http://www.cnr.it/ontology/cnr/individuo/prodotto/ID54226
New dithieno[3,2-b:2',3'-d]thiophene oligomers as promising materials for organic field-effect transistor (Articolo in rivista)
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- New dithieno[3,2-b:2',3'-d]thiophene oligomers as promising materials for organic field-effect transistor (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.synthmet.2004.08.004 (literal)
- Alternative label
Iosip M.D.; Destri S.; Pasini M.; Porzio W.; Pernstich K.P.; Batlogg B. (2004)
New dithieno[3,2-b:2',3'-d]thiophene oligomers as promising materials for organic field-effect transistor
in Synthetic metals; Elsevier Science SA, Lausanne (Svizzera)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Iosip M.D.; Destri S.; Pasini M.; Porzio W.; Pernstich K.P.; Batlogg B. (literal)
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- Organic Field-Effect Transistors: Towards Molecular Scale. Proceedings of Symposium E. E-MRS Spring Meeting.
Strasbourg, France
24-28 May 2004 (literal)
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- http://www.sciencedirect.com/science/article/pii/S0379677904003017 (literal)
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- Destri S., Pasini M., Porzio W., ISMAC-CNR
Iosip M.D Univ Milano Bicocca, Dipartimento Sci Mat, Milan, Italy and Inst Macromol Chem, Iasi 6600, Romania
Pernstich K.P., Batlogg B. ETH, Solid State Phys Lab, Swiss Fed Inst Technol, CH-8093 Zurich, Switzerland (literal)
- Titolo
- New dithieno[3,2-b:2',3'-d]thiophene oligomers as promising materials for organic field-effect transistor (literal)
- Abstract
- We designed and synthesized new organic semiconductors for organic field-effect transistor (OFET) using the fused thiophene derivative, dithieno[3,2-b:2',3'-d]thiophene (DTT), as a core of the molecules. In order to understand the influence of dithienothiophene unit on the chemical, physical and electronic properties of the final oligomer we synthesized a related molecule having a fluorene unit as the core, which is known to display different chemical and electronic characteristics. The target co-oligomers based on dithienothiophene and thiophene or fluorene derivatives have been obtained by Suzuki coupling reactions. Electrochemical characterization of these molecules as films evidenced their reversible oxidation, a necessary condition for OFET active material. Their electronic energy scheme is well matched to the high work-function electrodes, gold or platinum. A closely packed face-to-face or face-on stacking arrangements in cast films and highly ordered vacuum-evaporated films are expected in view of the structural packing observed in similar compounds (literal)
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