Search results for "Oxidizing agent"
showing 10 items of 71 documents
Synthesis and Comparative Catalytic Study of Zirconia-MnCO3or -Mn2O3for the Oxidation of Benzylic Alcohols
2016
Abstract We report on the synthesis of the zirconia–manganese carbonate ZrO x (x %)–MnCO3 catalyst (where x=1–7) that, upon calcination at 500 °C, is converted to zirconia–manganese oxide ZrO x (x %)–Mn2O3. We also present a comparative study of the catalytic performance of the both catalysts for the oxidation of benzylic alcohol to corresponding aldehydes by using molecular oxygen as the oxidizing agent. ZrO x (x %)–MnCO3 was prepared through co‐precipitation by varying the amounts of Zr(NO3)4 (w/w %) in Mn(NO3)2. The morphology, composition, and crystallinity of the as‐synthesized product and the catalysts prepared upon calcination were studied by using scanning electron microscopy, tr…
Modeling hexanal production in oxido-reducing conditions by the yeast Yarrowia lipolytica
2009
International audience; Hexanal produced by cells of a recombinant Yarrowia lipolytica yeast expressing the hydroperoxide lyase (HPL) from green bell pepper fruit was studied under oxido-reducing conditions using the reducing dithiotreitol and oxidizing potassium ferricyanide compounds. The combined effect of pH, linoleic acid 13-hydroperoxides concentration, temperature and oxido-reducing molecules on the hexanal production was studied. Significant positive effects for the hexanal production were found using high concentrations of hydroperoxides (100 mM, 30 g/L). Adding reducing molecules enhanced significantly hexanal production while the oxidizing molecules had an inhibitory effect. Comb…
Carboranylphosphinic Acids: A New Class of Purely Inorganic Ligands
2015
Purely inorganic carboranyl phosphinates were prepared, and the influence of the cluster on the reactivity of the phosphinate group was studied. Electron-withdrawal by the carboranyl carbon atoms, combined with space-filling efficiency and enhanced aromaticity of the cluster cage, renders the phosphorus more difficult to oxidize. This enables carboranyl phosphinates to survive harsh oxidizing conditions, a property which is uncommon in organic phosphinates.
Oxygen Availability, Energy Metabolism, and Metabolic Rate in Invertebrates and Vertebrates
1988
It has often been emphasized that primitive life originated in an environment devoid of oxygen. The first eukaryotic cells, however, appeared some 1.4 billion years ago when the earth’s atmosphere had already turned from a mildly reducing to an oxidizing one by the photosynthetic action of prokaryotes that used H20 as reducing agent (see Harold 1986, for review). The presence of free oxygen obviously was a major force shaping the evolution of eukaryotic cells. As a consequence all animals are primarily aerobes, using respiratory chains with oxygen as electron acceptor (oxidant) and membrane-bound ATP synthases for the production of ATP.
Modular Access to 9,9-Spirobifluorenes by Oxidative Coupling Using Molybdenum Pentachloride
2013
The strong oxidizing agent molybdenum pentachloride was used for an efficient direct C–C bond formation of 9,9-diarylfluorenes to the corresponding 9,9-spirobifluorenes. Thus, a versatile method that is compatible with labile groups, such as iodo moieties, was established. By this approach important building blocks for light emitting polymers were synthesized in high yields.
The abundance of Au, Pt, Pd, and the mode of heavy metal fixation in highly polluted sediments from the Rhine River near Mainz, West Germany
1984
The Au, Pt and Pd contents of the sediments of Ginsheimer‐Altrhine River, a channel of the Rhine river which drains one of the most industrialized regions of western Europe, have been determined by flameless atomic absorption spectrophotometry. The abundances of these noble metals range from 96–460 ppb Au; 734 ppb‐31 ppm Pt and 32 ppb‐4 ppm Pd. The extremely high concentrations, particulary those of Pt and Pd, are attributed to their use in industry and are due to the formation and concentration of metal‐organic complexes, mainly at the interface between an extremely reducing and an oxidizing aquatic environment. Differential thermal analyses of the polluted sediments in comparison to the p…
Oxidative cyclization of some aldehyde semicarbazones induced by metallic salts
1993
The oxidative cyclization of some aldehyde semicarbazones 10 with four different oxidizing agents has been effected. The structure of the semicarbazones and the nature of cyclizing agent affected the rate and yield of cyclization but they did not show any influence on the regiochemistry of reaction. In fact, 1,2,4-triazoline 20 was the only heterocyclic ring obtained by the cyclization reaction.
ChemInform Abstract: Oxidative Cyclization of Some Aldehyde Semicarbazones Induced by Metallic Salts.
2010
The oxidative cyclization of some aldehyde semicarbazones 10 with four different oxidizing agents has been effected. The structure of the semicarbazones and the nature of cyclizing agent affected the rate and yield of cyclization but they did not show any influence on the regiochemistry of reaction. In fact, 1,2,4-triazoline 20 was the only heterocyclic ring obtained by the cyclization reaction.
Chemoenzymatic synthesis of a poly(hydroquinone)
1999
Chemoenzymatic synthesis of a poly(hydroquinone) was achieved by enzymatic oxidative polymerization of 4-hydroxyphenyl benzoate, followed by alkaline hydrolysis of the resulting polymer. The polymerization of 4-hydroxyphenyl benzoate was performed using a peroxidase and hydrogen peroxide as catalyst and oxidizing agent, respectively, in an aqueous organic solvent. Soybean peroxidase afforded the polymer in good yields. IR analysis of the polymer showed the formation of the polymer consisting of a mixture of phenylene and oxyphenylene units. By alkaline hydrolysis of the resulting polymer, benzoate moiety was completely removed to give poly(hydroquinone).
Studies on the UV-photolytic decomposition of some tensides and complexones inhibiting the inverse-voltammetric determination of metal ions
1993
The UV-photolytic decomposition of some tensides and complexones has been investigated using the DPASV peak of indium as an indicator. The results show that UV-irradiation alone can completely decompose these compounds at lower concentrations within a short time. Higher concentrations need an additional oxidising agent.