TY - JOUR
T1 - Design and synthesis of 2-substituted-8-hydroxyquinline zinc complexes with hole-transporting ability for highly effective yellow-light emitters
AU - Ouyang, Xinhua
AU - Wang, Guangrong
AU - Zeng, Heping
AU - Zhang, Weiming
AU - Li, Jing
N1 - Funding Information:
Financial support from the National Natural Science Foundation of China (Nos. 20671036, 2007A010500008 and 2008B010800030) are gratefully acknowledged. Ouyang X H would like to acknowledge the receipt of the Doctorate Foundation from South China University of Technology (SCUT), Guangzhou and the China Scholarship Council. J.L. is a Cheung Kong Guest Chair Professor associated with SCUT.
PY - 2009/10/1
Y1 - 2009/10/1
N2 - Four multifunctional 8-hydroxyquinoline derivatives were designed and synthesized, their structures were identified by FT-IR, 1H NMR, MS and elemental analysis. Among them are (E)-2-(2-(9-(4-methoxyphenyl)-9H-carbazol-3-yl)vinyl) quinolato-zinc (1), (E)-2-(2-(9-p-tolyl-9H-carbazol-3-yl)vinyl)quinolato-zinc (2), (E)-2-(2-(9H-fluoren-2-yl)vinyl)quinolato-zinc (3), and (E)-2-(2-(phenanthren-9-yl)vinyl)quinolato-zinc (4). The electroluminescence (EL) and hole-transporting characteristics of these materials were investigated on four configurations: (A) ITO/2-TNATA/NPB/1, 2, 3 or 4/Alq3/LiF/Al; (B) ITO/2-TNATA/NPB/1, 2, 3 or 4/LiF/Al; (C) ITO/2-TNATA/1, 2, 3 or 4/Alq3/LiF/Al; and (D) ITO/2-TNATA/1 or 2/NPB/Alq3/LiF/Al. The maximum luminescence and current efficiencies of are 3556 cd m-2 (at 13 V) and 2.17 cd A-1 (at 9 V) for compound 2, 4624 cd m-2 (at 15 V) and 2.1 cd A-1 (at 7 V) for compound 3, and 3164 cd m-2 (at 14 V) and 1.83 cd A-1 (at 13 V) for compound 4 in the configuration D, respectively, indicating that they are good multifunctional materials with strong hole-transporting abilities and luminescence properties.
AB - Four multifunctional 8-hydroxyquinoline derivatives were designed and synthesized, their structures were identified by FT-IR, 1H NMR, MS and elemental analysis. Among them are (E)-2-(2-(9-(4-methoxyphenyl)-9H-carbazol-3-yl)vinyl) quinolato-zinc (1), (E)-2-(2-(9-p-tolyl-9H-carbazol-3-yl)vinyl)quinolato-zinc (2), (E)-2-(2-(9H-fluoren-2-yl)vinyl)quinolato-zinc (3), and (E)-2-(2-(phenanthren-9-yl)vinyl)quinolato-zinc (4). The electroluminescence (EL) and hole-transporting characteristics of these materials were investigated on four configurations: (A) ITO/2-TNATA/NPB/1, 2, 3 or 4/Alq3/LiF/Al; (B) ITO/2-TNATA/NPB/1, 2, 3 or 4/LiF/Al; (C) ITO/2-TNATA/1, 2, 3 or 4/Alq3/LiF/Al; and (D) ITO/2-TNATA/1 or 2/NPB/Alq3/LiF/Al. The maximum luminescence and current efficiencies of are 3556 cd m-2 (at 13 V) and 2.17 cd A-1 (at 9 V) for compound 2, 4624 cd m-2 (at 15 V) and 2.1 cd A-1 (at 7 V) for compound 3, and 3164 cd m-2 (at 14 V) and 1.83 cd A-1 (at 13 V) for compound 4 in the configuration D, respectively, indicating that they are good multifunctional materials with strong hole-transporting abilities and luminescence properties.
KW - 2-Substituted-8-hydroxyquinolate-zinc
KW - Multifunctional material
KW - Yellow-light emitting material
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U2 - 10.1016/j.jorganchem.2009.06.022
DO - 10.1016/j.jorganchem.2009.06.022
M3 - Article
AN - SCOPUS:68949221586
SN - 0022-328X
VL - 694
SP - 3511
EP - 3517
JO - Journal of Organometallic Chemistry
JF - Journal of Organometallic Chemistry
IS - 21
ER -