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101.
Dr. Changfeng Hong Takahiro Otabe Saki Matsumoto Dr. Chikara Dohno Dr. Asako Murata Dr. Masaki Hagihara Prof. Dr. Kazuhiko Nakatani 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(18):5282-5287
The hairpin structure is one of the most common secondary structures in RNA and holds a central position in the stream of RNA folding from a non‐structured RNA to structurally complex and functional ribonucleoproteins. Since the RNA secondary structure is strongly correlated to the function and can be modulated by the binding of small molecules, we have investigated the modulation of RNA folding by a ligand‐assisted formation of loop–loop complexes of two RNA hairpin loops. With a ligand (NCT6), designed based on the ligand binding to the G–G mismatches in double‐stranded DNA, we successfully demonstrated the formation of both inter‐ and intra‐molecular NCT6‐assisted complex of two RNA hairpin loops. NCT6 selectively bound to the two hairpin loops containing (CGG)3 in the loop region. Native polyacrylamide gel electrophoresis analysis of two doubly‐labeled RNA hairpin loops clearly showed the formation of intermolecular NCT6‐assisted loop–loop complex. Förster resonance energy‐transfer studies of RNA constructs containing two hairpin loops, in which each hairpin was labeled with Alexa488 and Cy3 fluorophores, showed the conformational change of the RNA constructs upon binding of NCT6. These experimental data showed that NCT6 simultaneously bound to two hairpin RNAs at the loop region, and can induce the conformational change of the RNA molecule. These data strongly support that NCT6 functions as molecular glue for two hairpin RNAs. 相似文献
102.
Manganese‐Corrole Complexes as Versatile Catalysts for the Ring‐Opening Homo‐ and Co‐Polymerization of Epoxide 下载免费PDF全文
Dr. Carine Robert Takahiro Ohkawara Prof. Dr. Kyoko Nozaki 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(16):4789-4795
Manganese‐corrole complexes in combination with a co‐catalyst [PPN]X ([PPN]+=bis(triphenylphosphoranylidene)iminium) were found to be new versatile catalysts for the polymerization of epoxides, copolymerization of epoxides with CO2, and copolymerization of epoxides with cyclic anhydrides affording a wide range of polymeric materials. This work should allow the synthesis of new types of improved innovative (co)polymers with original properties and would clearly increase the number of applications for polyesters, polycarbonates, and polyethers. 相似文献
103.
Facile Synthesis of Dibenzopentalene Dianions and Their Application as New π‐Extended Ligands 下载免费PDF全文
Takuya Kuwabara Dr. Kazuya Ishimura Prof. Dr. Takahiro Sasamori Prof. Dr. Norihiro Tokitoh Prof. Dr. Masaichi Saito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(25):7571-7575
Reduction of phenyl(silyl)ethynes with potassium followed by quenching with iodine gave dibenzopentalenes in moderate yields. The intermediates of the reactions, dipotassium dibenzopentalenides, were isolated. The first dibenzopentalene–transition‐metal complex was successfully synthesized. The ruthenium atoms are located above the six‐membered rings. However, X‐ray diffraction analysis and theoretical calculations revealed that the aromatic nature of the five‐membered rings was retained. The cyclic voltammetry of the Ru complex revealed two oxidation waves with relatively large separation. 相似文献
104.
Back Cover: Motion Capture and Manipulation of a Single Synthetic Molecular Rotor by Optical Microscopy (Angew. Chem. Int. Ed. 38/2014) 下载免费PDF全文
105.
Takahiro Gunji Kengo Hirama Satoru Tsukada Yoshimoto Abe 《Journal of Sol-Gel Science and Technology》2014,72(1):80-84
An organic–inorganic hybrid was prepared by simply mixing a fullerene derivative with polymethoxysiloxane. First, C60 was subjected to a radical addition reaction with 4,4′-azobis(4-cyanovaleric acid) to provide a C60 derivative. Polymethoxysiloxane was prepared by a controlled hydrolytic condensation of tetramethoxysilane. These two compounds were mixed and heated to provide hybrid bulk body. The hybrid bulk body showed high mechanical strength and elastic modulus compared with polymethoxysiloxane or the C60/polymethoxysiloxane hybrid. The formation of a dense siloxane network was established by a homogeneous mixing of the C60 derivative with polymethoxysiloxane. 相似文献
106.
Inagaki Makoto Sekimoto Shun Tadokoro Takahiro Ueno Yuichiro Kani Yuko Ohtsuki Tsutomu 《Journal of Radioanalytical and Nuclear Chemistry》2020,324(2):681-686
Journal of Radioanalytical and Nuclear Chemistry - Amount estimation of production of 99Mo required for medical applications was carried out by utilizing an electron linear accelerator with... 相似文献
107.
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109.
Takahiro Miyata Kozo Matsumoto Takeshi Endo Shigeaki Yonemori Shoji Watanabe 《Journal of polymer science. Part A, Polymer chemistry》2012,50(15):3046-3051
A styrene‐based monomer having a five‐membered cyclic carbonate structure, 4‐vinylbenzyl 2,5‐dioxoran‐3‐ylmethyl ether (VBCE), was prepared by lithium bromide‐catalyzed addition of carbon dioxide to 4‐vinylbenxyl glycidyl ether (VBGE). Radical polymerization of the obtained VBCE was carried out using 2,2′‐azobisisobutyronitrile as an initiator. PolyVBCE with number‐averaged molecular weight higher than 13,800 was obtained by a solution polymerization in N,N‐dimethylformamide, N,N‐dimethylacetamide, dimethyl sulfoxide, and methyl ethyl ketone. The glass transition temperature and 5 wt % decomposition temperature of the polyVBCE were determined to be 52 and 305 °C by differential scanning calorimetry and thermal gravimetry analysis, respectively. It was confirmed that a polymer consisting of the same VBCE repeating unit can be also obtained via chemical modification of polyVBGE, that is, a lithium‐bromide‐catalyzed addition of carbon dioxide to a polyVBGE prepared from a radical polymerization of VBGE. Further copolymerization of VBCE with styrene gave the corresponding copolymer in a high yield. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
110.