Journal
CHEMICAL COMMUNICATIONS
Volume 58, Issue 69, Pages 9586-9593Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cc03516b
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Funding
- NSF Center for Sustainable Polymers [CHE-1901635]
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This article provides an overview of strategies for the polymerization of EVP to various polymer structures, utilizing the highly functionalized lactone, including radical polymerizations and ring-opening polymerizations.
3-Ethyl-6-vinyltetrahydro-2H-pyran-2-one (EVP) is a CO2-derived lactone synthesized via Pd-catalyzed telomerization of butadiene. As EVP is 28.9% by weight CO2, it has received significant recent attention as an intermediary for the synthesis of high CO2-content polymers. This article provides an overview of strategies for the polymerization of EVP to a wide variety of polymer structures, ranging from radical polymerizations to ring-opening polymerizations, that each take unique advantage of the highly functionalized lactone.
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