Journal
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 50, Issue 1, Pages 127-133Publisher
WILEY
DOI: 10.1002/pola.24996
Keywords
carbon dioxide; copolymerization; epoxides; in situ infrared spectroscopy; kinetic; polycarbonates; terpolymerization
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Funding
- National Science Foundation [CHE 05-43133]
- Robert A. Welch Foundation [A-0923]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1057743] Funding Source: National Science Foundation
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The selective transformation of CO2 and epoxides to afford completely alternating copolymers remains a topic of much interest for the potential utilization of carbon dioxide in chemical synthesis. The use of salicylaldimine (salen)-metal complexes and their saturated (salan)-metal versions have proven to be the most effective and robust single-site catalyst for these processes. Herein, we report on mechanistic aspects of the copolymerization of alicyclic and aliphatic epoxides with CO2 in toluene solution and in neat epoxides in the presence of a (salan) CrCl/onium salt catalyst system. The activation barriers for both cyclohexene oxide(CHO)/CO2 and propylene oxide(PO)/CO2 were shown to be significantly higher in toluene solution than those previously reported for reactions carried out under solventless conditions. Terpolymerization of CHO/vinylcyclohexene oxide/CO2 was shown via Fineman-Ross analysis at 60 degrees C to proceed with little monomer selectivity, for example, r(CHO) = 1.03 and r(VCHO) = 0.847. On the other hand, terpolymerization of CHO/PO/CO2 occurred at 25 degrees C with a propensity for incorporation of PO in the polymer. However, at 40 degrees C, Fineman-Ross analysis revealed r(CHO) and r(PO) values of 0.869 and 1.49, thereby affording a terpolymer with a more equal distribution of monomers. (C) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 50: 127-133, 2012
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