Abstract

Bennabi Lamia,Belarbi Lahcene,Bousalem Smain and Abederrezak Mesli

Poly (e-caprolactone) macromonomers carrying amide end groups were synthesed via a polycondensation reaction of functional carboxylic diacid terminated poly(ε-caprolactone) prepolymers (HOOC-PCL-COOH) with 1,4 phenylene bis (2-Oxazoline). The prepolymers were produced by the ring opening polymersation of ε-caprolactone by adipic acidic. This polymersation used a new one-step method that eliminated the need to isolate of the telechelic prepolymer intermediate. The expected structures of the polymers were confirmed by FTIR. Hydrolytic and enzymatic degradations of the materials were performed.

degradation; poly (ε-caprolactone); chain extender; coupling reaction

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