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Vinyl methyl ether, stereoregular polymerization

Since coordination of the ether oxygen is involved in the stereoregulating step, any factor which weakens this will decrease stereospecificity. This explains why the more hindered, higher alkyl vinyl ethers give less stereoregular polymerization than vinyl methyl ether. [Pg.565]

Stereoregular Polymerization. Chemists at GAF Corporation were first to suggest that stereoregularity or the lack thereof is responsible for both nontacky and crystalline or tacky and amorphous polymers generated from IBVE with BF2 0(C2H )2, depending on the reaction conditions (22,23). In addition, it was shown that the crystalline polymer is actually isotactic (24). Subsequentiy, the reaction conditions necessary to form such polymers have not only been demonstrated, but the stereoregular polymerization has been extended to other monomers, such as methyl vinyl ether (25,26). [Pg.516]


See other pages where Vinyl methyl ether, stereoregular polymerization is mentioned: [Pg.453]    [Pg.169]    [Pg.422]    [Pg.211]    [Pg.178]    [Pg.51]   
See also in sourсe #XX -- [ Pg.211 , Pg.212 ]




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Methyl polymerization

Methyl vinyl ether polymerization

Polymerization stereoregular

Polymerization vinylic

Stereoregularities

Stereoregularity

Vinyl ethers, polymerization

Vinyl methyl ether, stereoregular

Vinyl polymerization

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