Abstract
We describe synthesis and characterization of a series of novel multifunctional methacrylate-based dental monomers. Triethanolamine was reacted with glycidyl methacrylate and methacryloyl chloride to produce a series of multifunctional methacrylate-end-capped compounds for conversion to quaternary ammonium fluoride monomers with decyl-substituted side-chain to afford antibacterial dental monomers. The chemical structure of all samples was characterized by Fourier-transform infrared and proton nuclear magnetic resonance (1H NMR) spectroscopies. The obtained monomers have potential to replace 2,2-bis[4-(2-hydroxy-3-methacryloyloxypropyl)phenyl]propane as base monomer of universal resin-based dental composites in presence of diluting monomer (e.g., triethylene glycol dimethacrylate) due to their multifunctionality as well as possible antibacterial activity.
| Original language | English |
|---|---|
| Pages (from-to) | 5707-5722 |
| Number of pages | 16 |
| Journal | Research on Chemical Intermediates |
| Volume | 43 |
| Issue number | 10 |
| DOIs | |
| State | Published - May 2 2017 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2017, Springer Science+Business Media Dordrecht.
ASJC Scopus Subject Areas
- General Chemistry
Keywords
- Antibacterial activity
- Dental monomers
- Multifunctional methacrylate
- Quaternary ammonium fluoride
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