Organometallic compound, organic light-emitting device including the same, and diagnostic composition including the organometallic compound
US-2020044166-A1 · Feb 6, 2020 · US
US12598906B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12598906-B2 |
| Application number | US-202117192035-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 4, 2021 |
| Priority date | Mar 31, 2020 |
| Publication date | Apr 7, 2026 |
| Grant date | Apr 7, 2026 |
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Provided is an OLED having an anode, a cathode and an organic emissive layer disposed between the anode and the cathode. The emissive layer includes a first host; and a first emitter; wherein the first emitter is selected from the following group: (L 1 -L 2 ) n Ir(L A ) 3−n and (L B ) n Ir(L 3 -L 4 ) 3−n ; wherein (L 1 -L 2 ) n Ir(L A ) 3−n is and (L B ) n Ir(L 3 -L 4 ) 3−n is
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What is claimed is: 1 . An organic light emitting device (OLED), comprising: an anode; a cathode; and an organic emissive layer disposed between the anode and the cathode comprising: a first host; and a first emitter; wherein the first emitter is (L 1 -L 2 ) n Ir(L A ) 3−n ; wherein (L 1 -L 2 ) n Ir(L A ) 3−n is wherein L 1 -L 2 represents an anionic bidentate ligand; wherein n is 1 or 2; wherein each of R S1 , R S2 , R S3 , R S4 , R S5 , and R S6 is independently selected from the group consisting of alkyl, cycloalkyl, partially or fully fluorinated variants thereof, partially or fully deuterated variants thereof, and combinations thereof; wherein at least one of R S1 to R S6 is not CH 3 ; wherein any two substituents of R S1 , R S2 , R S3 , R S4 , R S5 , and R S6 can be joined or fused into a ring; wherein at least one of the following is true: (1) R S1 is joined with R S2 to form a ring; (2) R S1 is joined with R S2 to form a ring, and R S4 is joined with R S5 to form a ring; or (3) at least one of R S1 to R S6 is partially or fully fluorinated alkyl; and wherein the first host comprises at least one donor group G D , and at least one acceptor group G A . 2 . The OLED of claim 1 , wherein the ligand (L 1 -L 2 ) is selected from the group consisting of: wherein Y 1 to Y 10 are each independently selected from the group consisting of carbon and nitrogen; wherein Y′ is selected from the group consisting of BR e , BR e R f , NR e , PR e , O, S, Se, C═O, S═O, SO 2 , CR e R f , SiR e R f , and GeR e R f ; wherein R e and R f are optionally fused or joined to form a ring; wherein R a , and R b each independently represent zero, mono, or up to a maximum allowed substitution to its associated ring; wherein each of R a , R b , R e and R f is independently 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, boryl; and wherein two adjacent substituents of R a , and R b are optionally fused or joined to form a ring or form a multidentate ligand. 3 . The OLED of claim 1 , wherein the ligand (L 1 -L 2 ) is selected from the group consisting of: L 1 -L 2 -1-i based on Structure 1: L 1 -L 2 -2-i based on Structure 2: L 1 -L 2 -3-i based on Structure 3: L 1 -L 2 -4-i based on Structure 4: L 1 -L 2 -5-i based on Structure 5: L 1 -L 2 -6-i based on Structure 6: L 1 -L 2 -7-i based on Structure 7: L 1 -L 2 -8-i based on Structure 8: L 1 -L 2 -9-i based on Structure 9: L 1 -L 2 -10-i based on Structure 10: L 1 -L 2 -11-i based on Structure 11: L 1 -L 2 -12-i based on Structure 12: L 1 -L 2 -13-i based on Structure 13: L 1 -L 2 -14-i based on Structure 14: and L 1 -L 2 -15-i based on Structure 15: L 1 -L 2 -16-i based on Structure 16: L 1 -L 2 -17-i based on Structure 17: wherein i is an integer from 1 to 810, and for each i, R E , and G are as defined below: i R E G 1 R 1 G 1 2 R 2 G 1 3 R 3 G 1 4 R 4 G 1 5 R 5 G 1 6 R 6 G 1 7 R 7 G 1 8 R 8 G 1 9 R 9 G 1 10 R 10 G 1 11 R 11 G 1 12 R 12 G 1 13 R 13 G 1 14 R 14 G 1 15 R 15 G 1 16 R 16 G 1 17 R 17 G 1 18 R 18 G 1 19 R 19 G 1 20 R 20 G 1 21 R 21 G 1 22 R 22 G 1 23 R 23 G 1 24
Triplet emission · CPC title
characterised by the electroluminescent [EL] layers · CPC title
of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd · CPC title
containing one nitrogen atom as the heteroatom · CPC title
Non-condensed systems · CPC title
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