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Tungsten salts alkenes

More recently, a Pd(II) salt was shown to catalyze the 1,2-insertion polymerization of a 7-oxanorbornadiene derivative (Fig. 10-16) [50]. The resulting saturated polymer, when heated, gives polyacetylene via a retro-Diels-Alder reaction. (This reaction is reminiscent of the Durham route to polyacetylene discussed below). One advantage of this technique over other routes is that it employs a late transition metal polymerization catalyst. Catalysts using later transition metals tend to be less oxophilic than the d° early transition metal complexes typically used for alkene and alkyne polymerizations [109,110]. Whereas tungsten alkylidene catalysts must be handled under dry anaerobic conditions, the Pd(II)-catalyzed reaction of water-insoluble monomers may be run as an aqueous emulson polymerization. [Pg.366]


See other pages where Tungsten salts alkenes is mentioned: [Pg.465]    [Pg.1079]    [Pg.190]    [Pg.151]    [Pg.54]    [Pg.545]    [Pg.9]    [Pg.125]    [Pg.190]    [Pg.44]    [Pg.46]    [Pg.326]    [Pg.328]    [Pg.25]    [Pg.27]    [Pg.186]   
See also in sourсe #XX -- [ Pg.531 ]




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Tungsten alkenes

Tungsten salts

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