Journal of Organic Chemistry p. 2155 - 2159 (1990)
Update date:2022-08-02
Topics:
Young, Joseph G.
Onyebuagu, William
An improved approach to the synthesis of di-disubstituted phthalocyanines from two different phthalyl precursors is described.The method combines substituted 1,3-diiminoisoindoles and 6/7-nitro-1,3,3-trichloroisoindolenine to synthesize phthalocyanine.The method can be applied to the synthesis of hydrogen and metallo phthalocyanine.The yields are variable, ranging from 17percent to 72percent depending on the substituents.
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