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Synthesis and modeling of new phosphorus-containing acrylates

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WILEY
DOI: 10.1002/pola.20733

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adhesives; dental polymers; modeling; photopolymerization; radical polymerization; synthesis

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New methacrylate monomers containing phosphonic acid or both phosphonic and carboxylic acids were synthesized through the reaction of t-butyl alpha-bromomethyl acrylate with triethyl phosphite followed by the selective hydrolysis of the phosphonate or t-butyl ester groups with trimethylsilyl bromide and trifluoroacetic acid. The copolymerization of these monomers with 2-hydroxyethylmethacrylate was investigated with photodifferential scanning calorimetry at 40 degrees C with 2,2 '-dimethoxy-2-phenyl acetophenone as a photoinitiator. Quantum mechanical tools were also used to understand the mechanistic behavior of the polymerization reactions of these synthesized monomers. The propagation and chain-transfer reactions were considered and rationalized. A strong effect of the monomer structure on the rate of polymerization was observed. The polymerization reactivities of the monomers increased with decreasing steric hindrance and/or increasing hydrogen-bonding capacity because of the hydrolysis of the phosphonate and the t-butyl ester groups. (c) 2005 Wiley Periodicals, Inc.

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