Abstract

The evolution of the polymerization-induced shrinkage stress and mechanical properties of thiol−allyl ether−methacrylate ternary systems and their relationship to the polymerization kinetics have been investigated. Because of the two distinct polymerization regimes of the ternary systemsa methacrylate homopolymerization regime followed by a thiol−ene polymerization dominated regimethe mechanism for the evolution of polymerization induced shrinkage stress is unique as compared to other thiol−ene and methacrylate systems. During the first polymerization stage, only intermediate molecular weight methacrylate oligomers are produced, resulting in delayed gelation and near zero shrinkage stress. Immediately following the first polymerization stage, the allyl ether begins to polymerize, and shrinkage stress increases in correspondence with the increased allyl ether conversion. It is observed that the shrinkage stress of the ternary systems exhibits ∼50% of the shrinkage stress of the current dental restoration s...

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