“…A number of systems have been studied by NMR under similar solution conditions (0.1 M ionic strength, pH~7.1): the hetero-association of phenanthridine (EB, PI, ethidium mono-and di-azides) [189,[208][209][210][211], acridine (AO, PF) [74,207] and xanthene [212] dyes with the antibiotics DAU, TPT and quinolones; the hetero-association of antitumor antibiotics DAU-NOV [213], DAU-AMD [214,215], DAU-NOR [168], DAU-NOG [167,191], NOV-AMD [214], NOV-NOG [167,191], NOR-NOG [168], NOG-AMD [167,191], DAU-TPT [189], antimalarial drugs [216] and the hetero-association of mutagens: AO-PF [217], EB-PI [218], PF-EB [75,76], dyes [219] and some other aromatic drug molecules [13,220]. These molecules have a planar 3-or 4-ring aromatic chromophore (except the 2-ring NOR molecule) and must potentially be characterised by greater π-stacking interactions than that provided by the derivatives of nucleic acid bases and xanthines.…”