The reaction of (2-pyrrole)-(5,6-diphenyl-[1,2,4]-triazin-3-yl)hydrazone with trivalent 4f lanthanide metal ions (La(III), Pr(III), Nd(III), Sm(III), Eu(III), Gd(III), Tb(III), Dy(III), Ho(III), Er(III) and Yb(III)) and 5f actinide metal ion UO 2 (II) has been studied potentiometrically in 75% (v/v) dioxane-water; at 283, 293, 303 and 313K. The ligand behaves as mono-protic species with the dissociation of hydrazo group proton and reacts with metal ion in molar ratio 1:2; M:L in solution. The formation constants were caulculated, which decrease as temprerature increases. The negative values of ΔH and ΔG° indicate that the complexation process is exothermic and proceeds spontaneously, respectivily. The electrostatic forces are weaker than non-electrostatic forces, where-G°n on is lower than-G°e l. G°e l has negative comparable values and suggests that the complexation process is affected by the temperature and environment. The higher negative value of H 1non than H 2non for UO 2-complex would reflect that the bond strength from ligand to UO 2 ion, which is stronger in the 1 st coordination than the 2 nd coordination.