Electroluminescent devices based on phosphorescent iridium and related group VIII metal multicyclic compounds

US9520574B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9520574-B2
Application numberUS-201113643054-A
CountryUS
Kind codeB2
Filing dateApr 28, 2011
Priority dateApr 28, 2010
Publication dateDec 13, 2016
Grant dateDec 13, 2016

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Abstract

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Disclosed herein are phosphorescent materials comprising a complex of a metal atom M selected from Ir, Pt, Rh, Pd, Ru and Os and at least one ligand L, wherein the ligand L is represented by formula (1). Also disclosed are organic electroluminescent devices including such phosphorescent materials.

First claim

Opening claim text (preview).

The invention claimed is: 1. An organic electroluminescent device comprising: a pair of electrodes comprising an anode and a cathode, and one or more layers of organic compound arranged between the anode and the cathode, wherein at least one of the one or more layers of organic compound comprises a phosphorescent material; wherein the phosphorescent material comprises a complex of a metal atom M selected from Ir, Pt, Rh, Pd, Ru and Os and at least one ligand L, wherein the ligand L is represented by formula (1): wherein: ring A is a substituted or unsubstituted 5-membered heterocycle containing at least one ring nitrogen atom bound to the metal atom at the asterisk (*), wherein ring A may be substituted with one or more substituents selected from the group consisting of: halogen, cyano, amide, imine, imide, amidine, amine, nitro, hydroxy, ether, carbonyl, carboxy, carbonate, carbamate, phosphine, phosphate, phosphonate, sulphide, sulphone, sulphoxide, silyl, substituents containing a functional group that can be polymerised or a polymer chain, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, and substituted or unsubstituted alkynyl, wherein: one or more of the carbon atoms in the alkyl may be replaced, wherein each carbon atom that is replaced is independently replaced with an atom or group selected from the group consisting of: —C(═O)—, —O—, —S—, —N', —C═N—, —Si— and —P—; ring B is a substituted or unsubstituted 5- or 6-membered carbocycle or heterocycle containing a carbon atom as represented in formula (1) which is bound to the metal atom at the asterisk (*), rings A and B are joined by a direct covalent bond as represented in formula (1), rings A and B are joined via a tether Q, wherein Q is a tether of between 3 and 20 atoms in length, and is selected from the group consisting of: linear, branched or cyclic alkyl; linear or branched alkenyl; linear or branched alkynyl; aryl; and alkyl-aryl; wherein one or more of the carbon atoms in the alkyl, aryl or alkyl-aryl may be replaced, wherein each carbon atom that is replaced is independently replaced with an atom or group selected from the group consisting of: —C(═O)—, —O—, —S—, —N—, ═N—, —Si— and —P—; wherein when the atom is ═N—, the nitrogen double bond is to an adjacent carbon atom in the alkyl, aryl, or alkyl-aryl so as to form a —C═N— group; and wherein the tether may contain one or more substituents selected from the group consisting of halogen, cyano, amide, imine, imide, amidine, amine, nitro, hydroxy, ether, carbonyl, carboxy, carbonate, carbamate, phosphine, phosphate, phosphonate, sulphide, sulphone, sulphoxide, alkenyl, aryl, alkyl, heteroaryl, alkynyl, silyl, and substituents containing a functional group that can be polymerised, a polymer chain, or two substituents may together form a ring or fused ring system. 2. The device of claim 1 , wherein ring B may be substituted with one or more substituents selected from the group consisting of: halogen, cyano, amide, imine, imide, amidine, amine, nitro, hydroxy, ether, carbonyl, carboxy, carbonate, carbamate, phosphine, phosphate, phosphonate, sulphide, sulphone, sulphoxide, silyl, substituents containing a functional group that can be polymerised or a polymer chain, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl and substituted or unsubstituted alkyl-aryl, wherein: one or more of the carbon atoms in the alkyl, aryl or alkyl-aryl may be replaced wherein each carbon atom that is replaced is independently replaced with an atom or group selected from the group consisting of: —C(═O)—, —O—, —S—, —N—, —C═N—, —Si— and —P—, the substituents on the alkyl, aryl or alkyl-aryl are selected from the group consisting of: halogen, cyano, amide, imine, imide, amidine, amine, nitro, hydroxy, ether, carbonyl, carboxy, carbonate, carbamate, phosphine, phosphate, phosphonate, sulphide, sulphone, sulphoxide, alkenyl, alkynyl, silyl, and substituents containing a functional group that can be polymerised or a polymer chain, and the alkyl, aryl or alkyl-aryl may additionally be connected to the tether Q, or the alkyl, aryl or alkyl-aryl may be attached via two points to its core ring B to form a fused ring or ring system. 3. The device of claim 1 , wherein the phosphorescent material comprises 1, 2 or 3 ligands L of formula (1), and 0, 1 or 2 bidentate ligands L′ of a different identity to ligand L. 4. The device of claim 3 , wherein the ligand L′ of the phosphorescent material is a ligand of formula (5), a ligand of formula (6) or a ligand of formula (7): wherein: ring Y is a 5-, 6- or 7-membered heterocycle which is unsubstituted or substituted by one or more substituents, containing at least one nitrogen atom as represented in the formula, which is bound to the metal atom at the asterisk (*), ring Y′ is a 5-, 6- or 7-membered heterocycle which is unsubstituted or substituted by one or more substituents, and containing at least one nitrogen atom as represented in the formula which is bound to the metal atom at the asterisk (*), and rings Y and Y′ are either joined by a direct covalent bond or via a linker J as represented in formula (5), wherein J, when present, is a B, C, O, N, P, Si or S atom which is covalently bonded to both rings Y and Y′ and which may be substituted or unsubstituted depending on its valency; wherein: ring Y is as defined in formula (5), Z is a ligand component connected via a covalent bond to ring Y, and connected to the metal atom via X, and X is an N, O, S or P atom bound to the metal atom at the asterisk (*), wherein the N or P atom is unsubstituted or is substituted wherein G is a ligand component consisting of one or two substituted or unsubstituted carbon atoms in length, which is connected covalently to two O atoms, and the O atoms are each bound to the metal atom at the asterisk (*). 5. The device of claim 1 , wherein ligand L of the phosphorescent material is of the formula (3): wherein: A 1 and A 2 are each independently selected from the group consisting of: C, N, O and S, wherein the C or N may be substituted or unsubstituted, A 3 and A 4 are selected from the group consisting of: C and N, wherein the C may be substituted or unsubstituted. 6. The device of claim 5 , wherein the ligand L of the phosphorescent material is of the formula (4): wherein: B 1 and B 2 are each independently selected from the group consisting of: C, N, O and S, wherein the C or N may be substituted or unsubstituted, B 3 , when present, is selected from the group consisting of: C, N, O and S, wherein the C or N may be substituted or unsubstituted, b is 0 or 1, B 4 is selected from the group consisting of: C and N, wherein the C may be substituted or unsubstituted, and B 5 is C. 7. The device of claim 6 , wherein the ligand L of the phosphorescent material is selected from the group consisting of:

Assignees

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Classifications

  • with sulfur · CPC title

  • containing one nitrogen atom as the heteroatom · CPC title

  • Apparatus or processes specially adapted to the manufacture of electroluminescent light sources · CPC title

  • Non-condensed systems · CPC title

  • of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd · CPC title

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What does patent US9520574B2 cover?
Disclosed herein are phosphorescent materials comprising a complex of a metal atom M selected from Ir, Pt, Rh, Pd, Ru and Os and at least one ligand L, wherein the ligand L is represented by formula (1). Also disclosed are organic electroluminescent devices including such phosphorescent materials.
Who is the assignee on this patent?
Groarke Michelle, Ueno Kazunori, Bown Mark, and 2 more
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 Dec 13 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).