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By T.N. Lomova, G.E. Zaikov

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Dolphin, Can. J. , 72, 1005 (1994). 2. R. Bonnett, Chemical Aspects of Photodynamic Therapy, Gordon and Breach Science Publishers, UK. 3. C. Musewald, G. Hartwich, F. Pollinger-Dammer, H. Lossau, H. E. Michel-Beyerle, J. Phys. Chem. B, 102, 8336–8342 (1998). 4. W. ), R. Y. K. Bower, J. Am. Chem. , 91, 7485 (1969). 5. R. D. -J. C. Berenbaum, Biochem. , 261, 277–280 (1989). 6. R. Bonnett, P. D. Djelal, S. J. G. Truscott, J. Chem. A. F. Mironov Soc. , 2, 325–328 (1999). 7. L. W. Johnson and A. Sweeney, Chem.

S. Sobolev, Mol. Meditsina, 4, 43–47 (2005) (in Russian). A. F. S. A. I. Koifman Ivanovo State University of Chemistry and Technology, 1 F. ru Methods of synthesis of meso-mono-, di-, three- and tetraphenylporphyrins as well as methods of introducing the supplement substituents and their further modification are considered. Possible ways for fine regulation of the physicochemical properties of porphyrins are shown. Introduction Porphyrins and metalloporphyrins are widespread in nature and are of great biological significance.

Seregin, Dokl. Akad. Nauk, 384, 263–266 (2002) (in Russian). 66. F. A. G. Tsiprovskiy, R. Titeev, E. Nizhnik and I. , 5, 204–207 (2004). 67. A. Grichin, A. Feofanov, T. Karmakova, N. Kazachkina, E. Pecherskih, R. Yakubovskaya, A. Mironov, M. Egret-Charlier ana P. Vigny, Photochem. , 73, 267 (2001). 68. A. Feofanov, A. Grichin, T. Karmakova, V. Lebedeva, A. Filyasova, R. Yakubovskaya, A. Mironov, M. Egret-Charlier ana P. Vigny, Photochem. , 75, 633 (2002). 69. R. C. Berenbaum, R. , J. Chem. Soc.

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