Electron-accepting compound and composition for charge-transporting film, and luminescent element using same

Patent metadata

Field	Value
Publication number	US-11793069-B2
Application number	US-202217694143-A
Country	US
Kind code	B2
Filing date	Mar 14, 2022
Priority date	Mar 24, 2016
Publication date	Oct 17, 2023
Grant date	Oct 17, 2023

Abstract

The present invention provides with an electron-accepting compound having a structure of the following formula (1):

First claim

The invention claimed is:

1. An electron-accepting compound having a structure of the following formula (1):

wherein
Ar is each independently a substituted or unsubstituted aromatic ring group or a fluorine-substituted alkyl group,
at least one Ar has a crosslinkable group,
F 4 represents a substitution with four fluorine atoms,
F (5-a) represents a substitution with (5-a) fluorine atom(s),
k each independently represents an integer of 0 to 5,
a each independently represents an integer of 0 to 5,
k+a is 1 to 10, and
X + represents a counter cation having a structure of the following formula (2):

wherein Ar 5 and Ar 6 are each independently an aromatic ring group which may have a substituent,
wherein X + does not represent octyloxy diphenyl iodonium.

2. The electron-accepting compound according to claim 1 , wherein k is 0, a is 1, and Ar is each independently a substituted or unsubstituted aromatic ring group.

3. The electron-accepting compound according to claim 1 , wherein at least one Ar is represented by the following formula (3):

wherein Ar 7 is a substituent and F 4 represents a substitution with four fluorine atoms; and
wherein Ar 7 is represented by the following formula (4).

4. The electron-accepting compound according to claim 1 , wherein the formula (2) is represented by the following formula (5):

wherein Ar 8 and Ar 9 represent a substituent.

5. The electron-accepting compound according to claim 1 , wherein at least one Ar of the formula (1) has a crosslinkable group selected from the crosslinking groups represented by the following formulae (Z-1) to (Z-7):

wherein * represents a bonding point and wherein the formulae (Z-1) to (Z-7) optionally further comprises a cyclic or non-cyclic aliphatic group having 30 or less carbon atoms, an aryl group having 30 or less carbon atoms, an alkyloxy group having 30 or less carbon atoms, or an aralkyl group having 30 or less carbon atoms.

6. The electron-accepting compound according to claim 1 , wherein at least one Ar of the formula (1) has a crosslinkable group selected from the crosslinking groups represented by the following formulae (7) and (8):

wherein * represents a bonding point and wherein the formulae (7) and (8) optionally further comprise a substituent selected from the group consisting of a hydrogen atom, a halogen atom, a cyano group, an aromatic ring group having 1 to 5 aromatic rings, a hydrocarbon ring group, an alkyl group, an alkenyl group, an alkynyl group, an aralkyl group, an alkyloxy group, an aryloxy group, an alkylthio group, an arylthio group, an alkyl ketone group, and an aryl ketone group and adjacent substituents may be combined to form a ring, and the aromatic ring group having 1 to 5 aromatic rings, the hydrocarbon ring group, the alkyl group, the alkenyl group, the alkynyl group, the aralkyl group, the alkyloxy group, the aryloxy group, the alkylthio group, the arylthio group, the alkyl ketone group, or the aryl ketone group optionally further comprise a substituent selected from the group consisting of a halogen atom, an alkyl group, and an aryl group.

7. A composition suitable for a charge-transporting film, comprising the electron-accepting compound according to claim 1 and a hole-transporting compound.

8. The composition according to claim 7 , wherein the hole-transporting compound is an aromatic tertiary amine compound.

9. The composition according to claim 7 , wherein the hole-transporting compound has a crosslinkable group.

10. The composition according to claim 7 , wherein the hole-transporting compound is an aromatic tertiary amine polymer compound.

11. The composition according to claim 7 , which further comprises a solvent.

12. The composition according to claim 11 , wherein the solvent contains at least one solvent selected from the group consisting of an ether-based solvent and an ester-based solvent.

13. The composition according to claim 12 , wherein the solvent further contains an aromatic hydrocarbon-based solvent.

14. A method for forming a charge-transporting film comprising applying the composition of claim 11 to a substrate and drying the composition.

15. A method for manufacturing an organic electroluminescent element comprising a hole injection layer or a hole-transporting layer and a luminescent layer between an anode and a cathode and that emits light by electric energy, the method comprising applying the composition of claim 11 to a substrate and drying the composition to form the hole injection layer or the hole-transporting layer.

16. An organic electroluminescent element comprising a hole injection layer or a hole-transporting layer and a luminescent layer between an anode and a cathode and emitting light by electric energy, wherein the hole injection layer or the hole-transporting layer is a layer formed by applying and drying the composition for a charge-transporting film according to claim 11 to form a film.

17. A display, comprising the organic electroluminescent element according to claim 16 .

18. A lighting device, comprising the organic electroluminescent element according to claim 16 .

19. A light-emitting device, comprising the organic electroluminescent element according to claim 16 .

20. The composition according to claim 7 , which is used for a hole injection layer of an organic electroluminescent element or a hole-transporting layer of the organic electroluminescent element.

21. An electron-accepting compound having a structure of the following formula (1);

wherein
Ar is each independently a substituted or unsubstituted aromatic ring group and at least one Ar has a crosslinkable group,
F 4 represents a substitution with four fluorine atoms,
F (5-a) represents a substitution with (5-a) fluorine atom(s)
k is 0
a is 1,
k+a is 1, and
X + represents a counter cation having a structure of the following formula (2):

wherein Ar 5 and Ar 6 are each independently an aromatic ring group which may have a substituent, and
wherein X + does not represent octyloxy diphenyl iodonium.

22. The electron-accepting compound according to claim 21 , wherein at least one Ar of the formula (1) has a crosslinkable group selected from the crosslinking groups represented by the following formulae (Z-1) to (Z-7):

wherein * represents a bonding point and wherein the formulae (Z-1) to (Z-7) optionally further comprises a cyclic or non-cyclic aliphat

Assignees

• Mitsubishi Chem Corp

Inventors

• Gorohmaru Hideki
• Okabe Kazuki
• Iida Koichiro
• Umemoto Tomokazu
• Bando Yoshimasa
• Ishibashi Koichi
• KAJIYAMA Yoshiko
• Abe Tomohiro

Classifications

• H10K71/00

  Manufacture or treatment specially adapted for the organic devices covered by this subclass · CPC title

• H10K85/611 Primary

  Charge transfer complexes · CPC title

• C07F5/027 Primary

  Organoboranes and organoborohydrides · CPC title

• C08L65/02

  Polyphenylenes · CPC title

• G09F9/30

  in which the desired character or characters are formed by combining individual elements (panels comprising a number of electrodes in a single cell controlling light arriving from an independent light source, e.g. electro-optical or magneto-optical cell, G02F1/00) · CPC title