Abstract
Asymmetrically-substituted smectic liquid crystals with a small core of benzo[1, 2-b:4, 5-b']dithiophene (BDT) substituted with monoalkyl and phenyl groups, 6-alkyl-2-phenyl-benzo[1, 2-b:4, 5-b']dithiophene (Ph-BDT-Cn, n = 8, 14), were synthesized, and their mesomorphism and properties of crystalline films were characterized for solution-processed OFETs. Both compounds exhibited the SmE phase, and their crystalline films derived from SmE films exhibited the crystal-to-crystal transition from the monolayered crystals as-fabricated to the bilayered crystals when thermally annealed. The FET mobility was significantly enhanced by a factor of 2 to 10, accompanied with the phase transition to the bilayered crystals and reached up to 0.59 cm2 V-1 s-1 in spite of a small core of BDT. We discuss a new strategy of molecular design of soluble OFET materials behind the present results.
Original language | English |
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Pages (from-to) | 510-513 |
Number of pages | 4 |
Journal | Chemistry Letters |
Volume | 47 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2018 |
Externally published | Yes |
Keywords
- Benzodithiophene
- Bilayer
- Organic field effect transistor (OFET)
ASJC Scopus subject areas
- Chemistry(all)