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Metal hydroxides/oxides, reactions with alcohols

B. Reactions of Metal Hydroxides/Oxides with Alcohols... [Pg.239]

Difluoroethanol is prepared by the mercuric oxide cataly2ed hydrolysis of 2-bromo-l,l-difluoroethane with carboxyHc acid esters and alkaH metal hydroxides ia water (27). Its chemical reactions are similar to those of most alcohols. It can be oxidi2ed to difluoroacetic acid [381-73-7] (28) it forms alkoxides with alkaH and alkaline-earth metals (29) with alkoxides of other alcohols it forms mixed ethers such as 2,2-difluoroethyl methyl ether [461-57-4], bp 47°C, or 2,2-difluoroethyl ethyl ether [82907-09-3], bp 66°C (29). 2,2-Difluoroethyl difluoromethyl ether [32778-16-8], made from the alcohol and chlorodifluoromethane ia aqueous base, has been iavestigated as an inhalation anesthetic (30,31) as have several ethers made by addition of the alcohol to various fluoroalkenes (32,33). Methacrylate esters of the alcohol are useful as a sheathing material for polymers ia optical appHcations (34). The alcohol has also been reported to be useful as a working fluid ia heat pumps (35). The alcohol is available ia research quantities for ca 6/g (1992). [Pg.293]

Cobalt(II) chloride hexahydrate [7791-13-1], C0CI2 6H20 is a deep red monoclinic crystalline material that deflquesces. It is prepared by reaction of hydrochloric acid with the metal, simple oxide, mixed valence oxides, carbonate, or hydroxide. A high purity cobalt chloride has also been prepared electrolyticaHy (4). The chloride is very soluble in water and alcohols. The dehydration of the hexahydrate occurs stepwise ... [Pg.377]

By Reactions of Metal Hydroxides and Oxides with Alcohols and Phenols 338... [Pg.335]

Hydroxides and oxides of the non-metals and less electropositive metals behave as oxyacids and react with alcohols to form esters (alkoxides) and water. Typically such reactions involve an equilibrium and removal of the generated water by fractionation is necessary to obtain the pure... [Pg.338]

Reactions of metal oxides or hydroxides with alcohols (method 3)... [Pg.16]

Hydrolysis of metal alkoxides is the basis for the sol-gel method of preparation of oxide materials therefore, reactions of metal alkoxides with water in various solvents, and primarily in alcohols, may be considered as their most important chemical properties. For many years the sol-gel method was mosdy associated with hydrolysis of Si(OR)4, discussed in numerous original papers and reviews [242, 1793,243]. Hydrolysis of M(OR) , in contrast to hydrolysis of Si(OR)4, is an extremely quick process therefore, the main concepts well developed for Si(OR)4 cannot be applied to hydrolysis of alcoholic derivatives of metals. Moreover, it proved impossible to apply classical kinetic approaches successfully used for the hydrolysis of Si(OR)4 to the study of the hydrolysis of metal alkoxides. A higher coordination number of metals in their alcoholic derivatives in comparison with Si(OR)4 leads to the high tendency to oligomerization of metal alkoxides in their solutions prior to hydrolysis step as well as to the continuation of this process of oligomerization and polymerization after first steps of substitution of alkoxide groups by hydroxides in the course of their reactions with water molecules. This results in extremely complicated oligomeric and polymeric structures of the metal alkoxides hydrolysis products. [Pg.107]

Metal chlorides can also be produced from the oxides or hydroxides using SOCl2. Thionyl chloride will also react with many organic compounds. For example, the reaction with an alcohol can be shown as... [Pg.360]

Just as with hydrothermal synthesis, it is possible to carry out the reaction in non-aqueous media, it is possible to form micelles using alcohol as the polar phase. Using ethanol as the polar phase, it is possible to further tailor the solubihties of metal hydroxides. In the SrFei20i9 hexaferrite, simply coprecipitation strontium and iron to make the mixed metal hydroxide results in a mixed-oxide phase. Sr(OH)2 has such a high solubUity... [Pg.550]


See other pages where Metal hydroxides/oxides, reactions with alcohols is mentioned: [Pg.9]    [Pg.10]    [Pg.119]    [Pg.119]    [Pg.120]    [Pg.360]    [Pg.387]    [Pg.432]    [Pg.471]    [Pg.593]    [Pg.622]    [Pg.635]    [Pg.648]    [Pg.732]    [Pg.734]    [Pg.802]    [Pg.806]    [Pg.806]    [Pg.1005]    [Pg.74]    [Pg.709]    [Pg.711]    [Pg.579]    [Pg.662]    [Pg.103]    [Pg.437]    [Pg.10]    [Pg.265]    [Pg.83]    [Pg.553]    [Pg.59]    [Pg.535]    [Pg.35]    [Pg.224]    [Pg.535]    [Pg.338]    [Pg.553]    [Pg.4827]   
See also in sourсe #XX -- [ Pg.247 ]




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Alcohols, oxidation with

Hydroxides reactions

Hydroxides reactions with

Metal alcohol oxidation

Metal alcoholates

Metal alcohols

Metal hydroxides

Metal hydroxides reactions

Metal hydroxides reactions with

Metal hydroxides with alcohols

Metal oxide reactions

Metal oxides reactions with alcohols

Metalation alcohols

Metallic hydroxide

Metals reactions with alcohol

Oxidation reactions with alcohols

Oxidation reactions, alcohols

Oxide-hydroxides

Reaction with alcohols

Reactions of metal oxides or hydroxides with alcohols (method

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