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
Link To Document :
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