Anionic Ring-Opening Copolymerization of L-Lactide with a Five-Membered Cyclic Carbonate Having a Glucopyranoside Structure

The anionic ring-opening copolymerization of L-lactide (LL) with a five-membered cyclic carbonate having the glucopyranoside structure, methyl 4,6-O-benzilidene-2,3-O-carbonyl-α-D-glucopyranoside (MBCG), was carried out using potassium tert-butoxide (t-BuOK) as the initiator and tetrahydrofuran (THF...

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Veröffentlicht in:Polymer journal 2009-01, Vol.41 (9), p.702-708
Hauptverfasser: HABA, Osamu, FURUICHI, Nanako, AKASHIKA, Yosuke
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creator HABA, Osamu
FURUICHI, Nanako
AKASHIKA, Yosuke
description The anionic ring-opening copolymerization of L-lactide (LL) with a five-membered cyclic carbonate having the glucopyranoside structure, methyl 4,6-O-benzilidene-2,3-O-carbonyl-α-D-glucopyranoside (MBCG), was carried out using potassium tert-butoxide (t-BuOK) as the initiator and tetrahydrofuran (THF) as the solvent at 30°C for 12h. The mole fractions of LL in the copolymer (fLL ) of all copolymers were nearly equal to the corresponding mole fraction of LL in the feed (FLL ). Deprotection of the copolymer was performed using trifluoroacetic acid in dichloromethane. 1 H NMR spectra of the resulting product indicated that deprotection was completely achieved due to the absence of the aromatic proton signals.
doi_str_mv 10.1295/polymj.PJ2008327
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subjects Applied sciences
Carbonates
Copolymerization
Copolymers
Exact sciences and technology
Initiators
Moles
Organic polymers
Physicochemistry of polymers
Preparation, kinetics, thermodynamics, mechanism and catalysts
Solvents
Spectra
Tetrahydrofuran
title Anionic Ring-Opening Copolymerization of L-Lactide with a Five-Membered Cyclic Carbonate Having a Glucopyranoside Structure
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