Some flavylium compounds were synthesized and their spectral behavior was studied in acidic solutions.(1)The effects of two substituent groups, hydroxyl and methoxyl of the synthetic flavylium compounds, on the wavelengths of their absorption maxima in the visible region (λ
vis.max)were examined in an 0.1% HCl-MeOH solution. Hydroxylation at the 3-position gave larger bathochromic shift than that at the 5 and 7-positions. The substitution in the B-ring (3', 4' and 5'-positions)shifted the λ
vis.max to longer wavelengths than that in the benzopyrylium ring(3, 5 and 7-positions).(2)The flavylium compounds investigated could be classified, according to their structures and spectral behavior to the pH increase, into three groups as follows: (i)with 7-hydroxy, 5, 7-dihydroxy and 8-methoxy flavylium compounds, a decrease of absorption in the visible region(flavylium salt)and an increase in the near ultra violet region(chalcone)were observed.(ii)The flavylium compounds unsubstituted in the benzopyrylium ring demonstrated a decrease of absorption based on flavylium salts and an increase due to anhydro-bases in the visible region.(iii)With the flavylium compounds substituted in the 3-position such as penonidin, a decrease in absorbance at 515nm and 272nm (flavylium salt), and an increase in absorbance at 290nm were observed.
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