“…1. 2.2. Synthesis of 2,3,9,10,16,17,23,24-octa(n-hexyl)phthalocyaninatoruthenium(II) (2) A mixture of 4,5-di-n-hexylphthalonitrile (1.2 g, 3.64 mmol), ruthenium(III) chloride trihydrate (0.26 g, 1 mmol) and diazabicyclo [5.4.0]undec-7-ene (DBU) (0.45 g, 3 mmol) was stirred in 2-ethoxyethanol (10 ml) under nitrogen at reflux temperature for 22 h. The reaction mixture was then cooled to room temperature, methanol (7 ml) and water (10 ml) was added, and the mixture was stirred at room temperature for 4 h. The precipitated solid was filtered off, washed with a methanol/water mixture (1/1, v/v) and dried under vacuum. The crude product (0.48 g) was subjected to column chromatography (50 g of silica gel, chloroform eluent) to yield 0.37 g (30%) of compound 2 as blue violet powder.…”