Title of article
Pentacene precursors for solution-processed OFETs
Author/Authors
Hiroki Uoyama، نويسنده , , Hiroko Yamada، نويسنده , , Tetsuo Okujima، نويسنده , , Hidemitsu Uno، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
6
From page
6889
To page
6894
Abstract
15-Acetoxy- and 15-hydroxy-6,13-dihydro-6,13-ethanopentacenes sublimed over 300 °C and no pentacene was formed below the temperature. The precursors bearing chlorinated epithiomethano bridges suffered complicated decomposition to give oligomeric pentacene derivatives. The precursor bearing an epithio–oxomethano bridge underwent smooth and clean conversion to pentacene by heat or light. An organic field-effect transistor fabricated by the spin-coating method of the precursor followed by light irradiation at 120 °C showed a good FET performance of μ=2.5×10−2 cm2 V−1 s−1 and on/off ratio=3.8×104.
Keywords
retro-Diels–Alder reaction , Organic field-effect transistor , Photochemical cycloreversion , Thermolysis , Pentacene
Journal title
Tetrahedron
Serial Year
2010
Journal title
Tetrahedron
Record number
1101213
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