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Boron alkoxide hydrolysis

Although symmetrical dialkylborinic acids can be obtained from boron alkoxides or boronic esters and organolithium or RMgX reagents " , these compounds usually are more conveniently synthesized, either by partial hydrolysis of trialkylboranes , or by hydroboration of alkenes with monohalogenoboranes followed by hydrolysis (see also refs. 1-8, 5.3.2.4 and ref. 2, 5.3.2.4.1). Diarylborinic acids are prepared by the reaction of 2 mol of ArMgX with trialkoxyborane at low The products are... [Pg.74]

For most metal alkoxides, hydrolysis with excess water yields insoluble oxide or hydroxide precipitates that are useless for further polymerization reactions [Eqs. (5.21)-(5.23)]. However, if small amounts of water are added slowly to a sufficiently dilute solution, it is possible to form polymerizable molecular species from these alkoxides also. For example, when a dilute solution of boron alkoxide in alcohol is exposed to water, soluble transient molecular species such as B(0R)2(0H) and B(OR)(OH)2, representing various degrees of hydrolysis, form initially, e.g.. [Pg.313]

In the sol-gel process, ceramic polymer precursors are formed in solution at ambient temperature shaped by casting, film formation, or fiber drawing and then consolidated to furnish dense glasses or polycrystalline ceramics. The most common sol-gel procedures involve alkoxides of silicon, boron, titanium, and aluminum. In alcohol water solution, the alkoxide groups are removed stepwise by hydrolysis under acidic or basic catalysis and... [Pg.398]

Alkoxides are usually more difficult to hydrolyze than halides, although hydrolysis can be rapid in activated systems. Pyrimidinethiones can sometimes be hydrolyzed directly to pyrimidinones, but it is often better to convert the thiones into alkylsulfenyl, alkylsulfmyl, or alkylsulfonyl derivatives before hydrolysis <1994HC(52)1, 1996CHEC-II(6)93>. The formation of 5-hydroxypyrimidines is not normally performed using hydrolytic procedures, although it can be achieved by the oxidation of boronate species in aqueous solution <1996CC2719, 2006TL7363>. [Pg.143]


See other pages where Boron alkoxide hydrolysis is mentioned: [Pg.395]    [Pg.394]    [Pg.315]    [Pg.49]    [Pg.145]    [Pg.469]    [Pg.373]    [Pg.227]    [Pg.246]    [Pg.390]    [Pg.22]    [Pg.374]    [Pg.241]    [Pg.1718]   
See also in sourсe #XX -- [ Pg.83 , Pg.84 , Pg.85 , Pg.86 ]




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Boronates hydrolysis

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