9-Anthracene carboxylic acid (9ACA) shows two fluorescence spectra whi
ch have been variously attributed to twisted and planar molecular form
s or to excimers and excited tetramers. The study of the concentration
dependence shows that both emissions are of molecular origin. In alka
line solution the fluorescence is similar to that of anthracene, and t
his is explained by the wide energy gap between the antibonding orbita
ls of the aromatic ring and of the carbonyl group linked to the very s
trong donor O-.