Organic electroluminescent materials and devices

1. A compound having a formula:

Formula I;

wherein L 1 is selected from the group consisting of a direct bond, phenyl, biphenyl, terphenyl, fluorene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, naphthalene, anthracene, and combinations thereof;

wherein G 1 is selected from the group consisting of:

wherein X is selected from the group consisting of oxygen, sulfur, and selenium;

wherein R 1 , R 5 , R 7 , R 8 , R 12 , and R 13 each independently represent mono, di, tri, or tetra substitution, or no substitution;

wherein R 2 , R 3 , R 4 , R 5 , R 6 , R 9 , R 10 , and R 11 each independently represent mono, di, or tri substitution, or no substitution;

wherein R 1 to R 13 are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, alkoxyl, halogen, silyl, nitro, benzene, biphenyl, terphenyl, naphthalene, phenanthrene, benzofuran, benzothiophene, benzoselenophene, dibenzofuran, dibenzothiophene, dibenzoselenophene, fluorene, triphenylene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinoline, phenanthroline, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-fluorene, aza-triphenylene, aza-carbazole, and combinations thereof;

wherein Z 1 to Z 20 are each independently selected from the group consisting of carbon and nitrogen;

wherein at least one of Z 1 , Z 2 , Z 3 , Z 4 , Z 5 , Z 6 , Z 7 , and Z 8 is nitrogen; and at least one of Z 9 , Z 10 , Z 11 , Z 12 , Z 13 , Z 14 , Z 15 , Z 16 , Z 17 , Z 18 , Z 19 and Z 20 is nitrogen;

wherein when any of Z 1 to Z 20 is nitrogen, there is no substitution on that nitrogen;

wherein L 1 and G 1 are bonded together by a C—C bond;

wherein Ar 1 is selected from the group consisting of benzene, biphenyl, terphenyl, triphenylene, fluorene, dibenzofuran, dibenzothiophene, dibenzoselenophene, naphthalene, phenanthrene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, azatriphenylene, aza-fluorene, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-carbazole, quinolone, quinazoline, and combinations thereof;

wherein L 1 and Ar 1 are each optionally further substituted with one or more substituents selected from the group consisting of deuterium, alkyl, alkoxyl, halogen, silyl, nitro, benzene, biphenyl, terphenyl, naphthalene, phenanthrene, dibenzofuran, dibenzothiophene, dibenzoselenophene, fluorene, triphenylene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinolone, phenanthroline, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-fluorene and aza-triphenylene, aza-carbazole, and combinations thereof; and

wherein the compound of Formula I contains at most one non-fused carbazole moiety.

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

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

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

a direct bond,

wherein X 1 is selected from a group consisting of O, S, Se, CR L1 R L2 , and NR L3 ;

wherein R L1 , R L2 , and R L3 are each independently selected from the group consisting of hydrogen, deuterium, alkyl, aryl, and combinations thereof.

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

6. A compound having a formula,

Formula II;

wherein L 2 is selected from the group consisting of a direct bond, alkyl, alkoxyl, aryl, heteroaryl, and combinations thereof;

wherein R 21 represents mono, di, tri, or tetra substitution, or no substitution;

wherein R 22 , and R 23 each independently represent mono, di, or tri substitution, or no substitution;

wherein R 21 to R 23 are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, alkoxyl, halogen, silyl, nitro, benzene, biphenyl, terphenyl, naphthalene, phenanthrene, benzofuran, benzothiophene, benzoselenophene, dibenzofuran, dibenzothiophene, dibenzoselenophene, fluorene, triphenylene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinoline, phenanthroline, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-fluorene, aza-triphenylene, aza-carbazole, and combinations thereof;

wherein G 2 is selected from the group consisting of:

wherein Z 21 to Z 42 are each independently selected from the group consisting of C—R 20 and N;

wherein at least one of Z 21 to Z 42 is C—R 20 ;

wherein each R 20 can be same or different, and is independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

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

wherein Y is selected from the group consisting of: O, S, Se, BR B1 , NR B2 , PR B3 , and CR B4 R B5 ;

wherein R B1 , R B2 , R B3 , R B4 and R B5 are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, and combinations thereof;

wherein R B4 and R B5 are optionally jointed to form a ring;

wherein L 2 is optionally further substituted with one or more substituents selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

wherein the compound of Formula II contains at most one non-fused carbazole moiety.

7. The compound of claim 6 , wherein the compound is selected from the group consisting of:

8. 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 a formula selected from the group consisting of:

wherein L 1 is selected from the group consisting of a direct bond, phenyl, biphenyl, terphenyl, fluorene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, naphthalene, anthracene, and combinations thereof;

wherein G 1 is selected from the group consisting of:

wherein X is selected from the group consisting of oxygen, sulfur and selenium;

wherein R 1 , R 5 , R 7 , R 8 , R 12 , R 13 , and R 21 each independently represent mono, di, tri, or tetra substitution, or no substitution;

wherein R 2 , R 3 , R 4 , R 5 , R 6 , R 9 , R 10 , R 11 , R 22 , and R 23 each independently represent mono, di, or tri substitution, or no substitution;

wherein R 1 to R 13 and R 21 to R 23 are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, alkoxyl, halogen, silyl, nitro, benzene, biphenyl, terphenyl, naphthalene, phenanthrene, benzofuran, benzothiophene, benzoselenophene, dibenzofuran, dibenzothiophene, dibenzoselenophene, fluorene, triphenylene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinoline, phenanthroline, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-fluorene, aza-triphenylene, aza-carbazole, and combinations thereof;

wherein Z 1 to Z 20 are each independently selected from the group consisting of carbon and nitrogen;

wherein at least one of Z 1 , Z 2 , Z 3 , Z 4 , Z 5 , Z 6 , Z 7 and Z 8 is nitrogen; and at least one of Z 9 , Z 10 , Z 11 , Z 12 , Z 13 , Z 14 , Z 15 , Z 16 , Z 17 , Z 18 , Z 19 and Z 20 is nitrogen;

wherein when any of Z 1 to Z 20 is nitrogen, there is no substitution on that nitrogen;

wherein L 1 and G 1 are bonded together by a C—C bond;

wherein Ar 1 is selected from the group consisting of benzene, biphenyl, terphenyl, triphenylene, fluorene, dibenzofuran, dibenzothiophene, dibenzoselenophene, naphthalene, phenanthrene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, azatriphenylene, aza-fluorene, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-carbazole, quinolone, quinazoline, and combinations thereof;

wherein L 1 and Ar 1 are each optionally further substituted with one or more substituents selected from the group consisting of deuterium, alkyl, alkoxyl, halogen, silyl, nitro, benzene, biphenyl, terphenyl, naphthalene, phenanthrene, dibenzofuran, dibenzothiophene, dibenzoselenophene, fluorene, triphenylene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinolone, phenanthroline, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-fluorene and aza-triphenylene, aza-carbazole, and combinations thereof;

wherein L 2 is selected from the group consisting of a direct bond, alkyl, alkoxyl, aryl, heteroaryl, and combinations thereof;

wherein G 2 is selected from the group consisting of:

wherein Z 21 to Z 42 are each independently selected from the group consisting of C—R 20 and N;

wherein at least one of Z 21 to Z 42 is C—R 20 ;

wherein each R 20 can be same or different, and is independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

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

wherein Y is selected from the group consisting of: O, S, Se, BR B1 , NR B2 , PR B3 , and CR B4 R B5 ;

wherein R B1 , R B2 , R B3 , R B4 and R B5 are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, and combinations thereof;

wherein R B4 and R B5 are optionally jointed to form a ring;

wherein L 2 is optionally further substituted with one or more substituents selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

wherein the compounds of Formula I and Formula II each contains at most one non-fused carbazole moiety.

9. The first organic light emitting device of claim 8 , wherein the organic layer is an emissive layer and the compound of Formula I or Formula II is a host.

10. The first organic light emitting device of claim 8 , wherein the organic layer further comprises a phosphorescent emissive dopant; wherein the emissive dopant is a transition metal complex having at least one ligand or part of the ligand if the ligand is more than bidentate selected from the group consisting of:

wherein each X 1 to X 13 are independently selected from the group consisting of carbon and nitrogen;

wherein X 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′ and R″ are optionally fused or joined to form a ring;

wherein each R a , R b , R c , and R d may represent from mono substitution to the possible maximum number of substitution, or no substitution;

wherein R′, R″, R a , R b , R c , and R d 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 any two adjacent substituents of R a , R b , R c , and R d are optionally fused or joined to form a ring or form a multidentate ligand.

11. The first organic light emitting device of claim 8 , wherein the organic layer is a blocking layer and the compound having Formula I or Formula II is a blocking material in the organic layer.

12. The first organic light emitting device of claim 8 , wherein the organic layer is an electron transporting layer and the compound having Formula I or Formula II is an electron transporting material in the organic layer.

13. The first organic light emitting device of claim 8 , wherein the device is incorporated into a device selected from the group consisting of a consumer product, an electronic component module, an organic light-emitting device, and a lighting panel.

14. A formulation comprising a compound having a formula selected from the group consisting of:

wherein L 1 is selected from the group consisting of a direct bond, phenyl, biphenyl, terphenyl, fluorene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, naphthalene, anthracene, and combinations thereof;

wherein G 1 is selected from the group consisting of:

wherein X is selected from the group consisting of oxygen, sulfur and selenium;

wherein R 1 , R 5 , R 7 , R 8 , R 12 , R 13 , and R 21 each independently represent mono, di, tri, or tetra substitution, or no substitution;

wherein R 2 , R 3 , R 4 , R 5 , R 6 , R 9 , R 10 , R 11 , R 22 and R 23 each independently represent mono, di, or tri substitution, or no substitution;

wherein R 1 to R 13 and R 21 to R 23 are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, alkoxyl, halogen, silyl, nitro, benzene, biphenyl, terphenyl, naphthalene, phenanthrene, benzofuran, benzothiophene, benzoselenophene, dibenzofuran, dibenzothiophene, dibenzoselenophene, fluorene, triphenylene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinoline, phenanthroline, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-fluorene, aza-triphenylene, aza-carbazole, and combinations thereof;

wherein Z 1 to Z 20 are each independently selected from the group consisting of carbon and nitrogen;

wherein at least one of Z 1 , Z 2 , Z 3 , Z 4 , Z 5 , Z 6 , Z 7 and Z 8 is nitrogen; and at least one of Z 9 , Z 10 , Z 11 , Z 12 , Z 13 , Z 14 , Z 15 , Z 16 , Z 17 , Z 18 , Z 19 and Z 20 is nitrogen;

wherein when any of Z 1 to Z 20 is nitrogen, there is no substitution on that nitrogen;

wherein L 1 and G 1 are bonded together by a C—C bond;

wherein Ar 1 is selected from the group consisting of benzene, biphenyl, terphenyl, triphenylene, fluorene, dibenzofuran, dibenzothiophene, dibenzoselenophene, naphthalene, phenanthrene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, azatriphenylene, aza-fluorene, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-carbazole, quinolone, quinazoline, and combinations thereof;

wherein L 1 and Ar 1 are each optionally further substituted with one or more substituents selected from the group consisting of deuterium, alkyl, alkoxyl, halogen, silyl, nitro, benzene, biphenyl, terphenyl, naphthalene, phenanthrene, dibenzofuran, dibenzothiophene, dibenzoselenophene, fluorene, triphenylene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinolone, phenanthroline, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-fluorene and aza-triphenylene, aza-carbazole, and combinations thereof;

wherein L 2 is selected from the group consisting of a direct bond, alkyl, alkoxyl, aryl, heteroaryl, and combinations thereof;

wherein G 2 is selected from the group consisting of:

wherein Z 21 to Z 42 are each independently selected from the group consisting of C—R 20 and N;

wherein at least one of Z 21 to Z 42 is C—R 20 ;

wherein each R 20 can be same or different, and is independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

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

wherein Y is selected from the group consisting of: O, S, Se, BR B1 , NR B2 , PR B3 , and CR B4 R B5 ;

wherein R B1 , R B2 , R B3 , R B4 and R B5 are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, and combinations thereof;

wherein R B4 and R B5 are optionally jointed to form a ring;

wherein L 2 is optionally further substituted with one or more substituents selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

provided that the compound of Formula I and Formula II each contains at most one non-fused carbazole moiety.

15. A formulation comprising the compound in claim 1 .