IP Library Granted Patent US 11,398,604
Granted Patent B2
US 11,398,604 · App. 16/347,991 · Granted Jul 26, 2022

Organic electronic material, organic layer, organic electronic element, organic electroluminescent element, display element, illumination device, and display device

Inventors: Kazuyuki Kamo (Tsukuba, JP); Naoki Asano (Tsukuba, JP); Hiroshi Takaira (Hitachinaka, JP); Iori Fukushima (Tsukuba, JP); Shigeaki Funyuu (Tsuchiura, JP)
Assignee: SHOWA DENKO MATERIALS CO., LTD.
H01L51/0072G09F9/30H01L27/32H01L51/007H01L51/0054H01L51/0059H01L51/0067H01L51/0068H01L51/0097H01L51/50H01L51/5016H01L51/5092H05B33/02H01L51/5056H01L51/5072
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Quick Facts
Patent No.
US 11,398,604
App. No.
16/347,991
Granted
Jul 26, 2022
Kind
B2
Abstract

An organic electronic material containing a charge transport compound having a structural region represented by formula (I) and having a weight average molecular weight greater than 40,000. —Ar—X—Y—Z  (I) In the formula, Ar represents an arylene group or heteroarylene group of 2 to 30 carbon atoms, X represents a linking group, Y represents an aliphatic hydrocarbon group of 1 to 10 carbon atoms, and Z represents a substituted or unsubstituted polymerizable functional group.

Claims (29)

1. An organic electronic material comprising a charge transport compound having a weight average molecular weight greater than 40,000 measured by gel permeation chromatography (GPC) using a calibration curve of standard polystyrenes, and exhibiting a thermal weight reduction upon heating to 300° C. of not more than 5% determined by using a thermogravimetric-differential thermal analysis (TG-DTA) apparatus when a 10 mg of the charge transport compound is heated in the air to 300° C. under temperature increase conditions of 5° C./minute,

wherein the charge transport compound is a charge transport polymer having a divalent structural unit with charge transport properties, a trivalent or higher structural unit that constitutes a branched structure in three or more directions, and a monovalent structural unit that constitutes a terminal portion of the charge transport polymer, wherein the monovalent structural unit comprises a structural unit represented by formula (I-3) below:

—Ar—O—(CH 2 ) n —Z  (I-3)

wherein Ar represents an arylene group or heteroarylene group of 2 to 30 carbon atoms, Z represents a substituted or unsubstituted polymerizable functional group, and n is an integer from 1 to 10.

2. The organic electronic material according to claim 1 , wherein the polymerizable functional group includes at least one type of group selected from the group consisting of an oxetane group, an epoxy group, a vinyl group, an acryloyl group and a methacryloyl group.

3. The organic electronic material according to claim 1 , wherein the structural region represented by the formula (I-3) is positioned at a terminal of the charge transport compound.

4. The organic electronic material according to claim 1 , wherein the charge transport compound is a hole injection layer material.

5. The organic electronic material according to claim 1 , wherein the charge transport compound contains at least one type of structure selected from the group consisting of aromatic amine structures, carbazole structures, thiophene structures, bithiophene structures, benzene structures, phenoxazine structures and fluorene structures.

6. The organic electronic material according to claim 1 , wherein the charge transport compound is a charge transport polymer.

7. The organic electronic material according to claim 1 , further comprising a polymerization initiator.

8. The organic electronic material according to claim 7 , wherein the polymerization initiator comprises a cationic polymerization initiator.

9. The organic electronic material according to claim 8 , wherein the cationic polymerization initiator comprises an onium salt.

10. The organic electronic material according to claim 9 , further comprising a solvent.

11. The organic electronic material according to claim 10 , wherein the solvent is a non-polar solvent.

12. An organic layer formed from the organic electronic material according g to claim 1 .

13. An organic electronic element comprising the organic layer according to claim 12 .

14. An organic electroluminescent element comprising the organic layer according to claim 12 .

15. The organic electroluminescent element according to claim 14 , having a light-emitting layer containing a phosphorescent material.

16. The organic electroluminescent element according to claim 14 , having a light-emitting layer containing a thermally activated delayed fluorescent material.

17. The organic electroluminescent element according to claim 14 , also having a flexible substrate.

18. The organic electroluminescent element according to claim 14 , also having a resin film substrate.

19. A display element comprising the organic electroluminescent according to claim 14 .

20. An illumination device comprising the organic electroluminescent element according to claim 14 .

21. A display device comprising the illumination device according to claim 20 , and a liquid crystal element as a display unit.

22. The organic electronic material according to claim 1 , wherein the charge transport compound further contains a structural unit represented by formula (II) below:

—Ar-J-R1  (II)

wherein:

(i) Ar represents an arylene group or heteroarylene group of 2 to 30 carbon atoms, J represents an ester linkage (—COO—), and R1 is a cyclic alkyl group of 3 to 30 carbon atoms, or

(ii) Ar represents an arylene group or heteroarylene group of 2 to 30 carbon atoms, J represents a linking group (—NR—) having a structure in which an additional one hydrogen atom has been removed from an amino group that R is a phenyl group, and R1 represents an arylene group of 6 to 30 carbon atoms.

Assignments (4)
CHANGE OF ADDRESS Recorded Feb 14, 2024
From: RESONAC CORPORATION
To: RESONAC CORPORATION
Reel/Frame 066599/0037 →
CHANGE OF NAME Recorded Mar 8, 2023
From: SHOWA DENKO MATERIALS CO., LTD.
To: RESONAC CORPORATION
Reel/Frame 062992/0805 →
CHANGE OF NAME Recorded Apr 21, 2022
From: HITACHI CHEMICAL COMPANY, LTD.
To: SHOWA DENKO MATERIALS CO., LTD.
Reel/Frame 059746/0578 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2019
From: KAMO, KAZUYUKI; ASANO, NAOKI; TAKAIRA, HIROSHI; FUKUSHIMA, IORI; FUNYUU, SHIGEAKI
To: HITACHI CHEMICAL COMPANY, LTD.
Reel/Frame 049101/0760 →