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Reactions Promoted and Catalysed by Pd ll Compounds

The in situ regeneration of Pd(II) from Pd(0) should not be counted as being an easy process, and the appropriate solvents, reaction conditions, and oxidants should be selected to carry out smooth catalytic reactions. In many cases, an efficient catalytic cycle is not easy to achieve, and stoichiometric reactions are tolerable only for the synthesis of rather expensive organic compounds in limited quantities. This is a serious limitation of synthetic applications of oxidation reactions involving Pd(II). However it should be pointed out that some Pd(II)-promoted reactions have been developed as commercial processes, in which supported Pd catalysts are used. For example, vinyl acetate, allyl acetate and 1,4-diacetoxy-2-butene are commercially produced by oxidative acetoxylation of ethylene, propylene and butadiene in gas or liquid phases using Pd supported on silica. It is likely that Pd(OAc)2 is generated on the surface of the catalyst by the oxidation of Pd with AcOH and 02, and reacts with alkenes. [Pg.419]


See other pages where Reactions Promoted and Catalysed by Pd ll Compounds is mentioned: [Pg.419]    [Pg.420]    [Pg.422]    [Pg.424]    [Pg.426]    [Pg.428]    [Pg.430]    [Pg.432]    [Pg.434]    [Pg.436]    [Pg.438]    [Pg.440]    [Pg.442]    [Pg.444]    [Pg.446]    [Pg.448]    [Pg.450]    [Pg.452]    [Pg.454]    [Pg.419]    [Pg.420]    [Pg.422]    [Pg.424]    [Pg.426]    [Pg.428]    [Pg.430]    [Pg.432]    [Pg.434]    [Pg.436]    [Pg.438]    [Pg.440]    [Pg.442]    [Pg.444]    [Pg.446]    [Pg.448]    [Pg.450]    [Pg.452]    [Pg.454]   


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Catalysed reactions

Pd -catalysed reaction

Pd catalysed

Pd compounds

Promoters reaction

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