Binuclear metal complexes for use as emitters in organic electroluminescent devices

Patent metadata

Field	Value
Publication number	US-11136343-B2
Application number	US-201716335560-A
Country	US
Kind code	B2
Filing date	Sep 18, 2017
Priority date	Sep 21, 2016
Publication date	Oct 5, 2021
Grant date	Oct 5, 2021

Abstract

The present invention relates to binuclear metal complexes and electronic devices, in particular organic electroluminescent devices containing said metal complexes.

First claim

The invention claimed is:

1. A compound of formula (1):

wherein
M is the same or different in each instance and is iridium or rhodium;
D is the same or different in each instance and is C or N;
X is the same or different in each instance and is CR or N; or two adjacent X together in the cycle containing E are CR or N and the third X is CR or N when either one D in the cycle coordinates as an anionic nitrogen atom to M or when E is N;
E is C or N, wherein E can be N only when two adjacent X together in the cycle containing E are CR or N and the third X is CR or N;
V is the same or different at each instance and is a group of the formula (2) or (3)

wherein the dotted bond bonded directly to the cycle is the bond to the corresponding 6-membered aryl or heteroaryl group of formula (1) and the two dotted bonds to A are each the bonds to the sub-ligands L;
L is the same or different in each instance and is a bidentate monoanionic sub-ligand;
X 1 is the same or different in each instance and is CR or N;
X 2 is the same or different in each instance and is CR or N; or two adjacent X 2 groups together are NR, O, or S, so as to define a five-membered ring, and the remaining X 2 are the same or different in each instance and are CR or N; or two adjacent X 2 groups together are CR or N when one of the X 3 groups in the cycle is N, so as to define a five-membered ring; with the proviso that not more than two adjacent X 2 groups are N;
X 3 is C in each instance or one X 3 group is N and the other X 3 groups in the same cycle are C; with the proviso that two adjacent X 2 groups together are CR or N when one of the X 3 groups in the cycle is N;
A 1 is the same or different in each instance and is C(R) 2 or O;
A 2 is the same or different in each instance and is CR, P(═O), B, or SiR, with the proviso that, when A 2 is P, (═O), or SiR, A 1 is O and the A bonded to the A 2 is not —C(═O)—NR′— or —C(═O)—O—;
A is the same or different in each instance and is —CR═CR—, —C(═O)—NR′—, —C(═O)—O—,—CR 2 —CR 2 —, —CR 2 —O—, or a group of formula (4):

wherein the dotted bond is the position of the bond of a bidentate sub-ligand L to the group of formula (4) and * is the position of the linkage of the group of formula (4) to the central cyclic group;
R is the same or different in each instance and is 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 carbon atoms or an alkenyl or alkynyl group having 2 to 20 carbon atoms or a branched or cyclic alkyl group having 3 to 20 carbon atoms, wherein the alkyl, alkenyl, or alkynyl group is in each case optionally substituted by one or more radicals R 1 and wherein one or more nonadjacent 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 and which is optionally substituted in each case by one or more radicals R 1 ; and wherein two radicals R together optionally define a ring system;
R′ is the same or different in each instance and is H, D, a straight-chain alkyl group having 1 to 20 carbon atoms or a branched or cyclic alkyl group having 3 to 20 carbon atoms, wherein the alkyl group is in each case optionally substituted by one or more radicals R 1 and wherein one or more nonadjacent 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 and which is optionally substituted in each case by one or more radicals R 1 ;
R 1 is the same or different in each instance and is 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 carbon atoms or an alkenyl or alkynyl group having 2 to 20 carbon atoms or a branched or cyclic alkyl group having 3 to 20 carbon atoms, wherein the alkyl, alkenyl, or alkynyl group is in each case optionally substituted by one or more radicals R 2 , and wherein one or more nonadjacent 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 and which are optionally substituted in each case by one or more radicals R 2 ; and wherein two or more radicals R 1 together optionally define a ring system;
R 2 is the same or different in each instance and is H, D, F, or an aliphatic, aromatic, or heteroaromatic organic radical having 1 to 20 carbon atoms, wherein one or more hydrogen atoms is also optionally replaced by F;
cation is the same or different in each instance and is selected from the group consisting of proton, deuteron, alkali metal ions, alkaline earth metal ions, ammonium, tetraalkylammonium, and tetraalkylphosphonium;
anion is the same or different in each instance and is selected 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 both metals M are Ir(III) and the compound is an uncharged compound.

3. The compound of claim 1 , wherein the compound is selected from the group consisting of compounds of formulae (1′), (1″), and (1″):

wherein the radicals R in the position ortho to the groups D and in the position ortho to the coordinating nitrogen atom in formula (1″) are each the same or different in each instance and are selected from the group consisting of H, D, F, CH 3 , and CD 3 .

4. The compound of claim 1 , wherein the compound is selected from the group consisting of compounds of formulae (1a) through (1h):

wherein X in the five-membered ling of formulae (1d) through (1h) is the same or different in each instance and is CR or N.

5. The compound of claim 1 , wherein the compound is selected from the group consisting of compounds of formulae (1a′) through (1h′):

wherein the radicals R in position ortho to the coordinating carbon or nitrogen atoms are each the same or different in each instance and are selected from the group consisting of H, D, F, CH 3 , and CD 3 .

6. The compound of claim 1 , wherein the group of formula (2) is selected from the group consisting of structures of formulae (5) through (8) and the group of formula (3) is selected from the group consisting of stru

Assignees

• Merck Patent Gmbh

Inventors

• Stoessel Philipp
• Ehrenreich Christian
• Harbach Philipp
• Hayer Anna
• Breuning Esther

Classifications

• C07F15/0033 Primary

  Iridium compounds · CPC title

• C09K2211/185

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

• C09K11/06

  containing organic luminescent materials · CPC title

• C07F15/0073

  Rhodium compounds · CPC title

• H01L2251/5384

  Electricity · mapped topic