Halogen-containing perylenetetracarboxylic acid derivatives and the use thereof

Abstract

The invention relates to compounds of the formula (I) in which Y 1 and Y 2 are each O or, respectively, NR a or NR b , where R a and R b are each H or organyl; Z 1 to Z 4 are each O or S; R 11 to R 14 , R 21 to R 24 are each Cl, F; where 1 or 2 of the R 11 to R 14 , R 21 to R 24 radicals may also be CN and/or 1 R 11 to R 14 , R 21 to R 24 radical may be H; and where, when Y 1 is NR a , Z 1 or Z 2 may also be NR c , where R a and R c together are a bridging X group having from 2 to 5 atoms; and where, when Y 2 is NR b , Z 3 or Z 4 may also be NR d , where R b and R d together are a bridging X group having from 2 to 5 atoms; to a process for preparation thereof, and to their use as emitter materials, charge transport materials or exciton transport materials.

1 . (canceled) 
     
     
         2 . A method of transporting a charge, the method comprising:
 conducting an electron through a material comprising a compound of formula (I.Ba):   
       
         
           
           
               
               
           
         
         wherein
 R a  represents hydrogen; an unsubstituted or substituted cycloalkyl group; an unsubstituted or substituted aryl group; a 2,2,3,3,3-pentafluoropropyl group; a 2,2-difluoroethyl group; a 2,2,3,3,4,4,4-heptafluorobutyl group; a 2,2,3,3,3-pentafluoropropyl group; a 1H,1H-pentadecafluorooctyl group; a 3-bromo-3,3-difluoropropyl group; a 3,3,3-trifluoropropyl group; a 1H,1H,2H,2H-perfluorodecyl group; a 3-(perfluorooctyl)propyl group; a 4,4-difluorobutyl group; a 4,4,4-trifluorobutyl group; a 5,5,6,6,6-pentafluorohexyl group; a 2,2-difluoropropyl group; a 2,2,2-trifluoroethyl group, or a 2-bromo-2,2-difluoroethyl group; 
 R b  represents hydrogen; an unsubstituted or substituted cycloalkyl group; an unsubstituted or substituted aryl group; a 2,2,3,3,3-pentafluoropropyl group; a 2,2-difluoroethyl group; a 2,2,3,3,4,4,4-heptafluorobutyl group; a 2,2,3,3,3-pentafluoropropyl group; a 1H,1H-pentadecafluorooctyl group; a 3-bromo-3,3-difluoropropyl group; a 3,3,3-trifluoropropyl group; a 1H,1H,2H,2H-perfluorodecyl group; a 3-(perfluorooctyl)propyl group; a 4,4-difluorobutyl group; a 4,4,4-trifluorobutyl group; a 5,5,6,6,6-pentafluorohexyl group; a 2,2-difluoropropyl group; a 2,2,2-trifluoroethyl group, or a 2-bromo-2,2-difluoroethyl group; 
 
         and 
         each of R 11 , R 12 , R 13 , R 14 , R 21 , R 22 , R 23 , and R 24 , individually, represents chlorine or fluorine. 
       
     
     
         3 . The method according to  claim 2 , wherein each of R 11 , R 12 , R 13 , R 14 , R 21 , R 22 , R 23 , and R 24  represents chlorine. 
     
     
         4 . The method according to  claim 2 , wherein each of R 11 , R 12 , R 13 , R 14 , R 21 , R 22 , R 23 , and R 24  represents fluorine. 
     
     
         5 . The method according to  claim 2 , wherein each of R a  and R b  represents hydrogen. 
     
     
         6 . The method according to  claim 2 , wherein R a  represents an unsubstituted or substituted cycloalkyl group. 
     
     
         7 . The method according to  claim 2 , wherein R a  represents an unsubstituted or substituted aryl group. 
     
     
         8 . The method according to  claim 2 , wherein R a  and R b  represent the same group. 
     
     
         9 . The method according to  claim 2 , wherein each of R a  and R b  represents an unsubstituted or substituted aryl group. 
     
     
         10 . The method according to  claim 2 , wherein the compound of formula (I.Ba) is selected from the group consisting of 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
     
     
         11 . The method according to  claim 2 , wherein
 each of R a  and R b  represents a 2,2,3,3,3-pentafluoropropyl group; a 2,2-difluoroethyl group; a 2,2,3,3,4,4,4-heptafluorobutyl group; a 2,2,3,3,3-pentafluoropropyl group; a 1H,1H-pentadecafluorooctyl group; a 3-bromo-3,3-difluoropropyl group; a 3,3,3-trifluoropropyl group; a 1H,1H,2H,2H-perfluorodecyl group; a 3-(perfluorooctyl)propyl group; a 4,4-difluorobutyl; a 4,4,4-trifluorobutyl group; a 5,5,6,6,6-pentafluorohexyl group; a 2,2-difluoropropyl group; a 2,2,2-trifluoroethyl group; or a 2-bromo-2,2-difluoroethyl group.