Azabenzimidazole carbene complexes as efficiency booster in OLEDs

Patent metadata

Field	Value
Publication number	US-10374172-B2
Application number	US-201414778174-A
Country	US
Kind code	B2
Filing date	Mar 19, 2014
Priority date	Mar 20, 2013
Publication date	Aug 6, 2019
Grant date	Aug 6, 2019

Abstract

An organic electronic device comprising at least one hole-transport material and/or at least one electron/exciton blocker material, wherein said at least one hole-transport material and/or said at least one electron/exciton blocker material is an Ir metal-carbene complex comprising one, two or three specific bidentate azabenzimidazole ligands; a hole transport layer or an electron/exciton blocking layer, comprising at least one Ir metal-carbene complex, comprising one, two or three specific bidentate azabenzimidazole ligands; 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 furniture and units in wallpaper, comprising the organic electronic device of the present invention or the hole transport layer or the electron/exciton blocking layer of the present invention; and the use of an Ir metal-carbene complex comprising one, two or three specific bidentate azabenzimidazole ligands according to the present invention as hole-transport material and/or electron/exciton blocker material.

First claim

The invention claimed is:

1. An organic electronic device selected from organic light-emitting diodes (OLED), light-emitting electrochemical cells (LEEC), organic photovoltaic cells (OPV) and organic field-effect transistors (OFET),
comprising at least one hole-transport material and/or at least one electron/exciton blocker material, wherein said at least one hole-transport material and/or said at least one electron/exciton blocker material comprises at least one Ir metal-carbene complex of formula (II′)

wherein
R 1 , R 2 and R 3
are each independently hydrogen, deuterium, a linear or branched alkyl radical, optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of from 1 to 20 carbon atoms and/or heteroatoms, a substituted or unsubstituted cycloalkyl radical, optionally bearing at least one functional group and having from 3 to 20 carbon atoms, a substituted or unsubstituted heterocyclo alkyl radical, interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of from 3 to 20 carbon atoms and/or heteroatoms, a substituted or unsubstituted aryl radical, optionally bearing at least one functional group and having 6 to 30 carbon atoms, a substituted or unsubstituted heteroaryl radical, interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of from 5 to 18 carbon atoms and/or heteroatoms, a group with donor or acceptor action;
or
R 1 and R 2 , or R 2 and R 3 , form, independently of each other, together with a carbon atom to which they are bonded an optionally substituted saturated or unsaturated or aromatic ring, optionally interrupted by at least one heteroatom and having 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 and having a total of from 5 to 18 carbon atoms and/or heteroatoms;
A 1 is CR 4 or N;
A 2 is CR 5 or N;
A 3 is CR 6 or N;
A 4 is CR 7 or N;
A 1′ is CR 4′ or N;
A 2′ is CR 5′ or N;
A 3′ is CR 6′ or N;
A 4′ is CR 7′ or N;
R 4 , R 5 , R 6 , R 7 , R 4′ , R 5′ , R 6′ , and R 7′
are each independently hydrogen, deuterium, a linear or branched alkyl radical, optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of from 1 to 20 carbon atoms and/or heteroatoms, a substituted or unsubstituted cycloalkyl radical, optionally bearing at least one functional group and having from 3 to 20 carbon atoms, a substituted or unsubstituted heterocyclo alkyl radical, interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of from 3 to 20 carbon atoms and/or heteroatoms, a substituted or unsubstituted aryl radical, optionally bearing at least one functional group and having from 6 to 30 carbon atoms, a substituted or unsubstituted heteroaryl radical, interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of from 5 to 18 carbon atoms and/or heteroatoms, a group with donor or acceptor action;
or
R 4 and R 5 , R 5 and R 6 , R 6 and R 7 , R 4′ and R 5′ , R 5′ and R 6′ , or R 6′ and R 7′ , 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, 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 and having a total of from 5 to 18 carbon atoms and/or heteroatoms;
n is 3;
L is not present; and
o is 0;
wherein the OLED comprises
(a) an anode,
(b) a cathode,
(c) a light-emitting layer between the anode and the cathode,
(d) at least one layer, selected from a hole-transport layer (d1) and an electron/exciton blocking layer (d2), disposed between the anode (a) and the light-emitting layer (c);
wherein the at least one hole-transport material is present in the hole-transport layer of the OLED and/or the at least one electron/exciton blocker material is present in the electron/exciton blocking layer of the OLED.

2. The organic electronic device according to claim 1 , wherein the at least one hole-transport material is present in a hole transport layer of the organic electronic device and the at least one electron/exciton blocker material is present in an electron/exciton-blocking layer of the organic electronic device.

3. The organic electronic device according to claim 1 , wherein the radicals, groups and symbols in the at least one Ir metal-carbene complex have the following meanings:
R 1 , R 2 and R 3
are each independently hydrogen, a linear or branched alkyl radical, having from 1 to 6 carbon atoms, a substituted or unsubstituted aryl radical, having from 6 to 30 carbon atoms, a substituted or unsubstituted heteroaryl radical, having a total of from 5 to 18 carbon atoms and/or heteroatoms, a group with donor or acceptor action, selected from the group consisting of halogen radicals, CF 3 , CN, SiPh 3 and SiMe 3 ;
or
R 1 and R 2 , or R 2 and R 3 , form, independently of each other, together with a carbon atom to which they are bonded an optionally substituted saturated or unsaturated or aromatic ring, optionally interrupted by at least one heteroatom and having 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 and having a total of from 5 to 18 carbon atoms and/or heteroatoms;
A 1 is CR 4 ;
A 2 is CR 5 ;
A 3 is CR 6 ;
A 4 is CR 7 ;
A 1′ is CR 4′
A 2′ is CR 5′
A 3 is CR 6′
A 4′ is CR 7′
R 4 , R 5 , R 6 , R 7 , R 4′ , R 5′ , R 6′ and R 7′
are each independently hydrogen, deuterium, a linear or branched alkyl radical, optionally bearing at least one functional group, optionally interrupted by at least one heteroatom and having a total of from 1 to 20 carbon and/or heteroatoms, a substituted or unsubstituted aryl radical, having from 6 to 30 carbon atoms, a substituted or unsubstituted heteroaryl radical, having a total of from 5 to 18 carbon atoms and/or heteroatoms, a group with donor or acceptor action, selected from halogen radicals; CF 3 , CN and SiMe 3 ;
or
R 4 and R 5 , R 5 and R 6 , R 6 and R 7 , R 4′ and R 5′ , R 5′ and R 6′ , or R 6′ and R 7′ , form, independently of each other, with the carbon atoms to which they are bonded, a saturated, unsaturated or aromatic, optionally substituted ring, which is optionally interrupted by at least one heteroatom, has a total of from 5 to 18 carbon atoms and/or heteroatoms and may optionally be fused by at least one further optionally substituted saturated or unsaturated aromatic ring, optionally interrupted by at least one heteroatom and having a total of from 5 to 18 carbon atoms and/or heteroatoms.

4. The organic electronic device according to claim 1 , wherein the at least one Ir metal-carbene complex has the formula (II′a)

5. The organic electronic device accor

Assignees

• Udc Ireland Ltd

Inventors

• Metz Stefan
• Watanabe Soichi
• Gessner Thomas
• Dormann Korinna
• Murer Peter
• Lennartz Christian
• Heinemeyer Ute
• Battagliarin Glauco

Classifications

• C09K2211/185

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

• C09K2211/1029

  containing one nitrogen atom as the heteroatom · CPC title

• C07F15/0033

  Iridium compounds · CPC title

• C09K2211/1092

  containing sulfur as the only heteroatom · CPC title

• H05B33/10

  Apparatus or processes specially adapted to the manufacture of electroluminescent light sources · CPC title