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Oxygen in hydroxylations

Nitroso-5//-dibenz[/j,/ azepine (see Section 3.2.1.5.4.1.) in methanolic hydrochloric acid undergoes rearrangement and ring contraction to a mixture of acridine (59%), acridine-9-carbaldehyde (trace), and 2-nitro-5//-dibenz[/ ,/ azepine (3% mp 176-178 C).184 However, in acetone and hydrochloric acid, the aldehyde (57 %) becomes the major product. On thermolysis, (or photolysis in the presence of oxygen), in hydroxylic solvents, the nitroso compound yields mainly acridine (36-76%) together with minor amounts of either 2-nitrodibenzazepine (4-6% by thermolysis) or acridine-9-carbaldehyde (18% by photolysis). However, in non-hydroxylic solvents, e.g. cumene, acridine-9-carbaldehyde (64%) is the major product. [Pg.286]

Protic solvent (Section 8 12) A solvent that has easily ex changeable protons especially protons bonded to oxygen as in hydroxyl groups... [Pg.1292]

The primary side reaction at the anode is the oxidation of hydroxyl ion to oxygen. In an undivided ceU, a side reaction takes place also at the cathode, ie, the unwanted reduction of MnO and MnO to lower valent manganese species. [Pg.520]

The surface of activated alumina is a complex mixture of aluminum, oxygen, and hydroxyl ions which combine in specific ways to produce both acid and base sites. These sites are the cause of surface activity and so are important in adsorption, chromatographic, and catalytic appHcations. Models have been developed to help explain the evolution of these sites on activation (19). Other ions present on the surface can alter the surface chemistry and this approach is commonly used to manipulate properties for various appHcations. [Pg.155]

Conversely, in hydroxyl-free vitreous siUca, the oxidation is much slower and is controlled by the diffusion of oxygen through the soHd according to the following reaction ... [Pg.503]

Generation of radicals by redox reactions has also been applied for synthesizing block copolymers. As was mentioned in Section II. D. (see Scheme 23), Ce(IV) is able to form radical sites in hydroxyl-terminated compounds. Thus, Erim et al. [116] produced a hydroxyl-terminated poly(acrylamid) by thermal polymerization using 4,4-azobis(4-cyano pentanol). The polymer formed was in a second step treated with ceric (IV) ammonium nitrate, hence generating oxygen centered radicals capable of starting a second free radical polymeriza-... [Pg.751]

In wet corrosion ionisation of oxygen to hydroxyl must involve the hydronium ion or water. [Pg.18]

The explicit aims of boiler and feed-water treatment are to minimise corrosion, deposit formation, and carryover of boiler water solutes in steam. Corrosion control is sought primarily by adjustment of the pH and dissolved oxygen concentrations. Thus, the cathodic half-cell reactions of the two common corrosion processes are hindered. The pH is brought to a compromise value, usually just above 9 (at 25°C), so that the tendency for metal dissolution is at a practical minimum for both steel and copper alloys. Similarly, by the removal of dissolved oxygen, by a combination of mechanical and chemical means, the scope for the reduction of oxygen to hydroxyl is severely constrained. [Pg.832]

The oxidation of carotenes results in the formation of a diverse array of xanthophylls (Fig. 13.7). Zeaxanthin is synthesised from P-carotene by the hydroxylation of C-3 and C-3 of the P-rings via the mono-hydroxylated intermediate P-cryptoxanthin, a process requiring molecular oxygen in a mixed-function oxidase reaction. The gene encoding P-carotene hydroxylase (crtZ) has been cloned from a number of non-photosynthetic prokaryotes (reviewed by Armstrong, 1994) and from Arabidopsis (Sun et al, 1996). Zeaxanthin is converted to violaxanthin by zeaxanthin epoxidase which epoxidises both P-rings of zeaxanthin at the 5,6 positions (Fig. 13.7). The... [Pg.263]

In figure 3 and show that the relative thermal motion of the surface atoms is significantly greater than in the bulk metal over the range from 100 - 800 K, This result is expected considering the partial coordination, hence lack of constraint of the surface atoms. A similar result has been found from LEED measurements on a Pt surface. ( ) Significantly, the surface atom disorder when extrapolated to 0 K remains sizable. This static disorder or strain appears to be a result of the interaction of the Ft atoms with the support, a kind of epitaxy to the oxygen (or hydroxyl) surface of the support. [Pg.285]

The degradation of nicotine has been examined extensively in Arthrobacternicotinovorans (oxydans). In strain P34, the first metabolite was 6-hydroxynicotine, and experiments with 62 and H2 0 showed that the oxygen in the hydroxyl group was derived from H2O (Hochstein and Dalton 1965). [Pg.279]

The degradation of nicotine has been examined extensively in Arthrobacter nicotinovorans (oxydans) in which it is mediated by a plasmid (Brandsch et al. 1982 Schenk et al. 1998). In strain P34, the hrst metabolite was 6-hydroxynicotine, and experiments with 02 and H2 0 showed that the oxygen in the hydroxyl group was derived from H2O (Hochstein and Dalton 1965). Nicotine dehydrogenase has a molecular mass of 120,000 and contains FAD, Mo, Fe, and acid-labile sulfur (Freudenberg et al. 1988). Degradation involves a series of reactions ... [Pg.532]


See other pages where Oxygen in hydroxylations is mentioned: [Pg.280]    [Pg.426]    [Pg.134]    [Pg.72]    [Pg.684]    [Pg.137]    [Pg.280]    [Pg.187]    [Pg.473]    [Pg.280]    [Pg.426]    [Pg.134]    [Pg.72]    [Pg.684]    [Pg.137]    [Pg.280]    [Pg.187]    [Pg.473]    [Pg.1026]    [Pg.444]    [Pg.456]    [Pg.502]    [Pg.219]    [Pg.96]    [Pg.529]    [Pg.218]    [Pg.2391]    [Pg.79]    [Pg.565]    [Pg.240]    [Pg.240]    [Pg.1059]    [Pg.169]    [Pg.654]    [Pg.330]    [Pg.531]    [Pg.91]    [Pg.675]    [Pg.63]    [Pg.196]    [Pg.59]    [Pg.116]    [Pg.120]    [Pg.172]    [Pg.114]    [Pg.536]    [Pg.537]   
See also in sourсe #XX -- [ Pg.699 ]

See also in sourсe #XX -- [ Pg.59 , Pg.187 ]




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In hydroxylation

Oxygen hydroxyl

Oxygenation/hydroxylation

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