Binding of N-2 and CO by the FeMo-cofactor of nitrogenase depends on the redox level of the cluster, but the extent to which pure redox chemistry perturbs the affinity of high spin iron clusters for it pi-acids is not well understood. Here, we report a series of site-differentiated iron clusters that reversibly bind CO in redox states Fe-4(II) through (FeFe3III)-Fe-II. One electron redox events result in small changes in the affinity for (at most similar to 400-fold) and activation of CO (at most 28 cm(-1) for V-co). The small influence of redox chemistry on the affinity of these high spin, valence-localized clusters for CO is in stark contrast to the large enhancements (10(5)-10(22) fold) in pi-acid affinity reported for monometallic and low spin, bimetallic iron complexes, where redox chemistry occurs exclusively at the ligand binding site. While electron-loading at metal centers remote from the substrate binding site has minimal influence on the CO binding energetics (similar to 1 kca.morl(-1)), it provides a conduit for CO binding at an Fe-III center. Indeed, internal electron transfer from these remote sites accommodates binding of CO at an Fe-III, with a small energetic penalty arising from redox reorganization (similar to 2.6 kcal.mol(-1)). The ease with which these clusters redistribute electrons in response to ligand binding highlights a potential pathway for coordination of N-2 and CO by FeMoco, which may occur on an oxidized edge of the cofactor.