Aromatic amine derivative and organic electroluminescence device utilizing the same
US-10312452-B2 · Jun 4, 2019 · US
US10840450B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10840450-B2 |
| Application number | US-201515532883-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 3, 2015 |
| Priority date | Dec 4, 2014 |
| Publication date | Nov 17, 2020 |
| Grant date | Nov 17, 2020 |
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Disclosed are a polymer, and a mixture or a formulation and an organic electronic device containing same, and applications thereof, and further a monomer of which the polymer is made; the polymer comprises on its side chain a repeating structure unit E, characterizing in that its S1(E)−T1(E))≤0.35 eV or even less, which may allow the said polymer having thermally activated delayed fluorescence (TADF) property. Thus a TADF polymer suitable for printing processes is provided, thereby reducing OLED manufacturing costs.
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The invention claimed is: 1. A polymer having the following general structural formula: wherein E is a structural unit, the energy difference between the singlet energy level and the triplet energy level of the structural unit E, i.e. (S1(E)−T1(E)), is less than or equal to 0.35 eV, x and y are the molar fractions, x+y=1, and G is an organic functional group selected from the group consisting of a hole-injecting or hole-transporting group, a hole-blocking group, an electron-injecting or electron-transporting group, an electron-blocking group, an organic host group, a singlet emitter group, and a triplet emitter group. 2. The polymer according to claim 1 , wherein (S1(E)−T1(E))≤0.25 eV. 3. The polymer according to claim 1 , wherein the structural unit E contains at least one electron donating group D and at least one electron accepting group A. 4. The polymer according to claim 1 , wherein the structural unit E contains a structural unit represented by the structural formula (I): where Ar is an aromatic or heteroaromatic structural unit, D is an electron donating group, A is an electron accepting group, each of n and m is an integer between 1 and 6, when m>1, each D is independently selected from the same or different electron donating groups, and when n>1, each A is independently selected from the same or different electron accepting groups. 5. The polymer according to claim 3 , wherein the electron donating group D is selected from structural units containing any one of the following groups: 6. The polymer according to claim 3 , wherein the electron accepting group A is selected from the group consisting of F, cyano group, and structural units containing any one of the following groups: wherein n1 is an integer from 1 to 3, X 1 -X 8 are CR 1 or N, at least one of X 1 -X 8 is N, and R 1 is selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, aralkyl, heteroalkyl, aryl, and heteroaryl. 7. The polymer according to claim 4 , wherein Ar is selected from structural units containing any one of the following groups: where z is O or S. 8. The polymer according to claim 1 , wherein the structural unit E is selected from structural units containing any one of the following structural formulas: 9. A mixture, comprising: the polymer according to claim 1 ; and at least one organic functional material that is selected from the group consisting of a hole-injecting or hole-transporting material, a hole-blocking material, an electron-injecting or electron-transporting material, an electron-blocking material, an organic host material, a singlet emitter, and a triplet emitter. 10. The mixture according to claim 9 , wherein the at least one organic functional material is a singlet emitter or a triplet emitter. 11. A formulation comprising the polymer according to claim 1 and at least one organic solvent.
Nitrogen · CPC title
Oxygen · CPC title
Manufacturing or production processes characterised by the final manufactured product · CPC title
Macromolecular compounds · CPC title
containing two or more rings · CPC title
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