Synthesis of Block Copolymers of Varying Architecture Through Suppression of Transesterification during Coordinated Anionic Ring Opening Polymerization

Well-defined di- and triblock copolymers consisting of ε-caprolactone (CL), L-lactide (LA), and trimethylene carbonate (TMC) were synthesized via “PLA first route” in coordinated anionic ring opening polymerization/copolymerization (CAROP) with tin (II) octoate as catalyst. The desired block structu...

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Main Authors: Vitali T. Lipik, Marc J. M. Abadie
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:International Journal of Biomaterials
Online Access:http://dx.doi.org/10.1155/2012/390947
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spelling doaj-fe171e4bb89a42b29220c3680c2b91082020-11-24T20:41:24ZengHindawi LimitedInternational Journal of Biomaterials1687-87871687-87952012-01-01201210.1155/2012/390947390947Synthesis of Block Copolymers of Varying Architecture Through Suppression of Transesterification during Coordinated Anionic Ring Opening PolymerizationVitali T. Lipik0Marc J. M. Abadie1School of Materials Science and Engineering, Nanyang Technological University, Nanyang Avenue 50, 639798, SingaporeSchool of Materials Science and Engineering, Nanyang Technological University, Nanyang Avenue 50, 639798, SingaporeWell-defined di- and triblock copolymers consisting of ε-caprolactone (CL), L-lactide (LA), and trimethylene carbonate (TMC) were synthesized via “PLA first route” in coordinated anionic ring opening polymerization/copolymerization (CAROP) with tin (II) octoate as catalyst. The desired block structure was preserved by use of protective additive α-methylstyrene by preventing the transesterification side-reactions. MALDI-TOF analysis revealed that the protection mechanism is associated with α-methylstyrene and tin (II) octoate complexation. Additionally, it was shown that use of α-methylstyrene in ring opening polymerization allowed the formation of polyesters with high molar mass.http://dx.doi.org/10.1155/2012/390947
collection DOAJ
language English
format Article
sources DOAJ
author Vitali T. Lipik
Marc J. M. Abadie
spellingShingle Vitali T. Lipik
Marc J. M. Abadie
Synthesis of Block Copolymers of Varying Architecture Through Suppression of Transesterification during Coordinated Anionic Ring Opening Polymerization
International Journal of Biomaterials
author_facet Vitali T. Lipik
Marc J. M. Abadie
author_sort Vitali T. Lipik
title Synthesis of Block Copolymers of Varying Architecture Through Suppression of Transesterification during Coordinated Anionic Ring Opening Polymerization
title_short Synthesis of Block Copolymers of Varying Architecture Through Suppression of Transesterification during Coordinated Anionic Ring Opening Polymerization
title_full Synthesis of Block Copolymers of Varying Architecture Through Suppression of Transesterification during Coordinated Anionic Ring Opening Polymerization
title_fullStr Synthesis of Block Copolymers of Varying Architecture Through Suppression of Transesterification during Coordinated Anionic Ring Opening Polymerization
title_full_unstemmed Synthesis of Block Copolymers of Varying Architecture Through Suppression of Transesterification during Coordinated Anionic Ring Opening Polymerization
title_sort synthesis of block copolymers of varying architecture through suppression of transesterification during coordinated anionic ring opening polymerization
publisher Hindawi Limited
series International Journal of Biomaterials
issn 1687-8787
1687-8795
publishDate 2012-01-01
description Well-defined di- and triblock copolymers consisting of ε-caprolactone (CL), L-lactide (LA), and trimethylene carbonate (TMC) were synthesized via “PLA first route” in coordinated anionic ring opening polymerization/copolymerization (CAROP) with tin (II) octoate as catalyst. The desired block structure was preserved by use of protective additive α-methylstyrene by preventing the transesterification side-reactions. MALDI-TOF analysis revealed that the protection mechanism is associated with α-methylstyrene and tin (II) octoate complexation. Additionally, it was shown that use of α-methylstyrene in ring opening polymerization allowed the formation of polyesters with high molar mass.
url http://dx.doi.org/10.1155/2012/390947
work_keys_str_mv AT vitalitlipik synthesisofblockcopolymersofvaryingarchitecturethroughsuppressionoftransesterificationduringcoordinatedanionicringopeningpolymerization
AT marcjmabadie synthesisofblockcopolymersofvaryingarchitecturethroughsuppressionoftransesterificationduringcoordinatedanionicringopeningpolymerization
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