IP Library Granted Patent US 10,930,857
Granted Patent B2
US 10,930,857 · App. 15/780,402 · Granted Feb 23, 2021

Heterocyclic compound and organic light emitting device using same

Inventors: Jun-Tae Mo (Osan-si, KR); Yong-Geun Jung (Seoul, KR); Won-Jang Jeong (Hwaseong-si, KR); Dae-Hyuk Choi (Yongin-si, KR); Joo-Dong Lee (Seongnam-si, KR)
Assignee: LT MATERIALS CO., LTD.
H01L51/0067C07D215/04C07D401/14C07D471/04C07D519/00C09B57/00C09K11/06H01L51/0052H01L51/0054H01L51/0072H01L51/001H01L51/0081H01L51/0085H01L51/5004H01L51/5012H01L51/5056H01L51/5072H01L51/5088H01L51/5092H01L51/5096H01L51/5278H01L51/56H01L2251/552H01L2251/558
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Quick Facts
Patent No.
US 10,930,857
App. No.
15/780,402
Granted
Feb 23, 2021
Kind
B2
Abstract

The present application provides a hetero-cyclic compound which may significantly improve the service life, efficiency, electrochemical stability, and thermal stability of an organic light emitting device, and an organic light emitting device in which the hetero-cyclic compound is contained in an organic compound layer.

Claims (26)

1. A hetero-cyclic compound represented by the following Chemical Formula 1:

in Chemical Formula 1,

L1 is a direct bond; or a substituted or unsubstituted C 6 to C 60 arylene group,

Ar1 is a substituted pyridine group; a substituted pyrimidine group; a substituted triazine group; a substituted phenanthroline group; or is represented by any one of the following Chemical Formulae 2 to 5:

wherein in Chemical Formulae 2 to 5,

at least one of X1 to X4 is N, O, or S, and the others are CR12,

at least one of X5 to X10 is N, O, or S, and the others are CR13,

at least one of X11 to X14 is N, O, or S, and the others are CR14,

at least one of X15 and X16 is N, O, or S, and the other is CR15,

R12 to R15 are hydrogen,

R1 to R5 and R7 to R11 are hydrogen,

wherein R6 of Chemical Formula 1 is -(L2)m-(Z)n,

L2 is a substituted or unsubstituted C6 to C60 arylene; or a substituted or unsubstituted C2 to C60 heteroarylene,

Z is a substituted or unsubstituted phenyl group; a substituted or unsubstituted biphenyl group; a substituted or unsubstituted naphthyl group; a substituted or unsubstituted triphenylenyl group; a substituted or unsubstituted pyrenyl group; a substituted or unsubstituted anthracenyl group; a substituted or unsubstituted phenanthrenyl group; a substituted or unsubstituted pyridine group; a substituted or unsubstituted pyrimidine group; a substituted or unsubstituted triazine group; a substituted or unsubstituted benzoimidazole group; a substituted or unsubstituted quinoline group; or a substituted or unsubstituted phenanthrolinyl group,

in chemical formula 2, wherein when one of X1 or X4 is N, the others are CR12 and L1 is a direct bond, Z is a substituted or unsubstituted phenyl group; a substituted or unsubstituted biphenyl group; a substituted or unsubstituted naphthyl group; a substituted or unsubstituted triphenylenyl group; a substituted or unsubstituted pyrenyl group; a substituted or unsubstituted anthracenyl group; a substituted or unsubstituted phenanthrenyl group; a substituted pyridine group; a substituted or unsubstituted pyrimidine group; a substituted or unsubstituted triazine group; a substituted or unsubstituted benzoimidazole group; a substituted or unsubstituted quinoline group; or a substituted or unsubstituted phenanthrolinyl group,

m is an integer from 0 to 5, and

n is an integer from 1 to 3.

2. The hetero-cyclic compound of claim 1 , wherein Chemical Formula 1 is represented by any one of the following compounds:

3. An organic light emitting device comprising:

a positive electrode;

a negative electrode; and

an organic material layer having one or more layers disposed between the positive electrode and the negative electrode,

wherein one or more layers of the organic material layer comprise the hetero-cyclic compound of claim 1 .

4. The organic light emitting device of claim 3 , wherein the organic material layer comprises at least one layer of a hole blocking layer, an electron injection layer, an electron transferring layer, an electron transporting layer, and a charge producing layer, and at least one layer of the hole blocking layer, the electron injection layer, the electron transferring layer, the electron transporting layer, and the charge producing layer comprises the hetero-cyclic compound.

5. The organic light emitting device of claim 3 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the hetero-cyclic compound.

6. The organic light emitting device of claim 3 , wherein the organic material layer comprises one or more layers of a hole injection layer, a hole transporting layer, and a layer which injects and transports holes simultaneously, and one layer of the layers comprises the hetero-cyclic compound.

Assignments (2)
CHANGE OF NAME Recorded Feb 13, 2020
From: HEESUNG MATERIAL LTD.
To: LT MATERIALS CO., LTD.
Reel/Frame 051926/0419 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2018
From: MO, JUN-TAE; JUNG, YONG-GEUN; JEONG, WON-JANG; CHOI, DAE-HYUK; LEE, JOO-DONG
To: HEESUNG MATERIAL LTD.
Reel/Frame 045962/0897 →
Priority Claims (1)
KR 10-2015-0170140 · Dec 1, 2015 · national
Continuity (1)
Related Publication 20180366652A1 · Dec 20, 2018