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1.
Kazuki Komatsu Stefan Klotz Satoshi Nakano Shinichi Machida Takanori Hattori Asami Sano-Furukawa 《高压研究》2020,40(1):184-193
ABSTRACTA new high pressure cell for neutron diffraction experiments using nano-polycrystalline anvils is presented. The cell design, off-line pressure generation tests and a gas-loading procedure for this cell are described. The performance is illustrated by powder neutron diffraction patterns of ice VII to ~82?GPa. We also demonstrate the feasibility of single crystal neutron diffraction experiments of Fe3O4 at ambient conditions using this cell and discuss the current limitation and future developments. 相似文献
2.
??This article provides the readers with an introduction to the
spectral theory of ergodic one dimensional Schrodinger operators. The theorems
developed by the author are mainly discussed and their proofs are given in detail. 相似文献
3.
Ayumi Suzuki Dr. Yuichiro Mutoh Dr. Noriko Tsuchida Chi-Wai Fung Dr. Shoko Kikkawa Prof. Isao Azumaya Prof. Shinichi Saito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(17):3795-3802
Although the chemistry of transition-metal complexes with carbonyl (CO) and thiocarbonyl (CS) ligands has been well developed, their heavier analogues, namely selenocarbonyl (CSe) and tellurocarbonyl (CTe) complexes remain scarce. The limited availability of such CSe and CTe complexes has so far hampered our understanding of the differences between such chalcogenocarbonyl (CE: E=O, S, Se, Te) ligands. Herein, we report the synthesis and properties of a series of cationic half-sandwich ruthenium CE complexes of the type [CpRu(CE)(H2IMes)(CNCH2Ts)][BArF4] (Cp=η5-C5H5−; H2IMes=1,3-dimesitylimidazolin-2-ylidene; ArF=3,5-(CF3)2C6H3). A combination of X-ray diffraction analyses, NMR spectroscopic analyses, and DFT calculations revealed an increasing π-accepting ability of the CE ligands in the order O<S<Se<Te. A variable-temperature NMR analysis of the thus obtained chiral-at-metal CE complexes indicated high stereochemical stability. 相似文献
4.
Dr. Zachary T. Gossage Nanako Ito Prof. Tomooki Hosaka Prof. Ryoichi Tatara Prof. Shinichi Komaba 《Angewandte Chemie (International ed. in English)》2023,62(43):e202307446
The solid-electrolyte interphase (SEI) is key to stable, high voltage lithium-ion batteries (LIBs) as a protective barrier that prevents electrolyte decomposition. The SEI is thought to play a similar role in highly concentrated water-in-salt electrolytes (WISEs) for emerging aqueous batteries, but its properties remain unknown. In this work, we utilized advanced scanning electrochemical microscopy (SECM) and operando electrochemical mass spectrometry (OEMS) techniques to gain deeper insight into the SEI that occurs within highly concentrated WISEs. As a model, we focus on a 55 mol/kg K(FSA)0.6(OTf)0.4 electrolyte and a 3,4,9,10-perylenetetracarboxylic diimide negative electrode. For the first time, our work showed distinctly passivating structures with slow apparent electron transfer rates alike to the SEI found in LIBs. In situ analyses indicated stable passivating structures when PTCDI was stepped to low potentials (≈−1.3 V vs. Ag/AgCl). However, the observed SEI was discontinuous at the surface and H2 evolution occurred as the electrode reached more extreme potentials. OEMS measurements further confirmed a shift in the evolution of detectable H2 from −0.9 V to <−1.4 V vs. Ag/AgCl when changing from dilute to concentrated electrolytes. In all, our work shows a combined approach of traditional battery measurements with in situ analyses for improving characterization of other unknown SEI structures. 相似文献
5.
High-speed holographic microscopy is applied to take three successive photographs of fast propagating cracks in Homalite 100 or in Araldite B at the moment of bifurcation. Crack speed at bifurcation is about 540 m/s on Homalite 100, and about 450 m/s on Araldite B. From the photographs, crack speeds immediately before and after bifurcation are obtained, and it is found that discontinuous change of crack speed does not exist at the moment of bifurcation in the case of Homalite 100, but exists in the case of Araldite B. From the photographs, crack opening displacement (COD) is also measured along the cracks as a function of distance r from the crack tips. The measurement results show that the CODs are proportional to √r before bifurcation. After bifurcation, the CODs of mother cracks are proportional to √r, though the CODs of branch cracks are not always proportional to √r. The energy release rate is obtained from the measured CODs, and it is found that energy release rate is continuous at bifurcation point in both cases of Homalite 100 and Araldite B. Energy flux that shows the energy flow toward a crack tip is also obtained. 相似文献
6.
We present two types of relativistic Lagrangians for the Lorentz–Dirac equation written in terms of an arbitrary world-line parameter. One of the Lagrangians contains an exponential damping function of the proper time and explicitly depends on the world-line parameter. Another Lagrangian includes additional cross-terms consisting of auxiliary dynamical variables and does not depend explicitly on the world-line parameter. We demonstrate that both the Lagrangians actually yield the Lorentz–Dirac equation with a source-like term. 相似文献
7.
Surasak Seesukphronrarak Shinichi Kawasaki Shigeki Kuwata Toshikazu Takata 《Journal of polymer science. Part A, Polymer chemistry》2019,57(24):2602-2605
Two novel 9,9‐difunctionalized fluorene‐type monomers, 9,9‐bis(4‐hydroxyphenyl‐ and 4‐aminophenyl)‐2,3:6,7‐dibenzofluorenes, are synthesized by the reaction of dibenzenzofluorenone with phenol and aniline. These monomers are used for the preparation of polyester and polyimide as the typical polymers to evaluate the property change such as thermal stability caused by the benzene rings fused to the fluorene skeleton with keeping good solubility, in comparison with the polymers derived from simple fluorenone. In fact, these two new polymers have the fairly enhanced thermal stability and refractive index value along with satisfactory solubility in organic solvents, enough to emphasize the fusion effect. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 2602–2605 相似文献
8.
Secondary carbinamines have been prepared from alkylation of N-boryl imines which were generated in situ from partial reduction of nitriles with sodium brohydride modified by carboxylic acid. 相似文献
9.
Shoichi Kutsumizu Koushi Morita Tatsuya Ichikawa Shinichi Yano Shuichi Nojima Takanari Yamaguchi 《Liquid crystals》2013,40(11):1447-1458
The structure of the thermotropic cubic phases of 4′- n -alkoxy-3′-nitrobiphenyl-4-carboxylic acids (ANBC- n , where n indicates the number of carbon atoms in the alkoxy group) was studied by X-ray diffraction. For the homologues with n = 15, 16, 17, and 18, the cubic phase was of an Ia 3 d type, whereas the homologues with n = 19, 20, and 21 exhibited an Im 3 m cubic structure; for these seven homologues the same type of cubic structure was observed both on heating and cooling. Further lengthening of the alkoxy chain to n = 22 and 26, however, gave two types of cubic structure in the cubic phase region on heating, one with Im 3 m symmetry in the low temperature region and the other with Ia 3 d symmetry in the high temperature region. On cooling, the two homologues exhibited the Ia 3 d cubic structure only. This is the first example in the cubic phase region of a series of homologues containing two types of structure, dependent on temperature and n . Such a complicated phase diagram in the cubic region is clearly understood qualitatively in terms of Gibbs free energy-temperature diagrams. The dependence of structural parameters such as the cubic lattice constant on the alkoxy chain length n are also presented and discussed. 相似文献
10.
Highly active polymeric organocatalyst: Chiral ionic polymers prepared from 10,11‐didehydrogenated cinchonidinium salt 下载免费PDF全文
Md. Mehadi Hassan Naoki Haraguchi Shinichi Itsuno 《Journal of polymer science. Part A, Polymer chemistry》2016,54(5):621-627
Since few examples of 10,11‐didehydrogenated (3‐ethynyl) cinchona alkaloids have been utilized as organocatalysts in asymmetric reaction, we synthesized 10,11‐didehydrogenated cinchonidine. The 3‐vinyl group of cinchonidine was transformed into a 3‐ethynyl functionality. Based on the resulting 10,11‐didehydrogenated cinchonidine, the corresponding quaternary ammonium salt and its dimers were prepared. The ion‐exchange reaction between the quaternary ammonium salt and sodium sulfonate produced the quaternary ammonium sulfonate as a stable ionic compound. Chiral ionic polymers were then synthesized by the ion‐exchange polymerization of the 10,11‐didehydrogenated cinchonidinium salt dimer and a disulfonate. The chiral ionic polymers were found to be capable of efficiently catalyzing the asymmetric alkylation of N‐(diphenylmethylene)glycine tert‐butyl ester. The enantioselectivities obtained with the polymeric catalysts were higher than those obtained with the corresponding monomeric catalyst. Dimers of 10,11‐didehydrogenated cinchonidinium salts were prepared. Treatment of the dimer with disodium disulfonate gave the chiral ionic polymers, which showed high catalytic activity in asymmetric benzylation of N‐(diphenylmethylen)glycine tert‐butyl ester. The polymeric catalysts were reused several times without the loss of catalytic activity. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 621–627 相似文献