Biomacromolecules · 2004 · 80 citations · 19 references
Natural SciencesChemical EngineeringChemistryPolymer ChemistryPolymer EngineeringPolymer MaterialsOlefin PolymerizationPolymer FunctionalizationPolymer StructurePolymerization ChemistryPolymerization ProcessesLow-toxicity MaterialsLow-toxicity ReagentsPolylactide SynthesisPolymer-monomer RatioStar PolymersTime Conversion
L-lactide was polymerized as concentrated solution in chlorobenzene with Bi(OAc)3 as initiator. When tetra(ethylene glycol) was added as co-initiator (CoI), telechelic polylactides having two CH-OH end groups were obtained. With 1,1,1-tri(hydroxy methyl)propane (THMP) as co-initiator, three-armed stars having three CH-OH end groups were formed. Analogously, tetrafunctional star-shaped poly(L-lactide)s were obtained with pentaerythritol as co-initiator. The chain lengths were varied via the monomer/CoI ratio. Time-conversion curves proved that Bi(OAc)3 is slightly less reactive as initiator than tin(II) 2-ethylhexanoate. However, bismuth acetate (or other carboxylates) have a particularly low toxicity as documented in the literature and by numerous Bi3+-containing pharmaceutical products.
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Polymerization of <scp>l</scp>,<scp>l</scp>-Dilactide Initiated by Tin(II) Butoxide
Adam Kowalski, Jan Libiszowski, Andrzej Duda et al. · Macromolecules · 2000 · 268 citations
Configurational structures of lactic acid stereocopolymers as determined by 13C{1H} n.m.r.
F. Chabot, Michel Vert, Stella Chapelle et al. · Polymer · 1983 · 233 citations