The reaction of two equivalents each of bisphenol A with 1,5-dichloroa
nthraquinone in the presence of base leads to a molecular box designed
to be electroactive. The compound is fully characterized, it exhibits
reversible redox behavior, and its solid state structure has been obt
ained. Two molecules of toluene are present in the crystal lattice but
these are not located within the receptor's cavity. Evidence for an i
nteraction of ferrocene (guest) with a precursor to the molecular box
is described.