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Effects of Thiophene-Fused Isomer on High-Layered Crystallinity in π‑Extended and Alkylated Organic Semiconductors

Here, we systematically investigated the effects of the thiophene-fused isomer and the end-cap substitution on high-layered crystallinity, film formability, and field-effect transistor characteristics in π-extended and alkylated organic semiconductors (OSCs). We developed four kinds of unsymmetric r...

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Published in:Chemistry of materials 2024-01, Vol.36 (2), p.848-859
Main Authors: Higashino, Toshiki, Inoue, Satoru, Arai, Shunto, Tsuzuki, Seiji, Matsui, Hiroyuki, Kumai, Reiji, Takaba, Kiyofumi, Maki-Yonekura, Saori, Kurokawa, Hirofumi, Inoue, Ichiro, Tono, Kensuke, Yonekura, Koji, Hasegawa, Tatsuo
Format: Article
Language:English
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Summary:Here, we systematically investigated the effects of the thiophene-fused isomer and the end-cap substitution on high-layered crystallinity, film formability, and field-effect transistor characteristics in π-extended and alkylated organic semiconductors (OSCs). We developed four kinds of unsymmetric rod-like OSCs based on syn-/anti-isomers of benzothieno­[6,5-b]-/benzothieno­[5,6-b]-benzothieno­[3,2-b]­thiophene (BTBTT) with phenyl/alkyl substitutions with different alkyl chain lengths: synCn and antiCn (n = 6, 10). The layered molecular packing motifs of the compounds are distinct from the thiophene orientation of isomeric π-cores but are unaffected by the alkyl chain length. The synCn forms a bilayer-type layered herringbone (b-LHB) packing composed of head-to-head arrangement of unidirectionally aligned molecular layers showing high-layered crystallinity and high carrier mobility over 10 cm2 V–1 s–1. By contrast, the antiCn forms an antiparallel alkyl-interdigitated herringbone (aai-HB) structure in which the respective π-core layer is composed of alternating antiparallel alignment of π-cores and the alkyl chains are interdigitated with each other between the adjacent π-core layers. The latter shows relatively poor crystalline-film formability and moderate carrier mobility. Dispersion-corrected density functional theory calculations of intermolecular interaction energy reveal that the overall shape of the rigid π-core components is crucial for achieving unidirectionally aligned and closely packed 2D π-core layers and that the flexible end-cap substituents strengthen and balance the layered crystallinity. The findings will be crucial for designing and developing the highly layered crystalline and high-performance OSCs.
ISSN:0897-4756
1520-5002
DOI:10.1021/acs.chemmater.3c02500