“…The neutral intermediates G1‐2R 1 , G2‐4R 1 , and G4‐8R 1 were synthesized by a simple esterification reaction of G1‐OH , G2‐2OH , and G4‐4OH with the carboxyl compound 1 , respectively, which were then reacted with iodomethane (CH 3 I) and followed by an anion exchange reaction with LiTFSI according to the procedures in literature, providing three 1,6‐heptadiyne derivatives, called as ionic monomers M1 , M2 , and M3 with di‐, tetra‐, or octo‐substituents of 1,2,3‐triazolium bearing short OEG segments. Lastly, MCP of monomers was carried out by the catalysis of Ru ‐ III at 30 °C to afford the corresponding iPAs, as shown in Scheme .…”