4.7 Article

Original route to polylactide-polystyrene diblock copolymers containing a sulfonyl group at the junction between both blocks as precursors to functional nanoporous materials

Journal

REACTIVE & FUNCTIONAL POLYMERS
Volume 72, Issue 8, Pages 495-502

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.reactfunctpolym.2012.04.012

Keywords

Semi-hydrolyzable diblock copolymers; Sulfonyl-functionalized junction point; Ring-opening polymerization/atom transfer radical polymerization tandem approach; Selective hydrolysis; Functional nanoporous materials

Funding

  1. Groupe Chimique Tunisien

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Novel functionalized nanoporous polymeric materials could be derived from poly(D,L-lactide)-block-polystyrene (PLA-b-PS) diblock copolymers with a sulfonyl group at the junction between both blocks were synthesized by a combination of ring-opening polymerization (ROP) and atom transfer radical polymerization (ATRP) using a synthetic difunctional initiator through a three-step sequential methodology. Different omega-bromo PLA polymers with various molar masses ranging from 3640 to 11,440 g mol(-1) were first produced by coupling omega-hydroxy PLA precursors to a chlorosulfonyl-functionalized ATRP initiator previously prepared, thus leading to the formation of suitable macroinitiators for the subsequent ATRP polymerization of styrene. Consequently, PLA-b-PS diblock copolymers were obtained with a finely tuned PLA volume fraction (f(PLA)) in order to develop a microphased-separation morphology. The resulting copolymers as well as the intermediate compounds were carefully analyzed by size exclusion chromatography and H-1 NMR. Upon shear flow induced by a channel die processing, oriented copolymers were generally afforded as characterized by small-angle-X-ray scattering (SAXS). Such copolymers were finally submitted to mild alkaline conditions so as to hydrolyze the sacrificial PLA block, and the presence of the sulfonic acid functionality on the pore walls of the resulting nanoporous materials was evidenced by means of a post-modification reaction consisting in the corresponding sulfonamide formation. (C) 2012 Elsevier Ltd. All rights reserved.

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