“…In a few cases mechanistic studies were also performed using ESR spectroscopy at low temperatures (Kriminskaya et al, 1987a(Kriminskaya et al, , 1991. Pulse radiolysis studies have been conducted in aqueous and aqueous-alcoholic (ethanol, isopropanol) solutions of tetrazolium molecules containing three phenyl substituents (2,3,5-triphenyl-tetrazolium chloride, TTC) (Kriminskaya et al, 1984(Kriminskaya et al, , 1988aKová cs et al, 1996), two phenyl and one pnitrophenyl substituent (2-p-nitrophenyl-3.5-diphenyltetrazolium chloride (p-NTC) (Kriminskaya et al, 1988a) and with a ditetrazolium compound having phenyl, p-nitrophenyl and mmethoxyphenyl substituents (nitro blue tetrazolium chloride, NBTC) (Bielski et al, 1980;Ková cs et al, 1999a). It was shown that under reducing conditions in aqueous solutions the solvated electron, while in aqueous-alcoholic solutions both the solvated electron and the a-hydroxyalkyl radicals reduce the tetrazolium ring into the electron adduct tetrazolinyl radical.…”