Volume 62, Issue 2 pp. 90-101
Research Paper

Isocyanate-free Route to Starch-graft-Polycaprolactone via Carbonyldiimidazole (CDI)-mediated End Group Conversion

Loubna Najemi

Loubna Najemi

Ingénierie des Matériaux Polymères/LRMP, UMR CNRS 5223, Université Jean Monnet, Saint-Etienne, France

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Thomas Jeanmaire

Thomas Jeanmaire

Département de Chimie, Université Jean Monnet, Saint-Etienne, France

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Amar Zerroukhi

Corresponding Author

Amar Zerroukhi

Département de Chimie, Université Jean Monnet, Saint-Etienne, France

Université Jean Monnet, Département de Chimie, 23 rue du Dr Paul Michelon, 42023 Saint-Etienne, Cedex 2, France. Tel: 0033477485100Search for more papers by this author
Mustapha Raihane

Mustapha Raihane

Faculté des Sciences et Techniques Guéliz, Laboratoire de Chimie Bioorganique et Macromoléculaire, Université Cadi Ayyad, Marrakech, Morocco

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First published: 17 February 2010
Citations: 12

Abstract

This paper reports on the synthesis of biodegradable starch-graft-poly ϵ-caprolactone (starch-g-PCL) in two steps. First, poly ϵ-caprolactone (PCL) was modified on the terminal groups by using carbodiimidazole (CDI) as coupling agent. Then, the starch graft copolymers with PCL were prepared through a carbonate bond using carboimidazole function. Monofunctional and bifunctional reactive end-group PCL terminated with carboimidazole groups were prepared and reacted with hydroxyl groups of starch. The resulting starch-g-PCL copolymers were characterized by FT-IR, NMR, HR-MAS-NMR, DSC, MEB and XRD.

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