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New Ground for Organic Catalysis: A Ring-Opening Polymerization Approach to Hydrogels
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文摘
Herein, we describe an organocatalytic living polymerization approach to network and subsequent hydrogelformation. Cyclic carbonate-functionalized macromolecules were ring-opened using an alcoholic initiator in thepresence of an organic catalyst, amidine 1,8-diazabicyclo[5.4.0]undec-7-ene. A model reaction for the cross-linking identified monomer concentration-dependent reaction regimes, and enhanced kinetic control wasdemonstrated by introducing a comonomer, trimethylene carbonate. The addition of the comonomer facilitatednear-quantitative conversion of monomer to polymer (>96%). Resulting poly(ethylene glycol) networks swellsignificantly in water, and an open co-continuous (water-gel) porous structure was observed by scanning electronmicroscopy. The organocatalytic ring-opening polymerization of cyclic carbonate functional macromonomersusing alcoholic initiators provides a simple, efficient, and versatile approach to hydrogel networks.

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