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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Series: | International Journal of Biomaterials |
Online Access: | http://dx.doi.org/10.1155/2012/390947 |
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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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1716825277181460480 |