Abstract
The deoxygenation of environmental pollutants CO2 and NO2- to form value-added products is reported. CO2 reduction with subsequent CO release and NO2- conversion to NO are achieved via the starting complex Fe(PPhPDI)Cl2 (1). 1 contains the redox-active pyridinediimine (PDI) ligand with a hemilabile phosphine located in the secondary coordination sphere. 1 was reduced with SmI2 under a CO2 atmosphere to form the direduced monocarbonyl Fe(PPhPDI)(CO) (2). Subsequent CO release was achieved via oxidation of 2 using the NOx- source, NO2-. The resulting [Fe(PPhPDI)(NO)]+ (3) mononitrosyl iron complex (MNIC) is formed as the exclusive reduction product due to the hemilabile phosphine. 3 was investigated computationally to be characterized as {FeNO}7, an unusual intermediate-spin Fe(III) coupled to triplet NO- and a singly reduced PDI ligand.
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