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Title: Closing the “One Monomer–Two Polymers–One Monomer” Loop via Orthogonal (De)polymerization of a Lactone/Olefin Hybrid
Award ID(s):
1904962
PAR ID:
10335180
Author(s) / Creator(s):
; ; ;
Date Published:
Journal Name:
Journal of the American Chemical Society
Volume:
144
Issue:
5
ISSN:
0002-7863
Page Range / eLocation ID:
2264 to 2275
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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  1. Stereoselective polymerization of chiral or prochiral monomers is a powerful method to produce high-performance stereoregular crystalline polymeric materials. However, for monomers with two stereogenic centers, it is generally necessary to separate diastereomers before polymerization, resulting in substantial material loss and added energy cost associated with the separation and purification process. Here we report a diastereoselective polymerization methodology enabled by catalysts that directly polymerize mixtures of eight-membered diolide (8DL) monomers with varying starting ratios of chiral racemic (rac) and achiralmesodiastereomers into stereosequenced crystalline polyhydroxyalkanoates with isotactic and syndiotactic stereodiblock or stereotapered block microstructures. These polymers show enhanced ductility and toughness relative to polymers of purerac-8DL, subject to tuning by variation of the diastereomeric ratio and structure of the 8DL monomers. 
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