Host materials for electroluminescent devices

1. A composition comprising:

a first compound of Formula I

wherein ring A is fused to a structure of Formula II:

wherein each Ar 1 , Ar 2 , and Ar 3 is independently a substituted or unsubstituted six-membered aromatic ring; and

a second compound capable of functioning as a phosphorescent emitter at room temperature;

wherein the second compound emits light with a peak emission wavelength equal to or greater than 550 nm;

wherein at least one of the following two conditions is true:

(i) the highest occupied molecular orbital of the second compound has an energy level equal to or less than −5.1 eV; and

(ii) the difference in energy between the highest occupied molecular orbital of the first compound and the highest occupied molecular orbital of the second compound is less than 0.3 eV.

2. The composition of claim 1 , wherein the second compound emits light with a peak emission wavelength equal to or greater than 600 nm, wherein at least one of the following two conditions is true:

(iii) the highest occupied molecular orbital of the second compound has an energy level equal to or less than −5.3 eV; and

(iv) the difference in energy between the highest occupied molecular orbital of the first compound and the highest occupied molecular orbital of the second compound is less than 0.1 eV.

3. The composition of claim 1 , wherein Ar 1 , Ar 2 , and Ar 3 are phenyl rings.

4. The composition of claim 1 , wherein at least one of Ar 1 , Ar 2 , and Ar 3 comprises a fused carbocyclic or heterocyclic ring.

5. The composition of claim 1 , wherein the second compound is an Ir or Pt complex having a metal-carbon bond.

6. The composition of claim 1 , wherein the first compound is selected from the group consisting of:

7. The composition of claim 1 , wherein the second compound has the formula of M(L 1 ) x (L 2 ) y (L 3 ) z ;

wherein M is a metal;

wherein L 1 , L 2 , and L 3 can be the same or different;

wherein x is 1, 2, or 3;

wherein y is 0, 1, or 2;

wherein z is 0, 1, or 2;

wherein x+y+z is the oxidation state of the metal M;

wherein at least one of L 1 , L 2 , and L 3 has Formula III

wherein ring A is a 5-membered or 6-membered carbocyclic or heterocyclic ring;

wherein R represents two adjacent substituents that are joined together to form a ring that is fused to ring B and R has a structure of Formula IV

or Formula V

wherein the wavy lines indicate bonds to ring B;

wherein R A and R B each independently represents no substitution to a maximum possible number of substitutions;

wherein R A and R B are each independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein A 1 , A 2 , A 3 , and A 4 are each independently CR C or N;

wherein Z 1 , Z 2 , Z 3 , and Z 4 are each independently C or N;

wherein at least two adjacent of Z 1 , Z 2 , Z 3 , and Z 4 are C and fuse to R;

wherein when R is Formula V, at least one of A 1 , A 2 , A 3 , A 4 , Z 1 , Z 2 , Z 3 , and Z 4 is N;

wherein Y is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO 2 , CR′R″, SiR′R″, and GeR′R″;

wherein R C , R 13 , R 14 , and R″ are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein any two adjacent substituents are optionally joined to form into a ring.

8. The composition of claim 7 , wherein R A and R B are each independently a hydrogen or a substituent selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof; and

R C , R 13 , R 14 , R′, and R″ are each independently selected from the group consisting of hydrogen, deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof.

9. The composition of claim 7 , wherein the second compound has a formula of M(L 1 ) 2 L 2 , wherein L 1 has a formula according to Formula III, and L 2 is an unsubstituted or substituted acetylacetonate ligand.

10. The composition of claim 1 , wherein the second compound is a transition metal complex comprising at least one ligand or part of the ligand if the ligand is more than bidentate selected from the group consisting of:

wherein R 1 and R 2 represent mono to a maximum possible number of substitutions, or no substitution; wherein each R 1 and R 2 is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

wherein any two substituents may be joined or fused together to form a ring.

11. The composition of claim 1 , wherein the second compound is selected from the group consisting of:

12. The composition of claim 1 , wherein the first compound is a host, and wherein the composition comprises a third compound, which serves as a co-host.

13. The composition of claim 12 , wherein the third compound is selected from the group consisting of the following compounds:

wherein R 3 to R 12 each independently represents no substitution to a maximum possible number of substitutions on a ring carbon the substituents are attached thereto;

wherein each of R 3 to R 12 is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein Ar 4 -Ar 8 are each independently a 6-membered carbocyclic or heterocyclic ring;

wherein m=0, 1, 2, or 3; and

wherein any two substituents may be joined or fused together to form a ring.

14. The composition of claim 12 , wherein the third compound is selected from the group consisting of:

15. An organic light emitting device comprising:

a cathode;

an anode; and

an emissive layer, disposed between the anode and cathode;

wherein the emissive layer comprises a composition comprising:

a first compound of Formula I

wherein ring A is fused to a structure of Formula II:

wherein each Ar 1 , Ar 2 , and Ar 3 is independently a substituted or unsubstituted six-membered aromatic ring; and

a second compound capable of functioning as a phosphorescent emitter at room temperature;

wherein the second compound emits light with a peak emission wavelength equal to or greater than 550 nm;

wherein at least one of the following two conditions is true:

(i) the highest occupied molecular orbital of the second compound has an energy level equal to or less than −5.1 eV; and

(ii) the difference in energy between the highest occupied molecular orbital of the first compound and the highest occupied molecular orbital of the second compound is less than 0.3 eV.

16. A consumer product comprising an organic light emitting device comprising:

an anode;

a cathode; and

an emissive layer, disposed between the anode and cathode;

wherein the emissive layer comprises a composition of claim 1 .

17. A composition comprising:

a first compound capable of functioning as a host in an emissive layer of an OLED device at room temperature; and

a second compound comprising a ligand L A of Formula III

wherein ring A is a 5-membered or 6-membered carbocyclic or heterocyclic ring;

wherein R represents two adjacent substituents that are joined together to form a ring that is fused to ring B, and R has a structure of Formula IV

or Formula V

wherein the wavy lines indicate bonds to ring B;

wherein R A and R B each independently represents no substitution to a maximum possible number of substitutions on a ring carbon the substituents are attached thereto;

wherein R A and R B are each independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein A 1 , A 2 , A 3 , and A 4 are each independently CR C or N;

wherein Z 1 , Z 2 , Z 3 , and Z 4 are each independently C or N;

wherein at least two adjacent of Z 1 , Z 2 , Z 3 , and Z 4 are C and fuse to R;

wherein when R is Formula V, at least one of A 1 , A 2 , A 3 , A 4 , Z 1 , Z 2 , Z 3 , and Z 4 is N;

wherein Y is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO 2 , CR′R″, SiR′R″, and GeR′R″;

wherein R C , R 13 , R 14 , R′ and R″ are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,

wherein any two adjacent substituents are optionally joined to form into a ring;

wherein the ligand L A is coordinated to a metal M;

wherein M is Ir or Pt;

wherein the ligand L A is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate, or hexadentate ligand; and

wherein M is optionally coordinated to other ligands; and

wherein at least one of the following two conditions is true:

(i) the highest occupied molecular orbital of the first compound has an energy level equal to or less than −5.1 eV; and

(ii) the difference in energy between the highest occupied molecular orbital of the first compound and the highest occupied molecular orbital of the second compound is less than 0.3 eV.

18. The composition of claim 17 , wherein at least one of R 13 and R 14 comprises a chemical group selected from the group consisting of alkyl, cycloalkyl, partially fluorinated alkyl, partially fluorinated cycloalkyl, and combinations thereof.

19. An organic light emitting device comprising:

a cathode;

an anode; and

an emissive layer, disposed between the anode and cathode;

wherein the emissive layer comprises a composition of claim 17 .

20. A consumer product comprising an organic light-emitting device comprising:

an anode;

a cathode; and

an emissive layer, disposed between the anode and cathode;

wherein the emissive layer comprises a composition according to claim 17 .