Synthesis and Characterization of Novel Quaternary Ammonium Urethane-Dimethacrylate Monomers-A Pilot Study

Six novel urethane-dimethacrylate analogues (QAUDMAs) were synthesized and characterized. They consisted of the 2,4,4,-trimethylhexamethylene diisocyanate (TMDI) core and two methacrylate-terminated wings containing quaternary ammonium groups substituted with alkyl chains of 8, 10, 12, 14, 16, or 18 carbon atoms. QAUDMAs, due to the presence of quaternary ammonium groups, may have possible antibacterial effects. Since they showed satisfactory physicochemical properties, they will be subjected to further research towards the development of dental composites with a capacity to reduce secondary caries. The synthesis of QAUDMAs included three stages: (i) transesterification of methyl methacrylate (MMA) with N-methyldiethanolamine (MDEA), (ii) N-alkylation of the tertiary amino group with alkyl bromide, and (iii) addition of TMDI to the intermediate achieved in the second stage. The formation of QAUDMAs was confirmed by H-1 and C-13 NMR. They were characterized for density (d(m)), viscosity (eta), refractive index (RI), glass transition temperature (T-g), polymerization shrinkage (S), and degree of conversion (DC). QAUDMAs were yellow, viscous resins (the eta values ranged from 1.28 x 10(3) to 1.39 x 10(4) Pa center dot s, at 50 degrees C). Their RI ranged from 1.50 to 1.52, T-g from -31 to -15 degrees C, DC from 53 to 78%, and S from 1.24 to 2.99%, which is appropriate for dental applications.

Automated summary

Six novel urethane-dimethacrylate analogues (QAUDMAs) were synthesized and characterized, with potential antibacterial effects for dental applications. They showed satisfactory physicochemical properties and will be further researched for dental composites development. The synthesis of QAUDMAs involved three stages, and their characteristics including density, viscosity, refractive index, glass transition temperature, polymerization shrinkage, and degree of conversion were determined.