Abstract
We synthesized complexones based on tetrapyridylporphin (I), namely, tetra(pyridinium-4-N-carboxymethylene) porphin tetrachloride (II), tetra(pyridinium-4-N-carboxymethylene)porphin tetrabromide (III), complete ethyl ester of (pyridinium-4-N-carboxymethylene)porphin tetrachloride (IV), and tetra(pyridinium- 4-N-methyl)porphin tetraiodide (V). Data on the electronic absorption spectra of the compounds, the enthalpies of their solution in water, and the enthalpies of complex formation with copper(II) and zinc acetates were obtained, and the acid properties of the ligands and their stability under thermooxidative destruction conditions were studied. The conclusion was drawn that the enthalpy of solution of complexone-porphyrins in water was determined by the strength of their crystal lattices and, when different anions (Cl−, Br−, and I−) were present, by the difference of the enthalpies of their hydration. As distinct from Cu2+, complex formation between Zn2+ and porphyrin ligands occurred with sensible energy expenditures likely caused by the electronic inconsistency between the zinc cation and porphyrin ligands. The stability of water-soluble porphyrins to thermooxidative destruction was limited by temperatures of 200–260°C.
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Original Russian Text © N.M. Berezina, M.I. Bazanov, A.S. Semeikin, M.B. Berezin, 2009, published in Zhurnal Fizicheskoi Khimii, 2009, Vol. 83, No. 5, pp. 903–910.
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Berezina, N.M., Bazanov, M.I., Semeikin, A.S. et al. The physicochemical properties of complexones, tetrapyridylporphin derivatives. Russ. J. Phys. Chem. 83, 785–791 (2009). https://doi.org/10.1134/S0036024409050185
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DOI: https://doi.org/10.1134/S0036024409050185