Organic electroluminescent materials and devices
A compound including a ligand L according to Formula I: as well as, a first device and a formulation containing the same, are disclosed. In the compound including the Ligand L of Formula I: R 1 and R 2 are independently selected from 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, cyano, and combinations thereof; two adjacent substituents of R 1 or R 2 are optionally joined to form a fused ring; ligand L is coordinated to transition metal M having an atomic number greater than 40; R 1 represent mono, di, tri, or tetra-substitution, or no substitution; R 2 represent mono, di, or tri-substitution, or no substitution; and at least one substituent of R 1 or R 2 is cyano.
1. A compound having the structure:
wherein each R 2 is independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;
wherein two adjacent substituents of R 2 are optionally joined to form a fused ring; and
wherein R 2 represents mono, di, or tri-substitution, or no substitution.
2. The compound of claim 1 , wherein
at least one substituent of R 2 is aryl or heteroaryl that is further substituted by a substituent selected from the group consisting of aryl, heteroaryl, cycloalkyl, and alkyl.
3. The compound of claim 2 , wherein
at least one substituent of R 2 is aryl or heteroaryl that is further substituted by a substituent selected from the group consisting of aryl, heteroaryl, cycloalkyl, and alkyl having three or more C atoms.
4. The compound of claim 1 , wherein the compound is a facial isomer.
5. The compound of claim 1 , wherein the compound is a meridional isomer.
6. The compound of claim 1 ,
wherein each R 2 is independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, and combinations thereof.
7. The compound of claim 1 , wherein two adjacent substituents of R 2 are joined to form a fused ring.
8. A first device comprising a first organic light emitting device, the 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 structure:
wherein each R 2 is independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;
wherein two adjacent substituents of R 2 are optionally joined to form a fused ring; and
wherein R 2 represents mono, di, or tri-substitution, or no substitution.
9. The first device of claim 8 , wherein the first device is a consumer product.
10. The first device of claim 8 , wherein the first device is an organic light emitting device.
11. The first device of claim 8 , wherein the first device comprises a light panel.
12. The first device of claim 8 , wherein the organic layer is an emissive layer and the compound is an emissive dopant.
13. The first device of claim 8 , wherein the organic layer is an emissive layer and the compound is a non-emissive dopant.
14. The first device of claim 8 , wherein the organic layer further comprises a host material.
15. The first device of claim 14 , wherein the host material comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan;
wherein any substituent in the host material 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≡C—C n H 2n+1 , Ar 1 , Ar 1 -Ar 2 , and C n H 2n —Ar 1 ;
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.
16. The first device of claim 14 , wherein the host material comprises at least one chemical group selected from the group consisting of carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.
17. The first device of claim 14 , wherein the host material is selected from the group consisting of:
and combinations thereof.
18. The first device of claim 14 , wherein the host material comprises a metal complex.
19. A formulation comprising a compound having the structure:
wherein each R 2 is independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, isonitrile, sulfanyl, sulfonyl, sulfonyl, phosphino, and combinations thereof;
wherein two adjacent substituents of R 2 are optionally joined to form a fused ring; and
wherein R 2 represents mono, di, or tri-substitution, or no substitution.