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 |
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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 |
format | Article |
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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 ). 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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 ). 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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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