IP Library Granted Patent US 10,680,186
Granted Patent B2
US 10,680,186 · App. 15/556,551 · Granted Jun 9, 2020

Polycyclic aromatic compound and light emitting layer-forming composition

Inventors: Takuji Hatakeyama (Hyogo, JP); Yasuhiro Kondo (Chiba, JP); Keiichi Nakamoto (Chiba, JP); Motoki Yanai (Chiba, JP)
Assignees: Kwansei Gakuin Educational Foundation; JNC Corporation
H01L51/008C07F5/02C07F5/027C09K11/025C09K11/06H01L51/0059H01L51/50H05B33/14H05B33/20H01L51/0007H01L51/0037H01L51/0085H01L51/5016H01L2251/308
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,680,186
App. No.
15/556,551
Granted
Jun 9, 2020
Kind
B2
Abstract

The present invention addresses the problem of providing a polycyclic aromatic compound which has improved solubility in solvents, film formability, wet coatability and in-plane orientation. The above-described problem is solved by a composition for forming a light emitting layer, which contains, as a first component, at least one compound selected from the group consisting of compounds represented by general formula (A-1) and compounds represented by general formula (A-2), as a second component, at least one compound that has a triplet energy (E T ) of 1.8-3.0 eV, and as a third component, at least one organic solvent. In the formulae, R represents a hydrogen atom, an aryl group, a heteroaryl group, a diarylamino group, a diheteroarylamino group or an aryl heteroarylamino group.

Claims (70)

1. A light emitting layer-forming composition for applying and forming a light emitting layer of an organic electroluminescent element, comprising:

at least one selected from the group consisting of a compound represented by the following general formula (A-1) and a compound represented by the following general formula (A-2) as a first component;

at least one compound having triplet energy (E T ) of 1.8 to 3.0 eV as a second component; and

at least one organic solvent as a third component

(In general formula (A-1),

R 1 to R 11 each independently represent a hydrogen atom, an aryl, a heteroaryl, a diarylamino, a diheteroarylamino, an arylheteroarylamino, or an aryloxy, while at least one hydrogen atom in these may be further substituted by an aryl, a heteroaryl, or a diarylamino,

adjacent groups among R 1 to R 11 may be bonded to each other to form an aryl ring or a heteroaryl ring together with ring a, ring b, or ring c, at least one hydrogen atom in the ring thus formed may be substituted by an aryl, a heteroaryl, a diarylamino, a diheteroarylamino, an arylheteroarylamino, or an aryloxy, at least one hydrogen atom in these may be further substituted by an aryl, a heteroaryl, or a diarylamino,

at least one hydrogen atom in a compound represented by the above formula (A-1) may be substituted by a group represented by the following general formula (FG-1), a group represented by the following general formula (FG-2), an alkyl having 1 to 24 carbon atoms, a halogen atom, or a deuterium atom,

any —CH 2 — in the alkyl may be substituted by —O— or —Si(CH 3 ) 2 —, any —CH 2 — excluding —CH 2 — directly bonded to a compound represented by the above formula (A-1) in the alkyl may be substituted by an arylene having 6 to 24 carbon atoms, and any hydrogen atom in the alkyl may be substituted by a fluorine atom)

(In general formula (A-2),

R 1 to R 16 each independently represent a hydrogen atom, an aryl, a heteroaryl, a diarylamino, a diheteroarylamino, an arylheteroarylamino, or an aryloxy, while at least one hydrogen atom in these may be further substituted by an aryl, a heteroaryl, or a diarylamino,

adjacent groups among R 1 to R 16 may be bonded to each other to form an aryl ring or a heteroaryl ring together with ring a, ring b, ring c, or ring d, at least one hydrogen atom in the ring thus formed may be substituted by an aryl, a heteroaryl, a diarylamino, a diheteroarylamino, an arylheteroarylamino, or an aryloxy, at least one hydrogen atom in these may be further substituted by an aryl, a heteroaryl, or a diarylamino,

at least one hydrogen atom in a compound represented by the above formula (A-2) may be substituted by a group represented by the following general formula (FG-1), a group represented by the following general formula (FG-2), an alkyl having 1 to 24 carbon atoms, a halogen atom, or a deuterium atom,

any —CH 2 — in the alkyl may be substituted by —O— or —Si(CH 3 ) 2 —, any —CH 2 — excluding —CH 2 — directly bonded to a compound represented by the above formula (A-2) in the alkyl may be substituted by an arylene having 6 to 24 carbon atoms, and any hydrogen atom in the alkyl may be substituted by a fluorine atom)

(In general formula (FG-1),

R's each independently represent a fluorine atom, a trimethylsilyl, a trifluoromethyl, an alkyl having 1 to 24 carbon atoms, or a cycloalkyl having 3 to 24 carbon atoms, any —CH 2 — in the alkyl may be substituted by —O—, any —CH 2 -excluding —CH 2 -directly bonded to a phenyl or a phenylene in the alkyl may be substituted by an arylene having 6 to 24 carbon atoms, at least one hydrogen atom in the cycloalkyl may be substituted by an alkyl having 1 to 24 carbon atoms or an aryl having 6 to 12 carbon atoms,

when two adjacent R's each represent an alkyl or a cycloalkyl, these R's may be bonded to each other to form a ring,

m's each independently represent an integer of 0 to 4,

n's each independently represent an integer of 0 to 5, and

p's each independently represent an integer of 1 to 5)

(In general formula (FG-2),

R's each independently represent a fluorine atom, a trimethylsilyl, a trifluoromethyl, an alkyl having 1 to 24 carbon atoms, a cycloalkyl having 3 to 24 carbon atoms, or an aryl having 6 to 12 carbon atoms, any —CH 2 — in the alkyl may be substituted by —O—, any —CH 2 — excluding —CH 2 — directly bonded to a phenyl or a phenylene in the alkyl may be substituted by an arylene having 6 to 24 carbon atoms, at least one hydrogen atom in the cycloalkyl may be substituted by an alkyl having 1 to 24 carbon atoms or an aryl having 6 to 12 carbon atoms, at least one hydrogen atom in the aryl may be substituted by an alkyl having 1 to 24 carbon atoms,

when two adjacent R's each represent an alkyl or a cycloalkyl, these R's may be bonded to each other to form a ring,

m's each independently represent an integer of 0 to 4, and

n's each independently represent an integer of 0 to 5).

2. The light emitting layer-forming composition described in claim 1 , in which the first component comprises a compound represented by the above formula (A-1).

3. The light emitting layer-forming composition described in claim 1 , in which

in the above formula (A-1),

R 1 to R 11 each independently represent a hydrogen atom, an aryl having 6 to 30 carbon atoms, a heteroaryl having 2 to 30 carbon atoms or a diarylamino (the aryl is an aryl having 6 to 12 carbon atoms), at least one hydrogen atom in these may be further substituted by an aryl having 6 to 30 carbon atoms, a heteroaryl having 2 to 30 carbon atoms or a diarylamino (the aryl is an aryl having 6 to 12 carbon atoms),

adjacent groups among R 1 to R 11 may be bonded to each other to form an aryl ring having 9 to 16 carbon atoms or a heteroaryl ring having 6 to 15 carbon atoms together with ring a, ring b, or ring c, at least one hydrogen atom in the ring thus formed may be substituted by an aryl having 6 to 30 carbon atoms, a heteroaryl having 2 to 30 carbon atoms or a diarylamino (the aryl is an aryl having 6 to 12 carbon atoms), at least one hydrogen atom in these may be further substituted by an aryl having 6 to 30 carbon atoms, a heteroaryl having 2 to 30 carbon atoms or a diarylamino (the aryl is an aryl having 6 to 12 carbon atoms), and

at least one hydrogen atom in a compound represented by the above formula (A-1) may be substituted by a group represented by the above formula (FG-1), a group represented by the above formula (FG-2), an alkyl having 1 to 24 carbon atoms, a halogen atom, or a deuterium atom.

4. The light emitting layer-forming composition described in claim 1 , in which

in the above formula (A-1),

R 1 to R 11 each independently represent any one selected from the group consisting of a hydrogen atom and groups represented by the following formulas (RG-1) to (RG-10), and

the groups represented by the following formulas (RG-1) to (RG-10) are each bonded to the above formula (A-1) at *, and

at least one hydrogen atom in a compound represented by the above formula (A-1) is substituted by a group represented by the above formula (FG-1), a group represented by the above formula (FG-2), or an alkyl having 7 to 24 carbon atoms.

5. The light emitting layer-forming composition described in claim 1 , in which

a compound represented by the above formula (A-1) is a compound represented by the following formula (1-1-z), (1-49-z), (1-91-z), (1-100-z), (1-152-z), (1-176-z), (1-1048-z), (1-1049-z), (1-1050-z), (1-1069-z), (1-1101-z), (1-1102-z), or (1-1103-z)

(z's in the above formulas each represent a hydrogen atom, a group represented by the above formula (FG-1), a group represented by the above formula (FG-2), or an alkyl having 7 to 24 carbon atoms, and not all z's represent hydrogen atoms).

6. The light emitting layer-forming composition described in claim 1 , in which the first component comprises a compound represented by the above formula (A-2).

7. The light emitting layer-forming composition described in claim 1 , in which

in the above formula (A-2),

R 1 to R 16 each independently represent a hydrogen atom, an aryl having 6 to 30 carbon atoms, a heteroaryl having 2 to 30 carbon atoms or a diarylamino (the aryl is an aryl having 6 to 12 carbon atoms), at least one hydrogen atom in these may be further substituted by an aryl having 6 to 30 carbon atoms, a heteroaryl having 2 to 30 carbon atoms or a diarylamino (the aryl is an aryl having 6 to 12 carbon atoms),

adjacent groups among R 1 to R 16 may be bonded to each other to form an aryl ring having 9 to 16 carbon atoms or a heteroaryl ring having 6 to 15 carbon atoms together with ring a, ring b, or ring c, at least one hydrogen atom in the ring thus formed may be substituted by an aryl having 6 to 30 carbon atoms, a heteroaryl having 2 to 30 carbon atoms or a diarylamino (the aryl is an aryl having 6 to 12 carbon atoms), at least one hydrogen atom in these may be further substituted by an aryl having 6 to 30 carbon atoms, a heteroaryl having 2 to 30 carbon atoms or a diarylamino (the aryl is an aryl having 6 to 12 carbon atoms), and

at least one hydrogen atom in a compound represented by the above formula (A-2) may be substituted by a group represented by the above formula (FG-1), a group represented by the above formula (FG-2), an alkyl having 1 to 24 carbon atoms, a halogen atom, or a deuterium atom.

8. The light emitting layer-forming composition described in claim 1 , in which

in the above formula (A-2),

R 1 to R 16 each independently represent any one selected from the group consisting of a hydrogen atom and groups represented by the above formulas (RG-1) to (RG-10),

the groups represented by the above formulas (RG-1) to (RG-10) are each bonded to the above formula (A-2) at *, and

at least one hydrogen atom in a compound represented by the above formula (A-2) is substituted by a group represented by the above formula (FG-1), a group represented by the above formula (FG-2), or an alkyl having 7 to 24 carbon atoms.

9. The light emitting layer-forming composition described in claim 1 , in which

in the above formula (FG-1), m and n each represent 0, and p represents an integer of 1 to 3, and

in the formula (FG-2), m and n each represent 0.

10. The light emitting layer-forming composition described in claim 1 , in which at least one hydrogen atom in a compound represented by the above formula (A-1) or a compound represented by the above formula (A-2) is substituted by a group represented by the above formula (FG-1).

11. The light emitting layer-forming composition described in claim 1 , in which the second component is at least one selected from the group consisting of a compound represented by the following general formula (B-1) and a compound represented by the following general formula (B-2)

(In general formula (B-1),

M represents at least one selected from the group consisting of Ir, Pt, Au, Eu, Ru, Re, Ag, and Cu, n represents an integer of 1 to 3, and “(X-Y)'s” each independently represent a bidentate monoanionic ligand)

ED-Ln-EA  (B-2)

(In general formula (B-2),

ED represents an electron-donating group, Ln represents a bonding group, EA represents an electron-accepting group, and an energy difference (ΔS 1 T 1 ) between singlet energy (S 1 ) and triplet energy (T 1 ) of a compound represented by formula (B-2) is 0.2 eV or less).

12. The light emitting layer-forming composition described in claim 1 , in which the boiling point of at least one organic solvent in the third component is from 130° C. to 300° C.

13. The light emitting layer-forming composition described in claim 1 , in which

the third component comprises a good solvent (GS) and a poor solvent (PS) for a compound represented by the above formula (A-1) and/or a compound represented by the above formula (A-2), and

the boiling point (BP GS ) of the good solvent (GS) is lower than the boiling point (BP PS ) of the poor solvent (PS).

14. The light emitting layer-forming composition described in claim 1 , in which

the content of the first component is from 0.0999% by weight to 8.0% by weight with respect to the total weight of the light emitting layer-forming composition,

the content of the second component is from 0.0001% by weight to 2.0% by weight with respect to the total weight of the light emitting layer-forming composition, and

the content of the third component is from 90.0% by weight to 99.9% by weight with respect to the total weight of the light emitting layer-forming composition.

15. An organic electroluminescent element comprising a light emitting layer formed using the light emitting layer-forming composition described in claim 1 .

16. A display apparatus comprising the organic electroluminescent element described in claim 15 .

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2021
From: JNC CORPORATION
To: SK MATERIALS JNC CO., LTD.
Reel/Frame 056038/0288 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2017
From: KONDO, YASUHIRO; NAKAMOTO, KEIICHI; YANAI, MOTOKI
To: JNC CORPORATION
Reel/Frame 043525/0956 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2017
From: HATAKEYAMA, TAKUJI
To: KWANSEI GAKUIN EDUCATIONAL FOUNDATION
Reel/Frame 043526/0218 →
Priority Claims (1)
JP 2015-045902 · Mar 9, 2015 · national
Continuity (1)
Related Publication 20180040821A1 · Feb 8, 2018
Cited By (3)
US 12,439,821 US 12,568,759 US 12,666,801