Issue 47, 2025

Synthesis of sterically unhindered Lewis acidic boron-doped π-conjugated polymers

Abstract

We report the synthesis of sterically unhindered boron-doped π-conjugated polymers via polymerization of organo-dilithium reagents with boron trichloride. The resulting polymer exhibits Lewis acidity and catalyzes the transesterification of methyl benzoate. This performance is attributed to the electron-accepting ability, and thermally labile Lewis acid–base interactions, facilitating catalytic turnover.

Graphical abstract: Synthesis of sterically unhindered Lewis acidic boron-doped π-conjugated polymers

Supplementary files

Article information

Article type
Communication
Submitted
06 Aug 2025
Accepted
08 Nov 2025
First published
17 Nov 2025
This article is Open Access
Creative Commons BY-NC license

Polym. Chem., 2025,16, 5035-5039

Synthesis of sterically unhindered Lewis acidic boron-doped π-conjugated polymers

N. Takahashi and Y. Nishina, Polym. Chem., 2025, 16, 5035 DOI: 10.1039/D5PY00783F

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