Synthesis, spectroscopy, and photophysical properties of newly magnesium (II) phthalocyanine

2(3),9(10),16(17),23(24)-tetrakis-2,6-dimethoxyphenoxy substituted magnesium (II) phthalocyanine, which has very good solubility in polar and non-polar solvents does not aggregate, was synthesized. Its structure characterized by spectroscopic methods such as elemental analysis, UV-vis, FT-IR, MALDI-TOF mass 1H NMR. It aprotic dimethyl sulfoxide, N, N- Dimethylformamide, tetrahydrofuran, dichloromethane, toluene, chloroform. aggregation properties have been studied both the mentioned above Dimethylformamide at different concentrations. photophysical were determined N-dimethyl formamide. The effects of nature presence 2,6-dimethoxyphenoxy group, is an antioxidant derivative, on phthalocyanine skeleton investigated comparing it with unsubstituted phthalocyanine. can be a nominee for various technological applications that aggregate solvents, well better favorable fluorescence than its analog previous study.