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Based on Friedel–Crafts acylation, nonstoichiometric polycondensation was achieved using 4,4′-dicarboxydiphenyl ether and 2,2′-dimethoxybiphenyl in trifluoromethanesulfonic acid. The decrease in the acylation reactivity of 2,2′-dimethoxybiphenyl by protonation and the increase in the acylation reactivity of the monoacylated species by deprotonation play a key role in successful nonstoichiometric polycondensations.

Graphical abstract: Nonstoichiometric polycondensation based on Friedel–Crafts acylation in superacids for the syntheses of aromatic polyketones

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