IP Library Granted Patent US 10,566,105
Granted Patent B2
US 10,566,105 · App. 13/642,522 · Granted Feb 18, 2020

Method for producing charge transport film

Inventors: Kenichi Ishitsuka (Tsukuba, JP); Shigeaki Funyuu (Tsuchiura, JP); Yousuke Hoshi (Tsukuba, JP)
Assignee: HITACHI CHEMICAL COMPANY, LTD.
H01B1/122C08K5/42C08K5/435C08L65/00C09D11/52H01L51/0039H01L51/0043C08G2261/1412C08G2261/1644C08G2261/3142C08G2261/3162C08G2261/411C08G2261/512C08G2261/5222C08G2261/76C08G2261/95H01L51/0085H01L51/5016H01L51/5036H01L51/5048H01L2251/308
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Quick Facts
Patent No.
US 10,566,105
App. No.
13/642,522
Granted
Feb 18, 2020
Kind
B2
Abstract

Disclosed is an organic electronic material comprising charge transporting compounds and ionic compounds having electron-accepting properties and high solubility in a solvent. The organic electronic material is characterized by comprising charge transporting compounds and ionic compounds, and in that at least one of the ionic compounds is any one kind of compounds represented by general formulas (1b)-(3b). (In the formulas Y 1 -Y 6 each independently represent a divalent linking group, R 1 -R 6 each independently represent an electron-attracting organic substituent (these structures can further have substituents and hetero-atoms, and R 1 , R 2 and R 3 , or, R 4 -R 6 can respectively combine and become a ring shape or a polymer shape) and L + represents a monovalent cation.)

Claims (12)

1. A method for producing a charge transport film, the method comprising:

adding at least one polymerization initiator to a charge transporting compound, the charge transporting compound including at least one of an aromatic amine comprising an aromatic ring directly bonded to a nitrogen atom, a carbazole and a thiophene compound, and

polymerizing the charge transporting compound after adding the at least one polymerization initiator to the charge transporting compound, such that polymerizing of the charge transporting compound takes place in the presence of the at least one polymerization initiator and forms the charge transport film so as to impart solvent resistance to the charge transport film,

wherein the at least one polymerization initiator includes at least one of Ionic compound A and Ionic compound J:

2. The method for producing a charge transport film according to claim 1 , wherein the charge transporting compound is a polymer or an oligomer, and has at least one polymerizable substituent.

3. The method for producing a charge transport film according to claim 1 , wherein the at least one polymerization initiator is added to the charge transporting compound in an amount of 0.1% to 50% by mass in the charge transport film.

4. A method for producing a charge transport film, the method comprising:

adding at least one polymerization initiator to a charge transporting compound, the charge transporting compound including at least one of an aromatic amine comprising an aromatic ring directly bonded to a nitrogen atom, a carbazole and a thiophene compound, and

polymerizing the charge transporting compound after adding the at least one polymerization initiator to the charge transporting compound, such that polymerizing of the charge transporting compound takes place in the presence of the at least one polymerization initiator and forms the charge transport film so as to impart solvent resistance to the charge transport film,

wherein the at least one polymerization initiator includes Ionic compound J:

5. The method for producing a charge transport film according to claim 1 , wherein the charge transport film comprises a property of a residual film ratio ranging from 75 to 99%, the residual film ratio being a ratio of an amount of a cured form of the charge transport film remaining after rinsing the cured form of the charge transport film with toluene to an amount of the cured form of the charge transport film before rinsing with toluene.

6. The method for producing a charge transport film according to claim 4 , wherein the charge transport film comprises a property of a residual film ratio ranging from 75 to 99%, the residual film ratio being a ratio of an amount of a cured form of the charge transport film remaining after rinsing the cured form of the charge transport film with toluene to an amount of the cured form of the charge transport film before rinsing with toluene.

Assignments (5)
CHANGE OF ADDRESS Recorded Feb 14, 2024
From: RESONAC CORPORATION
To: RESONAC CORPORATION
Reel/Frame 066599/0037 →
CHANGE OF NAME Recorded Mar 3, 2023
From: SHOWA DENKO MATERIALS CO., LTD.
To: RESONAC CORPORATION
Reel/Frame 062946/0125 →
CHANGE OF NAME Recorded Mar 2, 2023
From: HITACHI CHEMICAL COMPANY, LTD.
To: SHOWA DENKO MATERIALS CO., LTD.
Reel/Frame 062917/0865 →
CHANGE OF ADDRESS Recorded Nov 25, 2019
From: HITACHI CHEMICAL COMPANY, LTD.
To: HITACHI CHEMICAL COMPANY, LTD.
Reel/Frame 051103/0155 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2012
From: ISHITSUKA, KENICHI; FUNYUU, SHIGEAKI; HOSHI, YOUSUKE
To: HITACHI CHEMICAL COMPANY, LTD.
Reel/Frame 029163/0027 →
Priority Claims (1)
JP 2010-099035 · Apr 22, 2010 · national
Continuity (1)
Related Publication 20130037753A1 · Feb 14, 2013