Organic electroluminescent materials and devices

US9450195B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9450195-B2
Application numberUS-201414573722-A
CountryUS
Kind codeB2
Filing dateDec 17, 2014
Priority dateDec 17, 2014
Publication dateSep 20, 2016
Grant dateSep 20, 2016

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  1. Title

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  5. First independent claim

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Abstract

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Phosphorescent metal complexes comprising a pendant redox-active metallocene are disclosed. These complexes are useful as emitters for phosphorescent OLEDs.

First claim

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What is claimed is: 1. A compound comprising a first ligand L 1 having the Formula: wherein ring A is a 6-membered heteroaryl and ring B is a phenyl; wherein X 1 and X 2 is N, and the other X 1 and X 2 is C; wherein X 3 and X 4 are C; wherein R A and R B each independently represent mono, di, tri, or tetra substitution; wherein at least one of R A and R B has a structure according to the following formula:  wherein L is a direct bond or a linker selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein R 1 represents mono, di, tri, or tetra substitution, or no substitution; wherein R 2 represents mono, di, tri, tetra, or penta substitution, or no substitution; wherein M 2 is selected from the group consisting of Os, Ru, and Re; wherein R 1 and R 2 are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein at least one R A has the structure of Formula II; wherein when R A and R B is not Formula II, R A and R B are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein any two adjacent substituents are optionally joined to form a ring, which can be further substituted; wherein the ligand L 1 is coordinated to Ir; wherein the Ir can be coordinated to other ligands; and wherein the ligand L 1 is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand. 2. The compound of claim 1 , wherein at least one of R A and R B has a structure according to the following formula: and wherein R 5 and R 6 are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof. 3. The compound of claim 1 , wherein the ligand L 1 is wherein R 3 and R 4 each independently represent mono, di, tri, or tetra substitution, or no substitution; and wherein R 3 , R 4 , R 5 , and R 6 are each independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof. 4. The compound of claim 1 , wherein the compound is homoleptic. 5. The compound of claim 1 , wherein the compound is heteroleptic. 6. The compound of claim 1 , wherein the compound is neutral. 7. The compound of claim 1 , wherein the ligand L 1 is selected from the group consisting of: 8. The compound of claim 1 , wherein the compound has the formula of M(L 1 ) x (L 2 ) y (L 3 ) z ; wherein L 2 is a second ligand, and L 3 is a third ligand, and L 2 and L 3 can be the same or different; wherein x is 1, 2, or 3; wherein y is 0, 1, or 2; wherein z is 0, 1, or 2; wherein x+y+z is the oxidation state of the metal M; wherein the second ligand L 2 and the third ligand L 3 are independently selected from the group consisting of: wherein R a , R b , R c , and R d may represent mono, di, tri, or tetra substitution, or no substitution; wherein R a , R b , R c , and R d are independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and wherein two adjacent substituents of R a , R b , R c , and R d are optionally joined to form a fused ring or form a multidentate ligand. 9. The compound of claim 8 , wherein the compound has the formula of Ir(L 1 )(L 2 ) 2 . 10. The compound of claim 1 , wherein the compound is selected from the group consisting of: 11. A device comprising one or more organic light emitting devices, at least one of the one or more organic light emitting devices comprising: an anode; a cathode; and an organic layer, disposed between the anode and the cathode, the organic layer comprising a compound comprising a first ligand L 1 of Formula I: wherein ring A is a 6-membered heteroaryl and ring B is a phenyl; wherein one of X 1 and X 2 is N, and the other X 1 and X 2 is C; wherein X 3 and X 4 are C; wherein R A and R B each independently represent mono, di, tri, or tetra substitution

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What does patent US9450195B2 cover?
Phosphorescent metal complexes comprising a pendant redox-active metallocene are disclosed. These complexes are useful as emitters for phosphorescent OLEDs.
Who is the assignee on this patent?
Universal Display Corp
What technology area does this patent fall under?
Primary CPC classification C07F15/0033. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).