Benzo[1,2-b:4,5-b']bis[b]benzothiophene as solution processible organic semiconductor for field-effect transistors

Benzo[1,2-b:4,5-b']bis[b]benzothiophene as solution processible organic semiconductor for field-effect transistors

Coplanar benzo[1,2-b:4,5-b']bis[b]benzothiophenes (, ) for the application in organic field-effect transistors were synthesized by a simple two-step procedure involving triflic acid induced ring-closure reaction; such solution processed devices show a hole mobility of up to 0.01 cm(2) V(-1) s(-...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2008-01 (13), p.1548-1550
Hauptverfasser: Gao, Peng, Beckmann, Dirk, Tsao, Hoi Nok, Feng, Xinliang, Enkelmann, Volker, Pisula, Wojciech, Müllen, Klaus
Format: Artikel
Sprache:eng
Schlagworte:
Crystallography, X-Ray
Cyclization
Mesylates - chemistry
Models, Molecular
Molecular Structure
Semiconductors
Solutions - chemistry
Thiophenes - chemical synthesis
Thiophenes - chemistry
Transistors, Electronic
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Zusammenfassung:Coplanar benzo[1,2-b:4,5-b']bis[b]benzothiophenes (, ) for the application in organic field-effect transistors were synthesized by a simple two-step procedure involving triflic acid induced ring-closure reaction; such solution processed devices show a hole mobility of up to 0.01 cm(2) V(-1) s(-1).
ISSN:1359-7345
1364-548X
DOI:10.1039/b717608b