Typical bimolecular photoinitiators (PIs) for radical polymerization of acrylates show only poor photoreactivity because of the unwanted effect of back electron transfer. Therefore, a PI system consisting of benzaldoxime esters and 4‐methyl benzophenone was investigated by photo‐differential scanning calorimetry experiments. Surprisingly, reactivities are comparable to that of classical monomolecular Type I PIs like Darocur 1173, probably because of an energy transfer from the triplet state of the benzophenone‐based sensitizer to the oxime ester initiator. Furthermore, sufficient thermal stability was proven by TGA and storage stability experiments of a resin formulation under elevated temperature.
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Dworak et al. (2010) studied this question.
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