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31.
[reaction: see text]. An In(OTf)(3)-catalyzed addition of a beta-ketoester to acetylene in the presence of molecular sieves produces a alpha-vinylated ketoester in good to excellent yield. The vinylation reaction proceeds without any loss of elements in starting molecules under solvent-free conditions and allows the use of welding-grade acetylene, providing a practical method for synthetic utilization of acetylene gas. 相似文献
32.
Yamamoto T Mukai SR Endo A Nakaiwa M Tamon H 《Journal of colloid and interface science》2003,264(2):532-537
Growth of colloidal particles formed during the sol-gel transition of a resorcinol-formaldehyde (RF) solution was simulated based on the population balance equation by using the discrete-sectional model (DSM). During the early stage of the sol-gel transition, the transient change of sizes of colloidal particles estimated by this method agreed well with the previous experimental observation by dynamic light scattering (DLS), which confirmed the influence of the catalyst concentration of a starting RF solution on the growth rate of the particles. From the size distribution of colloidal particles predicted at the gelation time, the surface area of a RF hydrogel after the completion of the sol-gel transition was estimated, which coincided with the BET surface area of a RF aerogel because the porous structure of a hydrogel was maintained and few micropores were formed during supercritical drying. 相似文献
33.
A. Fukumi I. Endo T. Horiguchi Y. Ishida T. Kondo T. Kuwamoto H. Matsuzaki T. Nakamura T. Takahashi 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1997,42(4):243-249
Systematic study of hyperfine structures, Zeeman and Stark effects in Sm I is performed for the lowest 7G1-6 levels belonging to the configuration 4f 66s6p by atomic-beam laser spectroscopy with fluorescence detection. The hyperfine coupling constants of 7G2-6 levels are determined. From the Zeeman splittings for the 4f 66s 2 7F2-6 ? 4f 66s6p 7G2-6 transitions, g-values are determined for the 7G2.6 levels and the precision is improved by several orders of magnitude. From the Stark splittings for the 7F0-3 ? 7G1-3 transitions, tensor polarizabilities α 2(J) are determined for the upper 7G1-3 levels. Particularly for the 7G1 level (15 650.55 cm?1) which has close-lying opposite-parity level, the isotope dependence of α 2(J) is clearly observed for the first time. 相似文献
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Three acyclic polythioethers containing 2-thienyl units at both ends were synthesized and the effect of substituent on the extraction of copper(II) was studied. The methyl groups in the terminal thiophene ring have imparted an appreciable degree of increase in the percent extraction of copper(II), while the introduction of chlorine atoms into the 2-thienyl unit resulted in the reverse effect. Among the counter dye anions examined, tetrabromophenolphthalein ethylester was the best one for copper(II) extraction. The composition of extracted species was evaluated to be 122 (Cu(II)/polythioether/dye anion). Quantitative extraction of copper(I) was attained as complexes with various triphenylmethane dyes, i.e., bromocresol green, bromothymol blue, bromo-phenol blue and pyrogallol red. Copper(I) in organic phase was completely back-extracted with 2 mole/l sulfuric acid containing 10% hydrogen peroxide. 相似文献
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Wataru Ueda Damian Vitry Tomokazu Kato Nobufumi Watanabe Yusuke Endo 《Research on Chemical Intermediates》2006,32(3-4):217-233
Mo-V-O-based complex metal oxide catalysts were synthesized hydrothermally for the first time, characterized structurally and tested in the selective oxidation of propane to acrylic acid, and the results obtained were compared on the basis of catalyst crystal structures in order to clarify key aspects of alkane selective oxidation over multifunctional metal oxide catalysts. The catalysts tested were black solids of rod-shaped crystals, which had a layer structure in the direction of fiber axis and various high dimensional arrangements of metal octahedra in the cross-section plane. A strong dependency on the octahedra arrangements and a facet dependency were observed, and the roles of metal elements in the course of selective oxidation of propane were clarified by comparing the catalytic performance of various Mo-V-O-based catalysts. We discuss the multi-functional character derived from high dimensional structures of the catalysts and mechanism of the selective oxidation of propane. 相似文献
39.
Chemical conversion of some natural oxindoles (pteropodine, isopteropodine and isorhynchophylline) into the corresponding indole alkaloids has been made by way of a sequence of reactions which include formation of iminoethers of the natural oxindoles with Meerwein's reagent, reduction of the iminoethers to 2,3-seco-indoles and cyclization of 2,3-seco-indoles to the desired natural indole alkaloids. Sodium borohydride in acetic acid was found to be a specific reagent for the reduction of oxindole-iminoethers to 2,3-seco-indoles which were the key intermediates in these transformations. Yohimbine-oxindole iminoether was similarly converted to yohimbine and pseudoyohimbine. A number of by-products were obtained and their structures were elucidated. 相似文献
40.
Yoshihiko Kondo Ken Endo Nobuhiko Iki Sotaro Miyano Fumio Hamada 《Journal of inclusion phenomena and macrocyclic chemistry》2005,52(1-2):45-49
Even though it was obtained in poor yield, p-tert-butylthiacalix[8]arene (TC8A) has been synthesized as a new member of thiacalix[n]arenes by the terephthalate-induced cyclization of a mixture of acyclic oligomers, which was obtained by the reaction between p-tert-butylphenol and sulfur with CaO in ethylene glycol/diphenyl ether system. Slow evaporation of the chloroform solution of TC8A afforded guest-free crystals consisting of TC8A itself. The close-packed crystal structure of TC8A resembles that of p-tert-butylcalix[8]arene (C8A) closely, containing a plated loop molecular structure.This revised version was published online in July 2005 with a corrected issue number. 相似文献