IP Library Granted Patent US 9,478,750
Granted Patent B2
US 9,478,750 · App. 14/375,243 · Granted Oct 25, 2016

Anthracene derivative and organic electroluminescent element using the same

Inventors: Toshihiro Koike (Chiba, JP); Yohei Ono (Chiba, JP)
Assignee: JNC CORPORATION
H01L51/0058C07D213/06C07D213/16C07D401/10C09K11/06H01L51/0052H01L51/0072H01L51/0096H01L51/5072H01L51/5092Y02E10/549
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Quick Facts
Patent No.
US 9,478,750
App. No.
14/375,243
Granted
Oct 25, 2016
Kind
B2
Abstract

This organic electroluminescent element is manufactured by using an anthracene derivative having a pyridyl aryl group substituted with an alkyl represented by formula (1) as an electron transport material, and satisfies characteristics such as the following in an adequate and well-balanced manner: improves the external quantum efficiency of the light-emitting element, which is generally required by the electron transport material; reduces the drive voltage of the light-emitting element; and increases the life of the element. (In formula (1), Ar is a divalent or trivalent benzene or naphthalene; R is hydrogen or an alkyl with a carbon number of 1 to 6, but all of the Rs never simultaneously form hydrogen; and R 1 to R 4 are, individually, hydrogen, an alkyl with a carbon number of 1 to 6, a cycloalkyl with a carbon number of 3 to 6, or an aryl with a carbon number of 6 to 20.)

Claims (39)

1. An anthracene derivative represented by the following formula (1):

wherein

Ars are each independently divalent or trivalent benzene or naphthalene,

Rs are each independently hydrogen or an alkyl having a carbon number of 1 to 6, with which Ar or pyridine is substituted, and not all Rs are hydrogen simultaneously, and

R 1 , R 2 , R 3 and R 4 are each independently hydrogen, an alkyl having a carbon number of 1 to 6, a cycloalkyl having a carbon number of 3 to 6 or an aryl having a carbon number of 6 to 20.

2. The anthracene derivative according to claim 1 , wherein

moieties consisting of Ar and pyridine are each independently a group represented by any of the following formula (Py-1) to formula (Py-12):

wherein

Rs are each independently hydrogen or an alkyl having a carbon number of 1 to 4, with which a group represented by any of the formula (Py-1) to formula (Py-12) is substituted, and not all Rs are hydrogen simultaneously, and

R 1 is hydrogen, an alkyl having a carbon number of 1 to 6 or an aryl having a carbon number of 6 to 20, and R 2 , R 3 and R 4 are hydrogen.

3. The anthracene derivative according to claim 2 , wherein

moieties consisting of Ar and pyridine are both a group represented by any of the formula (Py-1) to formula (Py-9),

two Rs binding to Ar are both hydrogen and two Rs binding to pyridine are both an alkyl having a carbon number of 1 to 4, or two Rs binding to Ar are both an alkyl having a carbon number of 1 to 4 and two Rs binding to pyridine are both hydrogen, and

R 1 is hydrogen, an alkyl having a carbon number of 1 to 4, phenyl, biphenylyl, terphenylyl or naphthyl, and R 2 , R 3 and R 4 are hydrogen.

4. The anthracene derivative according to claim 2 , wherein

moieties consisting of Ar and pyridine are both a group represented by any of the formula (Py-1) to formula (Py-9),

two Rs binding to Ar are both hydrogen, and one of two Rs binding to pyridine is an alkyl having a carbon number of 1 to 4 and the other is hydrogen, and

R 1 is hydrogen, an alkyl having a carbon number of 1 to 4, phenyl, biphenylyl, terphenylyl or naphthyl, and R 2 , R 3 and R 4 are hydrogen.

5. The anthracene derivative according to claim 2 , wherein

moieties consisting of Ar and pyridine are both a group represented by any of the formula (Py-1) to formula (Py-6),

two Rs binding to Ar are both hydrogen, and two Rs binding to pyridine are both an alkyl having a carbon number of 1 to 4, and

R 1 is hydrogen, phenyl, terphenylyl or naphthyl, and R 2 , R 3 and R 4 are hydrogen.

6. The anthracene derivative according to claim 2 , wherein

moieties consisting of Ar and pyridine are both a group represented by any of the formula (Py-1) to formula (Py-6),

two Rs binding to Ar are both an alkyl group having a carbon number of 1 to 4, and two Rs binding to pyridine are both hydrogen, and

R 1 is hydrogen or phenyl, and R 2 , R 3 and R 4 are hydrogen.

7. The anthracene derivative according to claim 2 , wherein

moieties consisting of Ar and pyridine are both a group represented by any of the formula (Py-1) to formula (Py-6),

two Rs binding to Ar are both hydrogen, and one of two Rs binding to pyridine is an alkyl having a carbon number of 1 to 4 and the other is hydrogen, and

R 1 is hydrogen or phenyl, and R 2 , R 3 and R 4 are hydrogen.

8. The anthracene derivative according to claim 1 , which is represented by the following formula (1-34), formula (1-35), formula (1-38), formula (1-39), formula (1-40), formula (1-41), formula (1-50) or formula (1-51)

9. The anthracene derivative according to claim 1 , which is represented by the following formula (1-6), formula (1-36), formula (1-44), formula (1-45), formula (1-151), formula (1-164), formula (1-236), formula (1-249) or formula (1-262)

10. The anthracene derivative according to claim 1 , which is represented by the following formula (1-46), formula (1-68), formula (1-71), formula (1-72) or formula (1-110)

11. An electron transport material containing the anthracene derivative according to claim 1 .

12. An organic electroluminescent element having a pair of electrodes consisting of an anode and a cathode, a luminescent layer arranged between the pair of electrodes, and an electron transport layer and/or an electron injection layer, which are arranged between the cathode and the luminescent layer, and contain the electron transport material according to claim 11 .

13. The organic electroluminescent element according to claim 12 , wherein at least one of the electron transport layer and the electron injection layer further contains at least one selected from the group consisting of a quinolinol metal complex, a pyridine derivative, a bipyridine derivative, a phenanthroline derivative, a borane derivative and a benzimidazole derivative.

14. The organic electroluminescent element according to claim 12 , wherein at least one of the electron transport layer and the electron injection layer further contains at least one selected from the group consisting of an alkali metal, an alkaline earth metal, a rare earth metal, an oxide of an alkali metal, a halide of an alkali metal, an oxide of an alkaline earth metal, a halide of an alkaline earth metal, an oxide of a rare earth metal, a halide of a rare earth metal, an organic complex of an alkali metal, an organic complex of an alkaline earth metal and an organic complex of a rare earth metal.

15. A display device equipped with the organic electroluminescent element according to claim 12 .

16. A lighting device equipped with the organic electroluminescent element according to claim 12 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2021
From: JNC CORPORATION
To: SK MATERIALS JNC CO., LTD.
Reel/Frame 056079/0808 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2014
From: KOIKE, TOSHIHIRO; ONO, YOHEI
To: JNC CORPORATION
Reel/Frame 033412/0779 →
Priority Claims (2)
JP 2012-021657 · Feb 3, 2012 · national
JP 2012-107229 · May 9, 2012 · national
Continuity (1)
Related Publication 20150014671A1 · Jan 15, 2015