Binuclear and trinuclear metal complexes composed of two inter-linked tripodal hexadentate ligands for use in electroluminescent devices

US10889604B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10889604-B2
Application numberUS-201716329363-A
CountryUS
Kind codeB2
Filing dateAug 28, 2017
Priority dateAug 30, 2016
Publication dateJan 12, 2021
Grant dateJan 12, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

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The present invention relates to bi- and trinuclear metal complexes and to electronic devices, in particular organic electroluminescent devices, containing these complexes.

First claim

Opening claim text (preview).

The invention claimed is: 1. A compound of formula (1) or formula (2): wherein M is on each occurrence, identically or differently, iridium or rhodium; Q is an aryl or heteroaryl group having 6 to 10 aromatic ring atoms and which is coordinated to each of the two or three M identically or differently in each case via a carbon or nitrogen atom and which is optionally substituted by one or more radicals R; and wherein the coordinating atoms in Q are not bonded in the ortho position to one another; D is on each occurrence, identically or differently, C or N; X is on each occurrence, identically or differently, CR or N; p is 0 or 1; V is on each occurrence, identically or differently, a group of formulae (3) or (4): wherein one of the dashed bonds is the bond to the corresponding 6-membered aryl or heteroaryl ring group of formula (1) or (2) and the two other dashed bonds are each the bonds to part-ligands L; L is on each occurrence, identically or differently, a bidentate, monoanionic part-ligand; X 1 is on each occurrence, identically or differently, CR or N; A 1 is on each occurrence, identically or differently, C(R) 2 or O; A 2 is on each occurrence, identically or differently, CR, P(═O), B, or SiR, with the proviso that, when A 2 is P(═O), B, or SiR, A 1 is O and the A bonded to this A 2 is not —C(═O)—NR′— or —C(═O)—O—; A is on each occurrence, identically or differently, —CR═CR—, —C(═O)—NR′—, —C(═O)—O—, —CR 2 —CR 2 —, —CR 2 —O—, or a group of formula (5): wherein the dashed bond is the position of the bond from a bidentate part-ligand L or from the corresponding 6-membered aryl or heteroaryl ring group of formula (1) or (2) to this structure and * is the position of the linking of the unit of formula (5) to the central cyclic group of formulae (3) or (4); X 2 is on each occurrence, identically or differently, CR or N or two adjacent groups X 2 together are NR, O, or S, so as to define a five-membered ring, and the remaining X 2 are, identically or differently on each occurrence, CR or N; or two adjacent groups X 2 together are CR or N if one of the groups X 3 in the ring are N, so as to define a five-membered ring; with the proviso that a maximum of two adjacent groups X 2 are N; X 3 is on each occurrence C, or one group X 3 is N and the other group X 3 in the same ring is C; with the proviso that two adjacent groups X 2 together are CR or N if one of the groups X 3 in the ring is N; R is on each occurrence, identically or differently, H, D, F, Cl, Br, I, N(R 1 ) 2 , CN, NO 2 , OR 1 , SR 1 , COOH, C(═O)N(R 1 ) 2 , Si(R 1 ) 3 , B(OR 1 ) 2 , C(═O)R 1 , P(═O)(R 1 ) 2 , S(═O)R 1 , S(═O) 2 R 1 , OSO 2 R 1 , COO(cation), SO 3 (cation), OSO 3 (cation), OPO 3 (cation) 2 , O(cation), N(R 1 ) 3 (anion), P(R 1 ) 3 (anion), a straight-chain alkyl group having 1 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms or a branched or cyclic alkyl group having 3 to 20 C atoms, wherein the alkyl, alkenyl, or alkynyl group is in each case optionally substituted by one or more radicals R 1 , wherein one or more non-adjacent CH 2 groups are optionally replaced by Si(R 1 ) 2 , C═O, NR 1 , O, S, or CONR 1 , or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which in each case is optionally substituted by one or more radicals R 1 ; and wherein two radicals R also optionally define a ring system with one another; R′ is on each occurrence, identically or differently, H, D, a straight-chain alkyl group having 1 to 20 C atoms or a branched or cyclic alkyl group having 3 to 20 C atoms, wherein the alkyl group is in each case optionally substituted by one or more radicals R 1 and wherein one or more non-adjacent CH 2 groups are optionally replaced by Si(R 1 ) 2 , or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which is in each case optionally substituted by one or more radicals R 1 ; R 1 is on each occurrence, identically or differently, H, D, F, Cl, Br, I, N(R 2 ) 2 , CN, NO 2 , OR 2 , SR 2 , Si(R 2 ) 3 , B(OR 2 ) 2 , C(═O)R 2 , P(═O)(R 2 ) 2 , S(═O)R 2 , S(═O) 2 R 2 , OSO 2 R 2 , COO(cation), SO 3 (cation), OSO 3 (cation), OPO 3 (cation) 2 , O(cation), N(R 2 ) 3 (anion), P(R 2 ) 3 (anion), a straight-chain alkyl group having 1 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms or a branched or cyclic alkyl group having 3 to 20 C atoms, wherein the alkyl, alkenyl, or alkynyl group is in each case optionally substituted by one or more radicals R 2 , wherein one or more non-adjacent CH 2 groups are optionally replaced by Si(R 2 ) 2 , C═O, NR 2 , O, S, or CONR 2 , or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which is in each case optionally substituted by one or more radicals R 2 ; and wherein two or more radicals R 1 also optionally define a ring system with one another; R 2 is on each occurrence, identically or differently, H, D, F, or an aliphatic, aromatic, or heteroaromatic organic radical having 1 to 20 C atoms, wherein one or more H atoms are optionally replaced by F; cation is selected on each occurrence, identically or differently, from the group consisting of proton, deuteron, alkali metal ions, alkaline-earth metal ions, ammonium, tetraalkylammonium, and tetraalkylphosphonium; and anion is selected on each occurrence, identically or differently, from the group consisting of halides, carboxylates R 2 —COO − , cyanide, cyanate, isocyanate, thiocyanate, thioisocyanate, hydroxide, BF 4 − , PF 6 − , B(C 6 F 5 ) 4 − , carbonate, and sulfonates. 2. The compound of claim 1 , wherein the compound is selected from the group consisting of compounds of formulae (1a) and (2a): wherein the radical R in the ortho position to D is in each case selected, identically or differently on each occurrence, from the group consisting of H, D, F, CH 3 , and CD 3 . 3. The compound of claim 1 , wherein Q in formula (1) is a group of formulae (Q-1) through (Q3) and Q in formula (2) is a group of one of formulae (Q-4) through (Q-15) when p is 0 or a group of formulae (Q-16) through (Q-19) when p is 1: wherein the dashed bond in each case indicates the linking within the formula (1) or (2); and * indicates the position at which the group is coordinated to M. 4. The compound of claim 1 , wherein the group of formula (3) is selected from the group consisting of structures of formulae (6) through (9) and wherein the group of formula (4) is selected from group consisting of structures of formulae (10) to (14): 5. The compound of claim 1 , wherein the group of formula (3) has a structure of formula (6′) and wherein the group of formula (4) has a structure of formula (10′) or (10″): 6. The compound of claim 1 , wherein A is selected, identically or differently on each oc

Assignees

Inventors

Classifications

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

  • Iridium compounds · CPC title

  • containing organic luminescent materials · CPC title

  • comprising dopants · CPC title

  • comprising iridium · CPC title

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Frequently asked questions

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What does patent US10889604B2 cover?
The present invention relates to bi- and trinuclear metal complexes and to electronic devices, in particular organic electroluminescent devices, containing these complexes.
Who is the assignee on this patent?
Merck Patent Gmbh
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 Jan 12 2021 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).