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281.
Shin Nakamura Takaya Mitsui Kosuke Fujiwara Naoshi Ikeda Yasuhiro Kobayashi Susumu Shimomura 《Hyperfine Interactions》2016,237(1):157
A Mössbauer diffractometer has been developed by using 57Fe nuclear resonant scattering apparatus at SPring-8 BL11XU in order to obtain a crystal-site-selective Mössbauer spectrum. A ??-2?? goniometer was newly installed between the nuclear monochromator and a detector. From a single crystal Fe3 O 4 mounted on the goniometer, the 111, 222, and 220 reflected γ-rays were used to collect the diffraction spectra at room temperature. The intensity ratio of the two subspectra, corresponding to A- and B-site Fe ions, changes notably according to the reflection index. The diffraction spectrum is composed of a major absorption spectrum and a minor emission spectrum. The former is given by the γ-ray due to the electron scattering and nuclear absorption, whereas the latter is given by the γ-ray due to the nuclear resonant scattering. Interference effects between these two γ-rays are also seen as line broadenings, asymmetric line shapes, and slope of the base lines. These features can be successfully expressed by a Fano function. We consider that the emission spectrum due to the nuclear resonant scattering represents crystal-site-selective Mössbauer spectrum. 相似文献
282.
Marc Steinmetz Kirika Ueda Prof. Dr. Stefan Grimme Dr. Junichiro Yamaguchi Dr. Sylvia Kirchberg Prof. Dr. Kenichiro Itami Prof. Dr. Armido Studer 《化学:亚洲杂志》2012,7(6):1256-1260
Direct C? H phenylation of 2‐ethylthiophene and 2‐chlorothiophene with PhPdI(bipy) complex to form either the corresponding 4‐phenyl or 5‐phenylthiophene derivative is studied under stoichiometric conditions using various Lewis acids as additives. It is shown that reactions occur via the corresponding cationic Pd complex (PhPdbipy+) and that the counteranion determines the regioselectivity. High‐level DFT calculations reveal that C? C bond formation occurs via a carbopalladation pathway and not via electrophilic palladation. These calculations give some indications regarding the regioselectivity of the thiophene arylation. 相似文献
283.
284.
Ahmad Kusumaatmaja Tsuyoshi Ando Kayo Terada Shiho Hirohara Takuya Nakashima Tsuyoshi Kawai Takaya Terashima Masao Tanihara 《Journal of polymer science. Part A, Polymer chemistry》2013,51(12):2527-2535
Water‐soluble luminescent material was developed by introducing europium (Eu(III)) ions into the core of a star polymer. Living radical polymerization was used to obtain the star polymer. The strategy to introduce Eu(III) ions into the star polymer was studied using poly(methyl methacrylate) as an arm. The best Eu(III) ion introduction was obtained by simultaneous introduction, resulting in about 30 µmol/g‐polymer, which needed only one step for synthesis. The utilization of a hydrophilic polymer such as poly(ethylene oxide) (PEO) as an arm produced a water‐soluble star polymer. The Eu(III)‐bearing PEO star polymer obtained in this study was water soluble and showed fluorescence. In addition, it was stable in water after 1 month. The Eu(III)‐bearing star polymer exhibited luminescent properties under UV light irradiation with relatively high quantum yields of 60% in organic solution and 19% in aqueous solution. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 2527–2535 相似文献
285.
286.
Akira Yoshiasa Genta Yagyu Tomokazu Ito Takamitu Yamanaka Takaya Nagai 《无机化学与普通化学杂志》2000,626(1):36-41
Crystal structures of the ambient pressure and temperature phase (phase I) and high pressure phase (phase II) in CuGeO3 were studied by means of the high pressure single‐crystal X‐ray diffraction method in a diamond anvil cell using high power X‐ray generator and imaging plate detector. The pressure dependence of the atomic displacements in the phase I was investigated under the hydrostatic pressure of 0.1 MPa and 2.9 and 3.9 GPa. The lattice is particularly compressive in the b direction. In phase I the rippled layers are formed by the corner‐shared chains of GeO4 tetrahedra and edge‐linked planar CuO4. Major effects of pressure, directly related to the shortening of the b‐axis, consist of an enhanced folding of the rippled layers towards the b‐direction and of a shortening of the weak Cu–O bond. The crystal structure of phase II is monoclinic, a = 4.935(57), b = 6.754(14), c = 6.208(11) Å, β = 92.67(3)°, space group; P21/c. The transition from phase I to II involves a corrugated arrangement of the both cation with some oxygens around the c‐axis. Ge ion at the transition point of 6.4 GPa changes its coordination number from four‐fold to five‐fold, and Cu ion occupies a position of seven‐fold site. The structure of phase II is explained as a slab structure having unique edge‐ and corner‐sharing arrangements of GeO5 and CuO7 polyhedra. The average Ge–O and Cu–O distances in phase II is 1.92 and 2.17 Å, respectively, at 6.5 GPa. 相似文献
287.
Yoshitaka Yamaguchi Noriyuki Suzuki Arno Fries Takaya Mise Hiroyuki Koshino Yuji Ikegami Hiromichi Ohmori Akira Matsumoto 《Journal of polymer science. Part A, Polymer chemistry》1999,37(3):283-292
Stereospecific polymerization of 1‐hexene under high pressures (up to 1,000 MPa = ca. 10,000 atm) using metallocene/methylaluminoxane (MAO) catalysts was investigated. Several C2‐symmetric ansa‐metallocenes, their meso‐isomers, and two Cs‐symmetric ansa‐metallocenes were employed as catalyst precursors. In the course of this study, novel C2‐symmetric germylene‐bridged ansa‐metallocenes, (rac‐[Me2Ge(η5‐C5H‐2,3,5‐Me3)2MCl2] (M = Zr, rac‐4a; M = Hf, rac‐4b), have been prepared. High pressures induced enhancement of the catalytic activity and the molecular weight of the polymers in most of the catalysts. The maximum of both the catalytic activity and the molecular weight of the polymers was mostly observed at 100–500 MPa in each catalyst, although the enhanced ratio was smaller than that observed for nonbridged metallocenes. Isospecificity of the C2‐symmetric ansa‐metallocene catalysts was essentially maintained even under high pressure. Highly isotactic polyhexene ([mmmm] = 91.6%) with very high molecular weight (Mw = 2,360,000) was achieved by rac‐4b under 250 MPa. High pressures slightly decreased syndiotacticity when the Cs‐symmetric ansa‐metallocene, isopropylidene(1‐η5‐cyclopentadienyl)(9‐η5‐fluorenyl)zirconium dichloride 5, was employed. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 283–292, 1999 相似文献
288.
Patrick Achenbach Carlos Ayerbe Gayoso Ralph Böhm Olga Borodina Damir Bosnar Vakkas Bozkurt Luka Debenjak Michael O. Distler Anselm Esser Ivica Friščić Yuu Fujii Toshiyuki Gogami Mar Gómez Rodríguez Osamu Hashimoto Satoshi Hirose Hiroki Kanda Masashi Kaneta Eunhee Kim Junichiro Kusaka Amur Margaryan Harald Merkel Ulrich Müller Sho Nagao Satoshi N. Nakamura Josef Pochodzalla Christophe Rappold Joerg Reinhold Takehiko R. Saito Alicia Sanchez Lorente Salvador Sánchez Majos B. Sören Schlimme Matthias Schoth Florian Schulz Concettina Sfienti Simon Širca Liguang Tang Michaela Thiel Kyo Tsukada 《Few-Body Systems》2014,55(8-10):887-892
At the Mainz Microtron MAMI exploratory experiments on the spectroscopy of mesonic weak decays (MWD) of electroproduced Λ-hypernuclei were performed. A unique setup was realized to use the broad momentum-band kaon spectrometer Kaos at zero degree angle with respect to the high-intensity electron beam direction to tag strangeness producing processes. A sample of order 103 MWD from a beryllium target was collected by the coincidence technique with the high-resolution multi-spectrometer facility of the A1 Collaboration. It is conjectured that this sample contains monochromatic two-body decays from stopped hyperfragment decays as well as a wide momentum distribution of quasi-free produced Λ- and Σ-hyperon decays and three-body decays from hyperfragments. Stopped hyperfragments will be identified as monochromatic peaks in the π ? momentum spectrum from which their masses can be extracted with a precision of 50 keV/c 2. 相似文献
289.
Okimichi Yano Takaya Kamoshida Shigehiro Sekiyama Yasaku Wada 《Journal of Polymer Science.Polymer Physics》1978,16(4):679-688
Drawing of oxidized high-density polyethylene (HDPE) and subsequent annealing greatly reduce the low-temperature dielectric loss when the electric field is applied perpendicular to the draw direction. This supports our model (J. Polym. Sci. Polym. Phys. Ed., 15 , 43 (1977)) of the proton moving parallel to the c axis of the PE crystal. A particular antioxidant (Ionox 330) in unoxidized HDPE induces a dielectric loss with a frequency and temperature dependence which differs from that for the loss in oxidized HDPE. The antioxidant loss seems to be an overlapping of tunneling and a thermal activation process. The possibility that the hydroperoxide group in the PE crystal is the origin of the loss in oxidized HDPE was theoretically examined in a manner similar to that used for the hydroxyl group in the previous paper. Results suggest that the hydroperoxide group is less probable than hydroxyl as the origin of the low-frequency loss in HDPE. 相似文献
290.
Calculation of the Ratio Between the Second and First Harmonic Signals in Wavelength-Modulation Spectroscopy for Absorption Measurement 总被引:1,自引:0,他引:1
Takaya Iseki 《Optical Review》2003,10(1):24-30
The dependence of the ratio between the second and first harmonic signals in wavelength-modulation spectroscopy is calculated for the precise absorption measurement that is applied to gas sensing. In the calculation, the amplitude modulation of the laser is considered as well as the frequency modulation. First, the dependence of signals on peak optical depth is discussed for the Lorentzian and Gaussian lines. Next, the dependence of signals on gas concentration is calculated in a weak absorption-limit. Finally, a numerical example is explained taking into consideration both peak optical depth and gas concentration. 相似文献