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
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.