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71.
Calculations are reported for the symmetric bending and stretching vibrational states of H3O+ and D3O+ including coupling between these two modes. The calculations were carried out by using a potential surface calculated by the SCF CI method and expressed in terms of symmetric internal coordinates. The transition energy of the ν2 (1? ← 0+) inversion mode is found to be 985 cm?1, which is comparable to the experimental value of 954.417 cm?1 observed by Haese and Oka. The calculated inversion doubling of the lowest state is 51 cm?1. 相似文献
72.
Xu Q Tanaka K Mori M Helaleh MI Hu W Hasebe K Toada H 《Journal of chromatography. A》2003,997(1-2):183-190
A monolithic ODS-silica gel column modified by saturating it with lithium dodecylsulfate (Li-DS) was used to demonstrate the high-speed separation of H+ from other mono- and divalent cations, such as Na+, NH4+, K+, Mg2+ and Ca2+ using ion chromatography (IC). Using a 5 mM EDTA-2K solution containing 0.10 mM Li-DS (pH 4.80) as eluent, H+ was eluted with a sharp and symmetrical peak within 1.0 min before other cations at a flow-rate of 1.5 ml min(-1). The rapid elution of H+ and its conductimetric detection could be attributed to the presence of EDTA (HY2-), which can convert H+ ions as anions. i.e. H(+) + H2Y(2-) --> H3Y(-). The acidity of rainwater and deionized water samples was determined using this IC system with satisfactory results. 相似文献
73.
Kiyoshi Endo Hajime Tsujikawa Takayuki Otsu 《Journal of polymer science. Part A, Polymer chemistry》1986,24(7):1633-1642
5-Phenyl-2-pentene (5Ph2P) was found to undergo monomer-isomerization polymerization with TiCl3–R3Al (R = C2H5 or i-C4H9, Al/Ti > 2) catalysts to give a polymer consisting of exclusively 5-phenyl-1-pentene (5Ph1P) unit. The geometric and positional isomerizations of 5Ph2P to its terminal and other internal isomers were observed to occur during polymerization. The catalyst activity of alkylaluminum examined to TiCl3 was in the following order: (C2H5)3Al > (i-C4H9)3Al > (C2H5)2AlCl. The rate of monomer-isomerization polymerization of 5Ph2P with TiCl3–(C2H5)3Al catalyst was influenced by both the Al/Ti molar ratio and the addition of nickel acetylacetonate [Ni(acac)2], and the maximum rate was observed at Al/Ti = 2.0 and Ni/Ti = 0.4 in molar ratios. 相似文献
74.
Kiyoshi Hasebe Satoshi Hikima Hitoshi Yoshida 《Fresenius' Journal of Analytical Chemistry》1991,339(4):261-263
Summary The covalent bonding of l-lactate oxidase (no E.C.) to cross-linked copolymers of chitosan (Chitopearl) using the glutaraldehyde method is described and applied to the determination of l-lactate in serums of diseased and normal animals. The bioreactor packing of the immobilized enzyme is stable for at least 4 months and can be continuously used for the rapid and simple determination of l-lactate. The reduction current of pyruvate, corresponding to the product of enzymatic reaction, is determined by differential pulse polarography. The reproducibility (RSD) for 10 mol/l l-lactate is 0.78% (n=6) and the detection limit is 0.62 mol/l (k=2, confidence level 97.72%). 相似文献
75.
Li4Ti5O12 thin films for rechargeable lithium batteries were prepared by a sol-gel method with poly(vinylpyrrolidone). Interfacial properties of lithium insertion into Li4Ti5O12 thin film were examined by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and potentiostatic intermittent titration technique (PITT). Redox peaks in CV were very sharp even at a fast scan rate of 50 mV s−1, indicating that Li4Ti5O12 thin film had a fast electrochemical response, and that an apparent chemical diffusion coefficient of Li+ ion was estimated to be 6.8×10−11 cm2 s−1 from a dependence of peak current on sweep rates. From EIS, it can be seen that Li+ ions become more mobile at 1.55 V vs. Li/Li+, corresponding to a two-phase region, and the chemical diffusion coefficients of Li+ ion ranged from 10−10 to 10−12 cm2 s−1 at various potentials. The chemical diffusion coefficients of Li+ ion in Li4Ti5O12 were also estimated from PITT. They were in a range of 10−11-10−12 cm2 s−1. 相似文献
76.
Four 6-phenyl-5,6,7,8-tetrahydro-4H-1,3,2,6-dioxathiazocine 2-oxides were synthesized by the reaction of the corresponding N,N-bis(2-hydroxyethyl)aniline with thionyl chloride in the presence of triethylamine. 相似文献
77.
Ikuo Ashikawa Mariko Kito Kimiyuki Satoh Hiroyuki Koike Yorinao Inoue Kayoko Saiki Kiyoshi Tsukida Yasushi Koyama 《Photochemistry and photobiology》1987,46(2):269-275
All- trans β-carotene-5,6-epoxide has been found in the thylakoid membranes of spinach and of the cyanobacterium Synechococcus vulcanus Copeland. The epoxide was extracted from the thylakoid membranes with acetone, and was isolated by high-performance liquid chromatography (HPLC). The structure of the epoxide was identified by means of mass, Raman, and electronic absorption spectroscopy. Changes in the amount of the epoxide, as a result of epoxidation and (apparent) de-epoxidation reactions in the membranes, were traced by analysis of extracts on HPLC. In isolated thylakoid membranes, only the epoxidation reaction took place. The reaction was caused by irradiation or by the addition of ferricyanide, suggesting that electron transport reactions in the membranes are involved in the epoxidation. In intact spinach leaves, however, both epoxidation and de-epoxidation took place; the extent of epoxidation correlated with the intensity of light incident on the leaves. The epoxidation and de-epoxidation of all- trans β-carotene are contrasted with those of xanthophylls (in the violaxanthin cycle). 相似文献
78.
Koichiro Shirota Ichirou Yamaguchi Kiyoshi Kanie Tomiki Ikeda Tamejiro Hiyama Ichiro Kobayashi 《Liquid crystals》2013,40(5):555-558
The optical properties of two kinds of photochromic antiferroelectric liquid crystal (AFLC) containing an azo group have been examined. Depending on the substituting group at the chiral centre, these AFLCs showed different photoinduced phase transitions by Ar+ laser light irradiation. This phase transition has led to a new form of optical switching controlled by a bias voltage. In addition, it was found that these AFLCs caused an azimuthal photoalignment effect regulated by linearly polarized Ar+ laser light irradiation. These phenomena were applied to image storage. 相似文献
79.
Fujisawa Kiyoshi Okano Mitsuki Martín-Pastor Manuel López-Sánchez Rubén Elguero José Alkorta Ibon 《Structural chemistry》2021,32(1):215-224
Structural Chemistry - Experimental multinuclear determination of the chemical shifts, especially 15N and 109Ag, of five silver(I) trinuclear pyrazolate complexes, (PzAg)3, coupled with ZORA... 相似文献
80.