Organic light emitting materials
Novel phosphorescent metal complexes containing 2-phenylisoquinoline ligands with at least two substituents on the isoquinoline ring are provided. The disclosed compounds have low sublimation temperatures that allow for ease of purification and fabrication into a variety of OLED devices.
1. A compound having the formula:
wherein M is a metal having an atomic weight higher than 40;
wherein L is a second ligand;
wherein m is the maximum coordination number of the metal M;
wherein d is the denticity of L;
wherein n is at least 1;
wherein one of R 13 , R 14 , R 15 , R 16 , R 17 , and R 18 is hydrogen and the remainder are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfonyl, sulfonyl, phosphino, and combinations thereof;
wherein at least two of R 13 , R 14 , R 15 , R 16 , R 17 , and R 18 are independently selected from two to three carbon containing alkyl, silyl, germyl, cycloalkyl, and combinations thereof;
wherein each of R 22 , R 23 , R 24 , and R 25 is 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 at least one of the following (i)-(ii) is true:
(i) at least one of R 13 to R 18 is cycloalkyl or germyl; and
(ii) at least one of R 13 to R 18 is silyl, R 23 and R 25 are alkyl, and R 22 and R 24 are hydrogen.
2. The compound of claim 1 , wherein two of R 13 to R 18 are alkyl substitutions.
3. The compound of claim 1 , wherein at least one of R 13 to R 18 represents a silyl or a germyl substitution.
4. The compound of claim 1 , wherein the compound has the formula:
5. The compound of claim 1 , wherein at least one of R 13 , R 15 , R 16 , and R 18 is selected from the group consisting of ethyl and CH(CH 3 ) 2 , or
at least one of R 13 to R 18 is selected from the group consisting of cyclopentyl, cyclohexyl, trimethylsilyl, triethylsilyl, triisopropylsilyl, trimethylgermyl, triethylgermyl, and triisopropylgermyl.
6. The compound of claim 1 , wherein M is Ir.
7. The compound of claim 1 , wherein n is 2.
8. The compound of claim 1 , wherein L is a monoanionic bidentate ligand.
9. The compound of claim 8 , wherein L is
and
wherein R x , R y , and R z 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.
10. The compound of claim 9 , wherein R x , R y , and R z are independently selected from the group consisting of alkyl, hydrogen, deuterium, and combinations thereof.
11. The compound of claim 10 , wherein R z is hydrogen or deuterium, and R x and R y are independently selected from the group consisting of methyl, CH(CH 3 ) 2 , and CH 2 CH(CH 3 ) 2 .
12. The compound of claim 9 , wherein the compound has the formula:
13. The compound of claim 1 , wherein the compound is selected from the group consisting of:
14. A first device comprising a first organic light emitting device, comprising:
an anode;
a cathode; and
an organic layer, disposed between the anode and the cathode, comprising a compound having the formula:
wherein M is a metal having an atomic weight higher than 40;
wherein L is a second ligand;
wherein m is the maximum coordination number of the metal M;
wherein d is the denticity of L;
wherein n is at least 1;
wherein one of R 13 , R 14 , R 15 , R 16 , R 17 , and R 18 is hydrogen and the remainder are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;
wherein at least two of R 13 , R 14 , R 15 , R 16 , R 17 , and R 18 are independently selected from two to three carbon containing alkyl, silyl, germyl, cycloalkyl, and combinations thereof;
wherein each of R 22 , R 23 , R 24 , and R 25 is 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 at least one of the following (i)-(ii) is true:
(i) at least one of R 13 to R 18 is cycloalkyl or germyl; and
(ii) at least one of R 13 to R 13 is silyl, R 23 and R 25 are alkyl, and R 22 and R 24 are hydrogen.
15. The first device of claim 14 , wherein the first device is a consumer product or an organic light-emitting device.
16. The first device of claim 14 , wherein the organic layer is an emissive layer and the compound is a non-emissive dopant.
17. The first device of claim 14 , wherein the organic layer further comprises a host.
18. The first device of claim 17 , wherein the host is a metal 8-hydroxyquinolate.
19. The first device of claim 17 , wherein the host is selected from the group consisting of:
and combinations thereof.
20. The first device of claim 14 , wherein the compound is selected from the group consisting of: