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A. I. Fedoseev S. G. Lushnikov S. N. Gvasaliya S. Kojima 《Physics of the Solid State》2006,48(6):1102-1105
The behavior of acoustic phonons in crystals of a relaxor ferroelectric, namely, the lead scandium tantalate PbSc1/2Ta1/2O3 (PST), is studied in the vicinity of the diffuse phase transition. The behavior of longitudinal and transverse acoustic phonons in a PST single crystal is examined using Brillouin scattering. The phonon subsystem is found to behave anomalously in the vicinity of T = 297 K, which can probably be assigned to the existence of a phase transition. Analysis of the results obtained yields the values of the elastic moduli C11, C12, and C44 for the cubic phase of the crystal over a wide temperature range. 相似文献
4.
Joji Ohshita Ryosuke Taketsugu Yuki Nakahara Atsutaka Kunai 《Journal of organometallic chemistry》2004,689(20):3258-3264
Selective dehydrogenative coupling of di- and trihydrosilanes with alcohols catalyzed by PdCl2 or NiCl2 afforded alkoxyhydro- and dialkoxyhydrosilanes in good yield. Further treatment of the resulting alkoxyhydrosilanes with carbon tetrachloride or allyl bromide in the presence of the same catalyst led to the formation of alkoxychloro- and alkoxybromosilanes, respectively. Similar reactions of dialkoxyhydrosilanes with carbon tetrachloride afforded dialkoxychlorosilanes in good yield, although contamination of small amounts of trialkoxysilanes and alkoxydichlorosilanes was detected in the products. Selective substitution of the alkoxyhalosilanes with nucleophiles is also reported. 相似文献
5.
M. Wada Y. Ishida T. Nakamura Y. Kanai T. M. Kojima A. Takamine Y. Yamazaki K. Okada A. Yoshida T. Kubo I. Katayama S. Ohtani V. Varentsov H. Wollnik V. Lioubimov H. A. Schuessler 《Hyperfine Interactions》2006,173(1-3):153-163
A next-generation slow radioactive nuclear ion beam facility (SLOWRI) which provides slow, high-purity and small emittance ion beams of all elements is being build as one of the principal facilities at the RIKEN RI-beam factory (RIBF). High energy radioactive ion beams from the projectile fragment separator BigRIPS are thermalized in a large gas catcher cell. The thermalized ions in the gas cell are guided and extracted to a vacuum environment by a combination of dc electric fields and inhomogeneous rf fields (rf carpet ion guide). From there the slow ion beam is delivered via a mass separator and a switchyard to various devices: such as an ion trap, a collinear fast beam apparatus, and a multi-reflection time of flight mass spectrometer. In the R&D works at the present RIKEN facility, an overall efficiency of 5% for a 100A MeV 8Li ion beam from the present projectile fragment separator RIPS was achieved and the dependence of the efficiency on the ion beam intensity was investigated. Recently our first spectroscopy experiment at the prototype SLOWI was performed on Be isotopes. Energetic ions of 10Be and 7Be from the RIPS were trapped and laser cooled in a linear rf trap and the specific mass shifts of these isotopes were measured for the first time. 相似文献
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K. M. Kojima 《Applied magnetic resonance》1997,13(1-2):111-122
Muon spin relaxation (μSR) and nuclear magnetic resonance (NMR) are powerful probes of magnetism, which have been extensively applied to studies of spin gap systems. Comparison of results obtained with the two techniques gives complementary results, as each is sensitive to different aspects of spin gap magnetism. We discuss recent μSR measurements of the spin ladder compounds Sr n?1Cu n+1O2n , pure and doped Haldane materials (Y2?x Ca x )Ba(Ni1?y Mg y )O5, and doped spin Peierls compounds (Cu1?x Zn x )(Ge1?y Si y )O3. 相似文献
8.
Using temperature-modulated
differential scanning calorimetry, the melting behaviour of poly(oxytetramethylene)-alt-(aromatic oligoamide) (POTM-alt-AOA)
has been studied in comparison with that of polyoxytetramethylene glycohols
(POTMGs). The apparent melting temperature of the block copolymers is found
to be less than that of the corresponding POTMGs by approximately 30°C.
The relaxation time of melting of a POTM segment has been estimated and compared
with that of POTMG. The relaxation time of POTM-alt-AOA
is slightly shorter than that of POTMG when the molar mass of the POTM segment
is 2900; however, it is longer when the molar mass is 1400. 相似文献
9.
Kojima T. Inoue E. Tsuchiya M. Ishimaru K. 《Journal of Thermal Analysis and Calorimetry》2003,72(2):737-742
TG, swelling, and viscometric studies are presented for the residues, PTHF/IPDI polymer networks, and the extracts, the linear
polymers and unreacted IPDI, after Soxhlet extraction of PTHF/IPDI reaction products. The products are obtained by reacting
PTHF with 650, 1400, (2×650+1×2900), or 2900 of molecular mass with IPDI at various concentrations in bulk. The results on
the swelling and the viscosity experiments suggest that the PTHF/IPDI reaction products have a usual expectable structure.
All the TG curves are a double stage curve. The initial stage and the last stage seem to reflect decomposition of PTHF chains
and vaporization of the remainder, IPDI, respectively. These are analyzed by a trial-and-error construction, supposing double
event behavior. The values of ratio of mass loss associated with the initial event, W01, to the mass loss associated with the last event, W02, are smaller than the expectable those. This suggests that Event 2 involves vaporization of the decomposition products of
PTHF moieties bonded to IPDI in addition to vaporization of IPDI.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
10.
Ryosuke Sakai Issei Otsuka Toshifumi Satoh Ryohei Kakuchi Harumi Kaga Toyoji Kakuchi 《Journal of polymer science. Part A, Polymer chemistry》2006,44(1):325-334
The asymmetric polymerization of 4′‐isocyanatobenzo‐18‐crown‐6 with the lithium amide of (S)‐(2‐methoxymethyl)pyrrolidine successfully proceeded to afford end‐functionalized poly(4′‐isocyanatobenzo‐18‐crown‐6) with (S)‐(2‐methoxymethyl)pyrrolidine (polymer 2 ). In the circular dichroism (CD) spectrum of 2 , a clear positive Cotton effect was observed in the range of 240–350 nm corresponding to the absorption of the polymer backbone, indicating that 2 partially formed a one‐handed helical structure, which was preserved by the chirality of (S)‐(2‐methoxymethyl)pyrrolidine bonding to the terminal end in 2 . In the titration experiments for the CD intensity of 2 in the presence of D ‐ and L ‐Phe·HClO4 (where Phe is phenylalanine), a small but remarkable difference was observed in the amount of the chiral guest needed for saturation of the CD intensity and in the saturated CD intensity, indicating that the extremely stable, one‐handed helical part should exist in the main chain of 2 , which was not inverted even when the unfavorable chiral guest for the predominant helical sense, L ‐Phe·HClO4, was added. In addition, helical polymer 2 exhibited a chiral discrimination ability toward racemic guests; that is, the guests were extracted from the aqueous phase into the organic phase with enantiomeric excess. The driving force of the chiral discrimination ability of 2 should certainly be attributed to the one‐handed helical structure in 2 . © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 325–334, 2006 相似文献