Web Release Date: April 23,
Catalytic Polymerization of a Cyclic Ester Derived from a "Cool" Natural Precursor
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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