, trans-di-5,10-carboxyphenyl-di-15,20-tolyl-, and tetra-5,10,15,20-carboxyphenyl(metallo)porphyrin (metallo?=?chloroiron(III), nickel(II)) anions. Evidence for supramolecular assemblies between the carboxylates and the cluster is provided by 31P NMR and UV?Cvis spectroscopy. The binding constant, K1n, extracted from the UV?Cvis data via Benesi-Hildebrand, Scott and Scatchard plots are approximately 21,000?±?5,000?M?1 for the nickel(II) species, in agreement with the previously reported zinc(II) ones (K11?=?20,000?±?2,000?M?1), but those for the chloroiron(III) are measured to be lower (12,500?±?3,500?M?1). This association is accompanied by a complete quenching of the luminescence of the cluster which can only be due to an efficient energy transfer to the d?Cd states of the chloroiron(III) and nickel(II) species but an electron transfer from the nickel(II)-containing chromophore to the cluster is also possible. This work demonstrates the profound effect that supramolecular interactions may have on the photophysical properties despite the long donor?Cacceptor separation. 相似文献
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Christine A. Bange Prof. Dr. Rory Waterman 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(36):12598-12605
Despite significant advances, metal‐catalyzed hydrophosphination has ample room for discovery, growth, and development. Many of the key successes in metal‐catalyzed hydrophosphination over the last decade have indicated what is needed and what is yet to come. Reactivity that is absent from the literature also speaks to the challenges in catalytic hydrophosphination. This Concept article discusses and highlights recent developments that address the ongoing challenges, and identifies areas in metal‐catalyzed hydrophosphination that are underdeveloped. Advances in product selectivity, catalyst design, and both unsaturated and phosphine substrates illustrate the ongoing development of the field. Like all catalytic transformations, the benefits are realized through catalyst, ligand, and conditions, and consideration of those features are the route to a yet more efficient and broadly applicable reaction. 相似文献
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149.
Irene Bravo-Osuna Christine Vauthier Alessandra Farabollini Gioconda Millotti Gilles Ponchel 《Journal of nanoparticle research》2008,10(8):1293-1301
Surface modified nanoparticles composed of poly(isobutylcyanoacrylate) (PIBCA) cores surrounded by a chitosan and thiolated
chitosan gel layer were prepared and characterized in previous works. The presence of such biopolymers on the nanoparticle
surface conferred those nanosystems interesting characteristics that might partially overcome the gastrointestinal enzymatic
barrier, improving the oral administration of pharmacologically active peptides. In the present work, the antiprotease behaviour
of this family of core–shell nanoparticles was in vitro tested against two model metallopeptidases present in the gastrointestinal
tract (GIT): Carboxypeptidase A -CP A- (luminal protease) and Leucine Aminopeptidase M -LAP M- (membrane protease). As previous
step, the zinc-binding capacity of these nanoparticles was evaluated. Interestingly, an improvement of both the zinc-binding
capacity and the antiprotease effect of chitosan was observed when the biopolymers (chitosan and thiolated chitosan) were
used as coating component of the core–shell nanoparticles, in comparison with their behaviour in solution, thanks to the different
biopolymer chains rearrangement. The presence of amino, hydroxyl and thiol groups on the nanoparticle surface promoted zinc
binding and hence the inhibition of the metallopeptidases analysed. On the contrary, the occurrence of a cross-linked structure
in the gel layer surrounding the PIBCA cores of thiolated formulations, due to the formation of interchain and intrachain
disulphide bonds, partially limited the inhibition of the proteases. The low accessibility of cations to the active groups
of the cross-linked polymeric shell was postulated as a possible explanation of this behaviour. Results obtained in this work
make this family of surface-modified nanocarriers promising candidates for the successfull administration of pharmacologically
active peptides and proteins by the oral route. 相似文献
150.
LetX be a complex manifold with finitely many ends such that each end is eitherq-concave or (n−q)-convex. If
, then we prove thatH
pn−q
(X) is Hausdorff for allp. This is not true in general if
(Rossi’s example withn=2 andq=1). If all ends areq-concave, then this is the classical Andreotti-Vesentini separation theorem (and holds also for
). Moreover the result was already known in the case when theq-concave ends can be ‘filled in’ (again also for
). To prove the result we first have to study Serre duality for the case of more general families of supports (instead of
the family of all closed sets and the family of all compact sets) which is the main part of the paper. At the end we give
an application to the extensibility of CR-forms of bidegree (p, q) from (n−q)-convex boundaries,
.
This research was partially supported by TMR Research Network ERBFMRXCT 98063. 相似文献