Electronic device comprising metal complexes

Patent metadata

Field	Value
Publication number	US-9634268-B2
Application number	US-201013513592-A
Country	US
Kind code	B2
Filing date	Nov 9, 2010
Priority date	Dec 5, 2009
Publication date	Apr 25, 2017
Grant date	Apr 25, 2017

Abstract

Electronic devices, in particular organic electroluminescent devices, comprising metal complexes of the formula (1).

First claim

The invention claimed is:

1. An electronic device comprising an anode, a cathode and at least one compound of the formula (1)

containing a metal M coordinated to a ligand L of the formula (2)

where the following applies to the symbols and indices used:

M is selected from Cu(I), Ag(I), Au(I), Ni(0), or Pd(0);
a is 0 and V is N or P, and V is coordinated to M through an electron lone pair, or
a is 1 and V is not coordinated to M, and is selected from B, BR − , CR, CO − , SiR, NR + , or P(═O); or V is a cyclic group of one of the formulae (31) to (34)

Y is, identically or differently on each occurrence, a divalent group selected from CR 2 , BR, SiR 2 , NR, PR, P(═O)R, O or S;
b is 1;
L1 is selected from the groups of the formulae (3) to (30):

X is on each occurrence, identically or differently, CR or N;
D is on each occurrence, identically or differently, O − , S − , NR − , PR − , NR 2 , PR 2 , COO − , SO 3 − , —C(═O)R, —CR(═NR) or —N(═CR 2 );
and the groups are coordinated to the metal M via the position denoted by *; the position denoted by # indicates the position at which the part-ligand is bonded to Y or to V, and the position denoted by (#) indicates the position at which the part-ligand is optionally bonded to Y or to L4, and if a further bond of this type to Y or to L4 is present, the corresponding symbol X(#) is C, and there is no group R bonded to the symbol N(#) in the formulae (7), (8), (9), (21) and (23);

L2 and L3 are selected, identically or differently on each occurrence, from the group consisting of —NR 2 , —NR − , —N═C(R 1 ) 2 , —PR 2 , —PR(OR), P(OR) 2 , —S − , —SR and L1;
L4 is a carbon monoxide, nitrogen monoxide, alkyl cyanide, aryl cyanide, alkyl isocyanide, aryl isocyanide, amine, halophosphine, trialkylphosphine, triarylphosphine, alkylarylphosphine, phosphite, arsine, stibene, neutral or anionic nitrogen-containing heterocycles, carbene, hydride, deuteride, F − , Cl − , Br − , alkylacetylide, arylacetylide, cyanide, cyanate, isocyanate, thiocyanate, isothiocyanate, aliphatic or aromatic alcoholate, aliphatic or aromatic thioalcoholates, amide, carboxylate, or

wherein, in formula (56), X and D are as defined for formulae (3) to (30), * indicates the position of the coordination to M, and the position denoted by (#) indicates the position at which L4 is optionally bonded, optionally via —(Y) n —, one of the part-ligands L1, L2 and L3 and if L4 is bonded to the part-ligand L1, L2 or L3 directly or through Y n , the corresponding symbol X(#) is C;
n is on each occurrence, identically or differently, 0, 1 or 2;
R is on each occurrence, identically or differently, H, D, F, Cl, Br, I, N(R 1 ) 2 , CN, NO 2 , OH, Si(R 1 ) 3 , B(OR 1 ) 2 , C(═O)R 1 , P(═O)(R 1 ) 2 , S(═O)R′, S(═O) 2 R 1 , OSO 2 R 1 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 C atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 C atoms or an alkenyl or alkynyl group having 2 to 40 C atoms, each of which is optionally substituted by one or more radicals R 1 , where one or more non-adjacent CH 2 groups is optionally replaced by R 1 C═CR 1 , C≡C, Si(R 1 ) 2 , Ge(R 1 ) 2 , Sn(R 1 ) 2 , C═O, C═S, C═Se, C═NR 1 , P(═O)(R 1 ), SO, SO 2 , NR 1 , O, S or CONR 1 and where one or more H atoms is optionally replaced by F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 1 , or an aryloxy, heteroaryloxy, aralkyl or heteroaryalkyl group having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R 1 , or a diarylamino group, diheteroarylamino group or arylheteroarylamino group having 10 to 40 aromatic ring atoms, which is optionally substituted by one or more radicals R 1 ; two or more substituents R here may also form a mono- or polycyclic, aliphatic, aromatic, heteroaromatic and/or benzo-fused ring system with one another;
R 1 is on each occurrence, identically or differently, 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 C atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 C atoms or an alkenyl or alkynyl group having 2 to 40 C atoms, each of which may be substituted by one or more radicals R 2 , where one or more non-adjacent CH 2 groups is optionally replaced by R 2 C═CR 2 , C≡C, Si(R 2 ) 2 , Ge(R 2 ) 2 , Sn(R 2 ) 2 , C═O, C═S, C═Se, C═NR 2 , P(═O)(R 2 ), SO, SO 2 , NR 2 , O, S or CONR 2 and where one or more H atoms is optionally replaced by F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 2 , or an aryloxy, heteroaryloxy, aralkyl or heteroaryalkyl group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 2 , or a diarylamino group, diheteroarylamino group or arylheteroarylamino group having 10 to 40 aromatic ring atoms, which is optionally substituted by one or more radicals R 2 ; two or more substituents R 1 here may also form a mono- or polycyclic, aliphatic, aromatic, heteroaromatic and/or benzo-fused ring system with one another;
R 2 is on each occurrence, identically or differently, H, D, F, or an aliphatic, aromatic or heteroaromatic radical having 1 to 20 C atoms, in which, in addition, one or more H atoms is optionally replaced by F; two or more substituents R 2 here may also form a mono- or polycyclic, aliphatic, aromatic, heteroaromatic and/or benzo-fused ring system with one another.

2. The electronic device according to claim 1 , wherein the device is an organic electroluminescent device, organic integrated circuit (O-IC), organic field-effect transistor (O-FET), organic thin-film transistor (O-TFT), organic light-emitting transistor (O-LET), organic solar cell (O-SC), organic optical detector, organic photoreceptor, organic field-quench device (O-FQD), light-emitting electrochemical cell (LEC) or organic laser diode (O-laser).

3. The electronic device according to claim 1 , wherein the device is an organic light-emitting diode.

4. The electronic device according to claim 1 , wherein the device is an organic electroluminescent device and the compound of the formula (1) is employed as emitting compound in an emitting layer.

5. The electronic device according to claim 4 , wherein the compound of the formula (1) is employed in combination with one or more matrix materials which are selected from the group consisting of ketone, phosphine oxide, sulfoxide, sulfone, triarylamine, carbazole derivative, indolocarbazole derivative, indenocarbazole derivative, azacarbazole, bipolar matrix material, silane, azaborole, boronic ester, triazine derivative, zinc complex, diaza- or tetraazasilole derivative a

Assignees

• Stoessel Philipp
• Joosten Dominik
• Breuning Esther
• Merck Patent Gmbh

Inventors

• Stoessel Philipp
• Joosten Dominik
• Breuning Esther

Classifications

• C09K2211/1029

  containing one nitrogen atom as the heteroatom · CPC title

• C09K2211/1033

  with oxygen · CPC title

• C09K11/06

  containing organic luminescent materials · CPC title

• H01L51/5012

  Electricity · mapped topic

• C09B57/10 Primary

  Metal complexes of organic compounds not being dyes in uncomplexed form · CPC title