Catalytic polymerization of a cyclic ester derived from a "cool" natural precursor
(-)-Menthide, a seven-membered lactone derived from the natural product (-)-menthol, was polymerized using a structurally defined zinc-alkoxide catalyst to form an aliphatic polyester. The polymer was fully characterized by NMR spectroscopy, size exclusion chromatography, and matrix-assisted laser desorption ionization mass spectrometry. The polymerization reaction occurred in a controlled fashion and polymer samples with Mn values up to 90 kg mol-1 were obtained by varying the catalyst loading. Monitoring of the rate of polymerization by in situ FT-IR spectroscopy (ReactIR) revealed a first order dependence on (-)-menthide. The temperature dependence of the observed rate constant between 30 and 90 °C was well described by the Arrhenius equation and gave Ea = 38.4 ± 0.9 kJ mol-1. Thermodynamic parameters (ΔHp° = -16.8 ± 1.6 kJ mol-1, ΔSp° = -27.4 ± 4.6 J mol-1 K-1) for the polymerization of (-)-menthide were also determined by measuring the equilibrium monomer concentration at different temperatures ranging from 40 to 100 °C. The equilibrium monomer concentrations at 25 and 100 °C were calculated to be 0.031 ± 0.018 and 0.120 ± 0.063 M, respectively. © 2005 American Chemical Society.
Publication Source (Journal or Book title)
Zhang, D., Hillmyer, M., & Tolman, W. (2005). Catalytic polymerization of a cyclic ester derived from a "cool" natural precursor. Biomacromolecules, 6 (4), 2091-2095. https://doi.org/10.1021/bm050076t