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41.
Giuseppe Bruno Archimede Rotondo Giuseppe Tresoldi Francesco Nicol Santo Lanza 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(4):m169-m172
The crystal structure of the title compound, [Ru(C10H8N2S)2(C11H11N3S)](PF6)2·C2H3N, is composed of a bivalent octahedral RuII complex, two PF6− anions and an acetonitrile solvent molecule. Two PF6− units are found on a crystallographic binary axis, therefore contributing just one half each to the asymmetric unit cell. The structure displays a peculiar stereochemistry of the cation. Three bidentate ligands around the Ru centre, together with the coordination of the non‐symmetric S atom, mean that these two atoms are chiral. This would lead to four stereoisomers, but only an enantiomeric pair was found in the analyzed sample. 相似文献
42.
V. I. Burenkov P. D. Lamberti M. Lanza de Cristoforis 《Journal of Mathematical Sciences》2008,149(4):1417-1452
The survey is devoted to spectral stability problems for uniformly elliptic differential operators under the variation of
the domain and to the accompanying estimates for the difference of the eigenvalues. Two approaches to the problem are discussed
in detail. In the first one it is assumed that the domain is transformed by means of a transformation of a certain class,
and the spectral stability with respect to this transformation is investigated. The second approach is based on the notion
of a transition operator and allows direct comparison of the eigenvalues on domains which are close in that or another sense.
__________
Translated from Sovremennaya Matematika. Fundamental’nye Napravleniya (Contemporary Mathematics. Fundamental Directions),
Vol. 15, Differential and Functional Differential Equations. Part 1, 2006. 相似文献
43.
44.
S. C. L. Gerritzen M. Kaufman L. Rosenthaler M. Roy S. Camilla J. Großfeld S. H. Bertram C. Stiebel G. W. Jennings R. D. Lewis J. Pritzker R. Jungkunz P. Bruère A. Fourmont W. L. Roberts H. A. Schuette J. K. Chowdhury S. M. Das-Gupta A. L. Bernoullie 《Analytical and bioanalytical chemistry》1933,92(11-12):451-461
45.
Camilla Nilsson Eva Malmström Mats Johansson Stacy M. Trey 《Journal of polymer science. Part A, Polymer chemistry》2009,47(2):589-601
A series of well‐defined allyl‐ether functionalized polyester dendrimers has been synthesized via the divergent approach using traditional esterification reactions. Two commercially available trifunctional thiols, trimethylolpropane tri(3‐mercaptopropanoate) (TRIS) and ethoxylated trimethylolpropane tri(3‐mercaptopropanoate) (ETTMP), were incorporated with the dendrimers into the thiol‐ene polymer networks. The thiol‐ene reactions were conducted at room temperature and cured by UV light without the addition of photoinitiatior. Highly crosslinked films were obtained and characterized with respect to mechanical (DMA) and thermal (DSC and TGA) properties. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 589–601, 2009 相似文献
46.
Camilla Nilsson Neil Simpson Michael Malkoch Mats Johansson Eva Malmström 《Journal of polymer science. Part A, Polymer chemistry》2008,46(4):1339-1348
Well‐defined, allyl‐ether functional, first‐generation dendrimers have been synthesized. The convergent growth approach was utilized, using the anhydride of the allyl‐ether terminated building block. Three different core moieties were used: trimethylolpropane, trisphenol, and ditrimethylolpropane. The coupling reactions proceeded in good yields and all compounds were characterized by NMR, MALDI‐TOF, and SEC. The allyl‐terminated dendrimers were crosslinked by thiol–ene chemistry, using a multifunctional thiol, TriThiol, to give clear and smooth films. The photopolymerization was conducted in the presence of a photoinitiator, Irgacure 651, and no traces of either allyl‐ether groups or thiols were observed by FT‐Raman after cure. All crosslinked films were characterized with respect to mechanical (DMA) and thermal (DSC) properties. It was found that homogeneous networks were formed and that the core functionality and structure had little effect on the network properties. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1339–1348, 2008 相似文献
47.
48.
Johan Sjöblom Camilla Dagsgård Sébastien Simon Geir Sørland Morten Hana 《Journal of Dispersion Science and Technology》2017,38(2):206-215
The present study reports on the influence of partially hydrolyzed polyacrylamide (HPAM) on essential w/o emulsion properties. The characterization has been undertaken with low field NMR to follow droplet sizes and distributions, sedimentation and coalescence kinetic, bench-scale electrocoalescence (Ecrit) experiments to follow emulsion stability changes, and electrorheology to detect changes in the viscosity upon applying an external electric field. The result is that HPAM does not basically influence the droplet size distribution (DSD) and the stability level of the emulsions as can be expected of bulk polymers. However, there seems to be an interaction between added demulsifiers either through direct molecular interaction or via an interfacial complexation. 相似文献
49.
Synthetic studies devoted to the development of a convergent approach toward phoslactomycins and leustroducsins, a family of natural products inhibitors of serine/threonine phosphatase 2A, are reported. A formal synthesis of phoslactomycin B was achieved in which the key steps are a [2,3]-Wittig rearrangement to control the C4 and C5 stereocenters, a diastereoselective addition of an acetylenic Grignard reagent to an α-alkoxy ketone to create the C8 tertiary alcohol, and a relay ring-closing metathesis to construct the α,β-unsaturated δ-lactone. In this approach, all the stereocenters originate, either directly or indirectly, from catalytic enantioselective reductions of acetylenic ketones. 相似文献
50.
Camilla D. Buarque Boniek Gontijo Vaz Alcides J.M. da Silva 《Journal of organometallic chemistry》2010,695(18):2062-310
The Pd(OAc)2-catalyzed oxyarylation of electron-rich (8 and 12) and electron-poor (10) olefins by ortho-iodophenols (3a-d) was studied using Ag2CO3 as the base, in acetone, and in the presence and absence of PPh3. The corresponding adducts of oxyarylation were obtained in moderate yields. The reaction mechanism was examined by electrospray ionization mass spectrometry (ESI-MS). Cationic arylpalladium intermediate (14), formed by the oxidative insertion of Pd(0) into 3a, and the cationic palladacycles (15), obtained by reaction of 14 with olefins 8 and 12, were intercepted by ESI-MS and characterized by ESI-MS/MS. 相似文献