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Canadian Science Publishing, Canadian Journal of Chemistry, 4(89), p. 499-505, 2011

DOI: 10.1139/v11-002

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Flexible and rigid core molecules in the synthesis of poly(lactic acid) star polymers

Journal article published in 2011 by Mitchell R. Perry, Michael P. Shaver ORCID
This paper is available in a repository.
This paper is available in a repository.

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Abstract

This study presents the synthesis and physical characterization of a series of structurally well-defined star-shaped poly(lactic acids). Polymer stars are prepared from a series of multifunctional alcohol cores including flexible polyols pentaerythritol and dipentaerythritol (four-armed and six-armed cores, respectively) and rigid substituted arenes tri(hydroxymethyl)benzene and hexa(hydroxymethyl)benzene. Utilizing a tin(II) octanoate catalyst, arms of 10 monomer units long are built from rac-lactide and l-lactide to form atactic and isotactic star polymers. Polymers were subsequently characterized by means of NMR spectroscopy, gel permeation chromatography, differential scanning calorimetry, and thermogravimetric analysis. Our results support previous work that suggests that the length of the individual arms, not the total molecular weight, correlates to physical characteristics including glass, melt, crystallization, and decomposition temperatures. In addition, differences between core molecules suggest that the chemical nature of the core can significantly alter the physical properties of the star polymer. Trends in crystallization and glass transition temperatures relative to the core used merit further study and correlate closest to the molecular weight and the number of arms emanating from the star core. It is also clear that the rigidity provided by aromatic cores has a significant effect on the melting temperatures of these macromolecules.