Abstract
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-aryloxyphthalodinitriles. From these substances octasubstituted copper phthalocyanines were synthesized, and their physicochemical properties were studied.
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Original Russian Text © A.I. Fedotova, V.E. Maizlish, G.P. Shaposhnikov, C.N. Filimonov, I.G. Abramov, 2009, published in Zhurnal Obshchei Khimii, 2009, vol. 79, No. 5, pp. 846–851.
For communication VIII, see [1].
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Fedotova, A.I., Maizlish, V.E., Shaposhnikov, G.P. et al. Nucleophilic substitution in 4-bromo-5-nitrophthalodinitrile: IX. Synthesis of 4-(morpholin-4-yl)-5-aryloxyphthalodinitriles and copper phthalocyanines based thereon. Russ J Gen Chem 79, 1018–1023 (2009). https://doi.org/10.1134/S1070363209050260
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DOI: https://doi.org/10.1134/S1070363209050260