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

Tipo de material: TextoTextoSeries ; Macromolecules, 30, p.2422-2428, 1997Trabajos contenidos:
  • Thakur, K.Am
  • Kean, R.T
  • Hall, E.S
  • Kolstad, J.J
  • Lindgren, T.A
  • Doscotch, M.A
  • Siepmann, J.I
  • Siepmann, J.I
Recursos en línea: Resumen: High-resolution 500 MHz solution-state 1H and 13C 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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High-resolution 500 MHz solution-state 1H and 13C 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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