Two amidothiourea based receptors (L1 and L2) containing a π-acidic 3,5-dinitrophenyl chromophore have been synthesized in good yields and their anion recognition properties were evaluated both in organic and aqueous organic environment by spectroscopic techniques. Anions such as F−, AcO− and H2PO4− were examined to be suitable analytes for the receptor molecules, displaying optical signaling from colorless to orange/red, whereas anions of lower basicity such as Cl−, Br−, I−, NO3− and HSO4− did not cause any discernable spectral changes. The detailed 1H NMR titration experiments and single crystal X-ray structural analyses revealed that the receptor–anion(s) interaction encourages deprotonation of the amide –NH proton of the amidothiourea function. Interestingly, the highly basic OH− ion showed stepwise color changes with increasing equivalents, from colorless to red to green. The step wise color changes were found to be the outcome of OH− (1 equiv.) induced mono-deprotonation of the individual receptors (colorless to red), followed by anionπ interaction (red to green) with the π-acidic 3,5-dinitrophenyl ring of the receptors beyond one equiv. of OH− addition. This anionπ interaction between the OH− ion and the synthesized receptors has also been confirmed by monitoring the OH− induced absorption spectral changes of a control receptor (LC).