A quinoxalinone derivative capable of lactam-lactim tautomerization was designed as a new fluorescence probe for sensing of cation (M+ = Li+ and Na+) and anion (X- = F-, Cl-, Br-, and CH3COO-) in organic solvents. In THF, the minor lactam tautomer exhibited a weak fluorescence band at 425 nm with a typical Stokes shift of similar to 4400 cm(-1), whereas the major lactim tautomer exhibited an intense fluorescence band at 520 nm with large Stokes shift of similar to 8900 cm(-1) due to excited-state intramolecular proton transfer (ESIPT). The presence of either cations or anions was found to promote lactim-to-lactam conversion, resulting in the lowering of the ESIPT fluorescence. The lone pairs on the alkylamide oxygen and the quinoxalinone ring nitrogen of the lactam were found to bind Li+ to form a 1:2 coordination complex, which was confirmed by single crystal X-ray structural analysis and fluorescent titrations. In addition, the N-H bond of the lactam was able to recognize anions via N-H center dot center dot center dot X hydrogen bonding interactions. Where X = F- or CH3COO-, further addition of these anions caused deprotonation of the lactam to generate an anionic state, consistent with the crystal structure of the anion prepared by mixing tetrabutylammonium fluoride and the quinoxalinone derivative in THF. Dual cation-anion-sensing responses were found to depend on the ion-recognition procedure. The anionic quinoxalinone derivative and its Li+ complex, which are formed by the addition of CH3COO- and L+, respectively, displayed different fluorescence enhancement behavior due to the two anions exchanging with each other.