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排序方式: 共有260条查询结果,搜索用时 15 毫秒
1.
Stability Properties of Maps Between Hopf Spaces 总被引:1,自引:0,他引:1
2.
Maki Onoda Takefumi Uchiyama Ken-Ichi Mawatari Kiyoko Kaneko Kazuya Nakagomi 《Analytical sciences》2006,22(6):815-817
A simple batch method for the fluorometric determination of hydrogen peroxide using phosphine-based fluorescent reagents has been developed. A rapid, mild and selective derivatization reaction was achieved by adding sodium tungstate dihydrate to the reaction mixture of hydrogen peroxide and a phosphine-based fluorescent reagent. When 4-diphenylphosphino-7-methylthio-2,1,3-benzoxadiazole was used as a reagent, the derivatization reaction was completed after 2 min at room temperature. The calibration curve was linear between 12.5 and 500 ng hydrogen peroxide in a 10 microL sample solution. This method is accurate and has potential for on-line applications. 相似文献
3.
Shouji Iwatsuki Ken-Ichi Inukai 《Journal of polymer science. Part A, Polymer chemistry》1974,12(7):1437-1442
Formation of charge-transfer complexes with trinitrotoluene (TNT) as a common acceptor was studied in detail by using dimethyltoluidine (DMT), poly-N-dimethyl-p-aminostyrene (poly-ASt), and also copolymers of aminostyrene (ASt) and styrene (St) as donors. A smooth bathochromic shift in λmax was observed with increasing ASt unit content in copolymers. Values of the constant for charge transfer complex formation KCT were found to increase smoothly with ASt unit content. However, the KCT value with DMT did not coincide with the value extrapolated from the plot of KCT value versus ASt unit content to zero ASt unit content, but was found to be much higher than the limiting value, in contradiction to the results obtained with maleic anhydride (MAnh). The entropy of complex formation with DMT was found to be exceptionally small; this small value may be responsible for the high KCT value with DMT. 相似文献
4.
Onodera K Nakamura H Oba Y Ohizumi Y Ojika M 《Journal of the American Chemical Society》2005,127(29):10406-10411
Zooxanthellamide Cs (ZAD-Cs), C(128)H(220)N(2)O(53)S(2) (ca. 2.7 kDa), was obtained from a cultured marine dinoflagellate of the genus Symbiodinium as an inseparable isomeric mixture of polyhydroxylated 61- to 66-membered macrolides. The chemical structures of the components were clarified by detailed 2D NMR analysis to be the macrolactonized analogues of zooxanthellamide A (ZAD-A), which had been previously isolated from the same microalgae. Chemical lability of ZAD-Cs suggests that ZAD-A is an artifact derived from ZAD-Cs during the isolation steps. Three of the components possess the largest (63-, 64-, and 66-membered) ring sizes found to date among the natural macrolides. ZAD-Cs exhibited higher vasoconstrictive activity than that of the zooxanthellatoxins, the first vasoconstrictive macrolides from Symbiodinium sp. The structure-activity relationship suggests that the huge macrolactone structure is important for biological activity. The relationship between the structures of the polyol metabolites and the phylogenetic systematics of Symbiodinium sp. is also discussed. 相似文献
5.
The cyclic voltammetric study of 1,10-phenanthroline—copper(II) complex was carried out in acidic buffer solution. It was found from the current—mole ratio (copper (II): 1,10-phenanthroline) relationship that the maximum coordination number of 1,10-phenanthroline—copper(II) complex was four under the present experimental condition. The reduction mechanism and kinetics of copper(II) was studied in the presence of various concentrations of 1,10-phenanthroline. 相似文献
6.
Takushi Kurihara Mariko Sugiyama Hiroshi Hirano Ken-Ichi Tomita Masayoshi Sakaki 《Journal of heterocyclic chemistry》1975,12(3):541-545
Reaction of o-nitrobenzylideneacetylacetone ( 1a ) with hydrazine dihydrochloride in methanol gave 4-(α-methoxy-o-nitrobenzyl)-3,5-dimethylpyrazole hydrochloride ( 4a ), whose structure was unambigously confirmed by an X-ray crystallographic analysis, via 4-(o-nitrobenzylidene)-3,5-dimethylisopyrazole ( 2a ). Compound 2a was synthesized by condensation of 1a with hydrazine dihydrochloride in acetonitrile. Analogously the corresponding o-chloro derivatives ( 2b, 4b ) were obtained. These were converted to N-methyl ( 6b ) and N-acetyl ( 7a,b ) derivatives and the behaviors on bromination and pyrolysis were investigated. 相似文献
7.
Mitsuo Ishikawa Ken-Ichi Nakagawa Ryuichi Enokida Makoto Kumada 《Journal of organometallic chemistry》1980,201(1):151-163
Photolysis of 2-phenylheptamethyltrisilane (I) in the presence of acyclic and cyclic conjugated dienes has been investigated using both a high-pressure mercury lamp with a quartz filter and a low-pressure mercury lamp with a Vycor filter. Irradiation of I in the presence of 1,3-butadiene, isoprene or 2,3-dimethylbutadiene with a high-pressure mercury lamp gave a product arising from photochemical isomerization of a silacyclopropane derivative and a compound apparently formed by 1,4-silylene addition, along with a 1/1 “ene” adduct of the diene to a photo-rearranged intermediate containing the silicon—carbon double bond. Irradiation of I in the presence of the conjugated diene with a low-pressure mercury lamp, followed by treatment of the product with methanol, afforded a methoxysilane arising from methanolysis of the corresponding silacyclopropane, together with the isomerization product, silacyclopentene and rearranged addition product. Irradiation of I in the presence of cyclopentadiene with a high-pressure mercury lamp produced methylphenylsilylcyclopentadiene, while irradiation of a similar mixture with a low-pressure mercury lamp followed by treatment with methanol gave 4-(methoxymethylphenylsilyl)-1-cyclopentene. With 1,3-cyclooctadiene, the photochemically generated methylphenylsilylene afforded many types of addition product. Photolysis of I in the presence of 1,3-cyclohexadiene, however, afforded none of the silylene addition products. 相似文献
8.
Oka H Suzuki M Harada K Iwaya M Fujii K Goto T Ito Y Matsumoto H Ito Y 《Journal of chromatography. A》2002,946(1-2):157-162
pH-Zone-refining counter-current chromatography was successfully applied to the separation of the main components of Food Color Red No. 106 (R-106, acid red, Color Index No. 45100). A 300-mg quantity of sample was separated using the following two-phase solvent system: n-butanol-water, 40 mM sulfuric acid in organic stationary phase and 30 mM ammonia in aqueous mobile phase. The obtained fractions were analyzed by high-performance liquid chromatography and fast atom bombardment mass spectrometry. The separation yielded 261.9 mg of main component of acid red with purity of 99.9%. 相似文献
9.
High concentrations of arsenic were observed in the blubber of ringed seals (Pusa hispida) in our previous study. To better understand the arsenic accumulation in blubber of marine mammals, arsenicals in the blubber of ringed seal were characterized using high performance liquid chromatography–inductively coupled plasma mass spectrometry (HPLC–ICPMS). The most predominant water-soluble arsenical in the blubber was dimethylarsinic acid (DMA), in spite of the predominance of arsenobetaine in other tissues. Lipid-soluble fraction was hydrolyzed under mild (tetraethylammonium hydroxide (TEAH) hydrolysis) and strong (NaOH hydrolysis) conditions, and then an aliquot of hydrolysate was injected onto HPLC–ICPMS. Both TEAH-labile and TEAH-stable/NaOH-labile lipid-soluble fractions contained precursors of DMA. These results suggest that the blubber might be the pool of DMA and DMA-containing precursors in ringed seals. 相似文献
10.
Ken-Ichi Okamoto Kazuhiro Tanaka Michiaki Muraoka Hidetoshi Kita Yutaka Maruyama 《Journal of Polymer Science.Polymer Physics》1992,30(11):1215-1221
Gas permeability and permselectivity are investigated for polybenzoxazoles from bis(3-amino-4-hydroxyphenyl)-1,1,1,3,3,3-hexafluoropropane (BAHHP) and aromatic diacid chlorides. Effects of thermal cyclization on the permeation properties are also investigated. The polybenzoxazole from BAHHP and 4,4′-(1,1,1,3,3,3-hexafluoroisopropylidene)dibenzoyl chloride (HFDB) displays high performance for CO2/CH4 separation ( $ {\rm P}_{{\rm CO}_2 } $ = 6.1 × 10?9 cm3 (STP) cm?1 s?1 cm-Hg?1, and $ {{{\rm P}_{{\rm CO}_2 } } \mathord{\left/ {\vphantom {{{\rm P}_{{\rm CO}_2 } } {{\rm P}_{{\rm CH}_4 } }}} \right. \kern-\nulldelimiterspace} {{\rm P}_{{\rm CH}_4 } }} $ = 38 at 35°C). The polybenzoxazole from BAHHP and 2,6-naphthalene dicarbonyl chloride displays high performance for H2/CO or H2/CH4 separation ( $ {\rm P}_{{\rm H}_2 } $ = 2.4 × 10?9 cm3 (STP) cm?1 s?1 cm-Hg?1, $ {{{\rm P}_{{\rm H}_2 } } \mathord{\left/ {\vphantom {{{\rm P}_{{\rm H}_2 } } {{\rm P}_{{\rm CO}} }}} \right. \kern-\nulldelimiterspace} {{\rm P}_{{\rm CO}} }} $ = 71, and $ {{{\rm P}_{{\rm H}_2 } } \mathord{\left/ {\vphantom {{{\rm P}_{{\rm H}_2 } } {{\rm P}_{{\rm CH}_{\rm 4} } }}} \right. \kern-\nulldelimiterspace} {{\rm P}_{{\rm CH}_{\rm 4} } }} $ = 250). Permeation properties for the polybenzoxazole from BAHHP and HFDB are close to those for a polyimide of similar chemical structure. The permeation properties are discussed in connection with packing density and local segmental mobility. © 1992 John Wiley & Sons, Inc. 相似文献