SYNTHESIS OF POLY(NORBORNENE-G-EPSILON-CAPROLACTONE) COPOLYMERS BY SEQUENTIAL CONTROLLED RING-OPENING POLYMERIZATION

Citation
P. Lecomte et al., SYNTHESIS OF POLY(NORBORNENE-G-EPSILON-CAPROLACTONE) COPOLYMERS BY SEQUENTIAL CONTROLLED RING-OPENING POLYMERIZATION, Polymer bulletin, 40(6), 1998, pp. 631-638
Citations number
7
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
01700839
Volume
40
Issue
6
Year of publication
1998
Pages
631 - 638
Database
ISI
SICI code
0170-0839(1998)40:6<631:SOPCBS>2.0.ZU;2-B
Abstract
Poly(norbomene-g-epsilon-caprolactone) copolymers have been prepared b y the ''grafting from'' technique. Well controlled polynorbornene cont aining 5% acetate pendant groups has been firstly synthesized by ruthe nium complex-mediated ring opening metathesis polymerization. The acet ate groups have been derivatized into aluminum alkoxides by hydrolysis into alcohol followed by reaction of the alcohol with triethylaluminu m. The two polymerization steps are under complete control, so that gr aft copolymers have been synthesized with a narrow molecular weight di stribution and are free from any detectable traces of the parent homop olymers as stated by selective fractionation experiments. These origin al copolymers have been characterized by SEC, FTIR, H-1 NMR, DSC, TGA.