Abstract
Four novel small molecules featuring central 1,2,5,6-tetrathiocin (TTC) units fusing two oligothiophene chains have been prepared, characterised and their structures elucidated through X-ray crystallography. These compounds have been evaluated as p-channel semiconductors in organic field-effect transistor devices, representing the first time that any tetrathiocin-containing compound has been utilised in organic transistors. Through extensive optimisation, involving the screening of different processing solvents, surface treatments, post-processing conditions, dielectric materials, and device configurations, hole mobilities (μh) in the 10−2 cm2 V−1 s−1 range were obtained for the most optimised devices, with the highest value of 7.3 × 10−2 cm2 V−1 s−1 achieved in 5T-TTC. The double-cable design, established through two parallel oligothiophene chains in the same molecule bridged by a tetrathiocin core, provides improved device characteristics over analogous double-cable oligothiophenes with tetrathiafulvalene and germanium cores.
| Original language | English |
|---|---|
| Pages (from-to) | 19260-19270 |
| Number of pages | 11 |
| Journal | Journal of Materials Chemistry C |
| Volume | 13 |
| Issue number | 37 |
| Early online date | 19 Aug 2025 |
| DOIs | |
| Publication status | Published - 7 Oct 2025 |
Funding
RGDT, JC and PJS thank the EPSRC for funding (EP/L012200/1 and EP/T022477/1). The work at Wake Forest University (M. M. and O. D. J.) was supported by the National Science Foundation under Awards ECCS-1810273 and DMR 2323423. LRS acknowledges support from the National Science Foundation Research Experience for Undergraduates Programme under award number CHE-0755206.
Keywords
- oligothiophene chains
- organic transistors
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