Synthesis and electroluminescent properties of new amorphous cyclohexyl- and hexyl-substituted ter(9,9-dialkylfluorene)s

Cited 3 time in webofscience Cited 0 time in scopus
  • Hit : 387
  • Download : 0
A series of ter(9,9-dialkylfluorene)s (TFs) containing cyclohexyl and hexyl side groups has been synthesized via the Suzuki coupling reaction. Their chemical structures were characterized by (1)H NMR and (13)C NMR. All TFs were soluble in common organic solvents and showed good thermal stability up to 400 degrees C. In particular, T(CHC)F composed of two 9,9-bis(cyclohexylmethyl)fluorenes and one dihexylfluorene showed improved thermal stability over T(HHH)F and was found to be amorphous, unlikely with T(CCC)F. A light-emitting diode device fabricated with an ITO/2-TNATA/NPB/TFs/Alq3/Liq/Al configuration exhibited blue light emission with EL maxima at 450 nm and EL efficiency of 1.1 cd/A.
Publisher
CHEMICAL SOC JAPAN
Issue Date
2008-07
Language
English
Article Type
Article
Keywords

BLUE-LIGHT; ELECTRON INJECTION; TERFLUORENES; STABILITY; EMISSION; LITHIUM

Citation

CHEMISTRY LETTERS, v.37, no.7, pp.686 - 687

ISSN
0366-7022
DOI
10.1246/cl.2008.686
URI
http://hdl.handle.net/10203/87989
Appears in Collection
CH-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 3 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0