Reduction of (pddi)Cr reveals redox noninnocence via C-C bond formation amidst competing electrophilicity: [(cpta)CrMe n ] - ( n = 0, 1) and [(pta)Cr]

Reversible cyclopropane formation is probed as a means of redox noninnocence in diimine/diamide chelates reduction and complex anion formation. Competition from imine attack renders complications in the latter approach, and electrochemical measurements with calculational support provide the rationale.