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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 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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. |
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ISSN: | 0897-4756 1520-5002 |
DOI: | 10.1021/acs.chemmater.3c02500 |