An imidazole-based organocatalyst designed for bulk polymerization of lactide isomers: inspiration from Nature
The design of an imidazole-based salt by enzyme-mimicking allowed controlling the ring-opening polymerization of L- and D-LA monomers in bulk. Kinetic study supports a bifunctional activation process only slightly different from the one occurring in Nature.
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2012-12, Vol.48 (95), p.11695-11697 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The design of an imidazole-based salt by enzyme-mimicking allowed controlling the ring-opening polymerization of L- and D-LA monomers in bulk. Kinetic study supports a bifunctional activation process only slightly different from the one occurring in Nature. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c2cc37061a |