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排序方式: 共有258条查询结果,搜索用时 15 毫秒
1.
Gui Hong YAN Da XING* Shi Ci TAN Institute of Laser Life Science South China Normal University Guangzhou 《中国化学快报》2004,15(1):101-104
Electrochemiluminescence (ECL), like other chemiluminescence technique, offers high signal-to-noise ratio. Furthermore, it has the advantage over other chemiluminescence techniques of being initiated by a voltage potential. Thus, it provides a better-controlled luminescence. This technique has been used in measuring many kinds of organic and inorganic matters, and analyzing many kinds of antigen, antibody and hapten, such as carcinoembryonic antigen and alpha-fetoprotein, etc1-6. The ele… 相似文献
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Hogsett D. A. Ahn H. -J. Bernardez T. D. South R. Lynd L. R. 《Applied biochemistry and biotechnology》1992,34(1):527-541
Applied Biochemistry and Biotechnology - Process development is reviewed for ethanol production from cellulosic biomass via direct microbial conversion (DMC). Experimental data addressing cellulase... 相似文献
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The electro-oxidation of CO on model platinum-tin alloy catalysts has been studied by ex-situ electrochemical measurements following the preparation of the Pt(111)/Sn(2x2) and Pt(111)/Sn(radical3 x radical3)R30 degrees surfaces. A surface redox couple, which is associated with the adsorption/desorption of hydroxide on the Sn sites, is observed at 0.28 V(RHE)/0.15 V(RHE) in H(2)SO(4) electrolyte on both surfaces. Evidence that it is associated with the adsorption of OH comes from ex-situ photoemission measurements, which indicate that the Sn atoms are in a metallic state at potentials below 0.15 V(RHE) and an oxidized state at potentials above 0.28 V(RHE). Specific adsorption of sulfate anions is not associated with the surface process since there is no evidence from photoemission of sulfate adsorption, and the same surface couple is observed in the HClO(4) electrolyte. CO is adsorbed from solution at 300 K, with saturation coverages of 0.37 +/- 0.05 and 0.2 +/- 0.05 ML, respectively. The adsorbed CO is oxidatively stripped at the potential coincident with the adsorption of hydroxide on the tin sites, viz., 0.28 V(RHE). This strong promotional effect is unambiguously associated with the bifunctional mechanism. The Sn-induced activation of water, and promotion of CO electro-oxidation, is sustained as long as the alloy structure remains intact, in the potential range below 0.5 V(RHE). The results are discussed in the light of the requirements for CO-tolerant platinum-based electrodes in hydrogen fuel cell anode catalysts and catalysts for direct methanol electro-oxidation. 相似文献
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Michael S. South 《Journal of heterocyclic chemistry》1991,28(4):1003-1011
A synthesis of 2-chloro-4-(trifluoromethyl)-5-isocyanatothiazole and 2,5-dichloro-5-isocyanatothiazole is described via the “Curtius Rearrangement” performed under anhydrous conditions. The synthetic procedure described allows for the isolation, storage, and manipulation of these highly reactive isocyanates. A number of derivatives of the above isocyanates were prepared. These include: carbamates, thiocarbamates, ureas, amines, amidines, and amides. 相似文献
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South MS Case BL Dice TA Franklin GW Hayes MJ Jones DE Lindmark RJ Zeng Q Parlow JJ 《Combinatorial chemistry & high throughput screening》2000,3(2):139-151
A parallel solution-phase library synthesis of functionalized diaminobenzamides is described. The four-step library synthesis is accomplished using polymer-assisted solution-phase (PASP) synthesis techniques. This high-yielding, multi-step sequence utilizes sequestering resins for the removal of reactants, reactant by-products, and employs a resin capture/release strategy as a key library synthesis step. Step one of the sequence relies on the displacement of an activated fluoro-group from the aromatic ring of 1a, b with a variety of primary amines to introduce the first diversity position. Step two is hydrolysis of the benzoate ester to a benzoic acid which is subsequently captured on a polyamine resin, washed, and released to give 4a, b in pure form. Step three utilizes PASP resins to mediate the amide coupling of a benzoic acid with a variety of primary amines to give the aminonitrobenzamides 5a, b and introduces the second diversity position. Step four is the parallel reduction of the aminonitrobenzamides 5a, b to the functionalized diaminobenzamides 6a, b. This library synthesis proceeds with high overall purities which average 80 % over the 4-step sequence. 相似文献
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HongBingJI DuGuiHE JunSONG YuQIAN 《中国化学快报》2004,15(10):1241-1244
Clean liquid oxidation of aldehydes can be accomplished using solid catalyst in the presence of molecular oxygen at room temperature, which is a valuable alternative to traditional counterparts. 相似文献
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