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91.
I. Jánossy 《Pramana》2003,61(2):435-445
It is suggested that liquid crystal—polymer interfaces are coupled systems, in which the components mutually influence the
orientational state of each other. The photo-orientation process at liquid crystal-polymer interfaces provides a striking
example of such a coupling. Experiments show that the anisotropic structure generated by polarised light at a polymer surface
is strongly affected by the phase of the liquid crystal covering the polymer. Photo-orientation is significantly more efficient
when the liquid crystal is in the isotropic phase than when it exhibits orientational order. The observations are interpreted
by assuming that in the smectic and nematic phases the liquid crystal stabilises to a large extent polymer chain-segments
aligned parallel to the director, while it blocks the photo-induced formation of chain-segments in the perpendicular direction.
Other situations, in which the coupling between the liquid crystal and the polymer can be important, are also discussed briefly. 相似文献
92.
Use of ab initio X-ray powder diffraction (XRPD) methods in the study of magnetically active species of covalent nature is presented. Selected cases are chosen in order to underline the power of XRPD methodologies, highlighting the importance of independent physico-chemical information from ancillary techniques. 相似文献
93.
The use of reagent concentration has resulted in increased rates for all stages of the REM resin synthesis of tertiary amines. These increases in rate translate into faster reaction times, higher yields and lower reagent consumption. Of the methods examined, the most successful was the use of perfluorous solvents, either alone or with a small amount of organic co-solvent. 相似文献
94.
Yozo Miura Masamichi Dairoku 《Journal of polymer science. Part A, Polymer chemistry》2007,45(18):4364-4376
Dendritic multifunctional macroinitiators having six and 12 TIPNO‐based alkoxyamines, TIPNO‐6 and TIPNO‐12 , were synthesized and used in the living radical polymerization of styrene (St), methyl acrylate (MA), N,N‐dimethylacrylamide (DMAAm), and isoprene (IP). The polymerizations of St initiated with TIPNO‐6 gave 6‐arm star polymers with narrow polydispersities of 1.14–1.18. In the polymerizations of MA initiated with TIPNO‐6 and TIPNO‐12 , the influences of added TIPNO on the polydispersity indexes (PDIs) of the resulting star polymers were first investigated, and this led to the successful formation of poly(MA) star polymers with narrow polydispersities (1.10–1.18). Moreover, the polymerizations of DMAAm and IP from TIPNO‐6 in the presence or absence of TIPNO were briefly investigated. The benzyl ether bonds of the poly(St) and poly(MA) star polymers were cleaved by treating with Me3SiI or Pd/C, and the resulting arm's parts were analyzed with SEC. The PDIs of the resulting arm parts were low (1.19–1.23), and the Mns agreed with the Mn,theor, indicating that the poly(St) and poly(MA) star polymers had well‐controlled arms. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4364–4376, 2007 相似文献
95.
Michael C. W. Chan Dr. 《化学:亚洲杂志》2008,3(1):18-27
The notion of weak attractive ligand–polymer interactions is introduced, and its potential application, importance, and conceptual links with “cooperative” ligand–substrate interactions are discussed. Synthetic models of weak attractive ligand–polymer interactions are described, in which intramolecular weak C? H???F? C interactions (the existence of which remains contentious) have been detected by NMR spectroscopy and neutron and X‐ray diffraction experiments. These C? H???F? C interactions carry important implications for the design of catalysts for olefin polymerization, because they provide support for the practical feasibility of ortho‐F???Hβ ligand–polymer contacts proposed for living Group 4 fluorinated phenoxyimine catalysts. The notion of weak attractive noncovalent interactions between an “active” ligand and the growing polymer chain is a novel concept in polyolefin catalysis. 相似文献
96.
Andrei N. Yakunin 《Central European Journal of Physics》2004,2(3):535-555
A cubic structure of polymer colloid complexes is studied. The technique of the research includes i) an analysis of well-known
literature SAXS data; on this basis, ii) constructing a simple model to estimate geometric structure parameters and to obtain
a simulated scattering curve; and iii) comparing the model with the real structure obtained from the SAXS data, using the
reconstruction of electron density distribution. A bicontinuous structure in cubic mesophases is formed.
Dedicated to the memory of Alexander T. Dembo 相似文献
97.
简述了高聚物薄膜玻璃化转变的复杂性,并结合文章作者的的一些研究结果介绍了扫描力显微术(SFM)在研究高聚物玻璃化转变中的一些方法,包括观察高聚物薄膜形貌的变化,测量其摩擦力、粘附力和弹性模量等物理量的变化,最后指出SFM是研究高聚物薄膜玻璃化转变的有力工具。 相似文献
98.
Tsutomu Nakanishi Hajime Okamoto Maki Kasahara Kyozaburo Takeda 《Journal of Polymer Science.Polymer Physics》2003,41(22):2829-2849
We theoretically investigated the polymorphy of the stereostructures of a periodic polymer. Using the polymer's internal conformation parameters of bond lengths, bond angles, and internal rotation angles, we extended the mathematical treatment for designing polymer backbones. We considered those periodic polymers whose unit cell consists of one (m = 1), two (m = 2), or three (m = 3) kinds of atoms. Moreover, for these three types of polymers, we supposed two catenation types for the skeleton atoms; one is a “homorotatory” sequence and the other is a “heterorotatory” one. To specify the backbone's stereostructure, we introduced several conformation parameters such as the helical pitch number n, the translation distance d, and the inclination angle of the skeleton plane Θ. By combining these parameters, we can systematically understand the variety and the possible polymorphy in the stereostructure of a periodic polymer backbone. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 2829–2849, 2003 相似文献
99.
Monica Sorescu L Diamandescu D Tarabasanu-Mihaila 《Journal of Physics and Chemistry of Solids》2004,65(10):1719-1725
α-Fe2O3-In2O3 mixed oxide nanoparticles system has been synthesized by hydrothermal supercritical and postannealing route, starting with (1−x)Fe(NO3)3·9H2O·xIn(NO3)3·5H2O aqueous solution (x=0-1). X-ray diffraction and Mössbauer spectroscopy have been used to study the phase structure and substitutions in the nanosized samples. The concentration regions for the existence of the solid solutions in the α-Fe2O3-In2O3 nanoparticle system together with the solubility limits of In3+ ions in the hematite lattice and of Fe3+ ions in the cubic In2O3 structure have been evidenced. In general, the substitution level is considerably lower than the nominal concentration x. A justification of the processes leading to the formation of iron and indium phases in the investigated supercritical hydrothermal system has been given. 相似文献
100.
N. Fazeli F. Afshar Taromi 《Journal of polymer science. Part A, Polymer chemistry》2003,41(1):135-142
The basis of the two‐step in–in method is as follows: star polymers with poly(divinyl benzene) cores, synthesized by the arm‐first method, include many unreacted double bonds in their core, and these double bonds can be attacked by the carbanions of some monomers such as styrene and dienes. In this work, linear polyisoprene chains were used to attack the double bonds existing in the poly(divinyl benzene) cores of polystyrene star polymers, so that a heteroarm star polymer with polystyrene and polyisoprene arms was synthesized. It was later well characterized with size exclusion chromatography, light scattering, viscometry, UV spectroscopy, dynamic mechanical thermal analysis, and 1H NMR. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 135–142, 2003 相似文献