Abstract

Organic molecules are emerging candidates for the next generation of cost-effective active materials of Li-ion batteries. Small diimide building blocks such as pyromellitic diimide (PMDI) have attracted much attention because of their high theoretical capacity. Many strategies have been undertaken to limit the well-known phenomenon of dissolution of the active material in the electrolyte. Such strategies include the preparation of salts and the synthesis of polyimides or macrocycles. Since dibromopyromellitic dimiide exhibits almost no sp2 cross-coupling polymerization reaction by conventional synthetic routes (Suzuki–Miyaura or Migita–Stille), we used PMDI as an aromatic C–H bond-bearing unit for direct (hetero)arylation polymerization (DHAP) with 1,4-dibromobenzene as comonomer as a new stabilization strategy. DHAP proved to be an effective tool in the preparation of this polymer, yielding a number-average molecular weight of up to 31 kDa. We studied the effect of side-chain engineering using variable c...

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