The presence of redox innocent metal ions has been proposed to modulate the reactivity of metal ligand multiple bonds; however, insight from structure/function relationships is limited. Here, alkali metal reduction of the Fe(III) imido complex [Ph2B(BuIm)2Fe═NDipp] (1) provides the series of structurally characterized Fe(II) imido complexes [Ph2B(BuIm)2Fe═NDippLi(THF)2] (2), [Ph2B(BuIm)2Fe═NDippNa(THF)3] (3), and [Ph2B(BuIm)2Fe═NDippK]2 (4), in which the alkali metal cations coordinate the imido ligand. Structural investigations demonstrate that the alkali metal ions modestly lengthen the Fe═N bond distance from that in the charge separated complex [Ph2B(BuIm)2Fe═NDipp][K(18-C-6)THF2] (5), with the longest bond observed for the smallest alkali metal ion. In contrast to 5, the imido ligands in 2-4 can be protonated and alkylated to afford Fe(II) amido complexes. Combined experimental and computational studies reveal that the alkali metal polarizes the Fe═N bond, and the basicity of imido ligand increases according to 5 < 4 ≈ 3 < 2. The basicity of the imido ligands influences the relative rates of reaction with 1,4-cyclohexadiene, specifically by gating access to complex 5, which is the species that is active for HAT. All complexes 2-4 react with benzophenone form metastable Fe(II) intermediates that subsequently eliminate the metathesis product Ph2C═NDipp, with relative rates dependent on the alkali metal ion. By contrast, the same reaction with 5 does not lead to the formation of Ph2C═NDipp. These results demonstrate that the coordination of alkali metal ions dictate both the structure and reactivity of the imido ligand and moreover can direct the reactivity of reaction intermediates.