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991.
Koichi M.T. Yamada 《Journal of Molecular Spectroscopy》2009,254(2):87-93
Vibrational assignments for some of the lowest energy levels of the CO dimer have been derived purely spectroscopically on the basis of the molecular symmetry, nuclear spin statistics, observed selection rules, and sequence of the transition doublets. Most of the previous assignments of Surin et al. [L.A. Surin, D.N. Fourzikov, T.F. Giesen, S. Schlemmer, G. Winnewisser, V.A. Panfilov, B.S. Dumesh, G.W.M. Vissers, A. van der Avoird, J. Phys. Chem. A 111 (2007) 12238-12247] are confirmed in the present work, and are supported by much clear evidences. One significant revision of that analysis in the present work is identification of the torsional (out-of-plane) excited state, which had been assigned previously to an excited state of the geared (in plane) internal rotation. 相似文献
992.
Hideo Hosono Katsuro Hayashi Koichi Kajihara Peter V. Sushko Alexander L. Shluger 《Solid State Ionics》2009,180(6-8):550-555
12CaO·7Al2O3 (C12A7) with a unique nano-porous structure and free O2? ions entrapped in sub-nanometer-sized cages is a fast oxygen-ion-conducting material. These free O2– may be replaced by various oxygen-related species, OH?, O2? and O?, by tuning the atmosphere during the heat treatment. We examined the conduction mechanism for stoichiometric C12A7 (C12A7:O2?), in which O2? ions exist as counter anions in sub-nanometer-sized cages, by Raman measurement of C12A7:O2? annealed in a dry 18O2 atmosphere. It was revealed that the primary ion conducting species is an O2? ion which diffuses via exchange with O2? in the cage wall. An experimental result on the sample containing O? ions implied that O? is more mobile than O2? in C12A7. Ab initio calculations on the diffusion paths of O2? and O? ions in C12A7 supported the above experimental results. 相似文献
993.
Kazuya Itsuki Yoshitaka Michihiro Shigeki Endou Koichi Nakamura Takashi Ohno 《Solid State Ionics》2009,180(14-16):917-921
Under the harmonic approximation, the contributions from the indirect ionic interactions to the elastic constants are calculated for the alkali halide and silver halide crystals with the rock-salt structure. The coupling constants of the indirect ionic interactions are calculated by the self-consistent field treatment of the local density approximation and the spherical solid model. The calculated values of the coupling constants are large for the silver ion. The indirect ionic interaction significantly affects the elastic constants. It quantitatively explains the deviation from the Cauchy relation in alkali halide crystals. Moreover, it provides a clear account for the large values of the deviation from the Cauchy relation in AgCl and AgBr. 相似文献
994.
Three new cyanogenic glycosides named hydracyanosides A (1), B (2), and C (3) were isolated from the leaves and/or stems of Hydrangea macrophylla in China. The absolute stereostructures of hydracyanosides were characterized on the basis of chemical and physiochemical evidence including single crystal X-ray crystallographic analysis. To the best of our knowledge, this is the first scientific report of cyanogenic glycosides from Hydrangea plants. 相似文献
995.
o-Carboranyl aminoalcohols were synthesized using a standard Mannich reaction, and were tested for their anticancer properties using an in vitro test for CT26 cancer cells. The polar periphery of the aminoalcohols benefited from the high boron uptake in CT26 cancer cells with low toxicity, indicating their potential as BNCT agents. 相似文献
996.
The Stille cross-coupling reaction of [1-11C]acetyl chloride with tributylphenylstannane leading to [carbonyl-11C]acetophenone was studied with the goal of developing a new 11C-labeling method for positron emission tomography tracer synthesis. The coupled product [carbonyl-11C]acetophenone was synthesized using the Pd2(dba)3/P(MeNCH2CH2)3N·HCl system with a 60-61% radiochemical conversion from [1-11C]acetyl chloride (decay-corrected, n = 3). 相似文献
997.
Shinji Nakamura Dr. Ching‐Yuan Liu Dr. Atsuya Muranaka Dr. Masanobu Uchiyama Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(23):5619-5619
Density functional theory and fragment‐energy analysis have been used to probe the mechanism of the halogen–zinc exchange reaction. In their Full Paper on page 5686 ff. , M. Uchiyama, S. Nakamura et al. discuss three important factors in this reaction: The effect of the halogen species, the effect of the alkyl ligand on zinc, and the effect of the substrate nature.
998.
Ryoji Kobori Tomonori Ohba Takaomi Suzuki Taku Iiyama Sumio Ozeki Michio Inagaki Akihiro Nakamura Masato Kawai Hirofumi Kanoh Katsumi Kaneko 《Adsorption》2009,15(2):114-122
N2 adsorption isotherms of molecular sieve carbon were measured at 77 K and 303 K. The Ar adsorption isotherms of molecular
sieve carbon samples were also measured at 303 K. The grand canonical Monte Carlo (GCMC) simulation technique was applied
to calculate the N2 and Ar adsorption isotherms at 303 K using the ultramicropore volume determined by H2O adsorption. The comparative method of experimental and simulated isotherms of supercritical N2 and Ar at 303 K gave the width of the micropore mouth of the molecular sieve carbon, which can be applied to the ultramicropore
width determination for other noncrystalline porous solids. 相似文献
999.
Japanese cedar wood powder (CWP) was chemically modified to a tertiary-amine-type adsorbent and studied for the selective recovery of Pd(II) from various industrial waters. Batch adsorption tests performed from 0.1 M to 5 M HCl and HNO3 systems reveal stable performance with better results in HNO3 medium. The maximum loading capacity for Pd(II) was studied in HCl as well as in HNO3. A continuous-flow experiment taking a real industrial solution revealed the feasibility of using modified CWP for the selective uptake and preconcentration of traces of palladium contained in acidic effluents. In addition, stable adsorption performance even on long exposure to γ-irradiation and selective recovery of palladium from simulated high-level liquid waste (HLW) are important outcomes of the study. 相似文献
1000.
Kenichi Murata Masato Suzuki Kazuki Kajiya Nobuhumi Nakamura Hiroyuki Ohno 《Electrochemistry communications》2009,11(3):668-671
The direct electron transfer reaction of fructose dehydrogenase (FDH) from Gluconobacter sp. on alkanethiol-modified gold nanoparticles (AuNPs) was examined. AuNP-modified electrodes were simply fabricated by depositing citrate-reduced gold nanoparticles onto a gold electrode and carbon fiber paper and then covering the surface with a self-assembled monolayer of alkanethiols. The immobilization of AuNPs provided a large effective surface area for the adsorption of FDH. Catalytic oxidation currents based on the direct electron transfer reaction of FDH were observed from a potential about ?100 mV (vs. Ag/AgCl, 3 M NaCl) in the presence of d-fructose without a mediator. The current density reached as high as 14.3 ± 0.93 mA/cm2 (at +500 mV), which was achieved in the presence of 200 mM d-fructose by immobilization of FDH on 2-mercaptoethanol-modified AuNP/carbon fiber paper electrodes. 相似文献