Abstract
Bottlebrush polymers (BBPs) have gained wide attention for their special characters, such as rigid main/side chains, stemming from the exceedingly high graft density. This study aims to provide a simple synthetic approach to BBPs with polyester side chains by merging ring-opening alternating copolymerization (ROAP) and ring-opening metathesis polymerization (ROMP). A simple phosphazene base (tBuP1) is employed for the ROAP of phthalic anhydride and epoxide, after which Grubbs third-generation catalyst (G3) is added to in situ switch on ROMP of the macromonomer, i.e., norbornenyl-ended alternating polyester. The compatibility of tBuP1 with G3 and well-controlled ROMP is evidenced by DOSY-NMR of mixed catalysts, characterization of BBPs, and side-chain degradation. The method can also be extended to BBPs with one-step synthesized block copolyesters side chains. These results highlight the strength of the non-nucleophilic organobase catalyst for convenient construction of complex (degradable) polymers with compositional diversity.
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