Preparation and Characterization of Regioisomerically Pure 1,7-Disubstituted Perylene Bisimide Dyes

A detailed study on bromination and subsequent imidization of perylene bisanhydride with
cyclohexylamine is reported. The present results reveal that previously reported 1,7-difunctionalized
perylene bisimides are presumably contaminated with the respective 1,6 regioisomers. N,N‘-Dicyclohexyl-1,7-dibromoperylene bisimide 1,7-3 is obtained for the first time in isomerically pure
form, and its structure is unequivocally confirmed by X-ray analysis. By using regioisomerically
pure 1,7-dibromoperylene bisimide 1,7-3, 1,7-dipyrrolidinylperylene bisimides 4a−c and 1,7-dipyrrolidinylperylene bisanhydride 5 as well as the unsymmetrically difunctionalized 1-bromo-7-pyrrolidinyl- and 1-cyano-7-pyrrolidinylperylene bisimides 7 and 8 are synthesized in good yield.