Zn(II) coordination by the phenanthroline-containing macrocycle 2,6,10,14-tetraaza[15](2,9)cyclo(1,10)phenanthrolinophane (L4) has been studied by means of potentiometric measurements in aqueous solution. Its coordination properties have been compared with those of other phenanthroline- or dipyridine-containing open-chain (L1, L2) or cyclic (L3) ligands. ATP binding to the Zn(II) complexes with L1–L4 has been examined by means of potentiometric and ¹H and ³¹P NMR measurements in aqueous solution. In the ATP adducts with the [ZnL]²⁺ complexes, the nucleotide interacts with the metal via the terminal P_γ phosphate group; the equilibrium constants for the addition of ATP to the complexes depend on the number and arrangement of the nitrogen donors coordinated to the metal ion. Protonation of the [ZnL]²⁺ complexes gives [ZnH_xL]^{(x + 2)+} species, which contain two binding sites for the phosphate chain of ATP; while the P_γ phosphate group gives a coordination bond with the metal, the P_β one interacts via P–O⁻⋯H–N⁺ salt bridges with the ammonium functions of the complex. In consequence, protonated complexes are better ATP receptors than the simple [ZnL]²⁺ species and even than the protonated forms [H_xL]^x+ of the ligands, due to the synergetic action of the metal ion and of ammonium functions in ATP binding.