Abstract
Two kinds of ladder-type conjugated polymers were concisely synthesized by the formation of single-stranded conjugated polymers via Stille cross-couplings, followed by nitrogen-directed electrophilic borylations at electron-rich aromatic rings. The resulting BN-annulated polymers show good film-forming behaviors and high air and thermal stability. Their structurally shape-persistent rigid backbones render them with π-extended conjugation, allowing for efficient light harvesting in the low-energy regions, and emitting strong fluorescence with narrow emission widths.
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