Organic electroluminescent materials and devices
A novel type of blue emitter is described based on the azaphenanthridine imidazole ligand. The preferred use of this moiety for generating blue phosphorescence is as part of a symmetric platinum tetradentate complex.
1. A compound of
wherein A and B are independently selected from the group consisting of a 5-membered or 6-membered carbocyclic or heterocyclic ring; and one of A and B is an anionic coordinating atom, and the other of A and B is a neutral coordinating atom;
wherein at least one of linking groups X and Y is present;
X and Y are independently selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO 2 , CR′R″, alkylene, arylene, SiR′R″, and GeR′R″;
M is Pt or Pd;
R is 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;
R 1 and R 3 each independently represent mono, or di-substitution, or no substitution;
R 2 represent mono, di, tri, or tetra-substitution, or no substitution;
wherein R 1 , R 2 , R 3 , R′, and R″ 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; or any two adjacent R 1 , R 2 , R 3 , R′, and R″ are optionally joined to form a ring.
2. The compound of claim 1 , wherein M is Pt.
3. The compound of claim 1 , wherein R is selected from the group consisting of alkyl, cycloalkyl, silyl, aryl, heteroaryl, and combinations thereof.
4. The compound of claim 1 , wherein R is selected from the group consisting of methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, cyclopentyl, cyclohexyl, phenyl, 2,6-dimethylphenyl, 2,4,6-trimethylphenyl, 2,6-diisopropylphenyl, and combinations thereof.
5. The compound of claim 1 , wherein X is absent.
6. The compound of claim 1 , wherein Y is absent.
7. The compound of claim 5 , wherein the compound is selected from the group consisting of:
wherein R 6 represents mono, di, tri-substitution, or no substitution;
R 4 , R 5 , and R 6 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; or any two adjacent R 4 , R 5 , and R 6 are optionally joined to form a ring.
8. The compound of claim 6 , wherein the compound is selected from the group consisting of:
wherein R 6 represents mono, di, tri-substitution, or no substitution;
R 4 , R 5 , and R 6 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; or any two adjacent R 4 , R 5 , and R 6 are optionally joined to form a ring.
9. The compound of claim 1 , wherein A-B is selected from the group consisting of:
wherein each X 1 to X 13 are independently selected from the group consisting of carbon and nitrogen; and if carbon then R a , R b , R c , and R d independently represent from mono substitution to the possible maximum number of substitution, or no substitution
X is selected from the group consisting of NR′, O, S, Se, C═O, CR′R″, SiR′R″, and GeR′R″;
R L represents mono substitution, or no substitution;
R a , R b , R c , R d and R L 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; or independently R a , R b , R c , and R d represent at least di substitution, and two adjacent R a , two adjacent R b , two adjacent R c , and two adjacent R d , join to form a ring; and
optional linking group X or Y joins with A-B through R L or any one X 1 to X 13 indicated by the dotted lines.
10. The compound of claim 1 , wherein the compound is selected from the group consisting of:
11. An organic light emitting device comprising:
an anode;
a cathode; and
an organic layer disposed between the anode and the cathode, the organic layer comprising a compound of claim 1 .
12. The device of claim 11 selected from the group consisting of a consumer product, an electronic component module, and a lighting panel.
13. The device of claim 11 , wherein the organic layer further comprises a host; wherein the host comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan;
wherein any substituent in the host is an unfused substituent independently selected from the group consisting of C n H n2+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≡CC n H 2n+1 , Ar 1 , Ar 1 —Ar 2 , and C n H 2n —Ar 1 , or no substitution;
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.
14. The device of claim 11 , wherein the organic layer further comprises a host, wherein the host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.
15. The device of claim 11 , wherein the organic layer further comprises a host and the host is selected from the group consisting of:
and any one mixture thereof.
16. A formulation comprising the compound of claim 1 .