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161.
Oishi S Masuda R Evans B Ueda S Goto Y Ohno H Hirasawa A Tsujimoto G Wang Z Peiper SC Naito T Kodama E Matsuoka M Fujii N 《Chembiochem : a European journal of chemical biology》2008,9(7):1154-1158
The design, synthesis, and bioevaluation of fluorescence- and biotin-labeled CXCR4 antagonists are described. The modification of D-Lys8 at an epsilon-amino group in the peptide antagonist Ac-TZ14011 derived from polyphemusin II had no significant influence on the potent binding of the peptide to the CXCR4 receptor. The application of the labeled peptides in flow cytometry and confocal microscopy studies demonstrated the selectivity of their binding to the CXCR4 receptor, but not to CXCR7, which was recently reported to be another receptor for stromal cell-derived factor 1 (SDF-1)/CXCL12. 相似文献
162.
Silica (SiO2)‐crosslinked polystyrene (PS) particles possessing photofunctional N,N‐diethyldithiocarbamate (DC) groups on their surface were prepared by the free‐radical emulsion copolymerization of a mixture of SiO2 (diameter = 20 nm), styrene, divinyl benzene, 4‐vinylbenzyl N,N‐diethyldithiocarbamate (VBDC), and 2‐hydroxyethyl methacrylate with a radical initiator under UV irradiation. In this copolymerization, the inimer VBDC had the formation of a hyperbranched structure by a living radical mechanism. The particle sizes of such core–shell structures [number‐average particle diameter (Dn) = 35–40 nm] were controlled by the variation of the feed amounts of the monomers and surfactant, or emulsion system. The size distributions were relatively narrow (weight‐average particle diameter/Dn ≈ 1.05). These particles had DC groups on their surface. Subsequently, poly(methyl methacrylate) brush encapsulated SiO2 particles were synthesized by the grafting from a photoinduced atom transfer radical polymerization approach of methyl methacrylate initiated by SiO2‐crosslinked PS particles as a macroinitiator. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
163.
The adsorption of metal ions (Mo6+, Cu2+, Fe2+, and Fe3+) was examined on chemically modified chitosans with a higher fatty acid glycidyl (CGCs), and the adsorption of Cu2+ was examined on ethylenediamine tetraacetic acid dianhydride modified CGCs (EDTA‐CGCs) synthesized by the reaction of the CGCs with ethylenediamine tetraacetic acid dianhydride. The adsorption of phosphate ions onto the resulting substrate/metal‐ion complex was measured. Mo6+ depicted remarkable adsorption toward the CGCs, although all the Mo6+ was desorbed under the adsorption conditions of the phosphate ions. The other metal ions were adsorbed to some extent on CGCs by chelating to the amino group in the substrate, except for CGC‐1, which had the highest degree of substitution (83.9%). Considerable amounts of Fe2+ were adsorbed onto CGCs; however, only a limited number of phosphate ions was adsorbed onto the substrate/metal‐ion complex. As a result, the following adsorbent/metal‐ion complexes gave higher adsorption ability toward phosphate ions: CGC‐4/Cu2+, CGC‐4/Fe3+, and EDTA‐CGC‐3/Fe3+. Where, CGC‐3 is a chemically modified chitosan with the degree of substitution of 26.5 percentage, and CGC‐4 is one with the degree of substitution of 16.0 percentage. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
164.
Methanol decomposition to synthesis gas over supported Pd catalysts prepared from synthetic anionic clays 总被引:2,自引:0,他引:2
Ryuji Shiozaki Takashi Hayakawa Yan-yong Liu Tomoko Ishii Mikio Kumagai Satoshi Hamakawa Kunio Suzuki Tatehiko Itoh Tetsuya Shishido Katsuomi Takehira 《Catalysis Letters》1999,58(2-3):131-140
Supported Pd or Rh catalysts were prepared by the solid-phase crystallization method starting from hydrotalcite anionic clay minerals based on [Mg6Al2(OH)16CO 2 2− ]·4H2O as the precursors. The precursors were prepared by a coprecipitation method from the raw materials containing Pd2+ and various trivalent metal ions which can replace each site of Mg2+ and Al3+ in the hydrotalcite. Rh3+ was also used for preparing the catalyst as comparison. The precursors were then thermally decomposed and reduced to form supported Pd or Rh catalysts and used for the methanol decomposition to synthesis gas. Among the precursors tested, use of Mg–Cr hydrotalcite containing Pd2+ resulted in the formation of efficient Pd supported catalysts for the production of synthesis gas by selective decomposition of methanol at low temperature. Although Pd2+ cannot well replace the Mg2+ site in the hydrotalcite, the Pd supported catalyst (Pd/Mg–Cr) prepared by the solid-phase crystallization method formed highly dispersed Pd metal particles and showed much higher activity than that prepared by the conventional impregnation method. When the precursor was prepared under mild conditions, more fine particles of Pd metal were formed over the catalyst, resulting in high activity. It is likely that the high activity may be due to the highly dispersed and stable Pd metal particles assisted by the role of Cr as the co-catalyst. This revised version was published online in November 2006 with corrections to the Cover Date. 相似文献
165.
Satoshi Yoshida Jun Matsuoka Naohiro Soga 《Journal of the American Ceramic Society》1999,82(6):1621-1623
Subcritical crack growth in glass shows three characteristic regions, depending on crack velocity. Among three regions, in region III, where water does not affect crack-growth behavior, the slope of the crack-growth curve can be correlated with the intrinsic nature of glass fracture. In this study, to measure the crack velocity in region III, a periodic stress wave was applied to produce fracture-surface markings in the double-cleavage-drilled compression specimen. The crack-growth data obtained were compared with results obtained via direct observation of the crack front. As a result, this method, by using stress-wave fractography, was found to be effective to obtain the crack-growth curve in region III. 相似文献
166.
Satoshi Kaneco Kenji Iiba Nobu-hide Hiei Kiyohisa Ohta Takayuki Mizuno Tohru Suzuki 《Electrochimica acta》1999,44(26):4701
The electrochemical reduction of CO2 with a Cu electrode in CsOH/methanol-based electrolyte was investigated. The main products from CO2 were methane, ethylene, ethane, carbon monoxide and formic acid. A maximum Faradaic efficiency of ethylene was 32.3% at −3.5 V vs. Ag/AgCl saturated KCl. The best methane formation efficiency was 8.3% at −4.0 V. The ethylene/methane current efficiency ratio was in the range 2.9–7.9. In the CsOH/methanol, the efficiency of hydrogen formation, being a competitive reaction against CO2 reduction, was depressed to below 23%. 相似文献
167.
Yuzo Nishida Satoshi Nishino Li Li Guo Mami Kunita Hideaki Matsushima Tadashi Tokii 《Inorganic chemistry communications》1999,2(12):160
We have observed that binuclear cobalt(II) compounds with H(HPTP), Co2(HPTP)(CH3COO)(ClO4)2 and Co2(HPTP)Cl(ClO4)2, react with oxygen molecules when DNA is present in the solution, cleaving the DNA (H(HPTP) denotes N,N,N′,N′-tetrakis(2-pyridylmethyl)-1,3-diaminopropane-2- ol). 相似文献
168.
Melt pool behaviour and the characteristics of the surrounding metal powder during selective laser melting (SLM) are captured using high-speed imaging, and the influence of the substrate temperature and the line building sequence on the formation of the built structure and the generation of spatter particles is experimentally investigated. The results indicate that the substrate temperature has a measurable effect on the formation of droplets and the generation of spatter particles, while the volume specific energy density of the process was the principal factor affecting the built structure. 相似文献
169.
Eisuke Watanabe Junko Fujii Kaori Kojima Satoshi Iwatsuki Masahiko Inamo Hideo D. Takagi Koji Ishihara 《Inorganic chemistry communications》2010,13(12):1406-1409
Kinetic studies were performed on the reactions of phenylboronic acid with L-lactic acid and mandelic acid in acidic aqueous and alkaline solutions in order to specify reactive species in these reactions. It was confirmed that the diprotonated ligand (H2L: L-lactic acid or mandelic acid) is less reactive than the monoprotonated ligand (HL?: L-lactate ion or mandelate ion), which made possible direct determination of the rate constants of phenylboronic acid (PhB(OH)2) and its conjugate base, phenylboronate ion (PhB(OH)3?). It was found that PhB(OH)2 is more reactive than PhB(OH)3?. On the basis of kinetic results, it was concluded that the most reactive species are PhB(OH)2 and HL? at physiological pH 7.4, so the reaction in the boronic acid-based sensor for L-lactate mainly would occur between these species. 相似文献
170.
Tsunehisa Handa Satoshi Igi Kenji Oi Kimihiro Nishimura Hisakazu Tajika Tetsuya Tagawa 《Welding International》2013,27(7):460-468
ABSTRACTBrittle crack arrestability of the heavy gauge steel plates for shipbuilding is now an important issue for the recent mega container ships. In the present work, the brittle crack arrestability of the steel plate with different toughness distributions in thickness is examined in ultra-wide duplex ESSO tests. It is examined whether a running long brittle crack arrests or not in flat temperature condition in ultra-wide duplex ESSO test that are harder mechanical conditions similar to an actual ship hull condition. Test temperatures are selected at which arrest toughness, Kca, evaluated by temperature gradient type standard ESSO test is the same for two test plates. The steel plate with higher toughness in mid-thickness (t/2) than that in quarter thickness (t/4) could arrest a running long brittle crack although the plate with lower toughness in mid-thickness than that in quarter thickness could not arrest it. The typical split-nail shape appeared at the arrested crack front in the plate with higher toughness in mid-thickness than that in quarter thickness. The numerical analyses also demonstrate that the local stress intensity factor at the arrested crack tip is changing sensitively to the crack front shape. It suggests that the higher brittle crack arrestability appears due to the split-nail shape of the arrested crack front enhanced by the inhomogeneous toughness in thickness. 相似文献