Redox noninnocent ligands are known to be involved in altering the overall electronic nature of organometallic complexes by serving as an electron reservoir. Pyrazine(diimine) backbones in these complexes introduce enhanced pi acidity over their more well-studied pyridine(diimine) analogues and open up the opportunity for functionalization of the nitrogen at the 4-position of the ring. Herein we report the characterization of bischelated pyrazine(diimine) [((PDI)-D-z)(2)Fe](n+) (n = 0, 1, and 2) complexes for electronic and structural comparison to pyridine(diimine)complexes (PDI) with similar architectures. Cyclic voltammetry studies show three reductions, two of which are ligand-based and reversible. Reduction of [((PDI)-D-z)(2)Fe](2+) (1) to [((PDI)-D-z)(2)Fe](+) (2) and ((PDI)-D-z)(2)Fe (3) gives rise to characteristic structural changes, such as imine C=N bond lengthening, indicating the formation of a ligand radical, a conclusion which is further supported by electron paramagnetic resonance (EPR) and electronic structure calculations. Comparisons between the (PDI)-D-z and PDI systems are highlighted. Complex 1 can be protonated at the uncoordinated pyrazine nitrogen, resulting in changes to its spectroscopic and redox properties; efforts to further functionalize the ligand are discussed.