Abstract
Reduction of 6-coordinate ((Ph2PPr)DI)FeBr₂ under N2 results in formation of the terminal dinitrogen complex, ((Ph2PPr)DI)FeN2. Heating this product to 75 °C allows for C-H and C-P activation of the chelate to generate the cisoid and transoid isomers of [(μ-PrPPh-κ(5)-P,N,N,Cγ,P-(Ph2PPr)DI(PrPPh))Fe]2. Mechanistic possibilities for this transformation are discussed.
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