“…In the 6AC molecule, an amino group is substituted at position 6 of the 1,2-benzopyrone moiety. Therefore, in contrast to 7-aminocoumarins (often used as fluorescence probes [ 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 ], chemosensors [ 23 , 24 , 25 ] in biological and biomedical sciences [ 26 , 27 , 28 , 29 ] and in dye lasers [ 30 , 31 , 32 , 33 ]), the donor and acceptor groups are arranged along the same molecular axis and no other substituent groups (e.g., –CH 3 , –CF 3 ) are present in the molecule. In general, aromatic carbonyl compounds with amino group, such as aminocoumarins, can form intermolecular hydrogen bonds with solvents at different sites both in the ground and excited states [ 3 , 4 , 5 , 34 , 35 , 36 , 37 , 38 ].…”