Metal Complexes

Patent metadata

Field	Value
Publication number	US-2016126480-A1
Application number	US-201414776796-A
Country	US
Kind code	A1
Filing date	Feb 24, 2014
Priority date	Mar 16, 2013
Publication date	May 5, 2016
Grant date	—

Abstract

The present invention relates to metal complexes in accordance with formula (1), to use thereof in electronic devices and to electronic devices, particularly organic electroluminescent devices, containing said metal complexes.

First claim

1 - 14 . (canceled)

15 . A compound of formula (1):

wherein
M is selected from the group consisting of Cu, Ag, Au, Zn, and Al;
A is selected from the group consisting of N and P;
Y is the same or different in each instance and is a bivalent group selected from the group consisting of CR 2 , O, S, 1,2-vinylene, 1,2-phenylene, 1,3-phenylene, and ortho-bonded heteroarylene groups having 5 or 6 aromatic ring atoms, wherein each of these groups is optionally substituted by one or more R radicals;
L 1 , L 2 , and L 3
is the same or different in each instance and is a heteroaryl group having 5 to 25 aromatic ring atoms, is optionally substituted by one or more R radicals, and contains a nitrogen, sulphur, or oxygen atom optionally coordinated to M, or is an aryl or heteroaryl group having 5 to 18 aromatic ring atoms, is optionally substituted by one or more R radicals, and has an exocyclic donor atom selected from the group consisting of N, O, S, and P coordinated to M and is optionally substituted by one or more R radicals; and wherein L 1 , L 2 , and L 3 are optionally bridged to one another via R radicals;

n is the same or different in each instance and is 0, 1, 2, 3, 4, or 5;
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 , 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 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms, a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 carbon atoms, an alkenyl or alkynyl group having 2 to 40 carbon atoms, each of which is optionally substituted by one or more R 1 radicals, wherein one or more nonadjacent CH 2 groups is optionally replaced by R 1 C═CR 1 , C≡C, Si(R 1 ) 2 , C═O, C═S, C═NR 1 , P(═O)(R 1 ), SO, SO 2 , NR 1 , O, S, or CONR 1 , and wherein one or more hydrogen atoms is optionally replaced by F, Cl, Br, I, CN, or NO 2 , an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms optionally substituted by one or more R 1 radicals, an aryloxy, heteroaryloxy, aralkyl, or heteroaralkyl group having 5 to 60 aromatic ring atoms optionally substituted by one or more R 1 radicals, or a diarylamino group, diheteroarylamino group, or arylheteroarylamino group having 10 to 40 aromatic ring atoms optionally substituted by one or more R 1 radicals; and wherein two or more R substituents together optionally define a mono- or polycyclic, aliphatic, aromatic, heteroaromatic and/or benzofused ring system;
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 , OH, 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 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms, a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 carbon atoms, an alkenyl or alkynyl group having 2 to 40 carbon atoms, each of which is optionally substituted by one or more R 2 radicals, wherein one or more nonadjacent CH 2 groups are optionally replaced by R 2 C═CR 2 , C≡C, Si(R 2 ) 2 , C═O, C═S, C═NR 2 , P(═O)(R 2 ), SO, SO 2 , NR 2 , O, S, or CONR 2 , and wherein one or more hydrogen atoms are optionally replaced by F, Cl, Br, I, CN, or NO 2 , an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, optionally substituted by one or more R 2 radicals, an aryloxy, heteroaryloxy, aralkyl or heteroaralkyl group having 5 to 60 aromatic ring atoms optionally substituted by one or more R 2 radicals, or a diarylamino group, diheteroarylamino group or arylheteroarylamino group having 10 to 40 aromatic ring atoms optionally substituted by one or more R 2 radicals; and wherein two or more R 1 substituents together optionally define a mono- or polycyclic, aliphatic, aromatic, heteroaromatic, and/or benzofused ring system;
R 2 is the same or different at each instance and is H, D, F or an aliphatic, aromatic and/or heteroaromatic hydrocarbyl radical having 1 to 20 carbon atoms, in which one or more hydrogen atoms may also be replaced by F; two or more R 2 substituents together may also form a mono- or polycyclic, aliphatic, aromatic, heteroaromatic and/or benzofused ring system; and

wherein if the compound is a charged compound, the compound also comprises one or more counterions, wherein the one or more counterions are the same or different.

16 . The compound of claim 15 , wherein M is Cu(I).

17 . The compound of claim 15 , wherein the compound has no electrical charge.

18 . The compound of claim 15 , wherein the cycle which is formed by A, Y, M and L 1 or L 2 or L 3 has 5, 6, 7, 8, or 9 ring atoms.

19 . The compound of claim 18 , wherein the cycle which is formed by A, Y, M and L 1 or L 2 or L 3 has 5, 6, 7, or 8 ring atoms.

20 . The compound of claim 19 , wherein the cycle which is formed by A, Y, M and L 1 or L 2 or L 3 has 5, 6, or 7 ring atoms.

21 . The compound of claim 15 , wherein L 1 or L 2 or L 3 has 5 to 14 aromatic ring atoms and wherein the aryl and heteroaryl groups are optionally substituted by one or more R radicals.

22 . The compound of claim 21 , wherein L 1 or L 2 or L 3 has 5 to 13 aromatic ring atoms.

23 . The compound of claim 22 , wherein L 1 or L 2 or L 3 has 5 to 10 aromatic ring atoms.

24 . The compound of claim 15 , wherein L 1 , L 2 , and L 3 are the same or different in each instance and are selected from the group consisting of formulae (2) to (41):

wherein
the groups coordinate to the metal M via the position identified by *;
the position identified by # indicates the position where L 1 or L or L 3 is bonded to Y or to A;
X is the same or different in each instance and is CR or N;
D is the same or different in each instance and is OH, O − , SH, S − , NR 2 , NR − , PR − , PR 2 , OR, SR, COO − , —C(═O)R, —CR(═NR), or —N(═CR 2 ).

25 . The compound of claim 15 , wherein Y is the same or different in each instance a and is a bivalent group selected from CR 2 and O, with the proviso that Y is not O when A ═N.

26 . The compound of claim 25 , wherein Y is a bivalent group CR 2 .

27 . The compound of claim 24 , wherein:
not more than three X symbols in each group are N; Y is the same or different in each instance and is a bivalent group selected from CR 2 and O; n is the same or different in each instance and is 0, 1 or 2.

28 . The compound of claim 15 , wherein at least two of L 1 , L 2 , and L 3 are the same and have the same substitution.

29 . A process for preparing the compound of claim 15 , comprising the step of reacting a metal salt or metal complex of the metal M with the appropriate free ligand, wherein the free ligand is optionally in deprotonated form and wherein the reaction step is optionally followed by a deprotonation step.

30 . A formulation comprising at least one compound of claim 15 and at least one further compound.

Assignees

• Merck Patent Gmbh

Inventors

• Wesemann Lars
• Kleith Matthias
• Mayer Hermann August

Classifications

• Y02E10/549

  Organic PV cells · CPC title

• C07F19/005

  without metal-C linkages · CPC title

• C09K11/06

  containing organic luminescent materials · CPC title

• H01L51/5016

  Electricity · mapped topic

• H01L51/0091 Primary

  Electricity · mapped topic