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101.
Hiroki Kanda Brian Beckford Takeji Fujibayashi Takao Fujii Yu Fujii Kenta Futatsukawa Toshiyuki Gogami Yun-Cheng Han Osamu Hashimoto Kentaro Hirose Ryotaro Honda Kenji Hosomi Alan Iguchi Takatsugu Ishikawa Yusuke Kaneko Masashi Kaneta Yuma Kasai Daisuke Kawama Taito Kawasaki Chigusa Kimura Shogo Kiyokawa Takeshi Koike Kazushige Maeda Tomofumi Maruta Nayuta Maruyama Masao Matsubara Koji Miwa Yohei Miyagi Sho Nagao Satoshi N. Nakamura Akira Okuyama Kotaku Suzuki Tadaaki Tamae Hirokazu Tamura Nobuhiro Terada Kyo Tsukada Tie-Shang Wang Fumiya Yamamoto Takeshi O. Yamamoto Hirohito Yamazaki 《Few-Body Systems》2013,54(7-10):1175-1178
Photoproduction of the neutral kaon on the deuteron has been investigated at the Research Center for Electron Photon Science, Tohoku University. We constructed the Neutral Kaon Spectrometer-2 for the detection of charged particles from the decay of the neutral kaon and the hyperon. We obtained a momentum distribution of K 0 with the inclusive measurement. It was consistent with the previous measurement. The total cross section of γ + d → K 0 + Λ + p was estimated from the measured integral cross section of γ + d → Λ + X. The total cross section with respect to the photon energy was compared with the theoretical calculations. It favored the Saclay-Lyon A model calculation with the ratio of the neutral to charged coupling constants of the axial-vector meson, K 1, as ~ ?1.5. The energy dependence and the magnitude of the total cross section were similar to the total cross section of γ + p → K + Λ. 相似文献
102.
H. Matsubara M. Takaki T. Uesaka S. Shimoura N. Aoi M. Dozono T. Fujii K. Hatanaka T. Hashimoto T. Kawabata S. Kawase K. Kisamori Y. Kikuch Y. Kubota C. S. Lee H. C. Lee Y. Maeda S. Michimasa K. Miki H. Miya S. Noji S. Ota S. Sakaguchi Y. Sasamoto T. Suzuki L. T. Tang K. Takahisa H. Tokieda A. Tamii K. Yako Y. Yasuda N. Yokota R. Yokoyama J. Zenihiro 《Few-Body Systems》2013,54(7-10):1433-1436
Spectroscopy for neutron-rich nuclei 9He and 12Be has been performed by means of heavy-ion double charge exchange (HIDCX) (18O, 18Ne) reaction on stable target nuclei 9Be and 12C, respectively. Several clear peaks in 12Be at low excitation energy region even above neutron separation energy have been observed in one-shot measurement, whereas no prominent signals of 9He have been observed owing to the small cross section. It is shown that the HIDCX reaction is a new powerful spectroscopic tool for study of unstable neutron-rich nuclei. 相似文献
103.
T. Kawabata T. Adachi M. Fujiwara K. Hatanaka Y. Ishiguro M. Itoh Y. Maeda H. Matsubara H. Miyasako Y. Nozawa T. Saito S. Sakaguchi Y. Sasamoto Y. Shimizu T. Takahashi A. Tamii S. Terashima H. Tokieda N. Tomida T. Uesaka M. Uchida Y. Yasuda N. Yokota H. P. Yoshida J. Zenihiro 《Few-Body Systems》2013,54(1-4):93-97
The alpha inelastic scattering from 24Mg was measured to obtain the isoscalar natural-parity excitation strengths and to search for the α-condensed states. The multipole decomposition analysis for the measured cross sections was performed. The strength distributions for the ${{\Delta}L=0{-}3}$ were successfully obtained and the possible candidates for the α-condensed states around the 16O core were found. 相似文献
104.
Takigawa M Matsubara S Horvatić M Berthier C Kageyama H Ueda Y 《Physical review letters》2008,101(3):037202
We present 11B NMR studies of the 2D frustrated dimer spin system SrCu2(BO3)_{2} in the field range 27-31 T covering the upper phase boundary of the 1/8 magnetization plateau, identified at 28.4 T. Our data provide a clear evidence that above 28.4 T the spin superlattice of the 1/8 plateau is modified but does not melt even though the magnetization increases. Although this is precisely what is expected for a supersolid phase, the microscopic nature of this new phase is much more complex. We discuss the field-temperature phase diagram on the basis of our NMR data. 相似文献
105.
Michito Shiotsuka Takuto Hashimoto Kenta Matsubara Katsuya Sako 《Transition Metal Chemistry》2018,43(8):693-703
Novel platinum(II) organometallic dinuclear complexes and oligomers with two types of phenanthroline ligands, namely 3,8-diethynylphenanthroline (L1) and 3,8-bis-(4-ethynyl-phenylethynyl)-1,10-phenanthroline (L2), were synthesized from trans-Pt(PBu3)2(1-ethynyl-4-methyl-benzene)Cl and trans-Pt(PBu3)2Cl2 by transmetalation of copper ion. The alternative procedure targeted platinum oligomer termination selection of either chloride or respective phenanthrolines and was successfully performed with different purifications by extraction and column chromatography. The structural formulae of these platinum complexes and oligomers were revealed with by analysis of both 31P{1H}-NMR and 1H-NMR spectral data. Alternative preparations of platinum oligomers with two types between chloride and respective phenanthroline termination are very useful for the selective synthesis for hybrid polymers with the coupling reaction with two different platinum oligomers with different diethynylaryl ligands. The platinum organometallic compounds showed similar absorption bands in the UV–Vis region. Those prepared with L1 had a strong absorption band at around 400 nm, assignable to the lowest energy metal-perturbed 1[π–π*] transitions, while in compounds prepared with L2, the strong band appeared around 410 nm, because L2 has an extended π conjugation relative to L1. No distinct differences were observed in the absorption spectra of these platinum oligomers between the different terminal structures, chloride or various phenanthrolines. The luminescence spectra of the platinum compounds prepared with either L1 or L2, however, showed a distinct difference. Those with L1 showed only a phosphorescence assignable to a typical metal-perturbed 3[π–π*] transition with vibronic progressions centered at around 530 nm in deoxygenated CH2Cl2 at room temperature, while those with L2 showed weak dual emissions assignable to a mixture of typical metal-perturbed 1[π–π*] and 3[π–π*] transitions in the visible region. 相似文献
106.
Aratono M Mori A Koga I Shigehisa M Onimaru N Tsuchiya K Takiue T Matsubara H 《The journal of physical chemistry. B》2008,112(39):12304-12311
Aggregate formation of a didodecyldimethylammonium bromide (DDAB) and didodecyldimethylammonium chloride (DDAC) mixture in aqueous solution was investigated. The concentration vs composition diagram of aggregate formation was constructed by analyzing the surface tension, turbidity, and electrical conductivity data. The cryogenic transmission electron microscopy was applied to several representative points in the diagram and provided information of the morphology of aggregates. The sequence of monomer (m) - m + small aggregate (A) - m + A + vesicle (V) - m + V was concluded with increasing total concentration of surfactants at all mixing ratios. The compositions of counterions in A and V were estimated on the basis of thermodynamic consideration and examined from the viewpoint of asymmetry of constituents and uneven distribution between outer and inner monolayers of a vesicle bilayer. Vesicle surfaces were suggested to abound in chloride ions compared to bulk solution, which is opposite to spherical micelle surfaces. 相似文献
107.
Matsubara H Ohtomi E Aratono M Bain CD 《The journal of physical chemistry. B》2008,112(37):11664-11668
Wetting of water by hexadecane has been investigated by ellipsometry as a function of the concentration of the cationic surfactant dodecyltrimethylammonium bromide (DTAB) in the aqueous phase and temperature. Three phases are identified: a 2-D gas of hexadecane molecules and DTAB molecules, a 2-D liquid comprising a mixed monolayer of hexadecane and DTAB, and a 2-D 'solid' phase. Evidence is presented to support the hypothesis that the liquid-solid phase transition is actually a wetting transition in which a surface-frozen layer of pure hexadecane wets the liquid-like mixed monolayer of hexadecane and DTAB. The triple point, at which the three phases coexist, is located at a temperature of 17.3 degrees C and DTAB concentration of 0.75 mmol kg (-1). The slopes of the three phase boundaries are analyzed thermodynamically. 相似文献
108.
Yoshitane Imai Dr. Katuzo Murata Kakuhiro Kawaguchi Tomohiro Sato Nobuo Tajima Dr. Reiko Kuroda Dr. Yoshio Matsubara Dr. 《化学:亚洲杂志》2008,3(3):625-629
A solid‐state fluorescent host system was created by self‐assembly of a 21‐helical columnar organic fluorophore composed of (1R,2S)‐2‐amino‐1,2‐diphenylethanol and fluorescent 1‐pyrenecarboxylic acid. This host system has a characteristic 21‐helical columnar hydrogen‐ and ionic‐bonded network. Channel‐like cavities are formed by self‐assembly of this column, and various guest molecules can be included by tuning the packing of this column. Moreover, the solid‐state fluorescence of this host system can change according to the included guest molecules. This occurs because of the change in the relative arrangement of the pyrene rings as they adjust to the tuning of the packing of the shared 21‐helical column, according to the size of the included guest molecules. Therefore, this host system can recognize slight differences in molecular size and shape. 相似文献
109.
Hiroshi Matsubara 《Journal of fluorine chemistry》2008,129(10):951-954
Phase-vanishing (PV) method using perfluorohexanes as a screen phase was applied to cyclopropanation reactions with CH2I2/Et2Zn and CH2I2/Et3Al. When Et3Al was used as a carbenoid generator, the reaction proceeded smoothly and desired cyclopropane derivatives were obtained in high yield. The PV cyclopropanation took 2 or 3 days to complete, however, reduction of reaction time by a factor of 2-3 was also achieved by vigorous stirring after the bottom CH2I2 layer disappeared. 相似文献
110.