Cascade Ring Strain Release Polymerization of Cyclohexene Oxide and Derivatives Using a Mono(μ-Alkoxo)bis(alkylaluminum) Initiator

• Published in: Macromolecules 2023-07, Vol.56 (13), p.4884-4894
• Main Authors: Pedretti, Benjamin J., Zhu, Congzhi, Watanabe, Hironobu, Aoshima, Sadahito, Lynd, Nathaniel A.
• Format: Article
• Language: English
• Subjects: Polymer Science
• ISSN: 0024-9297; 1520-5835
• DOI: 10.1021/acs.macromol.3c00473

Cyclohexene oxide (CHO) is a useful building block for the synthesis of novel materials and is a model substrate for polymerization catalyst development. The driving force for CHO polymerization is derived from its bicyclic structure, which combines the release of the enthalpy from epoxide ring-opening (ca. −15 kcal/mol) and a twist-chair-to-chair conformation shift in the cyclohexane ring (ca. −5 kcal/mol) upon enchainment. The lack of regio-defined functional handles attached to the CHO monomer limits the ability to both pre- and post-functionalize the resultant materials and establish structure–property relationships, which reduces the versatility of currently accessible materials. We report the synthesis of two series of CHO derivatives with butyl, allyl, and halogen substituents in the α and β positions relative to the epoxide ring. Adding substituents to the CHO ring was found to affect polymerization kinetics, with 4-substituted (β) CHO being more reactive than 3-substituted (α) CHO analogs when initiated with a mono­(μ-alkoxo)­bis­(alkylaluminum) pre-catalyst. Polymer thermal properties depended on substituent location and identity. Halogenated CHO rings were most reactive and produced the highest glass transition temperatures in the resultant polymers (up to 105 °C). Density functional theory revealed a possible mechanistic explanation consistent with the observed differences in polymerization rate for the 3- and 4-substituted CHOs derived from a combination of steric and thermodynamic considerations.