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Polystyrene, living polymer 1,1-diphenylethylene reaction

A number of other unsaturated electrophilic compounds were used by Milkovich 18 as deactivators for living polystyrene or living polydienes. A characterization of the macromonomers obtained showed that the reaction of the living polymer with compounds such as maleic anhydride, vinyl chloroacetate, or 2-chloroethylvinyl ether yields the following unsaturated chain ends (in some cases the addition of 1,1-diphenylethylene is necessary) ... [Pg.13]

A structure resembling that of the dumbbell polymers was made by Frechet et al. In this case the connector is linked with polyether dendritic groups [272, 273]. The synthetic approach involved the preparation of a difunctional polystyrene chain in THF using potassium naphthalenide as initiator. The living polymer was end-capped with 1,1-diphenylethylene (DPE) to reduce its nucle-ophilicity and avoid side reactions with benzylic halomethyl groups. Addition of the fourth generation dendrimer [G-4] -Br led to the final product (Scheme 100). [Pg.98]


See other pages where Polystyrene, living polymer 1,1-diphenylethylene reaction is mentioned: [Pg.20]    [Pg.759]    [Pg.759]    [Pg.109]    [Pg.216]    [Pg.58]    [Pg.125]    [Pg.50]   
See also in sourсe #XX -- [ Pg.470 ]




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Diphenylethylene

Living polystyrene

Polymer live

Polymers living

Polystyrene polymers

Polystyrene reaction

Polystyrene, living polymer

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