Volume 5, Issue 12 pp. 867-872
Research Article

Synthesis of organo-soluble metallophthalocyanines bearing electron-withdrawing substituents

Muriel Sanchez

Muriel Sanchez

Laboratoire de Chimie de Coordination du CNRS, 205 route de Narbonne, 31077 Toulouse cedex 4, France

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Eric Fache

Eric Fache

RHODIA Recherches, 85 Avenue des Frères Perret, BP 62, 69192 Saint Fons cedex, France

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Didier Bonnet

Didier Bonnet

RHODIA Recherches, 85 Avenue des Frères Perret, BP 62, 69192 Saint Fons cedex, France

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Bernard Meunier

Corresponding Author

Bernard Meunier

Laboratoire de Chimie de Coordination du CNRS, 205 route de Narbonne, 31077 Toulouse cedex 4, France

Laboratoire de Chimie de Coordination du CNRS, 205 route de Narbonne, 31077 Toulouse cedex 4, FranceSearch for more papers by this author
First published: 31 December 2001
Citations: 1

Abstract

The syntheses of organo-soluble metallophthalocyanines having sulfo- and sulfonamido- electron-withdrawing substituents are reported. The simple cation exchange of the readily available tetrasodium salt of metallo-sulfophthalocyanines 1 (M = Ni, Co, Fe, Cr) by alkylammonium salts afforded the sulfophthalocyanines 2 and 3 in good yields. Complexes 2 featuring two long C18 alkyl chains are only soluble in organic solvents while tetrabutylammonium counter ions exhibit a dual solubility in both organic solvents and water for compounds 3. The tetrasulfonamidophthalocyanine complexes 57 with four C8, four C18 or eight C8 alkyl chains have been obtained after chlorination of the sulfophthalocyanines 1 leading to the chlorosulfonyl derivatives 4, followed by reaction with various substituted amines. The synthesis of the chromium precursors with tetrasulfo and tetrachlorosulfonyl substituents is also described. Copyright © 2001 John Wiley & Sons, Ltd.

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