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Ethene polymerization hydride elimination

Water and carbon monoxide can produce dihydrogen in situ (shift reaction), as has been shown in the synthesis of diethylketone (pentan-3-one) from ethene, CO and water in the presence of palladium(II) salts, triphenylphosphine and acids [37], Ether chain ends have been observed in some polymerization reactions [40] and low molecular weight products can also contain an ether moiety as an end group. Most likely ether chain ends are not formed by attack of alcohol at coordinated ethene in a Wacker type reaction, since this is usually followed by fast (3-hydride elimination. Instead we propose that a palladium-... [Pg.251]


See other pages where Ethene polymerization hydride elimination is mentioned: [Pg.284]    [Pg.3567]    [Pg.86]    [Pg.284]    [Pg.3566]    [Pg.784]    [Pg.786]    [Pg.818]    [Pg.28]    [Pg.233]    [Pg.179]    [Pg.906]   
See also in sourсe #XX -- [ Pg.43 ]




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3-Hydride elimination

Polymeric hydrides

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