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1.
Let ir(G) and γ(G) be the irredundance number and the domination number of a graph G, respectively. A graph G is called irredundance perfect if ir(H)=γ(H), for every induced subgraph H of G. In this article we present a result which immediately implies three known conjectures on irredundance perfect graphs. © 2002 Wiley Periodicals, Inc. J Graph Theory 41: 292–306, 2002 相似文献
2.
Vadim Kaimanovich 《Israel Journal of Mathematics》1995,89(1-3):77-134
Covering Markov operators are a measure theoretical generalization of both random walks on groups and the Brownian motion
on covering manifolds. In this general setup we obtain several results on ergodic properties of their Poisson boundaries,
in particular, that the Poisson boundary is always infinite if the deck group is non-amenable, and that the deck group action
on the Poisson boundary is amenable. For corecurrent operators we show that the Radon-Nikodym cocycles of two quotients of
the Poisson boundary are cohomologous iff these quotients coincide. It implies that the Poisson boundary is either purely
non-atomic or trivial, and that the action of any normal subgroup of the deck group on the Poisson boundary is conservative.
We show that the Poisson boundary is trivial for any corecurrent covering operator with a nilpotent (or, more generally, hypercentral)
deck group. Other applications and examples are discussed.
Supported by a British SERC Advanced Fellowship. A part of this work was done during my stay at MSRI, Berkeley supported by
NSF Grant DMS 8505550. 相似文献
3.
ZverovichIE ZverovichOI 《高校应用数学学报(英文版)》2004,19(2):125-132
Two new hereditary classes of P5-free graphs where the stability number can be found in polynomial time are proposed. They generalize several known results. 相似文献
4.
We consider a class of homogeneous manifolds including all semisimple coadjoint orbits. We describe manifolds of that class
admitting deformation quantizations equivariant under the action ofG and the corresponding quantum group. We also classify Poisson brackets relating to such quantizations.
Presented at the 11th Colloquium “Quantum Groups and Integrable Systems”, Prague, 20–22 June 2002. 相似文献
5.
Journal of Algebraic Combinatorics - A set $$S\subseteq V$$ is independent in a graph $$G=\left( V,E\right) $$ if no two vertices from S are adjacent. The independence number $$\alpha (G)$$ is the... 相似文献
6.
Chemo- and regioselectivity in the reactions between highly electrophilic fluorine containing dicarbonyl compounds (ethyl 4,4,4-trifluoroacetoacetate, 3,3,3-trifluoropyruvate and 1,1,1,5,5,5-hexafluoropentane-2,4-dione) and various benzylamines were systematically studied. The results obtained lead to the development of a generalized and practical method for large-scale synthesis of the corresponding imines/enamines, useful starting materials for preparation fluorinated amines and amino acid. 相似文献
7.
8.
Eugene A. Komissarov Yuri I. Baukov Eugeniya P. Kramarova Sergey Yu. Bylikin Vadim V. Negrebetsky Alexander A. Korlyukov 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(4):m144-m146
In the title compound, [Ge(C8H14NO)2Cl]CF3SO3, which is the first complex containing an eight‐membered lactam (enantholactam) as ligand, the coordination polyhedron of the GeIV atom is intermediate between trigonal–bipyramidal and square‐pyramidal. Quantum chemical calculations of the crystal structure indicate the absence of additional coordination bonding between the GeIV atom and the trifluoromethanesulfonate anion. 相似文献
9.
Konstantin N. Gavrilov Pavel V. Petrovskii AntonS. Safronov Vadim A. Davankov 《Tetrahedron》2005,61(44):10514-10520
Novel P-monodentate aryl phosphite ligands have been synthesised in one step from (R)-BINOL, (R)-H8-BINOL and (R)-H8-3,3′-dibromo-BINOL. With the new aryl phosphites, up to 86% ee was observed in the asymmetric Pd-catalysed amination of 1,3-diphenyl-2-propenyl acetate with sodium diformylamide. In the enantioselective alkylation of 1,3-diphenyl-2-propenyl acetate with dimethyl malonate, up to 97% enantioselectivity was achieved. 相似文献
10.
Specific sorption sites for nitrogen, N2, in NaLSX and LiLSX zeolites were investigated using a DRIFT spectroscopic method. Sorption of molecular hydrogen, H2, by NaLSX or LiLSX zeolite at 77 K with DRIFT control of perturbation of sorbed molecules allowed to discriminate two or three different types of specific sorption sites in the respective zeolites. Their H–H stretching frequencies are 4077 and 4081 cm–1 for NaLSX, and 4061, 4084 and 4129 cm–1 for LiLSX. With reference to an independent investigation by methods of both sorption thermodynamics and molecular modeling for N2 sorption on LiLSX, the first two of the corresponding bands were ascribed to H2 sorption on lithium cations, Li+, localized in supercages of the faujasite, FAU, zeolite framework at sites SIII and SIII, while the latter band most likely belongs to H2 sorption on Li+ cations at sites SII, and on hydroxyl groups, OH. Sorption of N2 by Li+ cations at sites SIII and SIII is the strongest, resulting in a decrease of intensity of the corresponding DRIFT bands that stem from subsequent H2 sorption. Nitrogen sorption by Li+ cations at sites SII is much weaker. Sorption of N2 on Na+ cations at sites SIII in NaLSX zeolite is also stronger than by Na+ cations at sites SII. 相似文献