The inclusion behavior of methylviologen (N,N'-dimethyl-4,4'-bipyridinium, MV) dication in cucurbit[7]uril (CB[7]) has been studied by using various spectroscopic and electrochemical methods. The inclusion complex of MV dication in CB[7] is stable thermodynamically and kinetically. The electrochemical study reveals that unlike beta-cyclodextrin, CB[7] prefers the charged species, MV dication (MV(2+)), and cation radical (MV(+)*) to the fully reduced neutral (MV(0) species as guests. Dimerization of MV(+)* is suppressed effectively by forming a stable complex with CB[7] in aqueous solution as confirmed by spectroelectrochemical experiments. Furthermore, the first redox process (MV(2+)/MV(+)*) of the MV(2+)-CB[7] complex occurs predominantly via the direct electron transfer pathway, whereas the second redox process (MV(+)*/MV(0)) occurs via both the direct and indirect pathway because of the low affinity of the fully reduced species MV(0) to CB[7].