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Синтез и спектральные свойства фталоцианинатов цинка и магния, содержащих диазенилфеноксильные группы
Optimal conditions have been selected for the production of new phenol—azo dyes of different compositions, namely 2-phenyldiazenyl-4-(2-phenylpropan-2-yl)phenol and (2,6-dibromo)phenyldiazenyl-4-(2-phenylpropan-2-yl)phenol. The synthesized dyes were used for nucleophilic substitution with 3- and 4-nitrophthalonitrile to form 3/4-[2-phenyldiazenyl-4-(2-phenyl)propan-2-yl]phenoxy- and 3/4-[2-(2,6-dibromo)phenyldiazenyl]-4-(2-phenylpropan-2-yl)phenoxypthalonitriles. The metal complexes were synthesized by template condensation in a solution of the corresponding phthalonitrile with zinc or magnesium acetate. The composition and structure of the obtained compounds were confirmed by mass spectrometry, NMR, IR spectroscopy, and electron absorption spectroscopy. The spectral-luminescent properties were studied, the singlet oxygen generation yield of the obtained phthalocyanines was determined, and the acid-base properties of the synthesized complexes were studied.