Self‐initiation of the UV photopolymerization of brominated acrylates

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Abstract
Brominated aromatic acrylates were found to polymerize rapidly upon exposure to UV light. Moreover, they are able to initiate the UV‐induced polymerization of acrylic formulations that do not contain a conventional photoinitiator. In contrast, the corresponding unbrominated homologues are not effective as initiators. Investigations by real‐time FTIR spectroscopy have shown that the addition of only 1 wt % of a brominated acrylate is sufficient for an efficient initiation. Fast photopolymerization is achieved even if irradiation is carried out at λ > 300 nm where most acrylates do not absorb. Short‐lived transients were studied by laser flash photolysis. The triplet was found to show low sensitivity to oxygen which is because of its very short lifetime. Bromine radicals split of from the acrylates were trapped with bromine ions from tetraethyl ammonium bromide and detected as Br. The resulting quantum yields for the formation of bromine radicals are in the range of up to 0.3. Quantum chemical modeling was carried out to establish a mechanism for the release of bromine radicals. Both bromine and bromophenyl radicals are able to initiate the polymerization reaction. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 4905–4916, 2008

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