Three Pt 4 L 2 L' 2 heteroleptic rectangles(1-3), containing ditopic redox-activeb is-pyridine functionalized perylene bisimide (PBI) ligands PBI-pyr 2 (L)a re reported. Coligand L' is ad icarboxylate spacero fv arying length, leading to modified overall size of the assemblies. 1 HNMR spectroscopy reveals at rend in the splitting andu pfield chemical shift of the PBI-hydrogens in the rectangles with respect to free PBI, mostp ronounced with the largest strut length (3) and least with the smallest strut length (1). This is attributed to increased rotational freedomo ft he PBI-pyr 2 ligand over its longitudinala xis (N py-N py), duet oi ncreased distance between the PBI-surfaces, whichi sc orroborated by VT-NMR measurements and DFT calculations. The intramolecular motion entails desymmetrization of the two PBI-ligands, in line with cyclic voltammetry (CV) data. The first (overall twoelectron) reductione vent and re-oxidation for 1 display a subtlep eak-to-peak splitting of 60 mV,w hilst increased splitting of this event is observedf or 2 and 3.T he binding of pyrenei n1 is probedt oe stablish proof of concept of hostguestc hemistry enabled by the two PBI-motifs. Fitting the binding curveo btained by 1 HNMR titration with a1 :1 complex formationm odel led to ab inding constant of 964 AE 55 m À1 .P yrene binding is shown to directly influence the redox-chemistry of 1,r esultingi nacathodic and anodic shift of approximately 46 mV on the first and second reduction event, respectively.