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Synthesis of Ultrahigh Molecular Weight PLAs Using a Phenoxy-Imine Al(III) Complex
Author(s) -
Feijie Li,
Sanjay Rastogi,
Dario Romano
Publication year - 2020
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.0c01952
Subject(s) - polymerization , monomer , polymer chemistry , imine , lactide , catalysis , benzyl alcohol , ring opening polymerization , molar mass distribution , chemistry , lactic acid , materials science , polymer , organic chemistry , biology , bacteria , genetics
l- and d-lactide polymerization kinetics using phenoxy-imine ligands of the type Me 2 Al[O-2- tert- Bu-6-(C 6 F 5 N=CH)C 6 H 3 ] in the presence of n -butanol and benzyl alcohol by ring-opening polymerization into polylactide are investigated. Effects of initiator concentration, catalyst concentration, polymerization temperature, and time on the molecular weight of poly-l-lactide are also investigated. Purification and drying of l-lactide are found to significantly influence the polymerization kinetics and the final molecular weight achieved. Ultrahigh molecular weight poly(l-lactic acid) PLLA ( M w = 1.4 × 10 6 g/mol with Đ = 1.8) and ultrahigh molecular weight poly(d-lactic acid) PDLA ( M w = 1.3 × 10 6 g/mol with Đ = 2.0) are obtained when polymerization is performed with a molar ratio of monomer to catalyst (LA/Al) of 8000 for 72 h at 120 °C in the presence of benzyl alcohol with conversions of 96 and 91%, respectively. We report for the first time the synthesis of ultrahigh molecular weight poly-l- and d-lactide using the Me 2 Al[O-2- tert -Bu-6-(C 6 F 5 N=CH)C 6 H 3 ] catalyst. The identified catalyst is found to be suitable for the synthesis of a broad range of molecular weights.

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