6
A 6H-indolo[2,3-b]quinoxaline derivative has a structure of formula (I). R 9 is a member selected from the group consisted of an aryl group having one or more substituents and a heteroaryl group having one or more substituents, and R 1 to R 8 are substituents. The 6H-indolo[2,3-b]quinoxaline derivative of the present invention incorporates an indole and a quinoxaline group therefore inherits good energy transfer ability from indole and good electron-injection ability from quinoxaline. The compound of the present invention may function as a host material or a dopant in the light-emitting layer. In addition, the compound of the present invention may function as hole transport material, electron transport material, hole blocking material, electron blocking material, hole injecting material or electron injecting material.
1. A 6H-indolo[2,3-b]quinoxaline derivative comprising a chemical formula represented by Formula (II), DPINQ, TPINQ or FINQ:
wherein each of R 1 to R 8 , R 10 to R 14 is independently selected from the group consisting of hydrogen, halogen, aryl group, alkenyl group, C1-C20 alkyl group, alkynyl group, cyano, trifluoromethyl, alkylamino, amino, alkoxy group, heteroaryl group, halogen substituted aryl group, halogen substituted aralkyl group, haloalkyl substituted aryl group, haloalkyl substituted aralkyl group, aryl substituted C1-C20 alkyl group, cycloalkyl group, C1-C20 alkoxy group, C1 -C20 alkyl substituted amino group, haloalkyl substituted amino group, aryl substituted amino group, heteroaryl substituted amino group, aryl substituted phosphine oxide, C1-C20 alkyl substituted phosphine oxide, haloalkyl substituted phosphine oxide, halogen substituted phosphine oxide, heteroaryl substituted phosphine oxide, nitro group, carbonyl group, aryl substituted carbonyl group, heteroaryl substituted carbonyl group, and halogen substituted C1-C20 alkyl group, and
at least one of R 11 to R 13 is selected from the group consisting of substituted or unsubstituted heteroaryl group, aryl or heteroaryl substituted boronic group, aryl or heteroaryl substituted silyl group and aryl or heteroaryl substituted phosphine oxide.
2. The 6H-indolo[2,3-b]quinoxaline derivative as claimed in claim 1 , wherein at least one of R 11 to R 13 is independently selected from the group consisting of aryl or heteroaryl substituted boronic group, aryl or heteroaryl substituted silyl group and aryl or heteroaryl substituted phosphine oxide.
3. The 6H-indolo[2,3-b]quinoxaline derivative as claimed in claim 1 , wherein at least one of R 11 to R 13 is selected from the group consisting of triphenylsilane and diphenylphosphine oxide
4. The 6H-indolo[2,3-b]quinoxaline derivative as claimed in claim 1 , wherein at least one of R 11 to R 13 is selected from the group consisting of 6H-indolo[2,3-b]quinoxaline, 1-phenyl-1H-benzol[d]imidazole and 9H-carbazole
5. The 6H-indolo[2,3-b]quinoxaline derivative as claimed in claim 1 , having a chemical formula represented as listed below
6. An organic light emitting diode, comprising:
a cathode;
an anode; and
an organic layer configured between the cathode and the anode and comprising a 6H-indolo [2,3-b]quinoxaline derivative comprising a chemical formula represented by Formula (II), DPINQ, TPINQ or FINQ:
wherein each of R 1 to R 8 , R 10 to R 14 is independently selected from the group consisting of hydrogen, halogen, aryl group, alkenyl group, C1-C20 alkyl group, alkynyl group, cyano, trifluoromethyl, alkylamino, amino, alkoxy group, heteroaryl group, halogen substituted aryl group, halogen substituted aralkyl group, haloalkyl substituted aryl group, haloalkyl substituted aralkyl group, aryl substituted C1-C20 alkyl group, cycloalkyl group, C1-C20 alkoxy group, C1-C20 alkyl substituted amino group, haloalkyl substituted amino group, aryl substituted amino group, heteroaryl substituted amino group, aryl substituted phosphine oxide, C1-C20 alkyl substituted phosphine oxide, haloalkyl substituted phosphine oxide, halogen substituted phosphine oxide, heteroaryl substituted phosphine oxide, nitro group, carbonyl group, aryl substituted carbonyl group, heteroaryl substituted carbonyl group, and halogen substituted C1-C20 alkyl group, and
at least one of R 11 to R 13 is selected from the group consisting of substituted or unsubstituted heteroaryl group, aryl or heteroaryl substituted boronic group, aryl or heteroaryl substituted silyl group and aryl or heteroaryl substituted phosphine oxide.
7. The organic light emitting diode as claimed in claim 6 , wherein at least one of R 11 to R 13 is independently selected from the group consisting of aryl or heteroaryl substituted boronic group, aryl or heteroaryl substituted silyl group and aryl or heteroaryl substituted phosphine oxide.
8. The organic light emitting diode as claimed in claim 6 , wherein at least one of R 11 to R 13 is selected from the group consisting of triphenylsilane and diphenylphosphine oxide
9. The organic light emitting diode as claimed in claim 6 , wherein at least one of R 11 to R 13 is selected from the group consisting of 6H-indolo[2,3-b]quinoxaline,-1-phenyl-1H-benzol[d]imidazole and 9H-carbazole
10. The organic light emitting diode as claimed in claim 6 , wherein the 6H-indolo[2,3-b]quinoxaline derivative has a chemical formula represented as listed below
11. The organic light emitting diode as claimed in claim 6 , wherein the organic layer comprises an emitting layer, and the 6H-indolo[2,3-b]quinoxaline derivative is a host emitting material.
12. The organic light emitting diode as claimed in claim 6 , wherein the organic layer comprises an emitting layer, and the 6H-indolo[2,3-b]quinoxaline derivative is a dopant.
13. The organic light emitting diode as claimed in claim 6 , wherein the organic light emitting diode comprises a red OLED, a green OLED, a red phosphorescent OLED or a green phosphorescent OLED.
14. The organic light emitting diode as claimed in claim 6 , further comprising an emitting layer configured between the cathode and the anode.
15. The organic light emitting diode as claimed in claim 14 , wherein the organic layer comprises a hole transport layer configured between the emitting layer and the anode, and the 6H-indolo[2,3-b]quinoxaline derivative is a hole transport material.
16. The organic light emitting diode as claimed in claim 14 , wherein the organic layer comprises an electron transport layer configured between the emitting layer and the cathode, and the 6H-indolo[2,3-b]quinoxaline derivative is an electron transport material.
17. The organic light emitting diode as claimed in claim 14 , wherein the organic layer comprises a hole transport layer configured between the emitting layer and the cathode, and the 6H-indolo[2,3-b]quinoxaline derivative is a hole blocking material.
18. The organic light emitting diode as claimed in claim 14 , wherein the organic layer comprises an electron blocking layer configured between the emitting layer and the anode, and the 6H-indolo[2,3-b]quinoxaline derivative is an electron blocking material.
19. The organic light emitting diode as claimed in claim 14 , wherein the organic layer comprises a hole injecting layer configured between the emitting layer and the anode, and the 6H-indolo[2,3-b]quinoxaline derivative is a hole injecting material.
20. The organic light emitting diode as claimed in claim 14 , wherein the organic layer comprises an electron injecting layer configured between the emitting layer and the cathode, and the 6H-indolo[2,3-b]quinoxaline derivative is an electron injecting material.