Heterocyclic compound, organic light-emitting device including the same, and electronic apparatus including the organic light-emitting device
US-2024373662-A1 · Nov 7, 2024 · US
US9985210B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9985210-B2 |
| Application number | US-201715649049-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 13, 2017 |
| Priority date | Nov 30, 2011 |
| Publication date | May 29, 2018 |
| Grant date | May 29, 2018 |
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Provided is an organic electronic material which is excellent in storage stability in the case as an ink composition, and able to prepare, at a high yield, an organic electronic element capable of reducing the driving voltage and of being driven stably for a long period of time, and an ink composition including the organic electronic material. The organic electronic material is characterized in that it contains at least an ionic compound represented by the following general formula (1), and a compound including a charge transporting unit, and the ink composition including the material. [In the general formula (1), R a to R c each independently represent a hydrogen atom (H), an alkyl group, or a benzyl group, and N is not bonded to an aryl group. A represents an anion.]
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The invention claimed is: 1. An organic electronic material comprising at least an ionic compound represented by the following general formula (1), and a charge transporting compound including a charge transporting unit: in the general formula (1), R a to R c each independently represent a hydrogen atom (H), an alkyl group, or a benzyl group, and A represents an anion, provided that at least one condition selected from the group consisting of: (i) at least two of R a to R c each independently represent an alkyl group having 5 or more carbon atoms, (ii) at least one of R a to R c represents a benzyl group, and (iii) at least one of R a to R c represents an alkyl group having 7 or more carbon atoms, is satisfied. 2. The organic electronic material according to claim 1 , wherein the anion is represented by the following formulas (1b) to (5b): in the general formulas (1b) to (5b), Y 1 to Y 6 each independently represent a divalent linking group; R 1 to R 16 each independently represent an electron attractive organic substituent, these structures may further have substituents and hetero atoms therein, and R 2 and R 3 , R 4 to R 6 , R 7 to R 10 , or R 11 to R 16 may be each linked to form a ring or a polymer; and E 1 , E 2 , E 3 , E 4 , and E 5 respectively represent an oxygen atom, a nitrogen atom, a carbon atom, a boron atom or a gallium atom, and a phosphorus atom or an antimony atom. 3. The organic electronic material according to claim 1 , wherein the charge transporting compound is an aromatic amine, a carbazole, or a thiophene. 4. The organic electronic material according to claim 1 , wherein the charge transporting compound is a polymer or an oligomer. 5. The organic electronic material according to claim 1 , wherein the charge transporting compound comprises one or more polymerizable substituents. 6. The organic electronic material according to claim 5 , wherein the polymerizable substituents are any of an oxetane group, and an epoxy group, and a vinyl ether group. 7. The organic electronic material according to claim 2 , wherein the charge transporting compound is an aromatic amine, a carbazole, or a thiophene. 8. The organic electronic material according to claim 2 , wherein the charge transporting compound is a polymer or an oligomer. 9. The organic electronic material according to claim 2 , wherein the charge transporting compound comprises one or more polymerizable substituents. 10. The organic electronic element according to claim 1 , wherein N is not bonded to an aryl group with the exception of a benzyl group.
Details · CPC title
characterised by the presence of specified groups {, e.g. terminal or pendant functional groups} · CPC title
Amines; Quaternary ammonium compounds · CPC title
Boron compounds · CPC title
of an acyclic saturated carbon skeleton · CPC title
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