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101.
Wang NH Taniguchi M Tsuji D Doi M Ohishi H Yoza K Baba K 《Chemical & pharmaceutical bulletin》2003,51(1):68-70
Four new guaianolides, sinodielides A-D (1-4), were isolated from Sinodielsia yunnanensis WOLFF together with a known polyacetylene, falcarindiol, and two known coumarins, bergapten and scopoletin. Their structures were established by spectral and X-ray analyses. 相似文献
102.
In this paper, the efficient application of high‐order weighted essentially nonoscillatory (WENO) reconstruction to the subsonic and transonic engineering problems is studied. On the basis of the physical considerations, two techniques are proposed to enhance the accuracy and efficiency of the WENO reconstruction. First, it is observed that the WENO scheme using characteristic variable has better accuracy and convergence speed than the scheme using primitive variable. For engineering problems with shock of moderate amplitude, on the basis of the Rankine–Hugoniot conditions, a simplified characteristic‐variable‐based WENO is developed. The simplified version significantly reduces the cost overhead without sacrificing the shock‐capturing capability. Second, in this work, it is found for viscous case that it is better to include the viscous effect. On the basis of a simple analysis, the viscous correction to the parameter ε in the WENO reconstruction is proposed. Numerical results indicate, with the proposed simplified characteristic‐variable‐based reconstruction and the viscous correction, that the nonlinear WENO interpolation is sharply activated in the region of shock jump, whereas in the shockless area, the WENO interpolation weights are tuned towards the designed optimal value for better accuracy. Compared with the original characteristic‐variable‐based WENO, the current implementation has similar accuracy and reduced cost. At the same time, compared with the primitive variable‐based WENO, better accuracy and convergence speed are obtained at marginal cost overhead. Several practical cases are calculated to demonstrate the accuracy and efficiency of the current methodology. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
103.
104.
Hisatoyo Morinaga Yusuke Ujihara Naho Yuto Daisuke Nagai Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2011,49(24):5210-5216
Metal‐free controlled ring‐opening polymerization of glycidyl phenyl ether (GPE) was achieved using tetra‐n‐butylammonium fluoride (Bu4NF) as an initiator in the presence of water and ethanol as chain transfer agents (CTAs). Number‐averaged molecular weight of poly(GPE) increased with an increase of [GPE]0/([Bu4NF]0 + [CTA]0) values, showing relatively narrow molecular weight distributions. NMR spectroscopic analysis exhibited a formation of ethoxy groups as well as FCH2 at the initiating polymer chain‐end when ethanol was used as the CTA in the polymerization. These results indicate that Bu4NF acts as a catalyst as well as the initiator for this polymerization system. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
105.
106.
Kazuhiro Nagata Daisuke Sano Yu Shimizu Michiko Miyazaki Takuya Kanemitsu Takashi Itoh 《Tetrahedron: Asymmetry》2009,20(21):2530-2536
The catalytic asymmetric alkylation of α-cyanocarboxylates and acetoacetates with an alkyl halide was performed under phase-transfer conditions to afford compounds which have a chiral quaternary carbon with up to 97% and 94% ee, respectively. As applications of this method, chiral 2-oxindole derivatives and a β-lactam derivative were synthesized. 相似文献
107.
108.
Daisuke Kamei Hiroharu Ajiro Mitsuru Akashi 《Journal of polymer science. Part A, Polymer chemistry》2010,48(16):3651-3657
The effects of stereoregularity, temperature, and solvent on the specific recognition of syndiotactic (st)‐poly(methacrylic acid) (PMAA) in macromolecularly porous isotactic (it)‐poly(methyl methacrylate) films were investigated to give important insights into the regularity and stability of nanospaces in the it‐PMMA films as well as template polymerization. The porous it‐PMMA films were fabricated on quartz crystal microbalance (QCM) substrates via the layer‐by‐layer (LbL) assembly of it‐PMMA/st‐PMAA, plus the st‐PMAA extraction from the assembly. QCM analysis and infrared spectroscopy revealed the first case of stereocomplex formation using st‐PMAA with lower stereoregularity (rr = 73%) in the LbL films, while st‐PMAA obtained with conventional free radical polymerization (rr = 62%) was barely incorporated into the porous it‐PMMA films. The maximum st‐PMAA incorporation increased from 25 to 40 °C, but there were almost no difference between 40 and 55 °C, indicating that the it‐PMMA crystallization would also be accelerated with increasing temperature. The studies on st‐PMAA incorporation with various complexing solvents revealed that the host it‐PMMA in the porous films could only form the original stereocomplex with 2/1 unit‐molar stoichiometry (st‐PMAA/it‐PMMA) in acetonitrile/water or ethanol/water. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3651–3657, 2010 相似文献
109.
Daisuke Nagai Asuka Fujii Masayoshi Tanaka Bungo Ochiai Atsushi Sudo Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2009,47(6):1510-1521
Anionic polymerization of methacrylates under sterically confined environment in a spherical beads‐shaped networked polystyrene (NwPS) matrix is described. The initiator used herein is a samarium (Sm) (III) enolate, which was formed by treatment of 2‐bromoisobutylate immobilized in the side chain of NwPS with Sm (II) iodide. By using this NwPS‐bound initiator, polymerization of a series of methacrylates (=solid‐supported polymerization) was studied to find its two aspects: (1) In the early stages, the rate constant for each methacrylate was comparable to that for its conventional solution‐phase polymerization using a Sm (III) enolate, suggesting that methacrylate can be efficiently supplied to the propagating end by its free permeation without any interference by the networked structure of the matrix. (2) After the early stages, the rate constant decreased remarkably, implying that permeation of methacrylate was sterically interfered by the formed poly(methacrylate) that filled the confined space in NwPS, as supported by a SEM image of the resulting beads, of which pores were filled with the formed polymers. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1510–1521, 2009 相似文献
110.
Minoru Umeda Hiroyuki Ojima Mohamed Mohamedi Isamu Uchida 《Journal of Polymer Science.Polymer Physics》2002,40(11):1103-1109
Methanol vapor‐induced membranous changes in a cast‐coated Nafion thin film were studied through current–voltage (I–V) characteristics with an interdigitated microarray (IDA) electrode and atomic force microscopy (AFM). The obtained I–V curves showed that the as‐prepared Nafion film was stable under humidified nitrogen gas; however, the I–V profile dramatically changed with exposure to methanol vapor. Next, the morphology of the film was compared before and after methanol exposure with AFM images. On the basis of our observations, we found that the as‐prepared film had an irregularly complicated microstructure, whereas the structure became homogeneous in appearance after 30 min of exposure to methanol gas. The alternating‐current conductivity data, showing almost the same magnitude before and after exposure, strongly suggested that the I–V profile shift was based on a change in an electrode reaction mechanism induced by a change in the junction at the Nafion/IDA electrode interface. Furthermore, the methanol vapor‐pre‐exposed Nafion was stable for further exposure to methanol vapor, water vapor, or both. With the stabilized film used in combination with the IDA electrode, a reversible change in the magnitude of the current was observed when the methanol/water vapor ratio was varied. This indicated that the electrode reaction had good reproducibility after the treatment. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 1103–1109, 2002 相似文献