Bm. Culbertson et al., PREPARATION AND EVALUATION OF VISIBLE-LIGHT-CURED MULTI-METHACRYLATESFOR DENTAL COMPOSITES, Journal of macromolecular science. Pure and applied chemistry, A34(12), 1997, pp. 2405-2421
To explore new VLC oligomers exhibiting low shrinkage, low water sorpt
ion, and improved mechanical properties, a family of multi-methacrylat
es, based on poly(isopropylidenediphenol) resin (BPA), was synthesized
, characterized, and evaluated. The BPA resin, having an average of ei
ght phenolic hydroxyl groups per molecule, was treated with ethylene c
arbonate and the resultant product esterified at four different grafte
d levels, using methacryloyl chloride. Structures of these EEBPA oligo
mers, were confirmed by FT-SR and C-13 NMR. The EEBPA oligomer/TEGDMA
(50/50, w/w) blends were combined with 0.5 wt% camphoroquinone(CQ) and
1.0 wt% N,N-dimethylaminoethyl methacrylate (DMAEM). The control was
BisGMA/TEGDMA (50/50, w/w) blends having the same levels of CQ/DMAEM.
Differential photocalorimetry (DPC) and differential scanning calorime
try (DSC) showed the multi-methacrylate/TEGDMA (neat resin) blends hav
e polymerization characteristics comparable to the BisGMA/TEGDMA contr
ol. These multi-functional oligomers have lower polymerization shrinka
ge and lower uptake of water and other liquids. In addition, two exper
imental oligomers EEBPA #2 and #3 have higher compressive strength tha
n the BisGMA and comparable diametral tensile strength to the BisGMA c
ontrol. These results suggest that the new type of multi-functional me
thacrylate oligomers (EEBPA) have potential application in formulating
dental composites with improved properties.