Procedures have been developed for the synthesis of a series of metal complexes derived from water-soluble anionic and cationic octa-4,5-carboxyphthalocyanine3taurine and choline conjugates.Phthalocyanines can be solubilized in water via introduction of sulfo [2], carboxy [3,4], or phosphono groups [5,6] into their molecules. In this way, anionic phthalocyanine dyes are obtained. Introduction of quaternary ammonium fragments gives rise to cationic phthalocyanine derivatives [2,7]. An interesting group of neutral water-soluble phthalocyanine derivatives includes those containing fragments of oligoethylene glycol ethers and esters [8]. In most cases, water-soluble phthalocyanine derivatives are mixtures of regioisomers or even products with different degrees of substitution, which are prepared, as a rule, via replacement in the macroring. Exceptions are octa-4,5-carboxyphthalocyanines which are individual compounds with a symmetric structure. It seems attractive to use octa-4,5-carboxyphthalocyanines as basis structures for building up symmetric derivatives [9], specifically those containing functional groups which make the resulting compounds soluble in water and aqueous solutions. We previously [1, 10] synthesized a series of covalent conjugates from octa-4,5-carboxyphthalocyanine metal complexes and a-amino acids, namely, the corresponding tetra(N-carboxymethyl)imides and octakis-4,5-(N-methyl-N-carboxymethyl)carbamoylphthalocyanines, which are soluble in both organic solvents and water.The goal of the present work was to synthesize previously unknown water-soluble conjugates of octa-4,5-carboxyphthalocyanines with a sulfo analog of a-amino acids, taurine (2-aminoethanesulfonic acid), and choline (anionic and cationic, respectively). By reaction of metal octa-4,5-carboxyphthalocyanine tetraanhydrides with taurine in anhydrous N-methylpyrrolidone at 1753180oC we obtained zinc, cobalt, iron, ÄÄÄÄÄÄÄÄÄÄÄÄ 1 For communication XXXVII, see [1]. and hydroxyaluminum complexes Ia3Id which were isolated in 40346% yield by chromatography. Taurinesubstituted phthalocyanines Ia3Id are fairly readily soluble in water, alcohol, and dilute hydrochloric acid. Their electronic absorption spectra in 0.1 N hydrochloric acid insignificantly differ from those recorded from aqueous solutions (see table). The spectra of complexes Ia3Id in 0.01% aqueous sodium hydroxide are characterized by a distinct vibrational structure, indicating a low degree of aggregation. Unlike 4,5-carboxyphthalocyanines, both neutral complexes Ia3Id and their sodium salts are weakly sensitive to calcium ions in aqueous solution. They remain soluble in water up to a calcium chloride concentration of 0.1 M.