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Updated: Oct 16, 2025

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
Published on: November 27, 2015
Accessing Divergent Main-Chain-Functionalized Polyethylenes via Copolymerization of Ethylene with a
Shan Tang1, Yajun Zhao1, Kyoko Nozaki1
1Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo 7-3-1- Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
Abstract:
Carbon dioxide (CO2) has been used as a sustainable comonomer in the synthesis of different functional polymers including polycarbonates, polyurea, and polyurethane. Until today, despite the great interest, little success has been made for incorporating CO2 into the most widely used polyethylene materials. Herein, we report the incorporation of CO2 to polyethylenes through the copolymerization of ethylene with a CO2/butadiene-derived lactone, 3-ethylidene-6-vinyltetrahydro-2H-pyran-2-one (EVP). Two-types of main-chain-functionalized polyethylenes can be synthesized through different copolymerization strategies. Palladium-catalyzed coordination/insertion copolymerization furnished polyethylenes bearing unsaturated lactones, while radical copolymerization afforded polyethylenes bearing bicyclic lactones. Modification of the polyethylene chains was successfully accomplished through Michael addition or aminolysis. This highly versatile copolymerization protocol provides access to a diverse range of polyethylene materials made from ethylene, CO2, and 1,3-butadiene.
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