Fused Hexacyclic Thienoquinoids Terminated by Indandione for Low Bandgap Organic Semiconductors

Abstract

Two indandione-terminated quinoidal compounds, Q4T and Q4T-4F, featuring a fused-ring thiophene-thieno[3,2-b]thiophene-thiophene (4T) as the central core, were designed and synthesized. The extended π-conjugation of the 4T unit, combined with the quinoidal framework, significantly broadens the absorption spectrum, achieving a low-energy onset of up to 1107 nm. Despite their extended π-conjugation, both Q4T and Q4T-4F exhibit good stability in air, even under UV irradiation. In organic thin-film transistors, both compounds demonstrate electron-transporting behavior. Notably, Q4T-4F exhibits higher electron mobility than Q4T, which is attributed to its closer three-dimensional molecular stacking, as revealed by single-crystal analysis. This unique packing facilitates more efficient electron hopping between molecules. These findings provide an effective strategy for designing and synthesizing low-bandgap n-type molecules with good stability.

Supplementary files

Article information

Article type
Paper
Submitted
18 Feb 2025
Accepted
06 May 2025
First published
07 May 2025

J. Mater. Chem. C, 2025, Accepted Manuscript

Fused Hexacyclic Thienoquinoids Terminated by Indandione for Low Bandgap Organic Semiconductors

Y. Xu, T. Du, Y. Deng and Y. Geng, J. Mater. Chem. C, 2025, Accepted Manuscript , DOI: 10.1039/D5TC00699F

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