RESUMO
Thermosetting materials generated by photopolymerization frequently suffer from significant shrinkage stress, are often brittle, and have a limited range of mechanical properties. Various classes of chain transfer agents (CTAs) have been investigated and developed to reduce the cross-linking density of photopolymers by terminating chains and initiating new chains in situ. Although CTAs are successful in manipulating the mechanical properties of photopolymers, they are traditionally consumed during the polymerization and are therefore required in high loadings (up to 20 wt % of the total formulation). Moreover, traditional CTAs frequently contain sulfur, which is malodorous and can create unstable formulations. Presented here is a catalytic, sulfur-free CTA that can be added in ppm quantities to existing commercial monomer feedstocks to create photopolymers similar to those prepared using traditional CTAs, but at 10â¯000-fold lower loadings. These catalysts, which are based on macrocyclic cobaloximes, were found to tunably reduce the molecular weight of the chain proportional to catalyst loading. It was shown, using only commercial monomers, that this catalyst could reduce the glass-transition temperature (Tg), rubbery modulus (E'rubbery), and stiffness of a cross-linked photopolymer while utilizing identical processing conditions and keeping 99.99 wt % of the formulation the same.
