3,5-di-tert-butyl substituted phthalocyanines: Synthesis and specific properties


JOURNAL OF MOLECULAR STRUCTURE, cilt.1214, 2020 (SCI İndekslerine Giren Dergi) identifier identifier


The photophysical and photochemical properties of tetrasubstituted 3,5-di-tert-butylphenoxy containing phthalocyanine (Pc) metal-free (H-2) as well as metal ions-containing (Mg, Zn, Co) compounds were synthesized and characterized using elemental analysis, Fourier-transform infrared, H-1 nuclear magnetic resonance, and electronic spectroscopies and mass spectrometry. The singlet oxygen, fluorescence and triplet quantum yields, and the fluorescence and triplet lifetimes of the complexes H2Pc, MgPc, and ZnPc were determined in dimethylsulfoxide, and the photodegradation quantum yield was calculated for the H-2-, Mg-, Zn-, and Co ions-containing phthalocyanine species. The fluorescence quantum yield values for the complexes ranged from 0.10 to 0.17 and the singlet oxygen quantum yields were found to be 0.11, 0.30, and 0.44 for H2Pc, MgPc, and ZnPc, respectively. ZnPc was found to have the longest triplet lifetime of 4260 ms. (C) 2020 Elsevier B.V. All rights reserved.