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Bismuth( III ) Alkoxide Catalysts for Ring‐Opening Polymerization of Lactides and ϵ‐Caprolactone
Author(s) -
Vuorinen Sirpa,
Lahcini Mohammed,
Hatanpää Timo,
Sundberg Markku,
Leskelä Markku,
Repo Timo
Publication year - 2013
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201200521
Subject(s) - alkoxide , polymerization , ring opening polymerization , polymer chemistry , chemistry , caprolactone , monomer , catalysis , bismuth , lactide , organic chemistry , polymer
Abstract Homoleptic bismuth alkoxide complexes, Bi(OR) 3 [R = i Pr ( 1 ), t Bu ( 2 ), and CMe 2 i Pr ( 3 )], are used as catalysts in the ring‐opening polymerization (ROP) of lactides. In contrast to 1 , two bulkier bismuth alkoxides, 2 and 3, show high activity in the ROP of lactides in toluene at 75 °C. Notably, Bi III alkoxides 2 and 3 are more active in lactide ROP than Sn II octoate activated with n ‐butanol under identical reaction conditions. Bismuth alkoxides 2 and 3 exhibit a living behavior in the ROP of lactides that is demonstrated both in homopolymerization and in a polymerization resumption experiment. Polymerization of rac ‐lactide using 2 and 3 yields polylactide with a slight heterotactic bias. In addition, 2 is an efficient initiator for the ROP of ϵ‐caprolactone in bulk at 120 °C. Variation of the monomer‐to‐catalyst ratio yielded poly(ϵ‐caprolactone) with M n s up to 120 000 g mol −1 in corrected gel‐permeation chromatography (GPC) data.