US2012184776A1PendingUtilityA1

Aromatic amine derivative and organic electroluminescent device using same

Assignee: YABUNOUCHI NOBUHIROPriority: Jan 5, 2005Filed: Mar 30, 2012Published: Jul 19, 2012
Est. expiryJan 5, 2025(expired)· nominal 20-yr term from priority
H10K 50/00C09K 11/06C09K 2211/1011C07C 211/61C09K 2211/1007C07C 2603/26C07C 211/58C07C 211/54H05B 33/20H05B 33/14C07C 2603/50C07C 2603/97Y10S428/917C07C 2603/18H10K 85/633H10K 85/324H10K 50/14H10K 85/626H10K 50/11H10K 85/649
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Claims

Abstract

Disclosed is an organic electroluminescence device in which an organic thin film which is composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. Since at least one layer of the organic thin film contains a novel aromatic amine derivative, which has an asymmetric structure wherein two different amine units are bonded through a linking group, by itself or as a component of a mixture, molecules are hardly crystallized thereby improving the production yield of the organic electroluminescence device. This organic electroluminescence device has a long life.

Claims

exact text as granted — not AI-modified
1 - 20 . (canceled) 
     
     
         21 . A process for producing an amine compound comprising reacting a halogenated aryl compound with an amine intermediate represented by the following general formula (1): 
       
         
           
           
               
               
           
         
         wherein 
         Ar 1  represents a substituted or unsubstituted aryl group having 6 to 50 ring atoms, 
         R 1  and R 2  each independently represent an alkyl group having 1 to 50 carbon atoms, and 
         the substituents of R 1  and R 2  may bond to each other to form a cyclic structure. 
       
     
     
         22 . The process according to  claim 21 , wherein said reacting is carried out in the presence of a base and a palladium compound. 
     
     
         23 . The process according to  claim 21 , wherein the halogenated aryl compound comprises a nitrogen atom. 
     
     
         24 . The process according to  claim 21 , wherein the halogenated aryl compound is selected from the group consisting of the following compounds: 
       
         
           
           
               
               
           
         
       
     
     
         25 . The process according to  claim 21 , wherein the amine intermediate is selected from the group consisting of the following compounds: 
       
         
           
           
               
               
           
         
       
     
     
         26 . The process according to  claim 21 , wherein the amine intermediate is represented by the following general formula (2): 
       
         
           
           
               
               
           
         
         wherein 
         R 1  to R 4  each independently represent an alkyl group having 1 to 50 carbon atoms, 
         provided that R 1  and R 2  may be bonded to each other to form a cyclic structure, and 
         R 3  and R 4  may be bonded to each other to form a cyclic structure. 
       
     
     
         27 . The process according to  claim 21 , wherein the amine intermediate is represented by the following general formula (3): 
       
         
           
           
               
               
           
         
         wherein 
         R 1  and R 2  each independently represent an alkyl group having 1 to 50 carbon atoms, 
         provided that R 1  and R 2  may be bonded to each other to form a cyclic structure. 
       
     
     
         28 . The process according to  claim 27 , wherein said reacting is carried out in the presence of a base and a palladium compound. 
     
     
         29 . The process according to  claim 27 , wherein the halogenated aryl compound comprises a nitrogen atom. 
     
     
         30 . The process according to  claim 27 , wherein the halogenated aryl compound is selected from the group consisting of the following compounds: 
       
         
           
           
               
               
           
         
       
     
     
         31 . The process according to  claim 27 , wherein the amine intermediate is selected from the group consisting of the following compounds: 
       
         
           
           
               
               
           
         
       
     
     
         32 . An organic electroluminescence device comprising an amine compound produced by the process according to  claim 21 . 
     
     
         33 . An organic electroluminescence device comprising an amine compound produced by the process according to  claim 27 . 
     
     
         34 . An amine intermediate represented by one or more of the following compounds:

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