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We show that photoinitiated electron/energy transfer–reversible addition–fragmentation chain transfer (PET-RAFT) enables vastly superior control over the polymerization of multiblock star copolymers compared to conventional techniques. Monomodal distributions with dispersities 95% conversion in each block extension. The improvement in control is likely due to the reabsorption of the free radical at the propagating chain end by the excited catalyst, which would otherwise lead to a termination product. Simple modeling shows the dramatic effect that this has in the case of star polymerizations. Because PET-RAFT is also tolerant to oxygen, we were able to automate the synthesis of up to heptablock stars at short block lengths, providing a useful technique for screening the effect of polymer composition on the solution structure.
Foster et al. (Wed,) studied this question.