Biomacromolecules, 6 (4), 2091 -2095, 2005. 10.1021/bm050076t S1525-7797(05)00076-0
Web Release Date: April 23, 2005

Copyright © 2005 American Chemical Society

Catalytic Polymerization of a Cyclic Ester Derived from a "Cool" Natural Precursor

Donghui Zhang, Marc A. Hillmyer,* and William B. Tolman*

Department of Chemistry, University of Minnesota, 207 Pleasant St. SE, Minneapolis, Minnesota 55455-0431

Received February 1, 2005

Revised March 10, 2005

Abstract:

(-)-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 (Hp = -16.8 ± 1.6 kJ mol-1, Sp = -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.


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