Poly( tert-butyl acrylate- b-isobutylene- b-styrene) terpolymer from a carbocationic initiator containing a latent radical initiating site

A poly(isobutylene- b-styrene) (PIB-PS) copolymer was synthesized via quasi-living carbocationic polymerization from an initiator containing a latent site for atom transfer radical polymerization (ATRP) initiation. The initiator, 3,3,5-trimethyl-5-chlorohexyl acetate (TMCHA), was synthesized in four...

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Veröffentlicht in:Polymer (Guilford) 2006-03, Vol.47 (6), p.1852-1860
Hauptverfasser: Breland, L. Krystin, Murphy, J. Chase, Storey, Robson F.
Format: Artikel
Sprache:eng
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Zusammenfassung:A poly(isobutylene- b-styrene) (PIB-PS) copolymer was synthesized via quasi-living carbocationic polymerization from an initiator containing a latent site for atom transfer radical polymerization (ATRP) initiation. The initiator, 3,3,5-trimethyl-5-chlorohexyl acetate (TMCHA), was synthesized in four steps from methyl 3,3-dimethyl-4-pentenoate. The PIB block was created at −70 °C in a methylcyclohexane/methyl chloride (60:40) cosolvent system, using TiCl 4 as the catalyst, followed by sequential addition of styrene. The acetate head group of the resulting block copolymer was converted to a hydroxyl group using a strong base and subsequently esterified with 2-bromopropionyl bromide to create an initiating site for ATRP of tert-butyl acrylate, which was carried out using a Cu(I)Br/1,1,4,7,7,-pentamethyl-diethylenetriamine (PMDETA) catalyst system. The final terpolymers had compositions that were very close to theoretical.
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2006.01.048