Iridium complex compound, solution composition containing the compound, organic electroluminescent element, display, and lighting

Patent metadata

Field	Value
Publication number	US-9799837-B2
Application number	US-201414330442-A
Country	US
Kind code	B2
Filing date	Jul 14, 2014
Priority date	Jan 13, 2012
Publication date	Oct 24, 2017
Grant date	Oct 24, 2017

Abstract

The present invention is to provide an iridium complex compound, which is soluble in an organic solvent, which can be stored for long periods without reprecipitation thereof and which secures a low driving voltage and a high luminescent efficiency of an organic electroluminescent element produced using the compound, to provide an organic electroluminescent element containing the compound and to provide a display and a lighting using the organic electroluminescent element. The present invention relates to the iridium complex compound having a specific chemical structure. Further, the invention also relates to the organic electroluminescent element produced using the compound, which requires a low operating voltage and has a long operating lifetime.

First claim

The invention claimed is:

1. An iridium complex compound represented by the following formula (1):

in the formula (1), the ring A represents a 6-membered or 5-membered aromatic hydrocarbon ring, containing the carbon atoms C 1 and C 2 or a 6-membered or 5-membered heteroaromatic ring containing the carbon atoms C 1 and C 2 , the ring B represents a 6-membered or 5-membered nitrogen-containing heteroaromatic ring containing the carbon atom C 3 and the nitrogen atom N 1 ; L represents an organic ligand; a and b each independently indicate an integer of from 1 to 4; n indicates an integer of from 1 to 3;
R 1 and R 2 each represent a substituent bonding to ring A and ring B, respectively, multiple R 1 s and R 2 s each are the same or different, and R 1 and R 2 represents a structure of formula (2) or any of a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an alkyl group having from 1 to 20 carbon atoms, a (hetero)aralkyl group having from 7 to 40 carbon atoms, an alkoxy group having from 1 to 20 carbon atoms, a (hetero)aryloxy group having from 3 to 20 carbon atoms, an alkylsilyl group having from 1 to 20 carbon atoms, a (hetero)arylsilyl group having from 3 to 20 carbon atoms, an alkylcarbonyl group having from 2 to 20 carbon atoms, a (hetero)arylcarbonyl group having from 4 to 20 carbon atoms, an alkylamino group having from 2 to 20 carbon atoms, a (hetero)arylamino group having from 3 to 20 carbon atoms, or a (hetero)aryl group having from 3 to 20 carbon atoms; these groups are optionally substituted with an atom or group selected from the group consisting of a fluorine atom, a chlorine atom, a bromine atom, an alkyl group having from 1 to 20 carbon atoms, a (hetero)aralkyl group having from 7 to 40 carbon atoms, an alkoxy group having from 1 to 20 carbon atoms, a (hetero)aryloxy group having from 3 to 20 carbon atoms, an alkylsilyl group having from 1 to 20 carbon atoms, a (hetero)arylsilyl group having from 3 to 20 carbon atoms, an alkylcarbonyl group having from 2 to 20 carbon atoms, a (hetero)arylcarbonyl group having from 4 to 20 carbon atoms, an alkylamino group having from 2 to 20 carbon atoms, a (hetero)arylamino group having from 3 to 20 carbon atoms, and a (hetero)aryl group having from 3 to 20 carbon atoms;
when a is 2 or more and multiple R's neighbor to each other, then the neighboring R 1 s may bond directly, or may bond via an alkylene group having from 3 to 12 carbon atoms, an alkenylene group having from 3 to 12 carbon atoms, or an arylene group having from 6 to 12 carbon atoms thereby to further form a ring; when b is 2 or more and multiple R 2 s neighbor to each other, then the neighboring R 2 s may bond directly, or may bond via an alkylene group having from 3 to 12 carbon atoms, an alkenylene group having from 3 to 12 carbon atoms, or an arylene group having from 6 to 12 carbon atoms thereby to further form a ring; R 1 and R 2 may bond directly, or may bond via an alkylene group having from 3 to 12 carbon atoms, an alkenylene group having from 3 to 12 carbon atoms, or an arylene group having from 6 to 12 carbon atoms thereby to further form a ring; the ring formed by bonding of R 1 s, R 2 s or R 1 and R 2 is optionally substituted with a fluorine atom, a chlorine atom, a bromine atom, an alkyl group having from 1 to 20 carbon atoms, a (hetero)aralkyl group having from 7 to 40 carbon atoms, an alkoxy group having from 1 to 20 carbon atoms, a (hetero)aryloxy group having from 3 to 20 carbon atoms, an alkylsilyl group having from 1 to 20 carbon atoms, a (hetero)arylsilyl group having from 3 to 20 carbon atoms, an alkylcarbonyl group having from 2 to 20 carbon atoms, a (hetero)arylcarbonyl group having from 4 to 20 carbon atoms, an alkyl amino group having from 2 to 20 carbon atoms, a (hetero)aryl amino group having from 3 to 20 carbon atoms, or a (hetero)aryl group having from 3 to 20 carbon atoms;
provided that at least one of R 1 is represented by the structure of formula (2):

in the formula (2), multiple Xs are the same or different, and X represents a (hetero)arylene group having from 6 to 20 carbon atoms, multiple Ar 1 s are the same or different, and Ar 1 represents a (hetero)aryl group having from 3 to 20 carbon atoms; wherein these groups are optionally substituted with an atom or group selected from the group consisting of a fluorine atom, an alkyl group having from 1 to 20 carbon atoms, a (hetero)aralkyl group having from 7 to 40 carbon atoms, an alkoxy group having from 1 to 20 carbon atoms, a (hetero)aryloxy group having from 3 to 20 carbon atoms, an alkylsilyl group having from 1 to 20 carbon atoms, a (hetero)arylsilyl group having from 3 to 20 carbon atoms, an alkylcarbonyl group having from 2 to 20 carbon atoms, a (hetero)arylcarbonyl group having from 4 to 20 carbon atoms, an alkylamino group having from 2 to 20 carbon atoms, a (hetero)arylamino group having from 3 to 20 carbon atoms, and a (hetero)aryl group having from 3 to 20 carbon atoms; Z is represented by the following formula (3); c indicates an integer of 1; d indicates an integer of from 1 to 3:

in the formula (3), multiple R's are the same or different, and R′ represents a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an alkyl group having from 1 to 20 carbon atoms, an alkoxy group having from 1 to 20 carbon atoms, a (hetero)aryloxy group having from 3 to 20 carbon atoms, or a (hetero)aryl group having from 3 to 20 carbon atoms; r indicates an integer of from 2 to 20.

2. The iridium complex compound according to claim 1 , wherein in the formula (1), at least one of the substituents R 2 s bonding to the ring B is represented by the formula (2).

3. The iridium complex compound according to claim 1 , wherein in the formula (1), the ring A is a benzene ring or a pyridine ring.

4. The iridium complex compound according to claim 1 , which is represented by the following formula (1-1):

in the formula (1-1), the ring B, R 2 , L, b and n each have the same meanings as in the formula (1);
R 3 to R 6 each are the same or different, and represent a structure of formula (2) or any of a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an alkyl group having from 1 to 20 carbon atoms, a (hetero)aralkyl group having from 7 to 40 carbon atoms, an alkoxy group having from 1 to 20 carbon atoms, a (hetero)aryloxy group having from 3 to 20 carbon atoms, an alkylsilyl group having from 1 to 20 carbon atoms, a (hetero)arylsilyl group having from 3 to 20 carbon atoms, an alkylcarbonyl group having from 2 to 20 carbon atoms, a (hetero)arylcarbonyl group having from 4 to 20 carbon atoms, an alkylamino group having from 2 to 20 carbon atoms, a (hetero)arylamino group having from 3 to 20 carbon atoms, or a (hetero)aryl group having from 3 to 20 carbon atoms; wherein these groups are optionally substituted with an atom or group selected from the group consisting of a fluorine atom, a chlorine atom, a bromine atom, an alkyl group having from 1 to 20 carbon atoms, a (hetero)aralkyl group having from 7 to 40 carbon atoms, an alkoxy group having from 1 to 20 carbon atoms, a (hetero)aryloxy group having from 3 to 20 carbon atoms, an alkylsilyl group having from 1 to 20 carbon atoms, a (hetero)arylsilyl group having from 3 to 20 carbon atoms, an alkylcarbonyl group having from 2 to 20 carbon atoms, a (hetero)arylcarbonyl group having from 4 to 20 carbon atoms, an alkyl

Assignees

• Mitsubishi Chem Corp

Inventors

• Nagayama Kazuhiro
• Komatsu Hideji
• MIGITA Akira
• Gorohmaru Hideki
• Iida Koichiro
• Oya Takashi
• Ishibashi Koichi

Classifications

• C09K2211/1007

  Non-condensed systems · CPC title

• C09K2211/1044

  containing two nitrogen atoms as heteroatoms · CPC title

• C09K2211/1011

  Condensed systems · CPC title

• C07F15/0033

  Iridium compounds · CPC title

• C09K2211/185

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