Issue 13, 2009

Bis(phenanthroimidazolyl)biphenyl derivatives as saturated blue emitters for electroluminescent devices

Abstract

Blue-emitting bis(phenanthroimidazolyl)biphenyl derivatives, 4,4′-bis(1-phenyl-1H-phenanthro[9,10-d]phenanthroimidazolyl-2-yl)biphenyl (PPIP), 4,4′-bis(1-p-tolyl-1H-phenanthro[9,10-d]phenanthroimidazolyl-2-yl)biphenyl (TPIP) and 4,4′-bis(1-p-anisyl-1H-phenanthro[9,10-d]phenanthroimidazolyl-2-yl)biphenyl (APIP) were effectively synthesized in high yields from commercially available starting materials through a simple two-step procedure without using expensive noble-metal catalysts. These compounds showed excellent thermal properties with a very high glass-transition temperature of 197–200 °C and emitted intense blue light in solution with emission peaks at ca. 428 and 446 nm. By using a different hole-transporting layer, we optimized the electroluminescent efficiencies of the PPIP-based devices. All the PPIP-based devices were turned on at very low applied voltages of <3.0 V and gave pure-blue light with a Commission Internationale d'Énclairage y-coordinate value (CIEy) ≤ 0.15. Among them, device C using TCTA (4,4′,4″-tris(N-carbazolyl)triphenylamine) as the hole-transporting layer reached a very high external quantum efficiency of 6.31% and power efficiency of 7.30 lm/W. When using TPIP or APIP as the emissive layer to replace PPIP in the optimal device C, the resulting devices also exhibited very high external quantum efficiencies of more than 5%, and highly saturated blue light can be obtained from the TPIP-based device with CIEy ≤ 0.10.

Graphical abstract: Bis(phenanthroimidazolyl)biphenyl derivatives as saturated blue emitters for electroluminescent devices

Supplementary files

Article information

Article type
Paper
Submitted
17 Sep 2008
Accepted
19 Dec 2008
First published
05 Feb 2009

J. Mater. Chem., 2009,19, 1865-1871

Bis(phenanthroimidazolyl)biphenyl derivatives as saturated blue emitters for electroluminescent devices

C. Kuo, T. Li, C. Lien, C. Liu, F. Wu and M. Huang, J. Mater. Chem., 2009, 19, 1865 DOI: 10.1039/B816327H

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