LUMINESCENCE STUDIES OF QUINIZARIN AND DAUNORUBICIN

Abstract

Abstract— The absorption and emission spectra of quinizarin (1,4‐dihydroxy‐anthraquinone) have been investigated in hydrocarbon and alcoholic solvents. Fluorescence spectra in 3 different Shpolskii matrices were recorded at 14 K. Vibrational analyses of these spectra revealed the presence of 3, 8, and 9 sites in octane, heptane, and hexane matrices, respectively. The fluorescence lifetime was found to be 6.5 ns in hexane and EPA. Fluorescence photoselection measurements in EPA (77 K) showed that the first 4 electronic transitions of quinizarin are polarized parallel, parallel, perpendicular, and parallel to the long molecular axis and can be assigned, in order of increasing energy, to 1 B 2 , 1 B 2 , 1 A 1 and 1 B 2 (ππ*)→ 1 A 1 (C 2v ,) transitions, respectively. The fluorescent transition is assigned as 1 B 1 (ππ*)→ 1 A 1 . The absence of phosphorescence is attributed to the intramolecular hydrogen bonding present which displaces the parent anthraquinone n →* states above the ππ* states, thereby rendering the intersystem crossing (S 1 ‐T 1 ) radiationless pathway inefficient. Photoselection measurements on daunorubicin, a substituted quinizarin and known anticancer drug, revealed an absorption band polarization pattern identical to that of quinizarin. These results are in part at variance with assumptions used in previous work on the intercalation specificity of daunorubicin with DNA.