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.
- This article is part of the themed collection: Polymer Chemistry Open Access Spotlight

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