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71.
72.
Ronald I. Becker Isabella Lari Andrea Scozzari Giovanni Storchi 《Annals of Operations Research》2007,150(1):65-78
In this paper we consider the location of a path shaped facility on a grid graph. In the literature this problem was extensively
studied on particular classes of graphs as trees or series-parallel graphs. We consider here the problem of finding a path
which minimizes the sum of the (shortest) distances from it to the other vertices of the grid, where the path is also subject
to an additional constraint that takes the form either of the length of the path or of the cardinality. We study the complexity
of these problems and we find two polynomial time algorithms for two special cases, with time complexity of O(n) and O(nℓ) respectively, where n is the number of vertices of the grid and ℓ is the cardinality of the path to be located.
The literature about locating dimensional facilities distinguishes between the location of extensive facilities in continuous
spaces and network facility location. We will show that the problems presented here have a close connection with continuous
dimensional facility problems, so that the procedures provided can also be useful for solving some open problems of dimensional
facilities location in the continuous case. 相似文献
73.
The Nd:YAG laser-induced breakdown of 20 μm glass microspheres was investigated using time-resolved optical shadow and Schlieren images. Time-resolved imaging showed the location of the initial breakdown and the shockwave motion over its first 400 μm of expansion. Measured shockwave velocities were in the range of 1–10 km/s and showed a linear dependency on laser fluence within 30 ns. 相似文献
74.
75.
76.
77.
Christian Kluger Wolfgang H. Binder 《Journal of polymer science. Part A, Polymer chemistry》2007,45(3):485-499
Block copolymers on basis of poly(oxanorbornenes) bearing functional moieties in their side‐chains are prepared via a combination of ROMP‐methods and 1,3‐dipolar‐“click”‐reactions. Starting from N‐substituted‐ω‐bromoalkyl‐oxanorbornenes and alkyl‐/perfluoroalkyl‐oxanorbornenes, block copolymers with molecular weights up to 25,000 g mol?1 were generated. Subsequent nucleophilic exchange‐reactions yielded the block‐copolymers functionalized with ω‐azidoalkyl‐moieties in one block. The 1,3‐azide/alkine‐“click” reactions with a variety of terminal alkynes in the presence of a catalyst system consisting of tetrakis(acetonitrile)hexafluorophosphate copper(I) and tris(1‐benzyl‐5‐methyl‐1H‐ [1,2,3]triazol‐4‐ylmethyl)‐amine furnished the substituted block copolymers in high yields, as proven by NMR‐spectroscopy. The resulting polymers were investigated via temperature‐dependent SAXS‐methods, revealing their microphase separated structure as well as their temperature‐dependent behavior. The presented method offers the generation of a large set of different block‐copolymers from only a small set of starting materials because of the high versatility of the “click” reaction, thus enabling a simple and complete functionalization after the initial polymerization reaction. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 485–499, 2007 相似文献
78.
Christian Buchgraber Alexander Pogantsch Stefan Kappaun Julia Spanring Wolfgang Kern 《Journal of polymer science. Part A, Polymer chemistry》2006,44(14):4317-4327
Light‐emitting diodes based on organic materials [organic light‐emitting diodes (OLEDs)] have attracted much interest over the past decade. Several different attempts have been made to realize multicolor OLEDs. This article describes a new approach based on energy transfer in a donor/acceptor system. A copolymer containing both donor and acceptor compounds as comonomer units is prepared. The polymer consists of a derivative of a luminescent dye [4‐dicyanmethylene‐2‐methyl‐6‐4H‐pyran (DCM); acceptor compound], which is copolymerized with fluorene (donor compound) to combine the properties of an electroactive polymer with a highly luminescent dye. Photochemical processing is achieved by UV irradiation of this copolymer in the presence of gaseous trialkylsilanes. This reagent selectively saturates the C?C bonds in the DCM comonomer units while leaving the fluorene units essentially unaffected. As a result of the photochemical process, the red electroluminescence of the acceptor compound vanishes, and the blue‐green electroluminescence from the polyfluorene units is recovered. Compared with previous approaches based on polymer blends, this copolymer approach avoids problems associated with phase‐separation phenomena in the active layer of OLEDs. © 2006Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4317–4327, 2006 相似文献
79.
Mousa Z. Al-Noaimi Raid J. Abdel-Jalil Mustafa M. El-Abadelah Salim F. Haddad Younis N. H. Baqi Wolfgang Voelter 《Monatshefte für Chemie / Chemical Monthly》2006,37(12):745-750
In the presence of RuCl3, N-phenylamidrazone underwent oxidative cyclization into 1,4-dihydro-1-phenyl-1,2,4-benzotriazine, the structure of which is
established by spectral and X-ray diffraction data. 相似文献
80.
Wolfgang H. Binder Laura Petraru Robert Sachenshofer Ronald Zirbs 《Monatshefte für Chemie / Chemical Monthly》2006,137(7):835-841
Summary. The surface modification of nanoparticles via azide/alkine-1,3-dipolar cycloaddition-reactions is described. Ligand exchange onto various nanoparticles was monitored by
1H NMR spectroscopy and formed the basis for the attachment of ligands onto the nanoparticles and their subsequent modification
by dipolar cycloaddition reactions. Nanoparticle-surfaces were monitored by binding onto self-assembled monolayers derivatized
with matching supramolecular interactions after derivatization. 相似文献