Carbazole-containing materials in phosphorescent light emitting diodes
Carbazole-containing compounds are provided. In particular, the compounds are oligocarbazole-containing compounds having an unsymmetrical structure. The compounds may be useful in organic light emitting devices, in particular as hosts in the emissive layer of such devices.
1. A carbazole-containing compound comprising:
wherein a is 1 to 20;
wherein b is 0 to 20;
wherein m is 0 to 2;
wherein n is 0 to 2;
wherein m+n is at least 1;
wherein X is selected from the group consisting of biphenyl, terphenyl, naphthalene, triphenylene, phenanthrene, fluorene, chrysene, dibenzothiophene, dibenzofuran, benzofuran, benzothiophene, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, indole, benzimidazole, indazole, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine; and
wherein X is substituted by R, where R is selected from the group consisting of hydrogen, alkyl, heteroalkyl, benzene, biphenyl, terphenyl, naphthalene, phenalene, phenanthrene, fluorene, chrysene, dibenzothiophene, dibenzofuran, benzofuran, benzothiophene, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, indole, benzimidazole, indazole, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine.
2. The compound of claim 1 , wherein a is 1 to 20 and n is 0.
3. The compound of claim 1 , wherein a is 1 or 2 and n is 0.
4. The compound of claim 1 , wherein a is 1, b is 1, and n is 1.
5. The compound of claim 1 , wherein X is selected from biphenyl, terphenyl, triphenylene, phenanthrene, fluorene, dibenzothiophene, dibenzofuran, pyridine, pyridazine, pyrimidine, pyrazine, triazine, benzimidazole, benzothiazole, quinoline, isoquinoline, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine.
6. The compound of claim 1 , wherein X is selected from the group consisting of dibenzothiophene, dibenzofuran, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, and triphenylene.
7. The compound of claim 1 , wherein R is selected from the group consisting of hydrogen, alkyl, benzene, biphenyl, terphenyl, triphenylene, phenanthrene, fluorene, dibenzothiophene, dibenzofuran, pyridine, pyridazine, pyrimidine, pyrazine, triazine, benzimidazole, benzothiazole, quinoline, isoquinoline, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine.
8. The compound of claim 1 wherein R is selected from the group consisting of hydrogen, alkyl, benzene, biphenyl, terphenyl, dibenzothiophene, dibenzofuran.
9. The compound of claim 5 , wherein R is selected from the group consisting of hydrogen, alkyl, benzene, biphenyl, terphenyl, triphenylene, phenanthrene, fluorene, dibenzothiophene, dibenzofuran, pyridine, pyridazine, pyrimidine, pyrazine, triazine, benzimidazole, benzothiazole, quinoline, isoquinoline, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine.
10. The compound of claim 6 , wherein R is selected from the group consisting of hydrogen, alkyl, benzene, biphenyl, terphenyl, dibenzothiophene, dibenzofuran.
11. The compound of claim 1 , wherein the compound is selected from the group consisting of:
12. The compound of claim 11 , wherein the compound is selected from the group consisting of:
13. The compound of claim 11 , wherein the compound is selected from the group consisting of:
14. The compound of claim 11 , wherein the compound is selected from the group consisting of:
15. The compound of claim 11 , wherein the compound is selected from the group consisting of:
16. The compound of claim 11 , wherein the compound is selected from the group consisting of:
17. The compound of claim 11 , wherein the compound is selected from the group consisting of:
18. An organic light emitting device, comprising:
an anode;
a cathode; and
a first organic layer disposed between the anode and the cathode, wherein the organic layer comprises a carbazole-containing compound, comprising
wherein a is 1 to 20;
wherein b is 0 to 20;
wherein m is 0 to 2;
wherein n is 0 to 2;
wherein m+n is at least 1;
wherein X is selected from the group consisting of biphenyl, terphenyl, naphthalene, triphenylene, phenanthrene, fluorene, chrysene, dibenzothiophene, dibenzofuran, benzofuran, benzothiophene, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, indole, benzimidazole, indazole, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine; and
wherein X is substituted by R, where R is selected from the group consisting of hydrogen, alkyl, heteroalkyl, benzene, biphenyl, terphenyl, naphthalene, phenalene, phenanthrene, fluorene, chrysene, dibenzothiophene, dibenzofuran, benzofuran, benzothiophene, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, indole, benzimidazole, indazole, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine.
19. The device of claim 18 , wherein the carbazole-containing compound is selected from the group consisting of:
20. The device of claim 19 , wherein the first organic layer is an emissive layer and the carbazole-containing compound is a host in the first organic layer.
21. The device of claim 20 , wherein the emissive layer further comprises a phosphorescent emitter.
22. The device of claim 21 , wherein the phosphorescent emitter is an iridium complex having the formula:
wherein n=1, 2 or 3;
wherein R 1a , R 1b , R 1c , R 1d , R 1e , R 1f , R 1g , R 1h , and R 1i are each, independently, H, hydrocarbyl, heteroatom substituted hydrocarbyl, cyano, fluoro, OR 2a , SR 2a , NR 2a R 2b , BR 2a R 2b , or SiR 2a R 2b R 2c , wherein R 2a-c are each, independently, hydrocarbyl or heteroatom substituted hydrocarbyl, and wherein any two of R 1a-i and R 2a-c may be linked to form a saturated or unsaturated, aromatic or non-aromatic ring; and
wherein X-Y is an ancillary ligand.
23. The device of claim 21 , wherein the phosphorescent emitter is a compound comprising a phosphorescent metal complex comprising a monoanionic, bidentate ligand having the formula:
wherein E 1a-q are selected from the group consisting of C and N and collectively comprise an 18 pi-electron system; provided that E 1a and E 1p are different;
wherein R 1a-i are each, independently, H, hydrocarbyl, heteroatom substituted hydrocarbyl, cyano, fluoro, OR 2a , SR 2a NR 2a R 2b , BR 2a , R 2b , or SiR 2a R 2b R 2c , where R 2a-c are each, independently, hydrocarbyl or heteroatom substituted hydrocarbyl, and where any two of R 1a-i and R 2a-c may be linked to form a saturated or unsaturated, aromatic or non-aromatic ring; provided that R 1a-i is other than H when attached to N;
wherein the metal is selected from the group consisting of the non-radioactive metals with atomic numbers greater than 40; and
wherein the bidentate ligand may be linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
24. The device of claim 20 , wherein the device further comprises a second organic layer that is a non-emissive layer.
25. The device of claim 24 , wherein the first organic layer is adjacent to the second organic layer.
26. The device of claim 21 , wherein the phosphorescent emitter has a triplet energy of 425 nm to 495 nm, X is selected from dibenzothiophene, dibenzofuran, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, and triphenylene, and R is selected from hydrogen, alkyl, benzene, biphenyl, terphenyl, dibenzothiophene, dibenzofuran.
27. The device of claim 26 , wherein the triplet energy is 440 nm to 480 nm.
28. The device of claim 21 , wherein the phosphorescent emitter has a triplet energy of 495 nm to 570 nm, X is selected from biphenyl, terphenyl, triphenylene, phenanthrene, fluorene, dibenzothiophene, dibenzofuran, pyridine, pyridazine, pyrimidine, pyrazine, triazine, benzimidazole, benzothiazole, quinoline, isoquinoline, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine, and R is selected from hydrogen, alkyl, benzene, biphenyl, terphenyl, triphenylene, phenanthrene, fluorene, dibenzothiophene, dibenzofuran, pyridine, pyridazine, pyrimidine, pyrazine, triazine, benzimidazole, benzothiazole, quinoline, isoquinoline, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine.
29. The device of claim 28 , wherein the triplet energy is 510 nm to 530 nm.
30. The device of claim 18 , wherein the oligocarbazole-containing compound has a concentration of 10-100 wt %.
31. The device of claim 30 , wherein the oligocarbazole-containing compound has a concentration of 40-99.9 wt %.
32. The device of claim 31 , further comprising a phosphorescent emitter having a concentration of 0.1 to 30 wt %.
33. A consumer product comprising a device, the device further comprising:
an anode;
a cathode; and
an organic layer, disposed between the anode and the cathode, the organic layer further comprising a carbazole-containing compound, comprising:
wherein a is 1 to 20;
wherein b is 0 to 20;
wherein m is 0 to 2;
wherein n is 0 to 2;
wherein m+n is at least 1;
wherein X is selected from the group consisting of biphenyl, terphenyl, naphthalene, triphenylene, phenanthrene, fluorene, chrysene, dibenzothiophene, dibenzofuran, benzofuran, benzothiophene, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, indole, benzimidazole, indazole, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine; and
wherein X is substituted by R, where R is selected from the group consisting of hydrogen, alkyl, heteroalkyl, benzene, biphenyl, terphenyl, naphthalene, phenalene, phenanthrene, fluorene, chrysene, dibenzothiophene, dibenzofuran, benzofuran, benzothiophene, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, indole, benzimidazole, indazole, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine.
34. A method of fabricating an organic light emitting device, comprising:
providing a first electrode;
co-depositing a host and a phosphorescent emitter to form an emissive layer;
wherein the emissive layer comprises an oligocarbazole-containing
compound, comprising:
wherein a is 1 to 20;
wherein b is 0 to 20;
wherein m is 0 to 2;
wherein n is 0 to 2;
wherein m+n is at least 1;
wherein X is selected from the group consisting of biphenyl, terphenyl, naphthalene, triphenylene, phenanthrene, fluorene, chrysene, dibenzothiophene, dibenzofuran, benzofuran, benzothiophene, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, indole, benzimidazole, indazole, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine; and
wherein X is substituted by R, where R is selected from the group consisting of hydrogen, alkyl, heteroalkyl, benzene, biphenyl, terphenyl, naphthalene, phenalene, phenanthrene, fluorene, chrysene, dibenzothiophene, dibenzofuran, benzofuran, benzothiophene, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, indole, benzimidazole, indazole, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, and thienodipyridine; and
depositing a second electrode.
35. The method of claim 32 , wherein the first electrode is an anode and the second electrode is a cathode.
36. The method of claim 32 , wherein an organic layer is deposited after the first electrode and before the emissive layer.
37. The method of claim 34 , wherein the organic layer is a hole transport layer.