SYNTHESIS OF WELL-DEFINED POLYSTYRENE WITH MULTIFUNCTIONAL END-GROUPSUTILIZING CYCLOTRIPHOSPHAZENE

Citation
K. Inoue et al., SYNTHESIS OF WELL-DEFINED POLYSTYRENE WITH MULTIFUNCTIONAL END-GROUPSUTILIZING CYCLOTRIPHOSPHAZENE, Macromolecular rapid communications, 18(3), 1997, pp. 225-231
Citations number
23
Categorie Soggetti
Polymer Sciences
ISSN journal
10221336
Volume
18
Issue
3
Year of publication
1997
Pages
225 - 231
Database
ISI
SICI code
1022-1336(1997)18:3<225:SOWPWM>2.0.ZU;2-F
Abstract
Telechelic polystyrenes with five benzyl chloride moieties at the poly mer end (PSt-E) were prepared by coupling reaction of polystyryllithiu m with hexakis(4-chloromethylphenoxy)cyclotriphosphazene (4). The coup ling reaction occurs almost quantitatively and unfavorable side reacti ons were not operative. When a mole ratio [4]/[sec-BuLi]=9.3 was used, polystyrenes with cyclophosphazene carrying five benzyl chloride moie ties at the polymer end (PSt-E) were obtained in more than 90% yield, which have narrow and predictable molecular weights (<(M)over bar (w)> /<(M)over bar (n)>=1.05). A star shaped polystyrene with phosphazene c ore could also be prepared by using excess polystyryl anions.