Organic electroluminescent materials and devices
The invention discloses novel polyheteroaromatic compounds derived from indolocarbazole core structures. These compounds can be used as hosts for PHOLEDs.
1. A compound of Formula I:
wherein X 1 and X 2 are independently selected from the group consisting from NR, O, Se, CRR′, and SiRR′; and at least one of X 1 or X 2 is NR having the structure selected from the group consisting of
R 1 and R 2 each independently represent mono, di, tri, or tetra substitution, or no substitution;
R 3 represents mono, or di substitution, or no substitution;
at least one of R 1 , R 2 or R 3 represents di substitution and fuses to the aryl ring that it attaches thereto, and is selected from the group consisting of
wherein the wave lines indicate bonds to the aryl ring that it fuses to;
R 1 , R 2 , R 3 , R, and R′ are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and any two adjacent substituents R 1 , R 2 , or R 3 are optionally joined to form a ring.
2. The compound of claim 1 , wherein X 1 and X 2 are each independently a NR.
3. The compound of claim 1 , wherein at least one of X 1 or X 2 is O.
4. The compound of claim 1 , wherein at least one of X 1 or X 2 is CRR′ or SiRR′.
5. The compound of claim 1 , wherein R 1 and R 2 each independently represent no substitution.
6. The compound of claim 1 , wherein R 3 represents no substitution.
7. The compound of claim 1 , wherein the compound is selected from the group consisting of
8. An organic light emitting device (OLED) comprising:
an anode;
a cathode; and
an organic layer, disposed between the anode and the cathode, comprising a compound of claim 7 .
9. The compound of claim 1 , wherein R 1 or R 3 is selected from the group consisting of
10. The compound of claim 1 , wherein one of R 1 , R 2 , or R 3 is selected from the group consisting of
the remaining two of R 1 , R 2 , and R 3 are unsubstituted.
11. The compound of claim 1 , wherein at least one of R 1 , R 2 , or R 3 represents disubstitution and is
12. The compound of claim 1 , wherein at least one of R 1 , R 2 , or R 3 represents disubstitution and is
13. The compound of claim 1 , wherein at least one of R 1 , R 2 , or R 3 represents disubstitution and is
14. An organic light emitting device (OLED) comprising:
an anode;
a cathode; and
an organic layer, disposed between the anode and the cathode, comprising a compound of Formula I:
wherein X 1 and X 2 are independently selected from the group consisting from NR, O, Se, CRR′, and SiRR′; and at least one of X 1 or X 2 is NR having the structure selected from the group consisting of
R 1 and R 2 each independently represent mono, di, tri, or tetra substitution, or no substitution;
R 3 represents mono, or di substitution, or no substitution;
at least one of R 1 , R 2 or R 3 represents di substitution and fuses to the aryl ring that it attaches thereto, and is selected from the group consisting of
wherein the wave lines indicate bonds to the aryl ring that it fuses to;
R 1 , R 2 , R 3 , R, and R′ are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and any two adjacent substituents R 1 , R 2 , or R 3 are optionally joined to form a ring.
15. The OLED of claim 14 , wherein the organic layer is an emissive layer and the compound of Formula I is a host.
16. The OLED of claim 14 , wherein the organic layer further comprises a phosphorescent emissive dopant; wherein the emissive dopant is a transition metal complex having at least one ligand or part of the ligand if the ligand is more than bidentate selected from the group consisting of
wherein each X 1 to X 13 are independently selected from the group consisting of carbon and nitrogen;
wherein X is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO 2 , CR′R″, SiR′R″, and GeR′R″;
wherein R′ and R″ are optionally fused or joined to form a ring;
wherein each R a , R b , R c , and R d may represent from mono substitution to the possible maximum number of substitution, or no substitution;
wherein R′, R″, R a , R b , R c , and R d are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and
wherein any two adjacent substituents of R a , R b , R c , and R d are optionally fused or joined to form a ring or form a multidentate ligand.
17. The OLED of claim 14 , wherein the organic layer is a blocking layer and the compound of Formula I is a blocking material in the organic layer, or the organic layer is a transporting layer and the compound of Formula I is a transporting material in the organic layer.
18. The OLED of claim 14 , wherein the OLED is incorporated into a device selected from the group consisting of a consumer product, an electronic component module, and a lighting panel.
19. The OLED of claim 14 , wherein R 3 represents no substitution.
20. A formulation comprising a compound of Formula I:
wherein X 1 and X 2 are independently selected from the group consisting from NR, O, Se, CRR′, and SiRR′; and at least one of X 1 or X 2 is NR having the structure selected from the group consisting of
R 1 and R 2 each independently represent mono, di, tri, or tetra substitution, or no substitution;
R 3 represents mono, or di substitution, or no substitution;
at least one of R 1 , R 2 or R 3 represents di substitution and fuses to the aryl ring that it attaches thereto, and is selected from the group consisting of
wherein the wave lines indicate bonds to the aryl ring that it fuses to;
R 1 , R 2 , R 3 , R, and R′ are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and any two adjacent substituents R 1 , R 2 , or R 3 are optionally joined to form a ring.