The bipyridine‐based constructs 4‐(pyridine‐2‐yl)‐3H‐pyrrolo[2,3‐c]quinoline (PPQ) and [6‐(3H‐pyrrolo[2,3‐c]quinolin‐4‐yl)pyridin‐2‐yl]methanol (PPQ‐OH) and their assemblies with surfactants are evaluated as turn‐on fluorescent sensors for Zn2+ ions in aqueous solution. This study strives to overcome the problem of low water solubility of the hydrophobic PPQ and PPQ‐OH by using micelles. Whereas the ligands show selective sensing behavior for Zn2+ over important biological cations including Na+, K+, Ca2+, Mg2+ in anionic sodium dodecyl sulfate and non‐ionic Tween 80 micelles, no Zn2+ sensing is observed in cationic cetyltrimethylammonium bromide micelles. Unlike in DMF, Cd2+ interference is observed in aqueous conditions, which can be avoided either by performing the study at pH≥9 or by carrying out a time‐resolved fluorescence study. Analysis of the Job plot data, the fluorescence lifetimes, and experiments on varying micellar shape and pH, confirms that the coordination volume of the resulting octahedral metal complex and formation of a five‐membered chelate ring are critical factors for Cd2+ interference. The described sensing systems are capable of detecting Zn2+ ions at the micromolar level. Additionally, it is shown that PPQ and PPQ‐OH can be used to detect Zn2+ in HeLa cells under physiological conditions in bioimaging studies.