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71.
Noboru Oyama Takeo Ohsaka Takeyoshi Okajima Tomoaki Hirokawa Tsuyoshi Maruyama Yukio Ohnuki 《Journal of Electroanalytical Chemistry》1985,187(1):79-96
Liquid crystalline/polymer composite membrane-coated electrodes were prepared by casting a 1,2-dichloroethane solution of N-(4-ethoxybenzylidene)-4′-n-butylaniline (EBBA) and polycarbonate (PC) on an electrode surface. The temperature-dependence of the permeability of the EBBA/PC composite membrane on electrodes to Fe(CN)3?6 ion as a solution-phase redox ion was investigated by means of hydrodynamic voltammetry at a rotating disk electrode. The permeability changed with temperature over the range of the crystalline-nematic-phase transition temperature of EBBA. It is demonstrated that the observed temperature-dependence of the permeability reflects the thermotropic properties of EBBA in the EBBA/PC composite membrane. Furthermore, the dependence of the limiting current of the steady-state current-potential curves for the reduction of Fe(CN)—6 at the EBBA/PC composite membrane-coated electrode upon the membrane thickness, the blend ratio of EBBA and PC and the concentration of Fe(CN)3?6 in a bulk solution was examined in order to understand the transport process of Fe(CN)?36 through the EBBA/PC composite membrane from the membrane/solution interface to the electrode/membrane interface. The transport process of Fe(CN)3?6 within the membrane was found to obey Fick's Law. 相似文献
72.
73.
Zircon-type compounds LnCrO4 (Ln=Nd, Sm, and Dy) were prepared. Their precise crystal structures at room temperature were determined from X-ray diffraction measurements. These compounds have a tetragonal system with space group I41/amd. Magnetic susceptibility and specific heat measurements have been performed for all the compounds in the temperature range between 1.8 and 300 K. For NdCrO4, an antiferromagnetic transition was found at 25.2 K. SmCrO4 and DyCrO4 show magnetic transitions at 15.0 and 22.8 K, respectively. In addition, structural phase transitions were observed at 58.5 and 31.2 K, respectively. For DyCrO4, the crystal structure below the transition temperature was determined by low-temperature powder X-ray diffraction measurements to be orthorhombic with space group Imma. 相似文献
74.
Per JensenSteven S. Wesolowski Nicole R. BrinkmannNancy A. Richardson Yukio YamaguchiHenry F. Schaefer III P.R. Bunker 《Journal of Molecular Spectroscopy》2002,211(2):254-261
The potential energy surface and dipole moment surfaces of the ã4A2 electronic state of CH2+ are calculated ab initio using an augmented correlation-consistent polarized valence quadruple-ζ (aug-cc-pVQZ) basis set, with the incorporation of dynamical correlation using the coupled cluster method with single and double excitations and perturbatively connected triple excitations [CCSD(T)]. We use these surfaces in the MORBID program system to calculate rotation and rotation-vibration term values for ã-state CH2+, CD+2, and CHD+ and to simulate the rotation and rotation-vibration absorption spectrum of CH2+ in the ã4A2 electronic state. Our work is motivated by studies of CH2+ that use the Coulomb explosion imaging technique and by the goal of predicting spectra that may be obtained from discharge sources. Although the ã state is the lowest-lying excited state above the X?/Ã ground state pair, it turns out to be relatively high-lying, and we determine that Te(ã)=30447.5 cm−1. The equilibrium bond angle for ã-state CH2+ is only 77.1°; as a result the asymmetric top κ value is close to 0, and the molecule is equally far from the oblate and prolate symmetric top limits in this electronic state. 相似文献
75.
[reaction: see text] A ruthenium catalyst precursor bearing a bulky and electron-donating pentamethylcyclopentadienyl (Cp) ligand, typically CpRuH3(PPh3), mediates hydrosilylation of several 1-alkynes with novel regioselectivity to give preferentially 2-silyl-1-alkenes. 相似文献
76.
The synthesis of MoVNbTe(Sb)O(x)() composite oxide catalysts based on the self-organization of polyoxometalates (POMs) was investigated. The catalysts which were synthesized via reduction of POMs by using reducing agents under mild conditions and/followed by calcination in an O(2)-excluded atmosphere which superior performance for propane (amm)oxidation. It was suggested that the metastable phase formed at an elevated temperature with a specific oxidation state corresponds to the catalytic activity. 相似文献
77.
78.
Soukil Mah Yukio Yamamoto Koichiro Hayashi 《Journal of polymer science. Part A, Polymer chemistry》1982,20(7):1709-1716
Radiation-induced cationic polymerization of styrene was studied in methylene chloride in the presence of triphenylsulfonium hexafluorophosphate. Acceleration in polymerization and an increase in molecular weight at a low temperature (?78°C) were observed in the presence of triphenylsulfonium salt. A study of pulse radiolysis revealed that both effects are due mainly to PF?6, which forms ion pairs with the cationic species involved in the polymerization. 相似文献
79.
80.
Shigeyuki Mayama Toshikazu Tani Tamio Ueno Kazumasa Hirabayashi Tadakazu Nakashima Hiroshi Fukami Yukio Mizuno Hiroshi Irie 《Tetrahedron letters》1981,22(22):2103-2106
The major phytoalexin from oat leaves has been identified as 2-[2-(4-hydroxyphenyDethenyl] -6-hydroxy-4H-3,1-benzoxazin-4-one (). 相似文献