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Haruyuki Okamura Minoru Kayanoki Kohei Takada Hideyuki Nakajiri Keiko Muramatsu Munenori Yamashita Masamitsu Shirai 《先进技术聚合物》2012,23(8):1151-1155
High‐resolution screen printing was devised. New resist formulation contains a base polymer, which consists of acid‐labile tetrahydropyranyl‐protected carboxylic acid, hydroxyl, and methacrylic functions. As crosslinkers, multifunctional acrylates were employed. Photoacid generators were used for pattern formation. A 10‐µm feature size of resist on a screen plate was obtained on irradiation at 365 nm and followed by development on a stainless steel screen. Post‐exposure curing improved the mechanical characteristics of the resist patterns. A 13‐µm feature size silver circuit was successfully printed on poly(ethylene terephthalate) film without defect. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
53.
Yang JH Song KS Zhang GJ Degawa M Sasaki Y Ohdomari I Kawarada H 《Langmuir : the ACS journal of surfaces and colloids》2006,22(26):11245-11250
Here, we report a novel method of micropatterning oligonucleotides via aromatic groups as linkers on partially amino-terminated diamond and the inherence on subsequent hybridization. The covalent immobilization of probe oligonucleotides and characterization of immobilized probe oligonucleotides with carboxylic compounds were investigated by X-ray photoelectron spectroscopy (XPS). To confirm the effects of linker flexibility in a low amino group on diamond for probe oligonucleotides, three kinds of dicarboxylic compound--adipic acid, terephthalic acid, and trimesic acid--were used for immobilization of probe oligonucleotides, like linkers; and these oligonucleotides were hybridized with target oligonucleotides labeled with Cy 5 on the micropatterned diamond surface. The hybridization intensities determined by epifluorescence microscopy were compared and analyzed. 相似文献
54.
We have exploited novel supramolecular wrapping techniques by helix-forming polysaccharides, β-1,3-glucans, which have strong tendency to form regular helical structures on versatile nanomaterials in an induced-fit manner. This approach is totally different from that using the conventional interpolymer interactions seen in both natural and synthetic polymeric architectures, and therefore has potential to create novel polymeric architectures with diverse and unexpected functionalities. The wrapping by β-1,3-glucans enforces the entrapped guest polymer to adopt helical or twisted conformations through the convergent interpolymer interactions. On the contrary, the wrapping by chemically modified semi-artificial β-1,3-glucans can bestow the divergent self-assembling abilities on the entrapped guest polymer to create hierarchical polymeric architectures, where the polymer/β-1,3-glucan composite acts as a huge one-dimensional building block. Based on the established wrapping strategy, we have further extended the wrapping techniques toward the creation of three-dimensional polymeric architectures, in which the polymer/β-1,3-glucan composite behaves as a sort of amphiphilic block copolymers. The present wrapping system would open several paths to accelerate the development of the polymeric supramolecular assembly systems, giving the strong stimuli to the frontier of polysaccharide-based functional chemistry. 相似文献
55.
Combination of supramolecular chemistry with molecular recognition has been successfully applied to creating large superstructures with a wide variety of morphologies. Control of shapes and patterns of ordered molecular assemblies in nano and micro scales has attracted considerable interest as promising bottom-up technology. It is known, however, that these molecular assembling superstructures are fragile, reflecting the characteristic of the non-covalent interaction, a driving force operating in these molecular systems. In fact, they easily collapse or change by small perturbation in the environmental conditions. Thus, over the last decade, researchers have been seeking possible methods for the immobilization these superstructures. This critical review focuses on recent advances in in situ post-modification under the influence of the molecular assemblies as templates and polymerization of ordered molecular assemblies such as organogel fibers and crystals to preserve their original superstructures and intensify their mechanical strength. 相似文献
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Prof. Dr. Munenori Numata Yusuke Takigami Momoko Takayama Tomohiro Kozawa Naoya Hirose 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(41):13008-13017
One of the fundamental problems in supramolecular chemistry, as well as in material sciences, is how to control the self‐assembly of polymers on the nanometer scale and how to spontaneously organize them towards the macroscopic scale. To overcome this problem, inspired by the self‐assembly systems in nature, which feature the dynamically controlled self‐assembly of biopolymers, we have previously proposed a self‐assembly system that uses a dynamic liquid/liquid interface with dimensions in the micrometer regime, thereby allowing polymers to self‐assemble under precisely controlled nonequilibrium conditions. Herein, we further extend this system to the creation of hierarchical self‐assembled architectures of polysaccharides. A natural polysaccharide, β‐1,3‐glucan (SPG), and water were injected into opposite “legs” of microfluidic devices that had a Y‐shape junction, so that two solvents would gradually mix in the down stem, thereby causing SPG to spontaneously self‐assemble along the flow in a head‐to‐tail fashion, mainly through hydrophobic interactions. In the initial stage, several SPG nanofibers would self‐assemble at the Y‐junction owing to the shearing force, thereby creating oligomers with a three‐way junction point. This unique structure, which could not be created through conventional mixing procedures, has a divergent self‐assembly capability. The dynamic flow allows the oligomers to interact continuously with SPG nanofibers that are fed into the Y‐junction, thus amplifying the nanostructure along the flow to form SPG networks. Consequently, we were able to create stable, centimeter‐length macroscopic polysaccharide strands under the selected flow conditions, which implies that SPG nanofibers were assembled hierarchically in a supramolecular fashion in the dynamic flow. Microscopic observations, including SEM and AFM analysis, revealed the existence of clear hierarchical structures inside the obtained strand. The network structures self‐assembled to form sub‐micrometer‐sized fibers. The long fibers further entangled with each other to give stable micrometer‐sized fibers, which finally assembled to form the macroscopic strands, in which the final stabilities in the macroscopic regime were governed by that of the network structures in the nanometer regime. Thus, we have exploited this new supramolecular system to create hierarchical polymeric architectures under precisely controlled flow conditions, by combining the conventional supramolecular strategy with microfluidic science. 相似文献
59.
Munenori Sumiyoshi Hiroko Kuritani Keiji Shingu Masazumi Nakagawa 《Tetrahedron letters》1980,21(30):2855-2856
The recently assigned diastereomeric configuration of 3,8-di-t-butylspiro[4.4]nonane-1,6-dione has been revised based on the X-ray analysis. 相似文献
60.
Haraguchi S Hasegawa T Numata M Fujiki M Uezu K Sakurai K Shinkai S 《Organic letters》2005,7(25):5605-5608
[chemical structure: see text]. Schizophyllan can interact with permethyldecasilane to produce the corresponding decasilane-nanofiber, in which the decasilane adopts helical conformations in a tubular hollow created by the helical superstructure of schizophyllan. 相似文献