The new tetradentate ligand H2L bis(5-(pyridine-2-yl)-1,2,4-triazol-3-yl)methane ligand H2L has been used to prepare corresponding Ln(III) complexes [Ln(L)(HL)H2O]·6H2O where Ln(III) is Tb(III), Sm(III), Eu(III), Gd(III), Nd(III). The resulting complexes were investigated by various means including elemental- and thermogravimetric analysis and IR-, UV-, VIS spectroscopy. The complexes form an isostructural series in the solid state according to X-ray diffraction. The optimal value of triple state energy of the ligand sensitizes both fluorescent visible and near-IR emissions of the lanthanides. However, the overall emission is moderate as a result of the quenching action of coordinated water molecules. The displacement of water molecules from the inner coordination sphere both in solid samples and the solutions results in a significant increase of the efficiency of the luminescence. The best value of the quantum yield was obtained for the Tb(III) complex with 41%. Luminescence titrations demonstrate that [Tb(L)(HL)H2O] is a pH-sensitive emitter which is able to detect pH values in both near neutral pH and acidic pH ranges.