http://www.cnr.it/ontology/cnr/individuo/prodotto/ID169162
First disubstituted dibenzothiophene-5,5-dioxide monodispersed molecular materials for efficient blue-electroluminescence. (Articolo in rivista)
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- Label
- First disubstituted dibenzothiophene-5,5-dioxide monodispersed molecular materials for efficient blue-electroluminescence. (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/b913628b (literal)
- Alternative label
Grisorio, R.; Melcarne, G.; Suranna, G. P.; Mastrorilli, P.; Nobile, C. F.; Cosma, P.; Fini, P.; Colella, S.; Fabiano, E.; Piacenza, M.; Della Sala, F.; Ciccarella, G.; Mazzeo, M.; Gigli, G. (2010)
First disubstituted dibenzothiophene-5,5-dioxide monodispersed molecular materials for efficient blue-electroluminescence.
in Journal of materials chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Grisorio, R.; Melcarne, G.; Suranna, G. P.; Mastrorilli, P.; Nobile, C. F.; Cosma, P.; Fini, P.; Colella, S.; Fabiano, E.; Piacenza, M.; Della Sala, F.; Ciccarella, G.; Mazzeo, M.; Gigli, G. (literal)
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- 1. Polytech Bari, Dept Water Engn & Chem, Bari, Italy
2. INFM, CNR, NNL, I-73100 Lecce, Italy (G. Melcarne, E. Fabiano, F. Della Sala, G. Ciccarella, M. Mazzeo, G. Gigli)
3. Univ Salento, Scuola Super ISUFI, I-73100 Lecce, Italy
4. Univ Bari, Dept Chem, Bari, Italy
5. Univ Salento, Dept Innovat Engn, I-73100 Lecce, Italy (literal)
- Titolo
- First disubstituted dibenzothiophene-5,5-dioxide monodispersed molecular materials for efficient blue-electroluminescence. (literal)
- Abstract
- This study reports oil the first monodispersed molecular materials embodying the dibenzothiophene-5,5-dioxide core for the achievement of blue electroluminescence. The core has been functionalised in its 2.8- or 3,7-positions with dimethyl-fluorene (2,8-DBTOF and 3,7-DBTOF) or methyl-carbazole (2,8-DBTOC and 3,7-DBTOC) groups. The obtained compounds were characterised by (1)H and (13)C NMR, APCI-MS, thermal analysis (TGA and DSQ and cyclic voltammetry. Their optical and photophysical properties were investigated by UV and PL measurements as well as by time-dependent density-functional theory calculations. The materials were successfully employed as active layers ill blue to purplish blue p-i-n OLED devices. that reached, in the case of 3,7-DBTOC, performances as high as 11 422 cd m(-2) and 3.25 cd A(-1). (literal)
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