The synthesis of seven crosslinking vinylcyclopropanes bearing urethane groups is described. These monomers were synthesized by esterification of 1-ethoxycarbonyl-2-vinylcyclopropane-1-carboxylic acid with either ethylene glycol or diethylene glycol, followed by a reaction with selected diisocyanates
In order to evaluate the reactivity of the synthesized vinylcyclopropanes, their photopolymerization behavior was investigated by photo-differential scanning calorimetry
Real-time-NIR-photorheology measurements were performed to evaluate rheological behavior and chemical conversion of the vinylcyclopropanes in situ. Composites based on these monomers show good to excellent mechanical properties and exhibit low shrinkage
The presence of urethane groups provides a significant improvement of the mechanical properties
The replacement of methacrylates by urethane vinylcyclopropanes appears to be a promising approach to develop low-shrinkage dental composites without sacrificing the mechanical properties
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