US2014225100A1PendingUtilityA1

Organic electroluminescent device

Assignee: YOKOYAMA NORIMASAPriority: Sep 12, 2011Filed: Sep 6, 2012Published: Aug 14, 2014
Est. expirySep 12, 2031(~5.1 yrs left)· nominal 20-yr term from priority
C07D 333/76C07D 213/38C09B 57/008C07C 211/54C07C 211/58H10K 50/858H10K 50/844H10K 85/615H10K 85/6572H10K 85/6576H10K 85/636H10K 85/633H10K 85/631H10K 85/00H10K 85/626C07D 209/88H10K 85/654H10K 50/15H10K 85/60H01L 51/0059H01L 51/0052H01L 51/006H01L 51/0058H01L 51/0067H01L 51/5275H01L 51/0074H01L 51/0061H01L 51/0072H01L 51/005
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Claims

Abstract

An organic electroluminescent device having a capping layer composed of material having a high refractive index, excelling in thin film stability and durability and having no absorption in the respective wavelength ranges of blue, green, and red is provided to improve device characteristics of the organic electroluminescent device, particularly to greatly improve light extraction efficiency. The organic electroluminescent device has at least an anode electrode, a hole transport layer, a light emitting layer, an electron transport layer, a cathode electrode, and the capping layer in this order, wherein the capping layer contains an arylamine compound (X) having a structure in which two triphenylamine structures are joined within a molecule via a single bond or a divalent group that does not contain a heteroatom.

Claims

exact text as granted — not AI-modified
1 . An organic electroluminescent device comprising at least an anode electrode, a hole transport layer, a light emitting layer, an electron transport layer, a cathode electrode, and a capping layer in this order, wherein the capping layer comprises an arylamine compound (X) having a structure in which two triphenylamine structures are joined within a molecule via a single bond or a divalent group that does not contain a heteroatom. 
     
     
         2 . The organic electroluminescent device according to  claim 1 , wherein the arylamine compound (X) having a structure in which two triphenylamine structures are joined within a molecule via a single bond or a divalent group that does not contain a heteroatom is an arylamine compound (X′) represented by the following general formula (1): 
       
         
           
           
               
               
           
         
       
       wherein R 1  to R 28  may be the same or different, and each represents a hydrogen atom, a deuterium atom, a fluorine atom, a chlorine atom, cyano, trifluoromethyl, nitro, linear or branched alkyl of 1 to 6 carbon atoms that may have a substituent, linear or branched alkenyl of 2 to 6 carbon atoms that may have a substituent, cycloalkyl of 5 to 10 carbon atoms that may have a substituent, linear or branched alkyloxy of 1 to 6 carbon atoms that may have a substituent, cycloalkyloxy of 5 to 10 carbon atoms that may have a substituent, a substituted or unsubstituted aromatic hydrocarbon group, a substituted or unsubstituted aromatic heterocyclic group, a substituted or unsubstituted condensed polycyclic aromatic group, or substituted or unsubstituted aryloxy, where these substituents may bind to each other to form a ring when a plurality of these substituents bind to the same benzene ring; R 1  to R 10  and R 19  to R 28  may form rings by binding to benzene rings to which the respective groups bind; and A represents a divalent group represented by the following structural formulae (B) to (F), or a single bond, where when A is a single bond, at least one of R 1  to R 28  is a substituted or unsubstituted aromatic hydrocarbon group, 
       
         
           
           
               
               
           
         
       
       wherein R 29  to R 32  may be the same or different, and each represents a hydrogen atom, a deuterium atom, a fluorine atom, a chlorine atom, cyano, trifluoromethyl, linear or branched alkyl of 1 to 6 carbon atoms, linear or branched alkenyl of 2 to 6 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group, a substituted or unsubstituted aromatic heterocyclic group, or a substituted or unsubstituted condensed polycyclic aromatic group, where these substituents may bind to each other to form a ring when a plurality of these substituents bind to the same benzene ring; 
       and n is an integer of 1 to 3, where when a plurality of each of R 29  to R 32  are present (when n is 2 or 3), R 29  to R 32  may be the same or different, 
       
         
           
           
               
               
           
         
       
       wherein R 33  to R 42  may be the same or different, and each represents a hydrogen atom, a deuterium atom, a fluorine atom, a chlorine atom, cyano, trifluoromethyl, linear or branched alkyl of 1 to 6 carbon atoms, linear or branched alkenyl of 2 to 6 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group, a substituted or unsubstituted aromatic heterocyclic group, or a substituted or unsubstituted condensed polycyclic aromatic group, where these substituents may bind to each other to form a ring, 
       
         
           
           
               
               
           
         
       
       wherein R 43  to R 50  may be the same or different, and each represents a hydrogen atom, a deuterium atom, a fluorine atom, a chlorine atom, cyano, trifluoromethyl, linear or branched alkyl of 1 to 6 carbon atoms, linear or branched alkenyl of 2 to 6 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group, a substituted or unsubstituted aromatic heterocyclic group, or a substituted or unsubstituted condensed polycyclic aromatic group, where these substituents may bind to each other to form a ring, 
       
         
           
           
               
               
           
         
       
       wherein R 51  to R 55  may be the same or different, and each represents a hydrogen atom, a deuterium atom, a fluorine atom, a chlorine atom, cyano, trifluoromethyl, linear or branched alkyl of 1 to 6 carbon atoms, linear or branched alkenyl of 2 to 6 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group, a substituted or unsubstituted aromatic heterocyclic group, or a substituted or unsubstituted condensed polycyclic aromatic group, where these substituents may bind to each other to form a ring. 
     
     
         3 . The organic electroluminescent device according to  claim 2 , wherein A is a divalent group represented by the structural formula (B) in the general formula (1). 
     
     
         4 . The organic electroluminescent device according to  claim 3 , wherein A is a divalent group represented by the structural formula (B), and n is 1 in the general formula (1). 
     
     
         5 . The organic electroluminescent device according to  claim 2 , wherein A is a single bond in the general formula (1). 
     
     
         6 . The organic electroluminescent device according to  claim 2 , wherein A is a divalent group represented by the structural formula (D) in the general formula (1). 
     
     
         7 . The organic electroluminescent device according to  claim 1 , wherein the thickness of the capping layer is within a range of 30 nm to 120 nm. 
     
     
         8 . The organic electroluminescent device according to  claim 1 , wherein the refractive index of the capping layer is 1.75 or more when the wavelength of light that transmits the capping layer is within a range of 530 nm to 750 nm. 
     
     
         9 . The organic electroluminescent device according to  claim 2 , wherein the thickness of the capping layer is within a range of 30 nm to 120 nm. 
     
     
         10 . The organic electroluminescent device according to  claim 3 , wherein the thickness of the capping layer is within a range of 30 nm to 120 nm. 
     
     
         11 . The organic electroluminescent device according to  claim 4 , wherein the thickness of the capping layer is within a range of 30 nm to 120 nm. 
     
     
         12 . The organic electroluminescent device according to  claim 5 , wherein the thickness of the capping layer is within a range of 30 nm to 120 nm. 
     
     
         13 . The organic electroluminescent device according to  claim 6 , wherein the thickness of the capping layer is within a range of 30 nm to 120 nm. 
     
     
         14 . The organic electroluminescent device according to  claim 2 , wherein the refractive index of the capping layer is 1.75 or more when the wavelength of light that transmits the capping layer is within a range of 530 nm to 750 nm. 
     
     
         15 . The organic electroluminescent device according to  claim 3 , wherein the refractive index of the capping layer is 1.75 or more when the wavelength of light that transmits the capping layer is within a range of 530 nm to 750 nm. 
     
     
         16 . The organic electroluminescent device according to  claim 4 , wherein the refractive index of the capping layer is 1.75 or more when the wavelength of light that transmits the capping layer is within a range of 530 nm to 750 nm. 
     
     
         17 . The organic electroluminescent device according to  claim 5 , wherein the refractive index of the capping layer is 1.75 or more when the wavelength of light that transmits the capping layer is within a range of 530 nm to 750 nm. 
     
     
         18 . The organic electroluminescent device according to  claim 6 , wherein the refractive index of the capping layer is 1.75 or more when the wavelength of light that transmits the capping layer is within a range of 530 nm to 750 nm. 
     
     
         19 . The organic electroluminescent device according to  claim 7 , wherein the refractive index of the capping layer is 1.75 or more when the wavelength of light that transmits the capping layer is within a range of 530 nm to 750 nm. 
     
     
         20 . The organic electroluminescent device according to  claim 9 , wherein the refractive index of the capping layer is 1.75 or more when the wavelength of light that transmits the capping layer is within a range of 530 nm to 750 nm.

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