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31.
Chi Feng Tomohiro Seki Shunichi Sakamoto Toshiyuki Sasaki Satoshi Takamizawa Hajime Ito 《Chemical science》2022,13(33):9544
Shape-memory materials can be mechanically deformed and subsequently reverse the deformation upon changing the temperature. Shape-memory materials have attracted considerable attention for basic research and industrial applications, and polymer and alloy shape-memory materials have been well studied; however, it is formidably challenging to develop functional shape-memory materials, such as materials with multi-stage and anisotropic shape changes and shape changes accompanied by changes in color and light emission. Here, we found a reversible multi-stage shape-changing effect after mechanical deformation in a molecular crystal induced by multi-step thermal phase transitions with reversible shape changes and luminescence-color changes. Using single-crystal structure and thermal analyses as well as mechanical property measurements, we found that the reversible multi-stage shape-changing effect was achieved by a combination of a twinning deformation and multi-step thermal phase transitions. The changes in the crystal shape and luminescence suggest novel strategies for imparting known shape-memory materials with additional functionalities.A reversible multi-stage shape-changing material based on an organic crystalline material is presented. Intriguingly, the interconversion among the three different shapes is accompanied by changes of the luminescence color. 相似文献
32.
Yoshimi Shioya Toshiyuki Ohdaira Ryoichi Suzuki Yutaka Seino Kazuhiko Omote 《Journal of Non》2008,354(26):2973-2982
Plasma-enhanced chemical vapor deposition (PE-CVD) low-dielectric (low-k) film was irradiated with ultra violet (UV) light of wavelength 172 nm to enhance mechanical strength and reduce dielectric constant (k value). The thickness measurement method for the UV annealed low-k film is discussed. The effects of UV irradiation on dielectric constant, shrinkage, stress, density, pore size, mechanical strength, and structure are clarified and the mechanism is discussed. 相似文献
33.
Yusuke Himei Tomohiro Nagakane Naoyuki Kitamura Akihiko Sakamoto 《Journal of Non》2008,354(27):3113-3119
Reduction in the temperature coefficient of the optical path length, dS/dT of Li2O-Al2O3-SiO2 glass-ceramics with near-zero thermal expansion coefficient was attempted using control of the temperature coefficient of electronic polarizability, ?, and the thermal expansion coefficient, α. The dS/dT value of 2.6 mol% B2O3-doped glass-ceramic was 12.5 × 10−6/°C, which was 0.9 × 10−6/°C smaller than that of B2O3-free glass-ceramic. On the other hand, reduction in dS/dT through B2O3 doping was not confirmed in precursor glasses. Results showed that reduction in dS/dT of the glass-ceramic through B2O3 doping is caused by the reduction in ?. The reduction in ? from B2O3 doping was probably attributable to numerical reduction in non-bridging oxide ions with larger ? value by the concentration of boron ions in the residual glass phase. In addition, application of hydrostatic pressure during crystallization was effective to inhibit precipitation of β-spodumene solid solution, which thereby decreases dS/dT. The dS/dT value of B2O3-doped glass-ceramic crystallized under 196 MPa was 11.7 × 10−6/°C. That value was slightly larger than that of silica glass. The α value of this glass-ceramic was smaller than that of silica glass. 相似文献
34.
Dr. Eiji Yamamoto Kiyotaka Izumi Ryosuke Shishido Prof. Dr. Tomohiro Seki Noriaki Tokodai Prof. Dr. Hajime Ito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(49):17547-17551
The first dimesitylboryl substitution of aryl halides with a silylborane bearing a dimesitylboryl group in the presence of alkali‐metal alkoxides is described. The reactions of aryl bromides or iodides with Ph2MeSi?BMes2 and Na(OtBu) afforded the desired aryl dimesitylboranes in good to high yields and with high borylation/silylation ratios. Selective reaction of the sterically less‐hindered C?Br bond of dibromoarenes provided monoborylated products. This reaction was used to rapidly construct a D‐π‐A aryl dimesityl borane with a non‐symmetrical biphenyl spacer. 相似文献
35.
36.
Hiroshi Nishikawa Ei-Ichi Terada Eishun Tsuchida Yoshimi Kurimura 《Journal of polymer science. Part A, Polymer chemistry》1978,16(10):2453-2463
The (alkyl)-bis(dimethylglyoximato)pyridinecobalt attached to polychloromethylstyrene by a cobalt–carbon bond was prepared by the reaction of Co(II)(DH)2Py with polychloromethylstyrene in benzene. The fraction of p-vinylbenzyl·Co(DH)2Py introduced to the polymer was 8.1 and 2.1 mole %. The photodecomposition of the polymer-bonded cobaloxime was investigated by following the change of the visible spectrum. The rate constant kdec of the polymer-bonded cobaloxime was 1.1 × 10?2 sec?1 in benzene; it is one-fourth of that of its monomeric analog, benzyl·Co(DH)2Py. The kdec values of the cobaloximes were also measured in benzene–dimethyl sulfoxide mixed solvents, and the polymer effects were discussed. The dependence of the photodecomposition on energy of the irradiation light was investigated, and it was found that the absorption band near 470 nm is important for the photodecomposition of the cobalt–carbon bond. Spectroscopic measurements of the ligand exchange reaction of polymer-bonded cobaloxime with pyridine in dimethyl sulfoxide gave a larger equilibrium constant (1.2 × 104 liter/mole) than that of benzyl·Co(DH)2Py (9.4 × 102 liter/mole). The kinetic data of the ligand exchange reaction indicated that the larger equilibrium constant for the polymeric system is due to the smaller rate constant of the reverse reaction. The thermodynamic parameters were also obtained. 相似文献
37.
38.
Hajime Maeda Hideki Ishida Yohtaro Inoue Abdurisit Merpuge Tomohiro Maeda Kazuhiko Mizuno 《Research on Chemical Intermediates》2009,35(8-9):939-948
Effects of trimethylsilyl, trimethylgermyl, and trimethylstannyl substituents attached to fused aromatic hydrocarbons such as pyrene, anthracene, phenanthrene, and naphthalene were studied in terms of UV absorption and fluorescence properties in aerated cyclohexane solutions. Absorption maxima of trimethylsilyl-, trimethylgermyl-, and trimethylstannyl-substituted aromatic hydrocarbons shifted to longer wavelengths than those of unsubstituted ones. Absorption maxima of mono-, bis-, tris-, and tetrakis(trimethylsilyl)pyrenes shifted to longer wavelength consecutively at intervals of 10 nm. Fluorescence intensities and fluorescence lifetimes of trimethylsilyl-substituted aromatic hydrocarbons were larger and longer than those of unsubstituted ones, and they decreased in the order of Me3SiAr > Me3GeAr > Me3SnAr. Fluorescence intensity of 1,3,6,8-tetrakis(trimethylsilyl)pyrene was largest among those of a series of mono-, bis-, tris-, and tetrakis(trimethylsilyl)pyrenes under aerated conditions. 相似文献
39.
Tomohiro Ohta Takeru Ito Masahiro Shimizu Lisa Tauchi Huy‐Danh Nguyen‐Tran Jong‐Chul Park Byoung‐Suhk Kim Ick‐Soo Kim Kazuchika Ohta 《先进技术聚合物》2011,22(12):2653-2658
We have developed a novel synthetic method that enables us to easily synthesize metal‐capsulated carbon nanotubes (CNTs) in a laboratory by using a combined technology of electrospinning‐metallization and microwave heating. These techniques greatly shorten the time for the synthesis of the CNTs in comparison with the conventional methods. TEM analysis confirmed a successful formation of the CNTs, and the resulting CNTs were multi‐walled and found to be about 25–100 nm in diameters. The products prepared by heating at 600 and 900°C exhibited less‐developed and strongly curved CNTs, whereas the products prepared by heating at 700 and 800°C relatively well‐developed long CNTs. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
40.
Tartaric acid catalyzes the asymmetric addition of vinylboronates to N-acyl quinoliniums, affording highly enantioenriched dihydroquinolines. The catalyst serves to activate the boronate through a ligand-exchange reaction and generates the N-acyl quinolinium in situ from the stable quinoline-derived N,O-acetal. 相似文献