IP Library Granted Patent US 11,508,909
Granted Patent B2
US 11,508,909 · App. 16/489,777 · Granted Nov 22, 2022

Organic electronic material and use of same

Inventors: Ryota Moriyama (Hitachi, JP); Naoki Asano (Tsukuba, JP); Iori Fukushima (Tsukuba, JP); Hiroshi Takaira (Hitachinaka, JP); Kazuyuki Kamo (Tsukuba, JP); Shunsuke Kodama (Tsukuba, JP)
Assignee: Showa Denko Materials Co., Ltd.
H01L51/0035C08G61/12C09D11/102G09F9/35H01L27/3232H01L51/0043C08G2261/124C08G2261/1412C08G2261/18C08G2261/228C08G2261/312C08G2261/3162C08G2261/3222C08G2261/334C08G2261/51C08G2261/95H01L51/5088
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Quick Facts
Patent No.
US 11,508,909
App. No.
16/489,777
Granted
Nov 22, 2022
Kind
B2
Abstract

An organic electronic material containing a charge transport compound having at least one of the structural regions represented by formulas (1), (2) and (3) shown below. In the formulas, Ar represents an arylene group or heteroarylene group of 2 to 30 carbon atoms, a represents an integer of 1 to 6, b represents an integer of 2 to 6, c represents an integer of 2 to 6, and X represents a substituted or unsubstituted polymerizable functional group. —Ar—O—(CH 2 ) a —O—CH 2 —X  (1) —Ar—(CH 2 ) b —O—CH 2 —X  (2) —Ar—O—(CH 2 ) c —X  (3)

Claims (25)

1. An organic electronic material comprising a charge transport compound having a divalent structural unit, a trivalent or higher structural unit, and a monovalent structural unit represented by formula (3) shown below:

—Ar—O—(CH 2 ) c —X  (3)

wherein Ar represents an arylene group or heteroarylene group of 2 to 30 carbon atoms, c represents an integer of 5 to 6, and X represents a substituted or unsubstituted polymerizable functional group,

wherein the polymerizable functional group comprises at least one group selected from an oxetane group, epoxy group, vinyl group, acryloyl group and methacryloyl group substituted with a saturated alkyl group with 1 to 4 carbon atoms or an unsubstituted oxetane group, epoxy group, vinyl group, acryloyl group and methacryloyl group,

wherein a proportion of the trivalent or higher structural unit based on a total of all the structural units is at least 1 mol % and not more than 50 mol %, and

wherein a thermal weight reduction upon heating at 300° C. of the charge transport compound is not more than 3.5% by mass relative to a mass of the charge transport compound prior to heating.

2. The organic electronic material according to claim 1 , wherein the structural unit represented by the formula (3) comprises a structure represented by formula 3-1 shown below:

wherein c represents an integer of 5 to 6, and R represents a methyl group or an ethyl group.

3. The organic electronic material according to claim 1 , wherein the charge transport compound has hole injection properties.

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

5. The organic electronic material according to claim 1 , wherein a molar ratio between the divalent structural unit, the monovalent structural unit, and the trivalent or higher structural unit is 100:(10 to 200):(10 to 100).

6. An ink composition comprising the organic electronic material according to claim 1 , and a solvent.

7. An organic layer formed using the organic electronic material according to claim 1 .

8. An organic electronic element comprising the organic layer according to claim 7 .

9. An organic electroluminescent element comprising the organic layer according to claim 7 .

10. A display element comprising the organic electroluminescent element according to claim 9 .

11. An illumination device comprising the organic electroluminescent element according to claim 9 .

12. A display device comprising the illumination device according to claim 11 , and a liquid crystal element as a display unit.

13. An organic layer formed using the ink composition according to claim claim 6 .

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

15. An organic electroluminescent element comprising the organic layer according to claim 13 .

16. A display element comprising the organic electroluminescent element according to claim 15 .

17. An illumination device comprising the organic electroluminescent element according to claim 15 .

18. A display device comprising the illumination device according to claim 17 , and a liquid crystal element as a display unit.

19. The organic electronic material according to claim 1 , wherein a proportion of the monovalent structural unit represented by formula (3) based on a total of all monovalent structural units is at least 50 mol %.

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 Oct 13, 2022
From: HITACHI CHEMICAL COMPANY, LTD.
To: SHOWA DENKO MATERIALS CO., LTD.
Reel/Frame 061669/0028 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 29, 2019
From: MORIYAMA, RYOTA; ASANO, NAOKI; FUKUSHIMA, IORI; TAKAIRA, HIROSHI; KAMO, KAZUYUKI; KODAMA, SHUNSUKE
To: HITACHI CHEMICAL COMPANY, LTD.
Reel/Frame 050216/0633 →
Priority Claims (1)
JP JP2017-039341 · Mar 2, 2017 · national
Continuity (1)
Related Publication 20200013956A1 · Jan 9, 2020