Journal
SYNTHETIC METALS
Volume 156, Issue 2-4, Pages 327-331Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.synthmet.2005.12.014
Keywords
organic semiconductors; organic field-effect transistors; heterocyclic synthesis; co-oligomers; thermal, optical and electrochemical measurement
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Novel five-membered heterocyclic or phenylene oligomers containing a thiazolothiazole ring system have been investigated as active materials of organic field-effect transistors (OFETs). The cyclic voltammetry and X-ray diffractogram studies revealed the relationship between the molecular structures of these co-oligomers and FET performance. The field-effect mobilities of 10(-4) to 10(-3) cm(2)/VS were obtained for the furyl derivatives and their FET performances as p-type semiconductors are presented as the first examples, of FET behavior of oligomers including furan rings. (c) 2006 Elsevier B.V. All rights reserved.
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