4.2 Article

Aluminum Schiff base catalysts derived from β-diketone for the stereoselective polymerization of racemic lactides

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WILEY
DOI: 10.1002/pola.21108

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biodegradable; crystal structures; enolic; ring-opening polymerization; stereoselective

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Two aluminum Schiff base catalysts with the formula LA1Et [L = bis(benzoylacetone)trimethylenediimine (1) or bis(benzoylacetone)ethylenediimine (2)] were designed and synthesized for a comparison of their catalytic properties in the polymerization of racemic lactides. Single-crystal data of catalyst 1 confirmed its trigonal bipyramidal configuration with a five-coordinated aluminum atom in the center. These catalysts were shown to be highly active and stereoselective for the controlled ring-opening polymerization of racemic lactides.

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