Synthesis, electrochemistry, spectroscopy and photophysical properties of a series of meso-phenylpyridylporphyrins with one to four pyridyl rings coordinated to [Ru(bipy)2Cl]+ groups

Abstract

A series of meso-phenylpyridylporphyrins and their respective supermolecular species obtained by the coordination of [ Ru ( bipy )2 Cl ]+ groups to the pyridyl substituents was synthesized and characterized. Their spectroscopic and electrochemical behavior were similar to that observed for the meso-tetra(4-pyridyl)porphyrin derivative, but the redox potential of the Ru (III/II) redox pair was about 70 mV more negative. The porphyrin centered fluorescence quantum yield exhibited a linear decrease as a function of the number of pyridyl substituents on the porphyrin ring. Efficient intramolecular energy transfer processes from the 3 MLCT state of the ruthenium complexes to the porphyrin center were observed at 77K in ethanol glass.