Organic electroluminescent materials and devices
Imidazophenanthridine ligands and metal complexes are provided. The compounds exhibit improved stability through a linking substitution that links a nitrogen bonded carbon of an imidizole ring to a carbon on the adjacent fused aryl ring. The compounds may be used in organic light emitting devices, particularly as emissive dopants, providing devices with improved efficiency, stability, and manufacturing. In particular, the compounds provided herein may be used in blue devices having high efficiency.
1. A compound having a structure (L A ) n ML m according to Formula 1:
wherein M is a metal having an atomic weight greater than 40, n has a value of at least 1 and m+n is the maximum number of ligands that may be attached to the metal;
wherein A is a linking group selected from the group consisting of —CR′R″—CR′R″—, —CR′R′—CR″R″—, and —CR′R′—CR′R′—CR′R′—;
wherein each R′ is independently selected from the group consisting of H, D, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof,
wherein each R″ is independently selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, partially or fully deuterated variants thereof, and combinations thereof,
wherein R′s and R″s are optionally connected to form a saturated five membered ring or a saturated six membered ring, and combinations thereof,
wherein R 1a to R 1g are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof;
wherein any one of the ring atoms to which R 1b to R 1g are attached may be replaced with a nitrogen atom, wherein when the ring atom is replaced with a nitrogen atom the corresponding R group is not present;
wherein L is a substituted or unsubstituted cyclometallated ligand,
wherein L can be joined to R 1g through a linking group L 2 ;
wherein L 2 is selected from the group consisting of a single bond, NR, O, S, CR 1 R 2 , and SiR 1 R 2 ;
wherein R, R 1 , and R 2 can be same or different, and are independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof; wherein any adjacent R 1 and R 2 are optionally connected to form a saturated five membered ring or a saturated six membered ring.
2. The compound of claim 1 , wherein A is selected from the group consisting of —CR′R″—CR′R″— and —CR′R′—CR″R″—.
3. The compound of claim 2 , wherein each of R′ and R″ is independently selected from the group consisting of undeuterated alkyl, partially deuterated alkyl, and fully deuterated alkyl.
4. The compound of claim 1 , wherein the compound has a peak emissive wavelength less than 500 nm.
5. The compound of claim 1 , wherein the linking group is selected from the group consisting of:
6. The compound of claim 1 , wherein at least one of R 1a to R 1g is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, partially or fully deuterated variants thereof, and combinations thereof.
7. The compound of claim 6 , wherein at least one of R 1b , R 1d and R 1e is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, partially or fully deuterated variants thereof, and combinations thereof.
8. The compound of claim 6 , wherein R 1d is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, partially or fully deuterated variants thereof, and combinations thereof.
9. The compound of claim 6 , wherein R 1a is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, partially or fully deuterated variants thereof, and combinations thereof.
10. The compound of claim 8 , wherein R 1d is selected from the group consisting of non-deuterated alkyl, partially deuterated alkyl, and fully deuterated alkyl.
11. The compound of claim 9 , wherein R 1a is selected from the group consisting of non-deuterated aryl, partially deuterated aryl, and fully deuterated aryl.
12. The compound of claim 11 , wherein R 1a is selected from the group consisting of non-deuterated phenyl, partially deuterated phenyl, and fully deuterated phenyl.
13. The compound of claim 10 , wherein R 1d is selected from the group consisting of —CH 3 , —CD 3 , and isopropyl.
14. The compound of claim 7 , wherein R 1f is selected from the group consisting of —CH 3 , —CD 3 , and isopropyl.
15. The compound of claim 1 , wherein the metal is Ir.
16. The compound of claim 1 , wherein the ligand L 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;
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 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.
17. The compound of claim 16 , wherein the ligand L is selected from the group consisting of:
18. The compound of claim 1 , wherein ligand L is selected from the group consisting of:
19. The compound of claim 16 , wherein the compound has a structure selected from the group consisting of (L A ) 3 Ir, (L A )Ir(L) 2 or (L A ) 2 Ir(L).
20. A compound having a structure according to Formula A:
wherein M is Ir;
wherein n is 3;
wherein A is a linking group selected from the group consisting of —CR′R″—CR′R″— and —CR′R′—CR″R″—;
wherein each or R′ and R″ is independently selected from the group consisting of undeuterated alkyl, partially deuterated alkyl, and fully deuterated alkyl;
wherein R′s and R″s are optionally connected to form a saturated five membered ring or a saturated six membered ring, and combinations thereof,
wherein R 1a to R 1g are each independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof;
wherein R 1a is selected from the group consisting of H, non-deuterated phenyl, partially deuterated phenyl, and fully deuterated phenyl;
wherein R 1d is selected from the group consisting of H, —CH 3 , —CD 3 , and isopropyl; and wherein 1f is selected from the group consisting of H, —CH 3 , —CD 3 , and isopropyl.