Synthesis and Properties of Tetra- and Octasubstituted Metal Pthalocyanines with Alkylsulfamoyl Groups
摘要:
Sulfochlorination of sulfophenyl- and halosulfo-substituted copper and cobalt phthalocyanines and the subsequent reaction of the resulting sulfonyl chlorides with various alkylamines afforded a series of tetra- and octasubstituted metal phthalocyanines containing alkylsulfamoyl groups. Their solubilities, spectral, and other physicochemical properties are dependent on the number and length of the alkyl radicals, the nature of the substituent combined with the alkylsulfamoyl group, and the nature of the complexing metal.