Materials for organic electroluminescent devices

Patent metadata

Field	Value
Publication number	US-2016190447-A1
Application number	US-201615060087-A
Country	US
Kind code	A1
Filing date	Mar 3, 2016
Priority date	Sep 15, 2010
Publication date	Jun 30, 2016
Grant date	—

Abstract

The present invention relates to compounds of the formula (1) which are suitable for use in electronic devices, in particular organic electroluminescent devices, and to electronic devices which comprise these compounds.

First claim

1 .- 14 . (canceled)

15 . A compound of formula (1),

where the following applies to the symbols and indices used:
Ar is, identically or differently on each occurrence, an aromatic ring system selected from the group consisting of benzene, naphthalene, phenanthrene, fluorene, spirobifluorene, dibenzofuran and dibenzothiophene, each of which is optionally substituted by one or more radicals R 1 ; Ar is optionally connected to Ar 1 and/or to Ar 2 by a group E;
Ar 1 and Ar 2 are, identically or differently on each occurrence, an aromatic or heteroaromatic ring system having 6 to 60 C atoms selected from the group consisting of benzene, naphthalene, phenanthrene, dibenzofuran and dibenzothiophene, each of which is optionally substituted by one or more radicals R 1 , or unsubstituted spirobifluorene or a combination of two, three, four or five of these groups, which may in each case be identical or different; or
Ar 1 and Ar 2 are, identically or differently on each occurrence, selected from formulae (9), (21), (26) or (27), where the dashed bond indicates the position of the bond to the nitrogen, and in each instance, Ar 1 and Ar 2 is optionally connected to one another, and/or Ar 1 is optionally connected to Ar, and/or Ar 2 is optionally connected to Ar, by a group E;

E is, identically or differently on each occurrence, selected from the group consisting of C(R 1 ) 2 , O, S and NR 1 ;
R is on each occurrence, identically or differently, and are H, D, F, Cl, Br, I, CN, Si(R 2 ) 3 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C atoms, each of which is optionally substituted by one or more radicals R 2 , where in each case one or more non-adjacent CH 2 groups is optionally replaced by Si(R 2 ) 2 , 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 D, F, Cl, Br or I, an aromatic or heteroaromatic ring system having 6 to 60 C atoms selected from the group consisting of benzene, naphthalene, phenanthrene, fluorene, spirobifluorene, dibenzofuran and dibenzothiophene, which may in each case be substituted by one or more radicals R 2 , or a combination of two, three, four or five of these groups, which may in each case be identical or different, an aryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 2 , or an aralkyl group having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 2 , where two or more adjacent substituents R or two or more adjacent substituents R 1 may optionally form a mono- or polycyclic, aliphatic ring system, which is optionally substituted by one or more radicals R 2 ;
R 1 is on each occurrence, identically or differently, is H, D, F, CN, a straight-chain alkyl group having 1 to 40 C atoms or a branched or cyclic alkyl group having 3 to 40 C atoms, or an aromatic ring or heteroaromatic ring system having 6 to 60 C atoms selected from the group consisting of benzene, naphthalene, phenanthrene, dibenzofuran, and dibenzothiophene, or a combination of two, three, four or five of these groups, which may in each case be identical or different;
R 2 is on each occurrence, identically or differently, is H, D, F, Cl, Br, I, Si(R 3 ) 3 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C atoms, each of which is optionally substituted by one or more radicals R 3 , where one or more non-adjacent CH 2 groups is optionally replaced by Si(R 3 ) 2 , C═NR 3 , P(═O)(R 3 ), SO, SO 2 , NR 3 , O, S or CONR 3 and where one or more H atoms is optionally replaced by D, F, Cl, Br or I, an aromatic ring system having 6 to 60 C atoms selected from the group consisting of benzene, naphthalene, phenanthrene, fluorene, spirobifluorene or a combination of two, three, four or five of these groups, which may in each case be identical or different, which may in each case be substituted by one or more radicals R 3 , an aryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 3 , or an aralkyl group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 3 , where two or more adjacent substituents R 2 may optionally form a mono- or polycyclic, aliphatic ring system, which is optionally substituted by one or more radicals R 3 ;
R 3 is selected from the group consisting of H, D, F, an aliphatic hydrocarbon radical having 1 to 20 C atoms, an aromatic ring system having 6 to 30 C atoms, in which one or more H atoms is optionally replaced by D or F, where two or more adjacent substituents R 3 may a mono- or polycyclic, aliphatic ring system with one another;
m is 0, 1, 2 or 3;
n is on each occurrence, identically or differently, 0, 1, 2, 3 or 4;
p is 0, 1 or 2;
the following compounds are excluded from the invention:

16 . The compound according to claim 15 of the formula (2), formula (3a), (3b), (4a) or formula (4b),

symbols and indices used have the meanings given in claim 15 .

17 . The compound according to claim 15 , wherein the groups Ar 1 and Ar 2 are selected, identically or differently on each occurrence, from the groups of the formulae (5) to (28),

where the symbols used have the meanings given in claim 15 , and the dashed bond indicates the position of the bond from the group to the nitrogen.

18 . The compound according to claim 15 , wherein the groups Ar 1 and Ar 2 are selected, identically or differently on each occurrence, from the groups of the formulae (5a) to (28a),

where the symbols used have the meanings given in claim 15 , and the dashed bond indicates the position of the bond from the group to the nitrogen.

19 . The compound according to claim 17 , wherein Ar 1 is a group of the formula (6), (7), (8), (9) or (21).

20 . The compound according to claim 18 , wherein Ar 1 is a group of the formula (6a), (7a), (8a), (9a) or (21a).

21 . The compound according to claim 15 , wherein the groups Ar 1 and Ar 2 are different from one another.

22 . The compound according to claim 15 , wherein the group —NAr 1 Ar 2 has the structure of one of the formulae (29), (30), (31) or (32) or in that the group —Ar—NAr 1 Ar 2 has the structure of one of the formulae (33), (34), (35) or (36),

where the symbols used have the meanings gi

Assignees

• Merck Patent Gmbh

Inventors

• Pflumm Christof
• Parham Amir Hossain
• Brocke Constanze
• Montenegro Elvira
• Voges Frank
• Heil Holger
• Buesing Arne

Classifications

• C09K2211/1011

  Condensed systems · CPC title

• C09K2211/1014

  bridged by heteroatoms, e.g. N, P, Si or B · CPC title

• C09K11/06

  containing organic luminescent materials · CPC title

• C07C2603/96

  containing at least one ring with less than six members · CPC title

• C07D219/02

  with only hydrogen, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system · CPC title