Journal
SYNTHETIC METALS
Volume 155, Issue 3, Pages 490-494Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.synthmet.2005.06.014
Keywords
pentacene precursor; alcohol soluble; organic transistors
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A novel pentacene precursor was synthesized by Diels-Alder reaction of pentacene and N-sulfinylbutylcarbamate. The adduct is highly soluble in isopropyl and higher alcohols and moderately soluble in ethanol and methanol. This precursor undergoes retro-Diels-Aider reaction in solid phase at low temperatures to give pentacene. Organic thin film transistors with pentacene channels obtained by solution deposition of this novel precursor from alcohols and subsequent thermal conversion, results in OTFTs with moderately high field effect mobilities. (C) 2005 Elsevier B.V. All rights reserved.
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