Nucleophilic Substitution in 4-Bromo-5-nitrophthalodinitrile: IX. Synthesis of 4-(Morpholin-4-yl)-5-aryloxyphthalodinitriles and Copper Phthalocyanines Based Thereon

摘要

Nucleophilic aromatic substitution of bromine in 4-bromo-5-nitrophthalodinitrile with the morpholine residue and the subsequent substitution of nitro group with the aryloxy one yielded 4-morpholyl-5-aryloxyphthalodinirriles. From these substances octasubstituted copper phthalocyanines were synthesized, and their physicochemical properties were studied.