Comparison of the difluoromethylene and carbonyl ligands in binuclear iron complexes

Abstract

The binuclear difluoromethylene iron carbonyl Fe2(CF2)(CO)8 has been isolated as a stable compound from the reaction of Na2Fe2(CO)8 with CF2Br2. The structures and energetics of its decarbonylation products Fe2(CF2)(CO)n (n=7, 6, 5) have now been investigated using density functional theory. These are possible products from the photolysis of Fe2(CF2)(CO)8 under suitable conditions. In the lowest energy Fe2(CF2)(CO)n (n=7, 6, 5) structures the CF2 group is always a bridging rather than terminal group and iron–iron triple and quadruple bonds are avoided in the highly unsaturated structures. The lowest energy Fe2(CF2)(CO)7 structure has a bridging CF2 group and two semibridging CO groups. However, a singly bridged Fe2(CF2)(CO)7 structure lies only ~2kcal/mol in energy above this global minimum. The lowest energy Fe2(CF2)(CO)6 structure is a doubly bridged structure with a four-electron donor bridging η2-μ-CO group, the usual bridging CF2 group, and an FeFe distance of ~2.44Å suggesting a formal double bond. An Fe2(CF2)(CO)6 structure with an FeFe distance of ~2.23Å suggesting a formal triple bond, analogous to the lowest energy Fe2(CO)7 structure, lies ~13kcal/mol in energy above this structure. The lowest energy Fe2(CF2)(CO)5 structures are doubly bridged triplet spin state structures having iron–iron single or double bonds. The lowest energy singlet Fe2(CF2)(CO)5 structure, lying ~12kcal/mol above the lowest energy triplet structure, has an unprecedented kind of four-electron donor η2-μ-CF2 group, which is bonded to the central Fe2 unit though both its carbon atom and one of its fluorine atoms.