In this work, the effect of functional groups on I 2 sorption kinetics is investigated using two different types of isostructural metal-organic frameworks, UiO-66-X series (X = H, Br, NO 2 , NH 2 , (OH) 2 , and (COOH) 2) and M 2 (m-DOBDC) series, (M = Co2+, Mg2+, and Ni2+; m-DOBDC 4− = 4,6-dioxo-1,3benzenedicarboxylate). Among the UiO-66-X series, UiO-66-(COOH) 2 exhibits the fastest sorption kinetics and the highest sorption capacity due to dipole-induced dipole interactions between carboxylic acid groups and I 2 molecules. In addition, faster I 2 chemisorption is observed in M 2 (m-DOBDC) because of electrophilic aromatic substitution of m-DOBDC 4− with I 2. The I 2 sorption mechanisms are further supported by fitting the I 2 adsorption kinetics data to pseudo-first-order and pseudo-second-order kinetic models.