Metal complexes, comprising carbene ligands having an O-substituted non-cyclometalated aryl group and their use in organic light emitting diodes

Patent metadata

Field	Value
Publication number	US-9862739-B2
Application number	US-201515300582-A
Country	US
Kind code	B2
Filing date	Mar 26, 2015
Priority date	Mar 31, 2014
Publication date	Jan 9, 2018
Grant date	Jan 9, 2018

Abstract

Cyclometallated Ir complex comprising three N,N diaryl substituted carbene ligands, bearing substituents in the 2 position of the non-cyclometallated aryl ring; an organic electronic device, preferably an organic light-emitting diode (OLED), comprising at least one cyclometallated Ir complex as described above, a light-emitting layer comprising said cyclometallated Ir complex preferably as emitter material, preferably in combination with at least one host material, use of said cyclometallated Ir complex in an OLED and an apparatus selected from the group consisting of stationary visual display units, mobile visual display units, illumination units, units in items of clothing, units in handbags, units in accessories, units in furniture and units in wallpaper comprising said organic electronic device, preferably said OLED, or said light-emitting layer. The present invention further relates to a process for the preparation of said cyclometallated Ir complex.

First claim

The invention claimed is:

1. A process for preparing cyclometallated Ir complex of formula (I):

wherein a weight ratio of mer to fac isomer of the cyclometallated Ir complex of formula (I) is 100% - 60% (mer) to 0% to 40% (fac),
wherein
A 1 is CH or N;
A 2 is CR 1 or N;
A 3 is CR 2 or N
wherein in the case that A 1 and/or A 3 are N, A 2 is CR 1 ;
R 1 , R 2 , R 3 , R 4 , R 6 and R 7 are each independently hydrogen; deuterium; a linear or branched, substituted or unsubstituted alkyl radical having from 1 to 20 carbon atoms, optionally interrupted by at least one heteroatom, selected from O, S and N; a substituted or unsubstituted cycloalkyl radical having a total of from 3 to 30 carbon atoms; a substituted or unsubstituted heterocyclo alkyl radical, interrupted by at least one heteroatom selected from O, S and N and having a total of from 3 to 30 carbon atoms and/or heteroatoms; a substituted or unsubstituted aryl radical, having a total of from 6 to 30 carbon atoms; a substituted or unsubstituted heteroaryl radical, having a total of from 5 to 30 carbon atoms and/or heteroatoms, selected from O, S and N; or a group with donor or acceptor action; selected from the group consisting of methoxy, phenyloxy, halogenated C 1 -C 4 -alkyl, halogen, CN, SiR 10 R 11 R 12 , diphenylamino and —C(O)OC 1 -C 4 -alkyl;
R 10 , R 11 , R 12 are each independently a linear or branched alkyl radical, having from 1 to 6 carbon atoms; a substituted or unsubstituted aryl radical, having from 6 to 12 carbon atoms; a substituted or unsubstituted heteroaryl radical, having a total of from 5 to 15 carbon atoms and/or heteroatoms; a substituted or unsubstituted cycloalkyl radical having a total of from 3 to 7 carbon atoms;

or
R 1 and R 2 , R 3 and R 4 and/or R 6 and R 7 may form, independently of each other, together with the carbon atoms to which they are bonded, a saturated or unsaturated or aromatic, optionally substituted ring, which is optionally interrupted by at least one heteroatom, selected from O, S and N, has a total of from 5 to 18 carbon atoms and/or heteroatoms, and may optionally be fused to at least one further optionally substituted saturated or unsaturated or aromatic ring, optionally interrupted by at least one heteroatom, selected from O, S and N, and having a total of from 5 to 18 carbon atoms and/or heteroatoms;
R 5 is a linear or branched, substituted or unsubstituted alkyl radical having from 1 to 20 carbon atoms, optionally interrupted by at least one heteroatom, selected from O, S and N; a substituted or unsubstituted cycloalkyl radical having a total of from 3 to 30 carbon atoms; a substituted or unsubstituted heterocyclo alkyl radical, interrupted by at least one heteroatom selected from O, S and N and having a total of from 3 to 30 carbon atoms and/or heteroatoms; a substituted or unsubstituted aryl radical, having a total of from 6 to 30 carbon atoms; a substituted or unsubstituted heteroaryl radical, having a total of from 5 to 30 carbon atoms and/or heteroatoms, selected from O, S and N; or a group with donor or acceptor action, selected from the group consisting of methoxy, phenyloxy, halogenated C 1 -C 4 -alkyl, halogen, CN, SiR 10 R 11 R 12 , diphenylamino and —C(O)OC 1 -C 4 -alkyl;

X is CH, CD or N;
Y is CR 8 or N;
R 8 is hydrogen; deuterium; a linear or branched, substituted or unsubstituted alkyl radical having from 1 to 20 carbon atoms, optionally interrupted by at least one heteroatom, selected from O, S and N; a substituted or unsubstituted cycloalkyl radical having a total of from 3 to 30 carbon atoms; a substituted or unsubstituted heterocyclo alkyl radical, interrupted by at least one heteroatom selected from O, S and N and having a total of from 3 to 30 carbon atoms and/or heteroatoms; a substituted or unsubstituted aryl radical, having a total of from 6 to 30 carbon atoms; a substituted or unsubstituted heteroaryl radical, having a total of from 5 to 30 carbon atoms and/or heteroatoms, selected from O, S and N; or a group with donor or acceptor action, selected from the group consisting of methoxy, phenyloxy, halogenated C 1 -C 4 -alkyl, halogen, CN, SiR 10 R 11 R 12 , diphenylamino and —C(O)OC 1 -C 4 -alkyl;
by contacting suitable compounds comprising Ir with appropriate ligand precursors,
wherein suitable compounds comprising Ir are complexes of iridium with halides, 1,5-cyclooctadiene, cyclooctene, phosphines, cyanides, alkoxides, pseudohalides and/or alkyl ligands, and appropriate ligand precursors are Ag-carbene complexes corresponding to the Ir complex of formula (I) or compounds of the general formula (IV)

wherein A 1 , A 2 , A 3 , R 3 , R 4 , R 6 , R 5 , R 7 , X and Y are each as already defined above for the compounds of the general formula (I), and R 13 is defined as follows:
R 13 is independently SiR 14 R 15 R 16 , aryl, heteroaryl, alkyl, cycloalkyl or heterocycloalkyl,
R 14 , R 15 , R 16 are each independently aryl, heteroaryl, alkyl, cycloalkyl or heterocycloalkyl.

2. The process according to claim 1 , wherein
R 1 , R 2 , R 3 , R 4 , R 6 and R 7 are each independently hydrogen; deuterium; methyl, ethyl, n-propyl, iso-propyl, n-butyl, tert-butyl, sec-butyl, iso-butyl, cyclopentyl, cyclohexyl, OCH 3 , OCF 3 ; phenyl, pyridyl, primidyl, pyrazinyl, carbazolyl, dibenzofuranyl, dibenzothiophenyl, benzofuranyl and benzothiophenyl wherein the aforementioned radicals may be unsubstituted or substituted by methyl, ethyl, n-propyl, iso-propyl, n-butyl, tert-butyl, sec-butyl, iso-butyl, methoxy, CF 3 or phenyl; a group with donor or acceptor action, selected from F, CF 3 , CN and SiPh 3 ; and
R 5 is methyl, ethyl, n-propyl, iso-propyl, n-butyl, tert-butyl, sec-butyl, iso-butyl, cyclopentyl, cyclohexyl, OCH 3 , OCF 3 ; phenyl, pyridyl, primidyl, pyrazinyl, wherein the aforementioned radicals may be substituted by, preferably monosubstituted, by methyl, ethyl, n-propyl, iso-propyl, n-butyl, tert-butyl, sec-butyl, iso-butyl, methoxy or phenyl or unsubstituted; a group with donor or acceptor action, selected from CF 3 and CN.

3. The process according to claim 1 , wherein
R 1 , R 2 , R 3 , R 4 , R 6 and R 7 are each independently hydrogen; deuterium; methyl, ethyl, n-propyl, iso-propyl, n-butyl, tert-butyl, sec-butyl, iso-butyl; phenyl, pyridyl, primidyl, pyrazinyl, carbazolyl, dibenzofuranyl, dibenzothiophenyl, wherein the aforementioned radicals may be unsubstituted or substituted by methyl, ethyl, iso-propyl, tert-butyl, iso-butyl or methoxy; CF 3 or CN; and
R 5 is methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl; phenyl, tolyl or pyridyl.

4. The process according to claim 1 , wherein
X, Y are each independently CH, CD or N.

5. The process according to claim 1 , wherein
X is N; and
Y is CR 8 .

6. The process according to claim 1 , wherein
X is N; and
Y is N.

7. The process according to claim 1 , wherein
X is CH or CD; and
Y is CR 8 .

8. The process according to claim 1 , wherein the cyclometallated Ir complex one of the following formulae:

Assignees

• Udc Ireland Ltd

Inventors

• Metz Stefan
• Dormann Korinna
• Battagliarin Glauco
• Eickhoff Christian
• Benedito Flavio Luiz
• Watanabe Soichi
• Wagenblast Gerhard
• Geβner Thomas
• Lennartz Christian
• Murer Peter

Classifications

• C09B69/008

  Dyes containing a substituent, which contains a silicium atom · CPC title

• C09K2211/1059

  containing three nitrogen atoms as heteroatoms · CPC title

• C09K2211/1044

  containing two nitrogen atoms as heteroatoms · CPC title

• C09K2211/185

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

• C09B57/00

  Other synthetic dyes of known constitution · CPC title