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Cp2ZrCl2 is presented as both an effective photoinitiator and additive for radical photopolymerization reactions in aerated conditions. This compound is characterized by remarkable properties: (i) an efficiency higher than that of a reference Type I photoinitiator (2,2-dimethoxy-2-phenylacetophenone, DMPA), (ii) an excellent ability, when added to DMPA, to overcome the oxygen inhibition of the polymerization, and (iii) a never reported in situ photoinduced and oxygen-mediated formation of zirconium-based nanoparticles (diameter ranging from 50 to 70 nm). The photochemical properties of Cp2ZrCl2 are investigated by steady state photolysis and electron spin resonance (ESR) experiments. The high reactivity of this compound is ascribed to a bimolecular homolytic substitution SH2 (clearly characterized by molecular orbital calculations) which converts the peroxyls into new polymerization-initiating radicals and oxygenated Zr-based nanoparticles. In conclusion, Cp2ZrCl2 is characterized by striking and unusual properties when used in a photopolymerization reaction: (i) this is a better initiator than DMPA for polymerization in aerated conditions; (ii) this structure can be used as an additive in combination with a commercial Type I initiator to overcome the oxygen inhibition (very good polymerization profiles were obtained); and (iii) zirconiumbased nanoparticles can be in situ generated, which can further increase the mechanical properties of the photosensible materials. |
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