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Updated: Sep 24, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Introducing random bio-terpene segments to high cis-polybutadiene: making elastomeric materials more sustainable
José Luis González-Zapata1, Francisco Javier Enríquez-Medrano1, Héctor Ricardo López González1
1Research Center for Applied Chemistry Blvd. Enrique Reyna 140, San José de los Cerritos 25294 Saltillo Coahuila Mexico Ricardo.lopez@ciqa.edu.mx Ramon.diazdeleon@ciqa.edu.mx.
Abstract:
In this work, we explore the statistical copolymerization of 1,3-butadiene with the terpenic monomers myrcene and farnesene, carried out via coordination polymerization using a neodymium-based ternary catalytic system. The resultant copolymers, poly(butadiene-co-myrcene) and poly(butadiene-co-farnesene), were synthesized at different monomer ratios, elucidating the influence of the bio-based monomer content over the kinetic variables, molecular and thermal properties, and the reactivity constants (Fineman-Ross and Kelen-Tüdös methods) of the resultant copolymers. The results indicate that through the herein employed conditions, it is possible to obtain "more sustainable" high-cis (≈95%) polybutadiene elastomers with random and tunable content of bio-based monomer. Moreover, the polymers exhibit fairly high molecular weights and a rather low dispersity index. Upon copolymerization, the T g of high-cis PB can be shifted from -106 to -75 °C (farnesene) or -107 to -64 °C (myrcene), without altering the microstructure control. This work contributes to the development of more environmentally friendly elastomers, to form "green" rubber materials.
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