IP Library Granted Patent US 11,637,250
Granted Patent B2
US 11,637,250 · App. 16/860,261 · Granted Apr 25, 2023

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; SK Materials JNC Co., Ltd.
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 11,637,250
App. No.
16/860,261
Granted
Apr 25, 2023
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 (34)

1. A compound represented by the following general formula (A-1)

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

3. The compound of 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.

4. The compound of 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.

5. The compound of 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.

6. The compound of claim 1 , in which 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).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2021
From: JNC CORPORATION
To: SK MATERIALS JNC CO., LTD.
Reel/Frame 056038/0288 →
Priority Claims (1)
JP 2015-045902 · Mar 9, 2015 · national
Continuity (2)
Division 15556551
Related Publication 20200259089A1 · Aug 13, 2020