Effects of Molecular Structure of the Resins on the Volumetric Shrinkage and the Mechanical Strength of Dental Restorative Composites

L. U. Kim, J. W. Kim, and C. K. Kim*
School of Chemical Engineering and Materials Science, Chung-Ang University, 221 Huksuk-dong. Dongjak-gu, Seoul, 156-756 Korea
Biomacromolecules, 2006, 7 (9), pp 2680–2687
DOI: 10.1021/bm060453h
Publication Date (Web): August 17, 2006
Copyright © 2006 American Chemical Society
*

 To whom correspondence should be addressed.

Abstract

Abstract Image

To prepare a dental composite that has a low amount of curing shrinkage and excellent mechanical strength, various 2,2-bis[4-(2-hydroxy-3-methacryloyloxy propoxy) phenyl] propane (Bis-GMA) derivatives were synthesized via molecular structure design, and afterward, properties of their mixtures were explored. Bis-GMA derivatives, which were obtained by substituting methyl groups for hydrogen on the phenyl ring in the Bis-GMA, exhibited lower curing shrinkage than Bis-GMA, whereas their viscosities were higher than that of Bis-GMA. Other Bis-GMA derivatives, which contained a glycidyl methacrylate as a molecular end group exhibited reduced curing shrinkage and viscosity. Methoxy substitution for hydroxyl groups on the Bis-GMA derivatives was performed for the further reduction of the viscosity and curing shrinkage. Various resin mixtures, which had the same viscosity as the commercial one, were prepared, and their curing shrinkage was examined. A resin mixture containing 2,2-bis[3,5-dimethyl, 4-(2-methoxy-3-methacryloyloxy propoxy) phenyl] propane] (TMBis-M-GMA) as a base resin and 4-tert-butylphenoxy-2-methyoxypropyl methacrylate (t-BP-M-GMA) as a diluent exhibited the lowest curing shrinkage among them. The composite prepared from this resin mixture also exhibited the lowest curing shrinkage along with enhanced mechanical properties.

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History

  • Published In Issue September 11, 2006
  • Received May 10, 2006
    Revised Manuscript Received July 2, 2006

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