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排序方式: 共有229条查询结果,搜索用时 187 毫秒
111.
Shota Miura Hikaru Sasaki Ken-ichi Takagi Takuya Fujima 《Journal of Physics and Chemistry of Solids》2014
Thermoelectric properties of AlMgB14-based materials prepared by spark plasma sintering were investigated. Al, Mg, and B powders were used as raw material powders. The raw powders were mixed using a V-shaped mixer, and then the mixture was sintered at 1673 K or 1773 K. The mixture ratio of raw powders was varied around stoichiometric ratio of AlMgB14. X-ray diffraction patterns of samples showed that all samples consist of AlMgB14 and MgAl2O4. The Seebeck coefficient of the samples exhibited significant change depending on the varying mixture ratio and sintering temperature. One sample exhibited a large negative value for the Seebeck coefficient (approximately −500 μV/K) in the temperature range from 573 K to 1073 K, while others showed positive value (250–450 μV/K). Thus n-type AlMgB14-based material has been realized by varying raw material ratio and sintering temperature. 相似文献
112.
Dr. Kazuteru Usui Nozomi Narita Ryosuke Eto Seika Suzuki Atsushi Yokoo Dr. Kosuke Yamamoto Prof. Dr. Kazunobu Igawa Naoko Iizuka Yuki Mimura Dr. Tomohiro Umeno Shota Matsumoto Dr. Masashi Hasegawa Prof. Dr. Katsuhiko Tomooka Prof. Dr. Yoshitane Imai Prof. Dr. Satoru Karasawa 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(65):e202202922
Small chiral organic molecules with CD properties are in high demanded due to their potential use in promising electronic and biological applications. Herein, we reveal a system in which the oxidation of a phosphino group to the corresponding phosphine oxide on the inner rim of a helicene derivative induces a CPL response. Laterally π-extended 7,8-dihydro[5]helicenes bearing phosphine and phosphine oxide groups on their inner helical rims (i. e., the C1 position) were synthesized, and their helical structures were unambiguously determined by X-ray crystallography. The photophysical (UV/visible and emission) and chiroptical properties of these compounds were investigated in various solvents. Despite their structural similarities, phosphine oxide showed a significantly better CPL response than phosphine, with a high dissymmetry factor for emission (|glum|=(1.3–1.9)×10−3) that can be attributed to structural changes in the interior of the helicene helix. 相似文献
113.
Prof. Dr. Keiichi Hirano Kensuke Morimoto Shota Fujioka Prof. Dr. Kazunori Miyamoto Dr. Atsuya Muranaka Prof. Dr. Masanobu Uchiyama 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(48):21632-21637
1-Boraphenalenes, a class of boron-doped polyaromatic hydrocarbons, were synthesized by nucleophilic diboration reaction of alkynes. Activation of diboron reagents with a highly basic sp2-carbanion results in very fast successive C−B bond formations to construct the boracycle. This methodology is characterized by high chemoselectivity, affording a wide variety of 1-boraphenarenes with diverse polar substituents. The endocyclic boron can be arylated conveniently in one pot, and the peripheral boron is available for various chemical transformations. Highly diastereoselective diboration gives pseudo-enantio-enriched boraphenarene, which emits circularly polarized fluorescence (CPL). 相似文献
114.
“Nondissociative” chain walking is a mechanism where an alkylmetal species undergoes rapid β-hydride elimination and reinsertion to move the metal center along the alkyl chain without dissociating an alkene intermediate during the migration process. This digest summarizes the unique characteristics of the nondissociative chain walking mechanism compared to the stepwise alkene isomerization mechanism and their use in catalytic organic synthesis. 相似文献
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117.
Shota Osumi Simcha E. Felder Hai Wang Yen‐Nan Lin Mei Dong Karen L. Wooley 《Journal of polymer science. Part A, Polymer chemistry》2019,57(3):432-440
Carbohydrates are the fundamental building blocks of many natural polymers, their wide bioavailability, high chemical functionality, and stereochemical diversity make them attractive starting materials for the development of new synthetic polymers. In this work, one such carbohydrate, d ‐glucopyranoside, was utilized to produce a hydrophobic five‐membered cyclic carbonate monomer to afford sugar‐based amphiphilic copolymers and block copolymers via organocatalyzed ring‐opening polymerizations with 4‐methylbenzyl alcohol and methoxy poly(ethylene glycol) as initiator and macroinitiator, respectively. To modulate the amphiphilicities of these polymers acidic benzylidene cleavage reactions were performed to deprotect the sugar repeat units and present hydrophilic hydroxyl side chain groups. Assembly of the polymers under aqueous conditions revealed interesting morphological differences, based on the polymer molar mass and repeat unit composition. The initial polymers, prior to the removal of the benzylidenes, underwent a morphological change from micelles to vesicles as the sugar block length was increased, causing a decrease in the hydrophilic–hydrophobic ratio. Deprotection of the sugar block increased the hydrophilicity and gave micellar morphologies. This tunable polymeric platform holds promise for the production of advanced materials for implementation in a diverse range of applications. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 432–440 相似文献
118.
Masaaki Motozawa Shota Ishitsuka Kaoru Iwamoto Hirotomo Ando Tetsuya Senda Yasuo Kawaguchi 《Flow, Turbulence and Combustion》2012,88(1-2):121-141
Turbulent drag reducing flow with blowing polymer solution from the channel wall was investigated experimentally using particle image velocimetry (PIV). Experiments were carried out with varying conditions of blowing polymer solution (e.g. weight concentration of polymer solution). Reynolds number based on the channel height and mean velocity was set to 20000 and 40000. When the polymer solution was blown from the channel wall, streamwise velocity fluctuation little increased, but wall-normal velocity fluctuation, Reynolds shear stress and correlation coefficient decreased significantly only near the blower wall. This behavior corresponds to the decrease of the ejection and sweep in the near-wall region observed by the investigation of instantaneous velocity map. On the contrary, this characteristic behavior was not observed at a position away from the blower wall (y/(H/2) > 0.4) and the scatter plot was almost the same as that of the water flow in this region. These results suggest that there are two regions in the drag reducing flow with blowing polymer solution from the wall; one is a non-Newtonian region which exists near the blower wall, and the other is a Newtonian region at a distance from the wall. The non-Newtonian region plays a key role in the drag reduction by the blowing polymer solution. 相似文献
119.
4-(4-Chlorophenyl)-4-hydroxypiperidine (CPHP), one of the metabolites of haloperidol, is considered to exhibit brain toxicity. CPHP concentrations in plasma and tissue homogenates (each 200 microL) from rats were analyzed by HPLC fluorescence detection after pre-column derivatization with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F). After basic extraction of the samples with benzene, the derivatization with NBD-F was conducted in borate buffer (pH 8.0) at 60 degrees C for 3 min. Mexiletine was carried through the procedure as an internal standard. The regression equation for CPHP showed a good linearity in the range of 0.03-1 microg/mL with a detection limit of 0.008 microg/mL. The coefficient of variation was less than 11.6%. Plasma concentration-time courses of CPHP after intraperitoneal or per oral administration of CPHP, haloperidol or reduced haloperidol were examined, and the pharmacokinetic parameters were estimated. Additionally, CPHP levels in various tissues at 8 h after intraperitoneal administration of these compounds were compared. The method was simple and sensitive, useful for determination of CPHP in rat biological samples using as little as 200 microL of sample volume and could be applied for pharmacokinetic study. 相似文献
120.
Qifeng Zheng Shota Miura Kasumi Miyazaki Seongjae Ko Eriko Watanabe Masaki Okoshi Chien‐Pin Chou Yoshifumi Nishimura Hiromi Nakai Takeshi Kamiya Tsunetoshi Honda Jun Akikusa Yuki Yamada Atsuo Yamada 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(40):14340-14345
Aqueous Na‐ or K‐ion batteries could virtually eliminate the safety and cost concerns raised from Li‐ion batteries, but their widespread applications have generally suffered from narrow electrochemical potential window (ca. 1.23 V) of aqueous electrolytes that leads to low energy density. Herein, by exploring optimized eutectic systems of Na and K salts with asymmetric imide anions, we discovered, for the first time, room‐temperature hydrate melts for Na and K systems, which are the second and third alkali metal hydrate melts reported since the first discovery of Li hydrate melt by our group in 2016. The newly discovered Na‐ and K‐ hydrate melts could significantly extend the potential window up to 2.7 and 2.5 V (at Pt electrode), respectively, owing to the merit that almost all water molecules participate in the Na+ or K+ hydration shells. As a proof‐of‐concept, a prototype Na3V2(PO4)2F3|NaTi2(PO4)3 aqueous Na‐ion full‐cell with the Na‐hydrate‐melt electrolyte delivers an average discharge voltage of 1.75 V, that is among the highest value ever reported for all aqueous Na‐ion batteries. 相似文献