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Synthesis and Functionalization of Isotactic Poly(propylene) Containing Pendant Styrene Groups
Author(s) -
Zou Junfeng,
Cao Chengang,
Dong JinYong,
Hu Youliang,
Chung TzeChiang
Publication year - 2004
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.200400284
Subject(s) - tacticity , styrene , polymer chemistry , atom transfer radical polymerization , copolymer , anionic addition polymerization , catalysis , polymer , butyllithium , divinylbenzene , polymerization , chemistry , materials science , organic chemistry
Summary: Copolymerization of propylene and 1,4‐divinylbenzene was successfully performed by a MgCl 2 ‐supported TiCl 4 catalyst, yielding isotactic poly(propylene) ( i ‐PP) polymers containing a few pendant styrene groups. With a metalation reaction with butyllithium and a hydrochlorination reaction with dry hydrogen chloride, the pendant styrene groups were quantitatively transformed into benzyllithium and 1‐chloroethylbenzene groups, respectively, which allowed the synthesis of i ‐PP‐based graft copolymers by living anionic and atom transfer radical (ATRP) polymerization mechanisms.The incorporation of styrene pendant groups into isotactic poly(propylene) using a Zeigler–Natta catalyst gave functionalized polymers able to undergo living anionic and atom transfer radical (ATRP) polymerizations.

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