articleJournal of the American Chemical SocietyJan 26, 2002Closed access

Stereochemistry of Lactide Polymerization with Chiral Catalysts:  New Opportunities for Stereocontrol Using Polymer Exchange Mechanisms

Cornell University

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Abstract

The synthesis of chiral aluminum and yttrium alkoxides and their application for lactide polymerization are reported. The complexes (SalBinap)MOR [4, M = Al, R = (i)Pr; 5, M = Y, R = (CH(2))(2)NMe(2)] are synthesized by reacting the ligand (SalBinap)H(2) [2,2'-[(1,1'-binaphthalene)-2,2'-diylbis(nitrilomethylidyne)]bisphenol] with the appropriate metal trisalkoxide. While enantiomerically pure yttrium complex 5 did not effect stereocontrol in the polymerization of either meso- or rac-lactide, homochiral 4 was found to exhibit excellent stereocontrol in a range of lactide polymerizations. Enantiomerically pure 4 polymerizes meso-lactide to syndiotactic poly(lactic acid) (PLA), while rac-4 polymerizes meso- and…

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Authors

2

Topics & keywords

Keywords
  • Lactide
  • Chemistry
  • Polymerization
  • Tacticity
  • Polymer chemistry
  • Yttrium
  • Ring-opening polymerization
  • Catalysis
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