Organic electroluminescent materials and devices
Organic electroluminescent materials and devices are disclosed. The organic electroluminescent materials are novel benzodithiophene or its analogous structure compounds, which can be used as charge transporting materials, hole injection materials, or the like in an electroluminescent device. These novel compounds can offer excellent performance compared with existing materials, for example, to further improve the voltage, efficiency and/or lifetime of the OLEDs.
1. A compound having Formula 1:
wherein
X 1 , X 2 , X 3 , and X 4 are each independently selected from the group consisting of CR, and N; when X 1 , X 2 , X 3 , and X 4 are each independently selected from CR, each R may be same or different, and at least one of R comprises at least one electron withdrawing group;
Z 1 and Z 2 are each independently selected from the group consisting of O, S, Se, S═O, and SO 2 ;
X and Y are each independently selected from the group consisting of S, Se, NR′, and CR″R′″;
R, R′, R″, and R″′ are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7 to 30 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 20 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 20 carbon atoms, a substituted or unsubstituted amino group having 0 to 20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a nitrile group, an isonitrile group, a sulfanyl group, a sulfinyl group, a sulfonyl group, a phosphino group, and combinations thereof;
Any adjacent substitution can be optionally joined to form a ring or fused structure.
2. The compound of claim 1 , wherein Z 1 and Z 2 are S.
3. The compound of claim 1 , wherein X 2 and X 3 are N.
4. The compound of claim 1 , wherein X 2 and X 3 are each independently selected from CR, each R may be same or different, and at least one of R comprises at least one electron withdrawing group.
5. The compound of claim 4 , wherein each R comprises at least one electron withdrawing group.
6. The compound of claim 4 , wherein R are selected from the group consisting of fluorine, chlorine, trifluoromethyl, trifluoromethoxyl, pentafluoroethyl, pentafluoroethoxyl, cyano, nitro group, methyl sulfonyl, trifluoromethyl sulfonyl, trifluoromethylthio, pentafluorosulfanyl, pyridyl, 3-fluorophenyl, 4-fluorophenyl, 3-cyanophenyl, 4-cyanophenyl, 4-trifluoromethylphenyl, 3-trifluoromethoxylphenyl, 4-trifluoromethoxylphenyl, 4-pentafluoroethylphenyl, 4-pentafluoroethoxylphenyl, 4-nitrophenyl, 4-methyl sulfonyl phenyl, 4-trifluoromethyl sulfonyl phenyl, 3-trifluoromethylsulfanylphenyl, 4-trifluoromethylsulfanylphenyl, 4-pentafluorosulfanylphenyl, pyrimidyl, 2,6-dimethyl-1,3,5-triazine, and combinations thereof.
7. The compound of claim 1 , wherein X and Y are each independently CR″R″′.
8. The compound of claim 7 , wherein R″ and R″′ are each independently selected from the group consisting of trifluoromethyl, cyano, pentafluorophenyl, 4-cyano-2,3,5,6-tetrafluorophenyl, and pyridyl.
9. The compound of claim 1 , wherein the compound has the formula:
10. The compound of claim 1 , wherein the compound is selected from the group consisting of:
11. An electroluminescent device comprising an anode, a cathode, and an organic layer disposed between the anode and the cathode, further comprising the compound of claim 1 .
12. The device of claim 11 , wherein the organic layer is a charge transporting layer.
13. The device of claim 12 , wherein the organic layer further comprises an arylamine compound.
14. The device of claim 11 , wherein the organic layer is a hole injection layer.
15. The device of claim 14 , wherein the organic layer further comprises an arylamine compound.
16. The device of claim 11 , wherein the device further comprises a light emitting layer.
17. An organic light-emitting device comprising a plurality of stacks between an anode and a cathode, the stacks comprise a first light-emitting layer and a second light-emitting layer,
wherein the first stack comprises a first light-emitting layer, the second stack comprises a second light-emitting layer, and a charge generation layer is disposed between the first stack and the second stack,
wherein the charge generation layer comprises a p type charge generation layer and an n type charge generation layer,
wherein the p type charge generation layer comprises the compound of claim 1 .
18. The compound of claim 1 , wherein Z 1 and Z 2 are O.