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141.
New chiral stationary phases of polydimethylsiloxane anchored with (S)-(-)-t-leucine derivatives were provided for use in enantiomer separation of pharmaceuticals by capillary gas chromatography. Fifteen pharmaceuticals were separated into their enantiomeric pairs by converting them into pentafluoropropionyl and heptafluorobutyryl derivatives. The separation factor and resolution obtained from the new phases were superior to those from the conventional Chirasil-Val capillary column. 相似文献
142.
Mitsuhiro Hirata Yutaka Abe Bungo Ochiai Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2010,48(20):4385-4392
Various star‐shaped poly(phenoxy propylene sulfide)s (PPSs) bearing curable end groups were synthesized by the functionalization of the propagating ends of star‐shaped poly(PPS) with various electrophilies. The functionalization with chloromethyl styrene proceeded quantitatively, and afforded polymers with Mn almost agreed with theoretical value and narrow Mw/Mn. The photocuring conditions were optimized, and the addition of 10 wt % of poly(ethylene glycol) diacrylate was effective to attain sufficient crosslinking. The photocuring reaction of the end‐functionalized poly(PPS) films cast on silicon wafers was conducted by UV irradiation. The cured poly (PPS)s became insoluble in THF, supporting the sufficient crosslinking. Developing of a cured polymer yielded a negative photoresist pattern. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
143.
Unlike polyhydroxyalkanoates (PHAs) copolymers, the controlled and efficient synthesis of PHA terpolymers from triglycerides and fatty acids are yet to be established. This study demonstrates the production of P(3HB-co-3HV-co-3HHx) terpolymer with a wide range of 3HV monomer compositions from mixtures of crude palm kernel oil and 3HV precursors using a mutant Cupriavidus necator PHB−4 transformant harboring the PHA synthase gene (phaC) of a locally isolated Chromobacterium sp. USM2. The PHA synthase of Chromobacterium has an unusually high affinity towards 3HV monomer. P(3HB-co-3HV-co-3HHx) terpolymers with 3HV monomer composition ranging from 2 to 91 mol% were produced. Generation of 3HHx monomers was affected by the concentration and feeding time of 3HV precursor. P(3HB-co-24 mol% 3HV-co-7 mol% 3HHx) exhibited mechanical properties similar to that of common low-density polyethylene. P(3HB-co-3HV-co-3HHx) terpolymers with a wide range of 3HV molar fraction had been successfully synthesized by adding lower concentrations of 3HV precursors and using a PHA synthase with high affinity towards 3HV monomer. 相似文献
144.
Vuthichai Ervithayasuporn Junichi Abe Toshinori Matsushima Yusuke Kawakami 《Tetrahedron》2010,66(48):9348-9355
Two new classes of mono- and oligo(p-phenylene ethynylene)s grafted with polyhedral oligomeric silsesquioxanes (POSS) were synthesized via ‘click’ chemistry and palladium-catalyzed Sonogashira cross-coupling. These materials with cubic silsesquioxanes are very robust with excellent thermal stability in air (T5%loss>330 °C) and exhibited Tg>80 °C. All the compounds showed high photoluminescence with a range of blue emission and quantum yield up to 80% in the solution. Extended π conjugation molecules of oligo-pPEs POSS maintain relatively high PL quantum efficiencies in the solid state, compared to mono-pPEs POSS. A preliminary report is made of some of the materials as multilayer OLED components with active dopants PVK and PBD. 相似文献
145.
This study examined the relationship between the functions of plant cells and the characteristics of cellulose microfibril
aggregates in the cell walls. For this purpose, the mature bamboo (Phyllostachys pubescens) culm was separated into fiber and parenchyma cells, and then the morphological and physical properties of the cellulose
microfibril aggregates isolated from both cells were compared. SEM observations revealed that both fiber and parenchyma cells
consist of similar microfibril aggregates approximately 15–20 nm in width. Moreover, X-ray analysis and the tensile tests
of the sheets prepared from the microfibril aggregates showed that the cellulose microfibrils isolated from fiber and parenchyma
cells had almost the same cellulose crystallinity and longitudinal Young’s modulus in the dry state. These results suggest
that all the cellulose microfibrils synthesized in the same individual exhibit the same characteristics in the dry state regardless
of cell function. 相似文献
146.
Bending tests and X-ray diffraction studies were conducted on oven-dried wood samples (Picea jezoensis Carr.) treated with various concentrations of aqueous NaOH solution to investigate the influence of alkali treatment on the
longitudinal contraction, bending properties, and cellulose structure. The length of the wood samples decreased and the density
increased at NaOH concentrations greater than 10%. The Young’s modulus and the specific Young’s modulus decreased and the
strain at yield increased for the same concentration range. However, the stress at yield was almost constant for all concentration
ranges. X-ray diffraction analysis showed that lattice transformation from cellulose I to cellulose II did not occur during
alkali treatment and the crystallinity index decreased at NaOH concentrations greater than 10%. The crystallinity index was
linearly correlated with the changes in longitudinal contraction and the bending properties, which indicates that the increase
in the proportion of amorphous components of the cellulose influences the longitudinal contraction and the bending properties
of wood samples during alkali treatment. 相似文献
147.
Takumi Abe Hiroyuki Takeda Yoshihisa Miwa Koji Yamada Reiko Yanada Minoru Ishikura 《Helvetica chimica acta》2010,93(2):233-241
It was shown that dichloramine‐T ( 1 ) reacted with cyclohexene in acetonitrile to give N1‐(2‐chlorocyclohexyl) amidine 2a and N‐(2‐chlorocyclohexyl)acetamide ( 3 ) via the competitive addition of acetonitrile and N‐chloro‐N‐tosylamino anion to cyclohexenechloronium ion. This reaction can be catalyzed by Cu(OAc)2, primarily affording 2a . Furthermore, the resulting 2a can be cyclized to benzimidazol 14a in good yield by treating with KOH in dioxane. 相似文献
148.
Nakamura H Abe Y Koizumi R Suzuki K Mogi Y Hirayama T Karube I 《Analytica chimica acta》2007,602(1):94-100
A new chemiluminescence biochemical oxygen demand (BODCL) determining method was studied by employing redox reaction between quinone and Baker's yeast. The measurement was carried out by utilizing luminol chemiluminescence (CL) reaction catalyzed by ferricyanide with oxidized quinone of menadione, and Saccharomyces cerevisiae using a batch-type luminometer. In this study, dimethyl sulfoxide was used as a solvent for menadione. After optimization of the measuring conditions, the CL response to hydrogen peroxide in the incubation mixture had a linear response between 0.1 and 100 μM H2O2 (r2 = 0.9999, 8 points, n = 3, average of relative standard deviation; R.S.D.av = 4.22%). Next, a practical relationship between the BODCL response and the glucose glutamic acid concentration was obtained over a range of 11-220 mg O2 L−1 (6 points, n = 3, R.S.D.av 3.71%) with a detection limit of 5.5 mg O2 L−1 when using a reaction mixture and incubating for only 5 min. Subsequently, the characterization of this method was studied. First, the BODCL responses to 16 pure organic substances were examined. Second, the influences of chloride ions, artificial seawater, and heavy metal ions on the BODCL response were investigated. Real sample measurements using river water were performed. Finally, BODCL responses were obtained for at least 8 days when the S. cerevisiae suspension was stored at 4 °C (response reduction, 69.9%; R.S.D. for 5 testing days, 18.7%). BODCL responses after 8 days and 24 days were decreased to 69.9% and 35.8%, respectively, from their original values (R.S.D. for 8 days involving 5 testing days, 18.7%). 相似文献
149.
Dr. Kazunobu Igawa Daisuke Yoshihiro Yusuke Abe Prof. Dr. Katsuhiko Tomooka 《Angewandte Chemie (International ed. in English)》2016,55(19):5814-5818
A variety of functionalized silacyclopentanes were synthesized by highly enantioselective β‐eliminations of silacyclopentene oxides followed by stereospecific transformations. The reaction mechanism of the β‐elimination was elucidated by DFT calculations. An in vitro biological assay with an oxy‐functionalized silacyclopentane showed substantial binding to a serotonin receptor protein. 相似文献
150.
Jianhuai Ye Dr. Sayaka Hatano Prof. Dr. Manabu Abe Prof. Dr. Ryohei Kishi Yusuke Murata Prof. Dr. Masayoshi Nakano Prof. Dr. Waldemar Adam 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(7):2299-2306
In the photochemical denitrogenation of 1,4‐diaryl‐2,3‐diazabicyclo[2.2.1]heptane ( AZ6 ) bearing sterically hindered substituents, a curious new absorption band at about 450 nm was observed under low‐temperature matrix conditions, together with the previously well‐characterized planar singlet diradical pl‐1 DR6 with λmax=≈580 nm. The 450 nm species was electron paramagnetic resonance (EPR)‐silent. Instead of generating the planar diradical pl‐1 DR6 and the precursor azoalkane AZ6 upon warming, the ring‐closed bicyclo[2.1.0]pentane derivative SB6 , that is, the AZ6 denitrogenation product was identified. Based on product analysis, low‐temperature spectroscopic observations, high‐level quantum‐mechanical computations, viscosity effect, and laser‐flash photolysis, the puckered singlet diradicaloid puc‐1 DR6 was assigned to the new 450 nm absorption. The latter was detected experimentally at the same time as the planar singlet diradical pl‐1 DR6 . Sterically demanding substituents as well as viscosity impediments were essential for the detection of the experimentally hitherto unknown puckered singlet cyclopentane‐1,3‐diyl diradicaloid puc‐1 DR6 , that is, the third isomer in homolysis. The present findings should stimulate future work on the mechanistically fascinating stereoselectivity documented in the formation of bicyclo[2.1.0]pentanes during the 2,3‐diazabicyclo[2.2.1]heptane denitrogenation. 相似文献