posted on 2022-07-06, 11:36authored byHenry Foster, Martina H. Stenzel, Robert Chapman
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 <1.3 could be achieved after the 10th block despite
pushing the polymerization to >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.