Photochemistry of norharmane in aqueous solution

M. MICAELA GONZALEZ, M. LAURA SALUM, YOUSEF GHOLIPOUR, FRANCO M. CABRERIZO AND ROSA ERRA-BALSELLS

Photochemical and Photobiological Sciences

The Royal Society of Chemistry and Owner Societies

Año: 2009 p. 1139 - 1149

1474-905X

The photochemistry of norharmane (9H-pyrido[3,4-b]indole) in acidic (pH 5.0 ± 0.1) and alkaline (pH 10.0 ± 0.1) aqueous solutions was studied. The photochemical reactions were monitored by TLC, UV/VIS absorption spectroscopy, high-performance liquid chromatography (HPLC), electronic ionization-mass spectrometry (EI-MS), UV-laser desorption/ionization-time of flight-mass spectrometry (UV-LDI-TOF-MS) and an enzymatic method for H2O2 determination. The neutral (nHoN) and the protonated (nHoH+) forms of norharmane irradiated under Ar atmosphere were photostable, but they suffered a photochemical transformation in the presence of O2, yielding as photoproducts norharmane dimers, trimers and tetramers. nHoN shown to be more photostable than nHoH+. The nHoH+ and nHoN consumption quantum yields were 1.82 x 10-3 and 0.51 x 10-3, respectively, and the mechanisms involved in its photochemistry are discussed. H2O2 and singlet oxygen (1O2) were also detected and quantified in irradiated solutions of norharmane, and their role in the photochemistry of norharmane is discussed.