Photophysics of 9-aminoacridinium hydrochloride

Abstract

The steady state and time domain spectroscopy of 9-aminoacridinium hydrochloride have been studied. 9-aminoacridine (I), 9-aminoacridinium (II) and the double protonated ion (III) follow Waterman’s principle with respect to their spectra and lifetimes. It is established that the excimer formation in (II) is from the ground state dimers which undergo either thermally-activated radiationless excimer conversion or a geometrical rearrangement in the excited state at room temperature. The quenching of monomer emission by dimers or foreign quenchers (KI) is found to be of transient nature as suggested by the continuum model.