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Molecular oxygen, oxidation organometallic compound

By coincidence, the oxygen problem is related to our present question. In the late 18th century, molecular oxygen (02) was a revolutionary discovery for chemists because of its involvement in oxidation, and because of the demonstration that a gas reacts chemically with liquids and solids. On the other hand, nitrogen gas (N2) is, as was already known at that time, inert towards most other chemicals, in particular towards all purely organic compounds (i. e., not organometallic compounds). [Pg.216]

Organometallic compounds asymmetric catalysis, 11, 255 chiral auxiliaries, 266 enantioselectivity, 255 see also specific compounds Organozinc chemistry, 260 amino alcohols, 261, 355 chirality amplification, 273 efficiency origins, 273 ligand acceleration, 260 molecular structures, 276 reaction mechanism, 269 transition state models, 264 turnover-limiting step, 271 Orthohydroxylation, naphthol, 230 Osmium, olefin dihydroxylation, 150 Oxametallacycle intermediates, 150, 152 Oxazaborolidines, 134 Oxazoline, 356 Oxidation amines, 155 olefins, 137, 150 reduction, 5 sulfides, 155 Oxidative addition, 5 amine isomerization, 111 hydrogen molecule, 16 Oxidative dimerization, chiral phenols, 287 Oximes, borane reduction, 135 Oxindole alkylation, 338 Oxiranes, enantioselective synthesis, 137, 289, 326, 333, 349, 361 Oxonium polymerization, 332 Oxo process, 162 Oxovanadium complexes, 220 Oxygenation, C—H bonds, 149... [Pg.196]

With regard to the susceptibility of many organometallics to aerial oxidation, it must be remembered that most compounds containing C-H bonds are thermodynamically unstable with respect to oxidation by molecular oxygen to produce water and carbon dioxide. The mechanisms whereby (for example) many alkyls are spontaneously flammable in air are necessarily difficult to determine the mechanisms involved in the combustion of hydrocarbons are still incompletely understood. Suffice it to say that the kinetic stability of ER to air seems to be low where E is of low electronegativity. [Pg.380]

Oxovanadium(V) compounds are potential Lewis acids with oxidation ability to induce one-electron oxidation reactions based on their characteristics. Oxidation capability and redox potential are effectively controlled by the substituent of oxovanadium(V) compounds. A catalytic system is allowed to be realized by the redox interaction with molecular oxygen. The oxidative ligand coupling proceeds via the intermetallic interaction between vanadium species and main-group organometallics. [Pg.152]


See other pages where Molecular oxygen, oxidation organometallic compound is mentioned: [Pg.263]    [Pg.27]    [Pg.717]    [Pg.64]    [Pg.4]    [Pg.5590]    [Pg.565]    [Pg.366]    [Pg.1723]    [Pg.169]    [Pg.2]    [Pg.316]    [Pg.438]    [Pg.264]    [Pg.5]    [Pg.2]    [Pg.7]    [Pg.302]    [Pg.1303]    [Pg.295]    [Pg.580]    [Pg.157]    [Pg.274]   


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Compounds oxygenated

Molecular compounds

Molecular organometallics

ORGANOMETALLIC COMPOUNDS oxide

Organometallic compounds, molecular

Organometallic oxidant

Oxidation molecular oxygen

Oxygen compounds

Oxygen, molecular, oxidant

Oxygenate compounds

Oxygenous compound

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