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Erythrodisyndiotactic polymer

All four diisotactic polymers (cis and trans, erythro and threo) are chiral and possess optical activity. Each of the four disyndiotactic polymers possesses a mirror glide plane and is achiral. For symmetric 1,4-disubstituted 1,3-butadienes (R = R ), only the cis and transthreo-diisotactic structures are chiral. Each of the erythrodiisotactic and threodisyndiotactic polymers has a mirror glide plane. Each of the erythrodisyndiotactic polymers has a mirror glide plane. [Pg.631]

Based on the mechanisms known from a-olefin polymerization, Ci-symmetric [Ph2C(Cp)(Flu)] ZrCl2 (3, Flu = 9-fluorenyl) should produce an erythrodisyndiotactic polymer and therefore favor the formation of the rac-hydrodimer, whereas C2-symmetric rac-[Me2Si(Ind)2]ZrCl2... [Pg.416]

SCHEME 16.2 Stereochemistry during the polymerization of a prochiral cycloolefin such as norbornene nsing Cs- (A) and C2-symmetiic (B) catalysts. Independent of the relative topicities of the single insertion events (contrasted by pathways a and b), apphcation of the mechanisms known from a-olefin polymerization predict an erythrodisyndiotactic polymer to be formed by C -symmetric catalysts and an erythrodiisotactic polymer to be formed by C2-symmetric catalysts. [Pg.417]

This polymer cannot be expressed as erythrodisyndiotactic or as threodisyndiotactic. Instead ABHHHHHH AHHHHBHH... [Pg.36]

Explain what is meant by erythrodiisotactic, threodiisotactic and polymers. Illustrate. Do the same for erythrodisyndiotactic and threodisyndiotactic. [Pg.33]


See other pages where Erythrodisyndiotactic polymer is mentioned: [Pg.626]    [Pg.626]    [Pg.847]    [Pg.626]    [Pg.626]    [Pg.847]    [Pg.400]    [Pg.843]    [Pg.846]    [Pg.853]   
See also in sourсe #XX -- [ Pg.625 , Pg.632 ]

See also in sourсe #XX -- [ Pg.625 , Pg.632 ]




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