The homoleptic complexes of cerium with the tris(piperidinyl)imidophosphorane ligand, [NP(pip)(3)](-), present the most negative Ce3+/4+ redox couple known (<-2.64 V vs Fc/Fc(+)). This dramatic stabilization of the cerium tetravalent oxidation state [>4.0 V shift from the Ce3+/4+ couple in 1 M HClO4(aq)] is established through reactivity studies. Spectroscopic studies (UV-vis, electron paramagnetic resonance, and Ce L-3-edge X-ray absorption spectroscopy), in conjunction with density functional theory studies, reveal the dominant covalent metal-ligand interactions underlying the observed redox chemistry and the dependence of the redox potential on the binding of potassium in the inner coordination sphere.