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Fully Conjugated Thiophene-Fused Oligo-BODIPYs: A Class of Intensely Near-Infrared Absorbing, Arc-Shaped Materials with up to 31 Linearly-Fused Rings

Qingbao Gong, Jinsong Shao, Wanwan Li, Xing Guo, Shizhang Ling, Yun Wu, Yaxiong Wei, Xinsheng Xu, Xiaochun Jiang, Lijuan Jiao, Erhong Hao

2025Journal of the American Chemical Society46 citationsDOI

Abstract

Structurally well-defined large π-conjugated systems attract significant interest in molecular materials both for their unique electronic/photophysical properties and unexplored structure–property relationships arising from synthetic challenges. Herein, we address this challenge by leveraging a series of polycondensed π-system doping with B, N and S heteroatoms. In our approach, a series of fully conjugated thiophene-fused oligo-BODIPYs with atomic precision have been efficiently synthesized through the combination of intermolecular S N Ar reactions followed by intramolecular aromatic oxidative couplings from halogenated BODIPY precursors. The largest architecture is a fully fused BODIPY octamer, featuring a coplanar backbone of 31 linearly fused rings. The extended π-conjugation causes a dramatic shift of the absorption event from about 500 nm (monomer) to 822 nm (octamer) with extremely high molar absorptivities reaching 800,000 M –1 cm –1, as well as maintaining intense fluorescence intensity (Φ FL up to 0.32), long triplet lifetime (τ T = 0.61–15.4 μs), efficient triplet quantum yields (Φ T = 0.24–0.81) and good singlet oxygen generation abilities. More interestingly, due to the weak aromaticity of thiophene, oligo-BODIPYs exhibit triplet state localization as their conjugation length increases, where the triplet energy remains constant while the singlet energy decreases significantly. Notably, intense near-infrared thermally activated delayed fluorescence (TADF) is observed even in tetramers, hexamers, and octamers. Our findings not only present a new series of heteroatom-doped condensed π-systems but also establish a precise regulation mechanism for singlet–triplet energy levels in molecules with large rigid π-conjugated structures. Furthermore, this work provides a novel strategy for designing next-generation TADF molecules with narrowband emission.

Topics & Concepts

ChemistryThiopheneConjugated systemInfraredArc (geometry)PhotochemistryPolymer chemistryOrganic chemistryPolymerOpticsGeometryMathematicsPhysicsLuminescence and Fluorescent MaterialsPorphyrin and Phthalocyanine ChemistryDendrimers and Hyperbranched Polymers
Fully Conjugated Thiophene-Fused Oligo-BODIPYs: A Class of Intensely Near-Infrared Absorbing, Arc-Shaped Materials with up to 31 Linearly-Fused Rings | Litcius