Abstract

The novel axially bis[4-(4-pyridinyl)phenol] substituted silicon(IV) phthalocyanine (3) and its quaternized derivative (3Q) were designed and synthesized. These phthalocyanines were fully characterized by elemental analysis and different spectroscopic methods, such as FT-IR, UV–Vis, MALDI-TOF and 1H NMR. The photophysical and photochemical properties, such as electronic absorption, fluorescence emission, fluorescence lifetimes, singlet oxygen generation and photostability, of these phthalocyanines were investigated. These properties were examined in DMSO for the non-ionic phthalocyanine (3) and in both DMSO and aqueous solution for the ionic phthalocyanine (3Q). The addition of bis[4-(4-pyridinyl)phenol] groups as axial ligands showed an improvement of the photophysical and photochemical properties. In addition, a spectroscopic investigation of the binding behavior of the quaternized silicon(IV) phthalocyanine complex to bovine serum albumin (BSA) and DNA was also studied in this work.

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