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High-Resolution 13C and 1H Solution NMR Study of Poly(lactide)

Thakur, Khalid A. M., Kean, Robert T., Hall, Eric S., Kolstad, Jeffrey J., Lindgren, Tim A., Doscotch, Matthew A., Siepmann, J. Ilja, Munson, Eric J.·1997·Macromolecules

Abstract

High-resolution 500 MHz solution-state 1 H and 13 C NMR spectra of various poly(lactides) indicate at least hexad stereosequence sensitivity. The poly(lactides) were prepared in vials by melt polymerization of various combinations of l -lactide, d -lactide, and meso -lactide at 180 °C for 3 h using tin(II) bis(2-ethylhexanoate) (tin(II) octoate) as the catalyst in a 1:10 000 ratio. The intensity distribution of the various stereosequence resonances in the NMR spectra indicates a preference for syndiotactic addition during the polymerization process. Minimal evidence of transesterification was observed for these polymerization conditions.

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Authors
Thakur, K. A. M., Kean, R. T., Hall, E. S., Kolstad, J. J., Lindgren, T. A., Doscotch, M. A., Siepmann, J. I., & Munson, E. J.
Venue
Macromolecules
Published
1997-04-01
Volume
30
Issue
8
Pages
2422-2428
ISSN
  • 0024-9297 (ISSN-L)
  • 1520-5835
OpenAlex
W1623501845
Cited by
241
References
0
FWCI
4.79
Type
journal article
Language
en
Open access
closed

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