Metal coordination compound, luminescence device and display apparatus

Abstract

An electroluminescence device having a layer containing a specific metal coordination compound is provided. The metal coordination compound is represented by formula (1) below: ML m L′ n   (1), wherein M is a metal atom of Ir, Pt, Rh or Pd; L and L′ are mutually different bidentate ligands; m is 1, 2 or 3 and n is 0, 1 or 2 with the proviso that m+n is 2 or 3; a partial structure MLm is represented by formula (2) shown below and a partial structure ML′ n is represented by formula (3) or (4) shown below: at least one of the optional substituent(s) of the cyclic groups, and the cyclic groups CyCl and CyC2 includes a benzofuran structure capable of having a substituent represented by the following formula (5): The metal coordination compound having the benzofuran structure is effective in providing high-efficiency luminescence and long-term high luminance.

1 . A metal coordination compound represented by formula (1) below: 
         ML m L′L n   (1), 
       wherein M is a metal atom of Ir, Pt, Rh or Pd; L and L′ are mutually different bidentate ligands; m is 1, 2 or 3 and n is 0, 1 or 2 with the proviso that m+n is 2 or 3; a partial structure MLm is represented by formula (2) shown below and a partial structure ML′ n  is represented by formula (3) or (4) shown below:  
       
         
           
           
               
               
           
         
       
       wherein CyN1 and CyN2 are each cyclic group capable of having a substituent, including a nitrogen atom and bonded to the metal atom M via the nitrogen atom; CyC1 and CyC2 are each cyclic group capable of having a substituent, including a carbon atom and bonded to the metal atom M via the carbon atom with the proviso that the cyclic group CyN1 and the cyclic group CyC1 are bonded to each other via a covalent bond and the cyclic group CyN2 and the cyclic group CyC2 are bonded to each other via covalent bond; 
 the optional substituent of the cyclic groups is selected from a halogen atom, cyano group, a nitro group, a trialkylsilyl group of which the alkyl groups are independently a linear or branched alkyl group having 1 to 8 carbon-atoms, a linear or branched alkyl group having 1 to 20 carbon atoms of which the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O—, —S—, —CO—, —CO—O—, —O—CO—, —CH═CH— or —C≡C—, and the alkyl group can include a hydrogen atom that can be optionally replaced with a fluorine atom, or an aromatic group capable of having a substituent (that is a halogen atom, a cyano atom, a nitro atom, a linear or branched alkyl group having 1 to 20 carbon atoms of which the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O—, —S—, —CO—, —CO—O—, —O—CO—, —CH═CH— or —C≡C—, and the alkyl group can include a hydrogen atom that can be optionally replaced with a fluorine atom);  
 E and G are independently a linear or branched alkyl group having 1 to 20 carbon atoms of which the alkyl group can include a hydrogen atom that can be optionally replaced with a fluorine atom, or an aromatic group capable of having a substituent (that is a halogen atom, a cyano atom, a nitro atom, a trialkylsilyl group of which the alkyl groups are independently a linear or branched alkyl group having 1-8 carbon atoms, a linear or branched alkyl group having 1 to 20 carbon atoms of which the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O—, —S—, —CO—, —CO—O—, —O—CO—, —CH═CH— or —C≡C—, and the alkyl group can include a hydrogen atom that can be optionally replaced with a fluorine atom; and  
 at least one of the optional substituent(s) of the cyclic groups, and the cyclic groups CyC1 and CyC2 includes a benzofuran structure capable of having a substituent represented by the following formula (5):  
                     
 wherein the benzofuran structure of the formula (5) is bonded to CyN1, CyN2, CyC1 or CyC2 via a single bond at any one of 2- to 7-positions when the benzofuran structure is the optional substituent(s) of the cyclic groups, and the benzofuran structure of the formula (5) is bonded to CyN1 or CyN2 via a single bond at any one of 2- to 7-positions and bonded to the metal atom M via a single bond at any one of 2- to 7-positions when the benzofuran structure is CyC1 or CyC2;  
 the optional substituent of the benzofuran structure of the formula (5) is selected from a halogen atom, cyano group, a nitro group, a trialkylsilyl group of which the alkyl groups are independently a linear or branched alkyl group having 1 to 8 carbon atoms, a linear or branched alkyl group having 1 to 20 carbon atoms of which the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O—, —S—, —CO—, —CO—O—, —O—CO—, —CH═CH— or —C≡C—, and the alkyl group can include a hydrogen atom that can be optionally replaced with a fluorine atom, or an aromatic group capable of having a substituent (that is a halogen atom, a cyano atom, a nitro atom, a linear or branched alkyl group having 1 to 20 carbon atoms of which the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O—, —S—, —CO—, —CO—O—, —O—CO—, —CH═CH— or —C≡C—, and the alkyl group can include a hydrogen atom that can be optionally replaced with a fluorine atom) with the proviso that an adjacent pair of substituents located at 4- to 7-positions of the benzofuran structure of the formula (5) can be bonded to form a cyclic structure.  
 
     
     
         2 . A metal coordination compound according to  claim 1 , wherein n is 0 in the formula (1).  
     
     
         3 . A metal coordination compound according to  claim 1 , including a partial structure ML′ n  represented by the formula (3) in the formula (1).  
     
     
         4 . A metal coordination compound according to  claim 1 , including a partial structure ML′ n  represented by the formula (4) in the formula (1).  
     
     
         5 . A metal coordination compound according to  claim 1 , wherein the cyclic groups CyC1 and CyC2 are independently selected from phenyl group, thienyl group, thianaphthyl group, naphthyl group, pyrenyl group, 9-fluorenonyl group, fluorenyl group, dibenzofuranyl group, dibenzothienyl group, carbazolyl group, or benzofuranyl group, as an aromatic cyclic group capable of having a substituent with the proviso that the aromatic cyclic group can include one or two CH groups that can be replaced with a nitrogen atom.  
     
     
         6 . A metal coordination compound according to  claim 5 , wherein the cyclic groups CyC1 and Cy2 are independently phenyl group or benzofuranyl group.  
     
     
         7 . A metal coordination compound according to  claim 1 , wherein the cyclic groups CyN1 and CyN2 are independently selected from pyridyl group, pyridazinyl group, and pyrimidinyl group, as an aromatic cyclic group capable of having a substituent.  
     
     
         8 . A metal coordination compound according to  claim 7 , wherein the aromatic cyclic group is pyridyl group.  
     
     
         9 . A metal coordination compound according to  claim 1 , wherein the cyclic groups CyN1, CyN2, CyC1 and CyC2 are independently non-substituted, or have a substituent selected from a halogen atom and a linear or branched alkyl group having 1 to 20 carbon atoms, {of which the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O—, —S—, —CO—, —CH═CH—, —C≡C—, or a divalent aromatic group capable of having a substituent (that is a halogen atom or a linear or branched alkyl group having 1 to 20 carbon atoms (of which the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O—, and the alkyl group can include a hydrogen atom that can be optionally replaced with a fluorine atom)), and the alkyl group can include a hydrogen atom that can be optionally replaced with a fluorine atom}.  
     
     
         10 . A metal coordination compound according to  claim 1 , wherein M in the formula (1) is iridium.  
     
     
         11 . A metal coordination compound according to  claim 1 , which is represented by the following formula (6) or (7):  
       
         
           
           
               
               
           
         
       
       wherein R 1 , R 2 , R 3 , R′ 3  and R 4  are independently a hydrogen atom; a fluorine atom; a linear or branched alkyl group of formula: C n H 2n+1 — in which n is an integer of 1-20, the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O— and also can include a hydrogen atom that can be optionally replaced with a fluorine atom; a phenyl group capable of having a substituent; or a benzofuranyl group capable of having a substituent; the optional substituent of phenyl group and benzofuranyl group is a fluorine atom or a linear or branched alkyl group of formula: C n H 2n+1 — in which n is an integer of 1-20, the alkyl group can include one or non-neighboring two or more methylene groups that can be replaced with —O— and also can include a hydrogen atom that can be optionally replaced with a fluorine atom.  
     
     
         12 . An electroluminescence device, comprising: a pair of electrodes disposed on a substrate, and a luminescence unit comprising at least one organic compound disposed between the electrodes, wherein the organic compound comprises a metal coordination compound represented by the formula (1) in  claim 1 .  
     
     
         13 . An electroluminescence device according to  claim 12  wherein a voltage is applied between the electrodes to emit phosphorescence.  
     
     
         14 . A picture display apparatus, comprising an electroluminescence device according to  claim 12 , and a means for supplying electric signals to the electroluminescence device.