Organic electroluminescent materials and devices
This invention discloses heteroleptic iridium complexes containing two tridentate ligands with three five- and one six-cyclometalated rings, showing desired device performance properties.
1. A compound selected from the group consisting of Formulae G1, G2, G3, G4, G5, G6, G7, G8, and G9:
wherein, in Formula G1, R 1 and R 3 to R 6 each independently represent mono-substitution to the possible maximum number of substitution, or no substitution;
wherein, in Formula G1, each R 1 and R 3 to R 6 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring;
wherein, in Formula G1, R 2 represents di-substitution to the possible maximum number of substitution;
wherein, in Formula G1, each R 2 is independently selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring, wherein each R 2 is optionally partially or fully deuterated;
wherein, in Formula G1, X is selected from the group consisting of BR, NR, PR, O, S, Se, C═O, S═O, SO 2 , SiRR′, and GeRR′;
wherein, in Formulae G2, G3, G4, G5, G6, G8, and G9, R 1 to R 9 each independently represent mono-substitution to the possible maximum number of substitution, or no substitution;
wherein, in Formulae G2, G3, G4, G5, G6, G8, and G9, each R 1 to R 9 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring;
wherein, in Formulae G2, G3, G4, G5, G6, G8, and G9, X is selected from the group consisting of BR, NR, PR, O, S, Se, C═O, S═O, SO 2 , CRR′, SiRR′, and GeRR′;
wherein, in Formula G7, R 1 to R 8 each independently represent mono-substitution to the possible maximum number of substitution, or no substitution;
wherein, in Formula G7, each R 1 and R 5 is independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, heteroaryl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and wherein any two adjacent substituents are optionally joined to form a ring or a fused ring;
wherein, in Formula G7, each R 2 , R 3 , R 4 , R 6 , R 7 , and R 8 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring;
wherein, in Formula G7, X is selected from the group consisting of BR, NR, PR, O, S, Se, C═O, S═O, SO 2 , CRR′, SiRR′, and GeRR′; and
wherein, in Formulae G1 to G9, substituent groups 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring.
2. The compound of claim 1 , wherein the compound is selected from the group consisting of Formulae G2, G3, G4, G5, G6, G7, G8, and G9.
3. The compound of claim 1 , wherein the compound is a compound of Formula G2.
4. The compound of claim 1 , wherein the compound is a compound of Formula G3.
5. The compound of claim 1 , wherein the compound is a compound of Formula G4.
6. The compound of claim 1 , wherein the compound is a compound of Formula G5.
7. The compound of claim 1 , wherein the compound is a compound of Formula G6 or Formula G7.
8. The compound of claim 1 , wherein the compound is a compound of Formula G8 or Formula G9.
9. The compound of claim 1 , wherein the compound is selected from the group consisting of:
10. A formulation comprising a compound of claim 1 .
11. A compound of one of the following:
a) a compound of Formula G10;
b) a compound of Formula G11;
or
c) a compound selected from the group consisting of
wherein R 1 to R 6 each independently represent mono-substitution to the possible maximum number of substitution, or no substitution;
wherein X is selected from the group consisting of NR, O, S, SiRR′, and GeRR′; and
wherein substituent groups R, R′, 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring.
12. The compound of claim 11 , wherein the compound is
13. 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 11 .
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 selected from the group consisting of Formulae G1, G2, G3, G4, G5, G6, G7, G8, and G9:
wherein, in Formula G1, R 1 and R 3 to R 6 each independently represent mono-substitution to the possible maximum number of substitution, or no substitution;
wherein, in Formula G1, each R 1 and R 3 to R 6 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring;
wherein, in Formula G1, R 2 represents di-substitution to the possible maximum number of substitution;
wherein, in Formula G1 , each R 2 is independently selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring, wherein each R 2 is optionally partially or fully deuterated;
wherein, in Formula G1, X is selected from the group consisting of BR, NR, PR, O, S, Se, C═O, S═O, SO 2 , SiRR′, and GeRR′;
wherein, in Formulae G2, G3, G4, G5, G6, G8, and G9, R 1 to R 9 each independently represent mono-substitution to the possible maximum number of substitution, or no substitution;
wherein, in Formulae G2, G3, G4, G5, G6, G8, and G9, each R 1 to R 9 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring;
wherein, in Formulae G2, G3, G4, G5, G6, G8, and G9, X is selected from the group consisting of BR, NR, PR, O, S, Se, C═O, S═O, SO 2 , CRR′, SiRR′, and GeRR′;
wherein, in Formula G7, R 1 to R 8 each independently represent mono-substitution to the possible maximum number of substitution, or no substitution;
wherein, in Formula G7, each R 1 and R 5 is independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, heteroaryl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and wherein any two adjacent substituents are optionally joined to form a ring or a fused ring;
wherein, in Formula G7, each R 2 , R 3 , R 4 , R 6 , R 7 , and R 8 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring;
wherein, in Formula G7, X is selected from the group consisting of BR, NR, PR, O, S, Se, C═O, S═O, SO 2 , CRR′, SiRR′, and GeRR′; and
wherein, in Formulae G1 to G9, substituent groups 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, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, wherein any two adjacent substituents are optionally joined to form a ring or a fused ring.
15. 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.
16. The OLED of claim 14 , wherein the organic layer is an emissive layer and the compound is an emissive dopant or a non-emissive dopant.
17. The OLED of claim 14 , wherein the organic layer further comprises a host,
wherein the host comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan;
wherein any substituent in the host is an unfused substituent independently selected from the group consisting of C n H 2n+1 , OC n H 2n+1 , OAr 1 , N(C n H 2n+1 ) 2 , N(Ar 1 )(Ar 2 ), CH═CH—C n H 2n+1 , C≡CC n H 2n+1 , Ar 1 , Ar 1 —Ar 2 , and C n H 2n —Ar 1 , or the host has no substitution;
wherein n is from 1 to 10; and
wherein Ar 1 and Ar 2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.
18. The OLED of claim 14 , wherein the organic layer further comprises a host,
wherein the host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.
19. The OLED of claim 14 , wherein the organic layer further comprises a host, wherein the host is selected from the group consisting of:
and combinations thereof.
20. The OLED of claim 14 , wherein the organic layer further comprises a host, wherein the host comprises a metal complex.