Understanding the Structure-Polymerization Thermodynamics Relationships of Fused-Ring Cyclooctenes for Developing Chemically Recyclable Polymers.

Polymers that can be chemically recycled to their constituent monomers offer a promising solution to address the challenges in plastics sustainability through a circular use of materials. The design and development of monomers for next-generation chemically recyclable polymers require an understanding of the relationships between the structure of the monomers/polymers and the thermodynamics of polymerization/depolymerization. Here we investigate the structure-polymerization thermodynamics relationships of a series of cyclooctene monomers that contain an additional ring fused at the 5,6-positions, including trans -cyclobutane, trans -cyclopentane, and trans -five-membered cyclic acetals. The four- and five-membered rings trans -fused to cyclooctene reduce the ring strain energies of the monomer, and the enthalpy changes of polymerizations are found to be in the range of -2.1 to -3.3 kcal mol -1 . Despite the narrow range of enthalpy changes, the ceiling temperatures at 1.0 M span from 330 to 680 °C, due to the low entropy changes, ranging from -2.7 to -5.0 cal mol -1 K -1 . Importantly, geminal substituents on the trans -five-membered cyclic acetal fused cyclooctenes are found to reduce the ceiling temperature by ∼300 °C, although they are not directly attached to the cyclooctene. The remote gem -disubstituent effect demonstrated here can be leveraged to promote depolymerization of the corresponding polymers and to tune their thermomechanical properties.