IP Library › Granted Patent US 11,925,105
Granted Patent B2
US 11,925,105 · App. 16/988,003 · Granted Mar 5, 2024

Organic electroluminescent materials and devices

Inventors: Tyler Fleetham (Newtown, PA); Hsiao-Fan Chen (Lawrence Township, NJ); Jerald Feldman (Cherry Hill, NJ)
Assignee: UNIVERSAL DISPLAY CORPORATION
H10K85/346C07D401/14H05B33/00H10K50/11H10K2101/10
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,925,105
App. No.
16/988,003
Granted
Mar 5, 2024
Kind
B2
Abstract

Provided is a new composition of matter for phosphorescent emitters containing a chelating ligand including five or more fused carbocyclic or heterocyclic rings that form two bonds to a metal forming a 7-membered chelate. This fused ring structure provides added rigidity to the molecule for enhanced stability in an OLED device and improve photophysical properties.

Claims (64)

1. A compound having a fragment with at least five rings fused next to each other consecutively wherein the fragment is a ligand L A of Formula I;

wherein:

rings A, B, C, D, and E are each independently a 5-membered or 6-membered carbocyclic or heterocyclic ring;

Z 1 -Z 12 are each independently C or N;

R A , R B , R C , R D , and R E each independently represents zero, mono, or up to a maximum allowed substitutions to its associated ring;

if an R A , R B , R C , R D , or R E represents no substitution, then said R A , R B , R C , R D , or R E is hydrogen;

if R A , R B , R C , R D , or R E represents a substituent, then each R A , R B , R C , R D , and R E is independently a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, fluorinated alkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

two substituents can be joined or fused together to form a ring;

wherein the ligand L A is complexed to a metal M at Z 1 and Z 6 ;

wherein the metal M is selected from the group consisting of Ir, Rh, Re, Ru, Os, Pt, Pd, Au, Ag, and Cu;

wherein M can be coordinated to other ligands; and

wherein the ligand L A can be linked with other ligands to form a tridentate, tetradentate, pentadentate, or hexadentate ligand.

2. The compound of claim 1 , wherein the at least five rings comprises two 5-membered rings and three 6-membered rings.

3. The compound of claim 1 , wherein the at least five rings comprises five aromatic rings.

4. The compound of claim 1 , wherein R A , R B , R C , R D , and R E are each independently selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, and combinations thereof.

5. The compound of claim 1 , wherein M is Ir, Pt or Pd.

6. The compound of claim 1 , wherein the ligand L A is linked with other ligands to form a tetradentate ligand.

7. The compound of claim 1 , wherein

ring A, ring C, and ring E are 6-membered rings, and ring B and ring D are 5-membered rings;

ring A, ring C, and ring E are 5-membered rings, and ring B and ring D are 6-membered rings;

ring A and ring E are 5-membered rings, and ring B, ring C, and ring D are 6-membered rings;

ring A and ring E are 6-membered rings, and ring B, ring C, and ring D are 5-membered rings; or

ring A, ring B, ring D, and ring E are 5-membered rings, and ring C is a 6-membered ring.

8. The compound of claim 1 , wherein Z 1 -Z 12 are C.

9. The compound of claim 1 , wherein at least one of Z 1 -Z 12 is N.

10. A compound having a fragment with at least five rings fused next to each other consecutively wherein the fragment is a ligand L A having a formula selected from the group consisting of:

wherein each X 1 -X 2 is independently selected from the group consisting of C and N; wherein no more than two N atoms are bonded to one another;

R A , R B , R C , R D , and R E each independently represents zero, mono, or up to a maximum allowed substitutions to its associated ring;

if an R A , R B , R C , R D , or R E represents no substitution, then said R A , R B , R C , R D , or R E is hydrogen;

if R A , R B , R C , R D , or R E represents a substituent, then each R A , R B , R C , R D , and R E is independently a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, fluorinated alkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein each Y 1 -Y 5 is selected from the group consisting of O, S, Se, NR, CRR′, SiRR′, GeRR′, and BR; and wherein R and R′ are independently selected from the group consisting of hydrogen, deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, and combinations thereof;

two substituents can be joined or fused together to form a ring;

wherein the dashed lines represent coordination to a metal M;

wherein the metal M is selected from the group consisting of Ir, Rh, Re, Ru, Os, Pt, Pd, Au, Ag, and Cu;

wherein M can be coordinated to other ligands; and

wherein the ligand L A can be linked with other ligands to form a tridentate, tetradentate, pentadentate, or hexadentate ligand.

11. The compound of claim 10 , wherein the ligand L A is selected from the group consisting of the following compounds:

wherein each X 1 -X 6 is independently selected from the group consisting of C and N; wherein no more than two N atoms are bond to one another; wherein each Y 1 -Y 7 is selected from the group consisting of O, S, Se, NR, CRR′, SiRR′, GeRR′, and BR; and wherein R and R′ are each independently selected from the group consisting of hydrogen, deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, and combinations thereof.

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

13. The compound of claim 1 , wherein the compound emits light upon photoexcitation at room temperature; wherein the emitted light has an emission spectrum characterized by a peak emission wavelength λ max when measured at a concentration of 0.1 mM in a solution of 2-methyl tetrahydrofuran; and wherein the full width at half maximum of the emission at λ max that is equal to or less than 20 nm.

14. An organic light emitting device (OLED) comprising:

an anode;

a cathode; and

an organic layer disposed between the anode and the cathode, wherein the organic layer comprises a compound having a fragment with at least five rings fused next to each other consecutively wherein the fragment is a ligand L A of Formula I;

wherein:

rings A, B, C, D, and E are each independently a 5-membered or 6-membered carbocyclic or heterocyclic ring;

Z 1 -Z 12 are each independently C or N;

R A , R B , R C , R D , and R E each independently represents zero, mono, or up to a maximum allowed substitutions to its associated ring;

if an R A , R B , R C , R D , or R E represents no substitution, then said R A , R B , R C , R D , or R E is hydrogen;

if R A , R B , R C , R D , or R E represents a substituent, then each R A , R B , R C , R D , and R E is independently a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, fluorinated alkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

two substituents can be joined or fused together to form a ring;

wherein the ligand L A is complexed to a metal M at Z 1 and Z 6 ;

wherein the metal M is selected from the group consisting of Ir, Rh, Re, Ru, Os, Pt, Pd, Au, Ag, and Cu;

wherein M can be coordinated to other ligands; and

wherein the ligand L A can be linked with other ligands to form a tridentate, tetradentate, pentadentate, or hexadentate ligand.

15. The OLED of claim 14 , wherein the organic layer further comprises a host, wherein host comprises at least one chemical group selected from the group consisting of metal complex, triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.

16. A consumer product comprising an organic light-emitting device (OLED) comprising:

an anode;

a cathode; and

an organic layer disposed between the anode and the cathode, wherein the organic layer comprises a compound according to claim 1 .

17. An organic light emitting device (OLED) comprising:

an anode;

a cathode; and

an organic layer disposed between the anode and the cathode, wherein the organic layer comprises the compound of claim 10 .

Assignments (1)
NUNC PRO TUNC ASSIGNMENT Recorded Aug 7, 2020
From: FLEETHAM, TYLER; CHEN, HSIAO-FAN; FELDMAN, JERALD
To: UNIVERSAL DISPLAY CORPORATION
Reel/Frame 053434/0441 →
Continuity (2)
Provisional Application 62891623 · Aug 26, 2019
Related Publication 20210066622A1 · Mar 4, 2021