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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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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
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Ewan Davies Rmi de Joannis de Verclos Ross J. Kang Franois Pirot 《Random Structures and Algorithms》2020,57(3):730-744
We prove two distinct and natural refinements of a recent breakthrough result of Molloy (and a follow‐up work of Bernshteyn) on the (list) chromatic number of triangle‐free graphs. In both our results, we permit the amount of color made available to vertices of lower degree to be accordingly lower. One result concerns list coloring and correspondence coloring, while the other concerns fractional coloring. Our proof of the second illustrates the use of the hard‐core model to prove a Johansson‐type result, which may be of independent interest. 相似文献
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Chemical reactions transform the reactant molecules by deleting existing and forming new bonds. The identification of these so-called reacting bonds is important for studying the reaction mechanism and for applications in metabolomics, e.g. for interpreting substrate labeling experiments. Here, we introduce an approach which suggests the simplest possible reaction center at the heavy atom level, with high accuracy. In contrast to current methods the approach is motivated by a simple theoretical model based on a crude approximation of the reaction energetics, and takes the complete reacting system into account. Finally, it recovers all optimal solutions to the problem while removing all symmetry-related, redundant solutions. We apply the method on the complete KEGG database of biochemical reactions, and compare our approach with previous methods. The resulting reaction centers are represented as imaginary transition states, which are molecule-like representations of reaction mechanisms. We provide the statistics of the calculations on the KEGG database and discuss some examples for the different types of alternative solutions found. 相似文献
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Joannis Papavassiliou 《Few-Body Systems》2016,57(6):417-423
The form of the kernel that controls the dynamics of the Bethe–Salpeter equations is essential for obtaining quantitatively accurate predictions for the observable properties of hadrons. In the present work we briefly review the basic physical concepts and field-theoretic techniques employed in a first-principle derivation of a universal (process-independent) component of this kernel. This “top-down” approach combines nonperturbative ingredients obtained from lattice simulations and Dyson–Schwinger equations, and furnishes a renormalization-group invariant quark-gluon interaction strength, which is in excellent agreement with the corresponding quantity obtained from a systematic “bottom-up” treatment, where bound-state data are fitted within a well-defined truncation scheme. 相似文献