Metal complex with fluorine substitution
A metal complex with fluorine substitution is disclosed, which employs a series of new ligands containing fluorine-substituted structure can be used as a luminescent material in an emissive layer of an electroluminescent device. By using the metal complex can provide much longer device lifetime, better thermal stability, no blue-shifted illumination, and higher luminous efficiency. An electroluminescent device and compound formulation are also disclosed.
1. A metal complex has a general formula of M(L a ) m (L b ) 3-m ;
wherein m is 1;
wherein M is iridium;
wherein the metal complex has a structure according to Formula 2:
R 1 , R a and R b can represent mono, di, tri, or tetra substitution, or no substitution;
R 3 represents mono, di, or no substitution;
R 4 represents mono, di or tri substitution;
wherein X is O;
wherein R 3 and R 4 are each independently selected from the group consisting of hydrogen, deuterium, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 12 carbon atoms; at least one of the R 4 is a substituted or unsubstituted aryl group having 6 to 12 carbon atoms;
R 1 is selected from the group consisting of hydrogen, deuterium, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 12 carbon atoms;
R a is selected from the group consisting of hydrogen, deuterium, and a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms;
R b is hydrogen or deuterium;
the alkyl and aryl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, aryl, heteroaryl, silyl, a nitrile group, and combinations thereof.
2. The metal complex of claim 1 ,
wherein R 1 , R 3 and R b are each hydrogen or deuterium;
R 4 is selected from the group consisting of hydrogen, deuterium, and a substituted or unsubstituted aryl group having 6 to 12 carbon atoms; at least one of the R 4 is a substituted or unsubstituted aryl group having 6 to 12 carbon atoms;
R a is selected from the group consisting of hydrogen, deuterium, and a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms;
the alkyl and aryl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, alkyl, silyl, and combinations thereof.
3. The metal complex of claim 1 , wherein R 4 is selected from the group consisting of hydrogen, and a substituted or unsubstituted aryl group having 6 to 12 carbon atoms, at least one of the R 4 is a substituted or unsubstituted aryl group having 6 to 12 carbon atoms;
R 1 , R 3 and R b are selected from hydrogen;
R a is selected from the group consisting of hydrogen, and unsubstituted alkyl group having 1 to 6 carbon atoms;
the aryl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, alkyl, silyl, and combinations thereof.
4. The metal complex of claim 1 , wherein ligand L a is selected from the group consisting of:
5. The metal complex of claim 4 , wherein L a can be partially or fully deuterated.
6. The metal complex of claim 4 , wherein the metal complex has the formula of IrL a (L b ) 2 , wherein L a is selected from the group consisting of
wherein L b is selected from the group consisting of:
7. The metal complex of claim 1 , wherein R 4 represents mono substitution, R 4 is a substituted or unsubstituted aryl group having 6 to 12 carbon atoms.
8. The metal complex of claim 1 , wherein
R 1 , R 3 and R b are each hydrogen;
R 4 is selected from the group consisting of hydrogen, and a substituted or unsubstituted phenyl; at least one of the R 4 is a substituted or unsubstituted phenyl;
R a is selected from the group consisting of hydrogen, and a substituted or unsubstituted methyl;
the methyl, phenyl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, alkyl, silyl, and combinations thereof.
9. The metal complex of claim 1 , wherein
R 1 , R 3 and R b are each hydrogen;
R 4 is selected from the group consisting of hydrogen, and a substituted or unsubstituted phenyl; at least one of the R 4 is a substituted or unsubstituted phenyl;
R a is selected from the group consisting of hydrogen, and methyl;
the phenyl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, methyl, silyl, and combinations thereof.
10. A formulation comprises the metal complex of claim 1 .
11. An electroluminescent device comprises an anode, a cathode, and an organic layer, disposed between the anode and the cathode, wherein the organic layer comprises the metal complex of claim 1 .
12. The electroluminescent device of claim 11 , wherein the organic layer is an emissive layer and the metal complex is an emitter.
13. The electroluminescent device of claim 11 , wherein the organic layer further comprises a host.
14. The electroluminescent device of claim 13 , wherein the host material comprises at least one the chemical group selected from the group consisting of: benzene, biphenyl, pyridine, pyrimidine, triazine, carbazole, azacarbazole, indolocarbazole, dibenzothiophene, azadibenzothiophene, dibenzofuran, azadibenzofuran, dibenzoselenophene, azadibenzoselenophene, triphenylene, azatriphenylene, fluorene, silicon fluorene, naphthalene, quinoline, isoquinoline, quinazoline, quinoxaline, phenanthrene, azaphenanthrene, and combinations thereof.
15. The electroluminescent device of claim 11 , wherein the electroluminescent device is incorporated into another device selected from the group consisting of a consumer product, an electronic component module, an organic light emitting device, and a lighting panel.
16. The electroluminescent device of claim 11 , wherein the organic layer comprises at least two hosts.