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91.
T. Shimoda K. Tajiri K. Kura A. Odahara M. Suga Y. Hirayama N. Imai H. Miyatake M. Pearson C. D. P. Levy K. P. Jackson R. Legillon C. Petrache T. Fukuchi N. Hamatani T. Hori M. Kazato Y. Kenmoku T. Masue H. Nishibata T. Suzuki A. Takashima R. Yokoyama 《Hyperfine Interactions》2014,225(1-3):183-191
Spin-polarized radioactive nuclear beams at TRIUMF enable a new spectroscopic method which efficiently assigns spins and parities of the daughter levels by taking advantage of the asymmetric β-decay of the polarized parent nucleus. This method was successfully applied to structure studies of 29Mg and 30Mg in connection with the physics of the “island of inversion”. In 29Mg, two low-lying levels with intruder configuration were assigned. In 30Mg, coexistence of spherical shape, prolate shape and γ-collectivity was strongly suggested. 相似文献
92.
Herein macromolecular recognition by cyclodextrins (CDs) is summarized. Recognition of macromolecules by CDs is classified as main‐chain recognition or side‐chain recognition. We found that CDs form inclusion complexes with various polymers with high selectivity. Polyrotaxanes in which many CDs are entrapped in a polymer chain were prepared. Tubular polymers were prepared from the polyrotaxanes. CDs were found to recognize side‐chains of polymers selectively. CD host polymers were found to form gels with guest polymers in water. These gels showed self‐healing properties. When azobenzene was used as a guest, the gel showed sol‐gel transition by photoirradiation. When ferrocene was used, redox‐responsive gels were obtained. Macroscopic self‐assembly through molecular recognition has been discovered. Photoswitchable gel association and dissociation have been observed. 相似文献
93.
Enhanced Phosphorescence Emission by Incorporating Aromatic Halides into an Entangled Coordination Framework Based on Naphthalenediimide 下载免费PDF全文
Dr. Virginia Martínez‐Martínez Rebeca Sola Llano Dr. Shuhei Furukawa Dr. Yohei Takashima Prof. Iñigo López Arbeloa Prof. Susumu Kitagawa 《Chemphyschem》2014,15(12):2517-2521
Phosphorescence emission at room temperature is turned on in an entangled porous coordination polymer (PCP) with naphthalenediimide (NDI) as chromophore, by incorporating halogenated guests into the pores. The phosphorescent efficiency is drastically increased by the incorporation of aromatic halide guests in comparison with the incorporation of nonaromatic derivatives. Aromatic halide guests trigger a structural transformation, which allows a strong interaction with the NDI ligand in the framework through charge‐transfer complexation, and provides an extra population process of the triplet state. The long‐lived photoinduced triplet states, with an emission wavelength in the red region of the visible spectrum, demonstrated by this PCP, may open the door for potential uses, for example, as singlet‐oxygen generators or for bio‐imaging applications. 相似文献
94.
Zheng Y Hashidzume A Takashima Y Yamaguchi H Harada A 《Langmuir : the ACS journal of surfaces and colloids》2011,27(22):13790-13795
Macroscopic molecular recognition observations were realized using polyacrylamide-based gels modified with α-cyclodextrin (α-CD), β-cyclodextrin (β-CD), 1-naphthylmethyl (1Np), and 2-naphthylmethyl (2Np) moieties, which are denoted as αCD(x)-gel, βCD(x)-gel, 1Np(y)-gel, and 2Np(y)-gel, where x and y indicate the mol % of CD and Np moieties, respectively. The αCD(5)-gel did not adhere to either the 1Np(5)-gel or 2Np(5)-gel, whereas the βCD(5)-gel interacted with both to form alternating or checkered assemblies. Although the difference in the association constants of β-CD for the model polymers was small, the βCD(x)-gel successfully discriminated between 1Np(y)-gel and 2Np(y)-gel at the appropriate x and y. 相似文献
95.
Goto Y Takashima H Takishita K Sawada H 《Journal of colloid and interface science》2011,362(2):375-381
Fluoroalkyl end-capped vinyltrimethoxysilane oligomeric nanocomposites having biphenylene units [R(F)-(VM-SiO(2))(n)-R(F)/Ar-SiO(2)] were prepared by the sol-gel reaction of the corresponding oligomer [R(F)-(VM)(n)-R(F)] with 4,4'-bis(triethoxysilyl)-1,1'-biphenyl [Ar-Si(OEt)(3)] under alkaline conditions. R(F)-(VM-SiO(2))(n)-R(F)/Ar-SiO(2) nanocomposites were applied to the surface modification of PMMA to exhibit not only a good oleophobicity imparted by fluorine but also a fluorescent emission ability on the surface. Methanol sol solutions of R(F)-(VM-SiO(2))(n)-R(F)/Ar-SiO(2) nanocomposites were effective for the surface modification of glass through the dipping technique to exhibit good oleophobicity with superhydrophobicity on the modified glass surface. On the other hand, 1,2-dichloroethane sol solutions enabled R(F)-(VM-SiO(2))(n)-R(F)/Ar-SiO(2) nanocomposites to exhibit both superhydrophobic and superoleophobic characteristics on the modified surface through dipping the glass in these sol solutions. 相似文献
96.
Tetsuaki Nishida Yoshimasa Takashima Yusuke Nakayama 《Journal of solid state chemistry》1980,33(2):141-144
Potassium borate glasses denoted by the formula xK2O · (100 ? x)B2O3 · 7Fe2O3 were irradiated with 60Co-γ-rays at room temperature. Mössbauer parameters for the irradiated glasses containing alkali equal to or higher than 20 mole% showed that the s-electron density at the iron nucleus increased without any change of the steric configuration of oxygen atoms around the iron nucleus. The increase of s-electron density was ascribed to electron transfer from the nonbridging oxygen to the iron nucleus. The presence of the nonbridging oxygen was also confirmed by the irradiation effect of the borate glass (x = 30) prepared using the enriched isotope of 57Fe2O3. Mössbauer parameters for the irradiated glass suggest that the newly observed Fe2+ ions are in tetrahedral symmetry. 相似文献
97.
K. Sakamoto Y. Hamajima S. Yamaguchi T. Takashima K. Itoh 《Journal of Radioanalytical and Nuclear Chemistry》1980,60(2):411-422
Samples of an andesite (Asama-yama, Japan) and a basalt (Kilauea, Hawaii) were finely fractioned by density and the U distributions
among the separates were determined by homogenized fission track method. Groundmass was found to be enriched with U; one half
of the andesite U and almost all of the basalt U are accounted for by the groundmass U. Cerium and other REE are correlated
with U. In the andesite separates Na is accompanied by these elements, but Fe and Co are rather anticorrelated. Uranium concentrations
in the bulk samples and some of the separates were then compared with those determined by133Xe extracted by heating at 1600°C. Fissiogenic133Xe seems to become labile in groundmass, especially of the andesite, during reactor irradiations for 5 h or more. Stepwise
heating experiments suggested that133Xe in U-rich groundmass tends to escape at low temperatures and the remaining133Xe is mostly retained in highly refractory sites in phenocryst rather poor in U. 相似文献
98.
Rikito Takashima Jumpei Kida Daisuke Aoki Hideyuki Otsuka 《Journal of polymer science. Part A, Polymer chemistry》2019,57(24):2396-2406
The maleimide structure is highly reactive, exemplified by thiol–ene click reactions with thiols and Diels–Alder reactions with furans. Although postpolymerization modifications and macromolecular conjugations involving maleimide units have been widely studied, mostly due to their selectivity and high reactivity, little has been reported on the one‐pot postpolymerization introduction of maleimides in polymer chains. Herein, we report p‐maleimidophenyl isocyanate and its derivatives as modification agents to introduce maleimide moieties by reaction with hydroxy groups into polymer chains. The high reactivity of the resulting modification agents and of the corresponding maleimide structures once inserted in the polymer chains was examined by studying their reaction kinetics. Furthermore, these modification agents were successfully applied to the synthesis of macromonomers for graft polymerization and various block copolymers, with, for example, AB‐type, star‐shaped, and H‐shaped architectures. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 2396–2406 相似文献
99.
The sorption of the chromium(III)-diphenylcarbazone complex (Cr-DPC) with XAD-2 has been investigated, for use in the separation of Cr(VI) from Cr(III) species in natural waters. Cr-DPC is formed from the reaction of Cr(VI) with diphenylcarbazide, but Cr(III) species give no reaction in aqueous solution. The addition of sodium chloride or sodium beta-naphthalenesulphonate markedly enhances the sorption. The Cr-DPC sorbed on XAD-2 can be almost completely eluted with organic solvents, especially methanol, but about 5% of it is irreversibly sorbed and cannot be eluted. The excess of diphenylcarbazide and some of the organic matter in natural waters are also sorbed on XAD-2 but most of this can also be eluted with methanol. Organic matter which interferes with measurement of the absorbance of Cr-DPC can almost all be removed by extraction with chloroform. By use of these techniques, Cr(VI) in sea-water has been determined by the standard-addition method. Although about 50 litres of sea-water are necessary for the analysis, organic and colloidal Cr(III) species do not interfere. 相似文献
100.
Masaki Takashima 《Fluid Dynamics Research》1996,17(6):293-310
The stability against small disturbances of the pressure-driven plane laminar motion of an electrically conducting fluid under a transverse magnetic field is investigated. Assuming that the outer regions adjacent to the fluid layer are electrically non-conducting and not ferromagnetic, the appropriate boundary conditions on the magnetic field perturbations are presented. The Chebyshev collocation method is adopted to obtain the eigenvalue equation, which is then solved numerically. The critical Reynolds number Rc, the critical wave number αc, and the critical wave speed cc are obtained for wide ranges of the magnetic Prandtl number Pm and the Hartmann number M. It is found that except for the case when Pm is sufficiently small, the magnetic field has both stabilizing and destabilizing effects on the fluid flow, and that for a fixed value of M the fluid flow becomes more unstable as Pm increases. 相似文献