This study investigates the electronic interactions and charge redistribution at the dopant−support interface using a Cu/Co 6 Se 8 cluster construct. Specifically, the redox cluster series [Cu 3 Co 6 Se 8 L 6 ] n ([1-Cu 3 ] n ; n = 0, −1, −2, −3; L = Ph 2 PNTol − , Ph = phenyl, Tol = p-tolyl) spanning four distinct oxidation states is synthesized and characterized using a multitude of techniques, including multinuclear NMR, UV−vis, XANES, and X-ray crystallography. Structural investigations indicate that the clusters are isostructural and chiral, adopting a pseudo-D 3 symmetry. Paramagnetic 31 P NMR spectroscopy and solution-phase magnetic measurements together with DFT calculations are employed to interrogate the electronic structure and spin-state changes across the [1-Cu 3 ] 3− to 1-Cu 3 redox series, revealing that the copper edge sites retain a +1 oxidation state while the Co/Se core becomes increasingly oxidized, yielding a highly zwitterionic cluster.