Organic electroluminescent materials and devices

1. A compound having the formula:

wherein:

(i) G 1 is an electron donor group and G 2 is an electron acceptor group, or

(ii) G 1 is an electron acceptor group and G 2 is an electron donor group;

wherein:

(A) the electron donor group comprises at least one chemical group selected from the group consisting of:

wherein n is an integer from 1 to 20,

wherein m is an integer from 1 to 20,

wherein X is selected from the group consisting of O, S, and NR 14 , and

wherein R 11 and R 12 are selected from the group consisting of aryl and heteroaryl; and

(B) the electron acceptor group is selected from the group consisting of:

wherein Z 1 to Z 8 independently comprise C or N,

wherein at least two of Z 1 to Z 8 are N,

wherein Y 1 to Y 8 independently comprise C or N,

wherein at least one of Y 1 to Y 8 is N,

wherein A 1 to A 8 independently comprise C or N,

wherein J 1 and J 2 independently comprise C or N,

wherein L 1 to L 4 independently comprise C or N,

wherein X 1 is O, S, or NR 14 , and

wherein R 14 is aryl or heteroaryl;

wherein the electron acceptor group is optionally substituted;

wherein R 1 and R 2 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 R 1 and R 2 are optionally joined to form a ring, which may be further substituted.

2. The compound of claim 1 , wherein the donor group is selected from the group consisting of:

3. The compound of claim 1 , wherein the acceptor group is selected from the group consisting of:

4. The compound of claim 1 , wherein the compound is selected from the group consisting of:

5. The compound of claim 1 , wherein the electron accepting group is selected from the group consisting of:

wherein the electron acceptor group is optionally substituted.

6. A first device comprising a first organic light emitting device, further comprising:

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode;

wherein the organic layer comprises a compound having the formula:

wherein:

(i) G 1 is an electron donor group and G 2 is an electron acceptor group, or

(ii) G 1 is an electron acceptor group and G 2 is an electron donor group;

wherein:

(A) the electron donor group comprises at least one chemical group selected from the group consisting of:

wherein n is an integer from 1 to 20,

wherein m is an integer from 1 to 20,

wherein X and Y are independently selected from the group consisting of O, S, and NR 14 , and

wherein R 11 , R 12 , R 13 and R 14 are selected from the group consisting of aryl and heteroaryl; and

(B) the electron acceptor group is selected from the group consisting of:

wherein Z 1 to Z 8 independently comprise C or N,

wherein at least two of Z 1 to Z 8 are N,

wherein Y 1 to Y 8 independently comprise C or N,

wherein at least one of Y 1 to Y 8 is N,

wherein A 1 to A 8 independently comprise C or N,

wherein J 1 and J 2 independently comprise C or N,

wherein L 1 to L 4 independently comprise C or N,

wherein X 1 is O, S, or NR 14 , and

wherein R 14 is aryl or heteroaryl;

wherein the electron acceptor group is optionally substituted;

wherein R 1 and R 2 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;

wherein R 1 and R 2 are optionally joined to form a ring, which may be further substituted; and

wherein the compound is an emissive dopant.

7. The first device of claim 6 , wherein the organic layer is an emissive layer.

8. The first device of claim 6 , wherein the electron acceptor group comprises at least one chemical group selected from the group consisting of a six-membered aromatic ring system having at least two nitrogen atoms and a 5-membered aromatic ring system containing at least one nitrogen atom, one oxygen atom, one sulfur atom, or one selenium atom.

9. The first device of claim 6 , wherein the first device emits a luminescent radiation at room temperature when a voltage is applied across the first organic light emitting device;

wherein the luminescent radiation comprises a delayed fluorescence process.

10. The first device of claim 6 , wherein the emissive layer further comprises a first phosphorescent emitting material.

11. The first device of claim 10 , wherein the first device emits a white light at room temperature when a voltage is applied across the organic light emitting device.

12. The first device of claim 11 , wherein the compound emits a blue light having a peak wavelength between about 400 nm to about 500 nm.

13. The first device of claim 11 , wherein the compound emits a yellow light having a peak wavelength between about 530 nm to about 580 nm.

14. The first device of claim 10 , wherein the emissive layer further comprises a second phosphorescent emitting material.

15. The first device of claim 6 , wherein the emissive layer further comprises a host material.

16. The first device of claim 6 , wherein the compound is a host.

17. The first device of claim 6 , wherein the first device comprises a second organic light-emitting device;

wherein the second organic light emitting device is stacked on the first organic light emitting device.

18. The first device of claim 6 , wherein the first device is a consumer product.

19. The first device of claim 6 , wherein the first device is an organic light-emitting device.

20. The first device of claim 6 , wherein the first device comprises a lighting panel.

21. A method of making a first organic light emitting device, comprising:

depositing an anode on a substrate;

depositing at least one organic layer comprising a compound of formula:

wherein:

(i) G 1 is an electron donor group and G 2 is an electron acceptor group, or

(ii) G 1 is an electron acceptor group and G 2 is an electron donor group;

wherein:

(A) the electron donor group comprises at least one chemical group selected from the group consisting of:

wherein n is an integer from 1 to 20,

wherein m is an integer from 1 to 20,

wherein X and Y are independently selected from the group consisting of O, S, and NR 14 , and

wherein R 11 , R 12 , R 13 and R 14 are selected from the group consisting of aryl and heteroaryl; and

(B) the electron acceptor group is selected from the group consisting of:

wherein Z 1 to Z 8 independently comprise C or N,

wherein at least two of Z 1 to Z 8 are N,

wherein Y 1 to Y 8 independently comprise C or N,

wherein at least one of Y 1 to Y 8 is N,

wherein A 1 to A 8 independently comprise C or N,

wherein J 1 and J 2 independently comprise C or N,

wherein L 1 to L 4 independently comprise C or N,

wherein X 1 is O, S, or NR 14 , and

wherein R 14 is aryl or heteroaryl;

wherein the electron acceptor group is optionally substituted;

wherein R 1 and R 2 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, sulfonyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein R 1 and R 2 are optionally joined to form a ring, which may be further substituted; and

wherein the compound is an emissive dopant

depositing a cathode;

wherein the emissive layer is deposited between the anode and cathode.

22. The method of claim 21 , wherein the at least one organic layer is deposited using a solution process.