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111.
112.
Shinshi M Sugihara T Osakai T Goto M 《Langmuir : the ACS journal of surfaces and colloids》2006,22(13):5937-5944
The transfer of proteins by the anionic surfactant bis(2-ethylhexyl) sulfosuccinate (AOT) at a polarized 1,2-dichloroethane/water (DCE/W) interface was investigated by means of ion-transfer voltammetry. When the tetrapentylammonium salt of AOT was added to the DCE phase, the facilitated transfer of certain proteins, including cytochrome c (Cyt c), ribonuclease A, and protamine, could be controlled electrochemically, and a well-defined anodic wave for the transfer was obtained. At low pH values (e.g., pH 3.4), the anodic wave was usually well-separated from the wave for the formation of protein-free (i.e., unfilled) reverse micelles. The anodic wave for the protein transfer was analyzed by applying the theory for facilitated transfer of ions by charged ligands and then supplying information regarding the number of AOT anions reacting with one protein molecule and the total charge carried by the protein transfer. However, controlled-potential electrolyses performed for the transfer of Cyt c, which is red, revealed that the protein-AOT complexes were unstable in DCE and liable to aggregate at the interface when the pH of the W phase was 3.4. At pH 7.0, when formation of unfilled reverse micelles occurred simultaneously, the protein-AOT complexes appeared to be stabilized, probably via fusion with unfilled reverse micelles. 相似文献
113.
A concise total synthesis of xestodecalactone A, utilizing a Diels-Alder strategy is described. The focal Diels-Alder reaction relied on an "ynoate" dienophile to rapidly assemble the required resorcylinic acid scaffold. During this study, Diels-Alder cycloaddition reactions involving 1,3-disubstituted nonequivalent allene dienophiles were studied, and some surprising results were encountered. 相似文献
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[reaction: see text] Efficient arylyne cyclization catalyzed by the Hg(OTf)(2)-(TMU)(3) complex has been developed. The reaction was carried out at ambient temperature in acetonitrile, and the catalytic cycle reaches up to 1000 turnovers. 相似文献
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118.
Treatment of radioactive waste phenol with Fenton's oxidation 总被引:1,自引:0,他引:1
A new procedure was developed for the waste treatment of radioactive phenol on a laboratory scale. Waste phenol was dissolved in water (2% as phenol), and ferrous ion (10 mg/l as Fe2+) was added. Hydrogen peroxide (6% as H2O2) was added separately in three steps, 20, 30, and 50% of the volume, in order to avoid rapid reaction. The solution was heated at 80-90 degrees C for several hours in a beaker covered with a watch glass till the color of the solution changes from red purple to pale yellow. Then, the solution was neutralized with sodium hydroxide and heated for 1 h to decompose excess hydrogen peroxide. When the procedure is carried out with four 2 l beakers on a hot plate, 100 ml of phenol (1,200 ml of the aqueous solution saturated with phenol) can be oxidized simultaneously. 相似文献
119.
Juzo Nakayama Ayako Tai Sachiko Iwasa Tomohiro Furuya Yoshiaki Sugihara 《Tetrahedron letters》2005,46(9):1395-1397
It was found that tetracyanoethylene oxide not only oxidizes sulfides to sulfoxides but also reduces sulfoxides to sulfides with generation of two molecules of carbonyl cyanide. The reaction thus also functions as a new method for generation of carbonyl cyanide. 相似文献
120.
A new type of photocatalytic reaction that splits water into H2 and O2 was designed using a two-step photoexcitation system composed of an iodate/iodide (IO3-/I-) shuttle redox mediator and two different photocatalysts, one for H2 evolution and the other for O2 evolution. Photocatalytic oxidation of water to O2 and reduction of IO3- to I- selectively proceeded with good efficiencies over TiO2-rutile and Pt-WO3 photocatalysts under UV and visible light irradiations, respectively. The O2 evolution selectively proceeded even in the presence of a considerable amount of I- in the solutions, although the oxidation of water is thermodynamically less favorable than oxidation of I-. Both the adsorption property of IO3- anions and the oxidation property of the photocatalysts are doubtless responsible for the selective oxidation of water. On the other hand, photocatalytic reduction of water to H2 and oxidation of I- to IO3- proceeded over Pt-TiO2-anatase and Pt-SrTiO3:Cr/Ta (codoped with Cr and Ta) photocatalysts under UV and visible light, respectively. The combination of two different photocatalysts results in a stoichiometric evolution of H2 and O2 via the redox cycle of IO3- and I-. The photocatalytic water splitting under visible light irradiation (lambda > 420 nm) was demonstrated by using the Pt-SrTiO3:Cr/Ta, Pt-WO3, and IO3-/I- shuttle redox mediator. 相似文献