Organic electroluminescent materials and devices
This invention relates to the development of heterocyclic materials with high triplet excitation energy, which can be used as host materials in electroluminescent devices such as a PHOLED. The materials improve the performance of such devices by enhancing the lifetime and efficiency of the device when the newly developed heterocyclic materials are utilized as a host.
1. A compound having a formula selected from the group consisting of Formula I and Formula II:
R 1 to R 6 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;
wherein R 5 and R 6 optionally join to form a phenyl ring or substituted phenyl ring
wherein at least one of R 1 to R 6 comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, and dibenzoselenophene;
wherein at least one of R 1 to R 6 comprises at least one chemical group selected from the group consisting of aza-triphenylene, aza-carbazole, aza-dibenzothiophene, aza-dibenzofuran, aza-dibenzoselenophene,
wherein each occurrence of X 1 and X 2 is independently selected from the group consisting of NR, SiRR′, GeRR′, O, S, and Se; and
wherein each occurrence of R and R′ is 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 adjacent substituents of R and R′ are optionally fused or joined to form a ring.
2. The compound of claim 1 , wherein the compound has triplet energy Tl of at least 3.2 eV.
3. The compound of claim 1 , wherein the compound is represented by Formula I.
4. The compound of claim 1 , wherein the compound is represented by Formula II.
5. The compound of claim 1 , wherein the compound is selected from the group consisting of:
wherein R 11 and R 12 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.
6. The compound of claim 1 , wherein R 1 to R 6 are each independently selected from the group consisting of hydrogen, aryl, substituted aryl, heteroaryl, and substituted heteroaryl.
7. The compound of claim 1 , wherein R 1 to R 6 are each independently selected from the group consisting of:
hydrogen,
8. A compound of Formula III or Formula IV
wherein X 1 is selected from the group consisting of NR, SiRR′, and GeRR′
X 2 is O;
R, R′, R 1 , R 2 , R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 are 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 adjacent substituents of R and R′ optionally join to form a ring; and
at least one of R 1 , R 2 , R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 comprises a chemical group selected from the group consisting of silyl, non-fused five-membered heteroaromatic ring, and tetraphenylene.
9. The compound of claim 8 , wherein the compound is selected from the group consisting of:
10. An organic light-emitting device (OLED) comprising:
an anode; a cathode; and an organic layer disposed between the anode and the cathode, the organic layer comprising a compound having a formula selected from the group consisting of Formula I and Formula II:
R 1 to R 6 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;
wherein R 5 and R 6 optionally join to form a phenyl ring or substituted phenyl ring
wherein at least one of R 1 to R 6 comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, and dibenzoselenophene;
wherein at least one of R 1 to R 6 comprises at least one chemical group selected from the group consisting of aza-triphenylene, aza-carbazole, aza-dibenzothiophene, aza-dibenzofuran, aza-dibenzoselenophene,
wherein each occurrence of X 1 and X 2 is independently selected from the group consisting of NR, SiRR′, GeRR′, O, S, and Se;
wherein each occurrence of R and R′ is 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 adjacent substituents of R and R′ are optionally fused or joined to form a ring.
11. The OLED of claim 10 , 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.
12. The OLED of claim 10 , wherein the organic layer further comprises a host, wherein host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, aza-triphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.
13. The OLED of claim 10 , wherein the organic layer further comprises a host, wherein the host is selected from the group consisting of:
and combinations thereof.
14. A formulation comprising a compound of claim 1 .
15. The compound of claim 1 , wherein X 1 and X 2 are each independently selected from the group consisting of NR, SiRR′, GeRR′, O, S, and Se;
R and R′ are independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof; and adjacent substituents of R and R′ are optionally fused or joined to form a ring;
R 1 to R 6 are independently selected from the group consisting of hydrogen, deuterium, alkyl, nitrile, amino, aryl, aryl, heteroaryl, and combinations thereof;
R 5 and R 6 optionally join to form a phenyl ring or substituted phenyl ring
at least one of R 1 to R 6 comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene; and
and at least of R 1 to R 6 comprises at least one chemical group selected from the group consisting of Formula I, Formula II, aza-triphenylene, aza-carbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.
16. The compound of claim 8 , wherein at least one of R 1 , R 2 , R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 comprises a chemical group selected from the group consisting of:
17. The compound of claim 8 , wherein at least one of R 1 , R 2 , R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, aza-triphenylene, aza-carbazole, aza-dibenzothiophene, aza-dibenzofuran, aza-dibenzoselenophene,
18. An organic light-emitting device (OLED) comprising: an anode; a cathode; and an organic layer disposed between the anode and the cathode, the organic layer comprising a compound of claim 8 .