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排序方式: 共有67条查询结果,搜索用时 15 毫秒
1.
Tzanetos NP Dracopoulos V Kallitsis JK Deimede VA 《Langmuir : the ACS journal of surfaces and colloids》2005,21(20):9339-9345
A detailed study of the self-assembly ability of triblock coil-rod-coil copolymers containing a rigid di(styryl)-anthracene segment covalently linked to oxadiazole-based blocks and their binary blends with oxadiazole-based homopolymers is presented here. The self-organized microdomains seem to pack into a fascinating ordered hexagonal structure obtained at a critical concentration without any significant influence of the sample preparation method, based on evidence obtained by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and fluorescence microscopy studies. The compatibilization efficiency of these coil-rod-coil copolymers in polymer blends composed of an electron-accepting polyoxadiazole and a luminescent polyanthracene-based pair was studied by atomic force microscopy (AFM). The common feature of all observed morphologies is the compatibilizing function of the rod-coil molecule, which intercalates between the incompatible domains to prevent the formation of well-defined phase separated nanostructured surfaces. 相似文献
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Radiation-induced and radical-initiated copolymerizations of norbornencarboxylic acid with maleic anhydride have been studied. In both cases decarboxylation occurs during the copolymerization; the composition of the copolymers is independent of the method of initiation and of the composition of the initial monomer feed. The decarboxylation is caused by the norbornencarboxylic acid and not by maleic anhydride. This result is supported by the observation that, during the radical homopolymerization of norbornencarboxylic acid also, carbon dioxide is split off. 相似文献
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Menger FM Zhang H de Joannis J Kindt JT 《Langmuir : the ACS journal of surfaces and colloids》2007,23(5):2308-2310
A molecular dynamics simulation was carried out involving a paclitaxel molecule, 987 peptoad molecules, and 35 938 water molecules (conditions shown experimentally to effect paclitaxel solubilization in water). The peptoads are shown to form large clumps, the centers of which are dry and thus favorable to hydrogen bonding between paclitaxel and peptoads. Hydrogen-bonding equilibrium among the peptoads themselves in the developing clumps is achieved in 2 ns. The number and position of hydrogen bonds between the paclitaxel and peptoads fluctuate randomly from two to six within a 2-5 ns time frame. Hydrophobic association between the peptoad chains and the apolar paclitaxel groups does not seem to be an important element of the solubilization. Instead, the hydrophobic chains of the peptoads encasing the paclitaxel extend outward into the dry interior of the peptoad clump where other chains in the clump are located. One hopes that studies such as this will ultimately allow rational predictions when designing new and specific drug solubilizers. 相似文献
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D. Apostolakis P. Ditsas S. Katsanevas 《Zeitschrift fur Physik C Particles and Fields》1997,76(2):201-211
We present and study the results for the standard model process $e^ + e^ - \to \nu \bar \nu b\bar b$ at c.m. energies 150 ≤ √s(GeV) ≤ 240 and for Higgs boson masses 60 GeV ≤ m H ≤ 110 GeV, obtained from all tree-level diagrams and including the most important radiative corrections. The matrix elements have been calculated by the ‘spinor bracket’ method without neglecting masses, which is presented in detail. The √s-dependence and the interference properties of the Higgs boson contributions and of various coherent background contributions to the total cross section are examined and compared. The important differential distributions for the Higgs boson and the background components are studied, providing information useful for choosing cuts in Higgs searches. We also examine the effect of a minimal set of cuts and evaluate the importance of the WW fusion for detecting a higher mass Higgs boson at LEP II. 相似文献
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Nikos P. Tzanetos Joannis K. Kallitsis 《Journal of polymer science. Part A, Polymer chemistry》2005,43(5):1049-1061
Atom transfer radical polymerization was used to prepare well‐defined vinyl polyoxadiazole homomacromonomers with a properly modified α‐dicarboxylic acid methyl ester as the initiator. Macromonomers of various molecular weights with narrow polydispersities in some cases were obtained, as proved by gel permeation chromatography (GPC). The structures of the obtained macromonomers were then identified with 1H NMR spectroscopy. These macromonomers were subsequently copolymerized with a dihydroxy anthracene based monomer by a polycondensation technique, and this resulted in polymacromonomers. Coil–rod–coil copolymers containing side‐chain anthracene and oxadiazole units were also synthesized by atom transfer radical polymerization. The resulting copolymers combined an anthracene derivative as the rigid block with a random copolymer of the desired anthracene‐ and/or oxadiazole‐based monomers as the flexible block. These copolymers were primarily characterized with GPC and 1H NMR techniques. Additionally, the optical properties of all these copolymers were investigated in detail, and they suggested energy transfer from the oxadiazole to the anthracene chromophores, which became much more efficient in the solid state. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1049–1061, 2005 相似文献
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Evdokia K. Oikonomou Aikaterini Bethani Georgios Bokias Joannis K. Kallitsis 《European Polymer Journal》2011,(4):752-761
A series of poly(sodium styrene sulfonate)-b-poly(methyl methacrylate), PSSNa-b-PMMA, amphiphilic diblock copolymers have been synthesized through atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) in N,N-dimethylformamide/water mixtures, starting from a PSSNa macroinitiator. The kinetics of the polymerization was followed by 1H NMR, while the chemical composition of the copolymers was verified by a variety of techniques, such as 1H NMR, FTIR and TGA. The MMA content of the copolymers ranges from 0 up to 60 mol%, while the number–average molecular weight of the PSSNa macroinitiator was 9000 g/mol. The self-association of the diblock copolymers in aqueous solution was compared to the respective behavior of similar random P(SSNa-co-MMA) copolymers through optical density measurements, pyrene fluorescence probing, dynamic light scattering and surface tension measurements. It is shown that the diblock copolymers form micellar structures in water, characterized by an increasing hydrophobic character and a decreasing size as the length of the PMMA block increases. These micelle-like structures turn from surface inactive to surface active as the length of the PMMA block increases. Moreover, contrary to the MMA-rich random copolymers, the respective diblock copolymers form water insoluble polymer/surfactant complexes with cationic surfactants such as hexadecyltrimethyl ammonium bromide (HTAB), leading to materials with antimicrobial activity. 相似文献