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Synthesis and field-effect properties of alfa,omega-disubstituted sexithiophenes bearing polar groups (Articolo in rivista)
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- Synthesis and field-effect properties of alfa,omega-disubstituted sexithiophenes bearing polar groups (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/b515583e (literal)
- Alternative label
Dell'Aquila, A., Mastrorilli, P., Nobile, C. F., Romanazzi, G., Suranna, G. P., Torsi, L., Tanese, M. C., Acierno, D., Amendola, E., Morales, P. (2006)
Synthesis and field-effect properties of alfa,omega-disubstituted sexithiophenes bearing polar groups
in Journal of materials chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Dell'Aquila, A., Mastrorilli, P., Nobile, C. F., Romanazzi, G., Suranna, G. P., Torsi, L., Tanese, M. C., Acierno, D., Amendola, E., Morales, P. (literal)
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- Department of Water Engineering and Chemistry (DIAC), Polytechnic
of Bari, via Orabona 4, I-70125, Bari, Italy.
Department of Civil and Environmental Engineering (DICA),
Polytechnic of Bari, via Orabona 4, I-70125, Bari, Italy
Department of Chemistry, T.I.R.E.S. Centre of Excellence, University
of Bari, via Orabona-4, I-70126, Bari, Italy
Department of Materials and Production Engineering (DIMP),
University of Naples Federico II, p.le Tecchio 80, I-80125, Naples, Italy
Institute of Composite and Biomedical Materials (IMCB), Italys
National Research Council, p.le Tecchio 80, I-80125, Naples, Italy
ENEA, Unita` Materiali e Nuove Tecnologie, Centro Ricerche della
Casaccia, 00060 S. Maria di Galeria, Roma, Italy (literal)
- Titolo
- Synthesis and field-effect properties of alfa,omega-disubstituted sexithiophenes bearing polar groups (literal)
- Abstract
- The synthesis of sexithiophenes bearing amide or ester groups in the Ñ,ç-terminal positions is described, along with their characterization in the solid state. The influence of the functional group on mobilities and on/off ratios of the org. FET devices was investigated. The oligomer bearing the ester functional group sepd. from the sexithiophene core by an ethylene spacer showed a hole field-effect mobility as high as 0.012 cm2 V-1 s-1, which is among the highest reported so far for org. FETs using sexithiophenes modified with polar groups. (literal)
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