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502 oxidation applicability proof

The discussion of the structure of the nitrones and the hydrazones received less attention. With the increased application of physical methods to structural problems, the three-membered ring structures for these compounds lost much of their attraction. The problem of the structure of the nitrones was satisfactorily solved with the open-chain A -oxide formulation. The compounds originally designated as diaziridines (2) were partly reformulated with the open-chain hydra-zone structures and partly were left without a. satisfactory proof of structure. [Pg.84]

Application of new types of graphite, found to be more oxidation-proof (in particular, TEG and TEG modified by boron), can largely increase the electrochemical stability of materials used in aqueous electrolyte media. Their high resistance to oxidation and enhanced long-term cycling stability create realistic prerequisites for wide range of applications for such graphite... [Pg.407]

Most applications of this compound are similar to those of the hydrochloride. It is primarily used as a reducing agent for organic synthesis and chemical analysis. Other uses are to purify aldehydes and ketones to inhibit oxidation of fatty acids in dehairing hides in synthesis of oximes for paints and varnishes in photographic developer solutions in rust proofing and as a catalyst. [Pg.386]

Added in proof. Recently the analysis of 13C-nmr spectra of polypropylene oxide provided a new information about the triad of methine carbon atom and dyad of methylene carbon in the main chain (9/). Applications of this analysis should give a valuable contribution to the more detailed understanding of the polymerization reaction of propylene oxide by organometallic catalysts. [Pg.104]

The most frequently reported oxidation reaction of isatins is the oxidation with alkaline hydrogen peroxide to give anthranilic acids. This procedure has been both as a proof of structure of isatins and as a method of synthesis of anthranilic acids. The oxidation has been applied to alkyl 8"10 11 23 33>38-40>46 49>50>118halo n.18.35.36-38-40.47.10 .11 . 119,136,240 alkoxy,26,a8 39,47,75.io7,ii8,i36 trifluoromethyl,33,38,137 and nitro8,120,217 isatins. Use of N-substituted isatins led to N-substituted anthranilic acids.66,71,125,158,169,243 In the oxidation of 5-bromo-l-(y-carbethoxypropyl)-7-ethylisatin, 60 was isolated after treatment with ethanol and acid.11 Oxidation of isatin derivatives 61 led, after treatment with diazomethane, to the acridine derivatives 62.67 Application of this oxidation method to 7-hydroxyisatins gave rise to benzoxazo-lones (63).2,41... [Pg.20]

Until recently the lactol ring structure of 2-desoxy-D-ribose in nucleic acid had been proved conclusively only for the thymidine nucleoside component and in this case it was furanose in form.26 Subsequently Brown and Lythgoe,27 by application of the periodate oxidation procedure to the 2 -desoxy ribosides of guanine, hypoxanthine, cytosine and thymine, afforded proof of the presence of a furanose sugar in each compound. [Pg.51]

Before the development and widespread application of spectroscopic methods for the elucidation of structure, confirmation of the class type of an unknown organic compound was completed by the preparation of two or more crystalline functional derivatives. If the compounds had been previously reported in the literature, agreement between the published physical constants of the derivatives with those prepared by the worker was accepted as proof of identity. In many cases, and particularly in natural product chemistry, functional group recognition led to oxidative, reductive, or hydrolytic breakdown into smaller carbon-containing fragments. These were, if necessary, separated, characterised and identified by derivative preparation. The reassembly of the jig-saw of fragments inferred by the identity of the fission products, then led to postulated structures. [Pg.1234]

These equilibrated silicone oils have valuable properties they are very stable to heat and oxidation, they have good electrical properties, and are water-repellent. They find application as vacuum oils and greases, water-proofing agents, and paint media. [Pg.802]

Proof of the location of the methoxyl group at C3 was established by application of periodate oxidation to methyl 2-acetamido-2-deoxy-3-0-methyl-a-D-glucopyranoside and to 2-amino-2-deoxy-3-0-methyl-D-gluconic acid. The first compound was resistant to oxidation, whereas the second consumed two equivalents of periodate per mole and released one mole of formaldehyde and one mole of formic acid per mole, but afforded no ammonia. ... [Pg.192]

OTHER COMMENTS Platinum metal is used in the manufacture of apparatus used in laboratories and industries, including thermocouples, acid-proof containers, chemical reaction vessels, platinum resistance thermometers, electrodes, etc. has found applications in dentistry, electroplating industry, and in the jewelry industry soluble platinum salts have been used as catalysts in the production of high octane gasoline, vinylesters, petrochemicals, and pharmaceuticals platinum metals, as well as soluble platinum salts, have been employed as oxidation catalysts in the manufacture of sulfuric acid, nitric acid from ammonia, and acetic acid soluble platinum salts have been used and reused in the reclamation of platinum ore. [Pg.855]

In summary, the goal of this combinatorial approach - the discovery of catalysts for the asymmetric epoxidation of olefins using dihydrogen peroxide as the terminal oxidant - was met The Fe-complexes of the ligands 12a-14f, 12a-14g, and 13c-14b indeed afforded up to 20% ee, at epoxide yields of up to 78 %. In this study proof-of-principle was clearly achieved. For practical applications in asymmetric synthesis, further improvement of the catalyst enantioselectivity appears desirable and represents the next challenge to be met. [Pg.10]

To summarize, Zachariasen s model has dominated glass science for several decades and is still extremely useful. However, diffraction methods do not actually provide definite proof for such a model they can only confirm that the results do not contradict this hypothesis. Remember also that the model was developed specifically for oxide glasses and is not necessarily applicable to other types of glasses. [Pg.117]


See other pages where 502 oxidation applicability proof is mentioned: [Pg.257]    [Pg.113]    [Pg.564]    [Pg.185]    [Pg.287]    [Pg.71]    [Pg.208]    [Pg.1021]    [Pg.95]    [Pg.268]    [Pg.281]    [Pg.723]    [Pg.875]    [Pg.937]    [Pg.1105]    [Pg.9]    [Pg.122]    [Pg.172]    [Pg.3]    [Pg.225]    [Pg.237]    [Pg.36]    [Pg.49]    [Pg.296]    [Pg.389]    [Pg.191]    [Pg.1116]    [Pg.5]    [Pg.655]    [Pg.44]    [Pg.364]    [Pg.264]    [Pg.100]    [Pg.358]   
See also in sourсe #XX -- [ Pg.178 ]




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