Abstract

Single-crystal X-ray diffraction studies on the triphosphaferrocene [Fe(η 5-C 5H 5)(η 5P 3C 2 t Bu 2)] and its [Rh(η 5-C 5Me 5)CO] complex reveal an unusual η 2-ring edge coordination mode in the latter resulting in a significant elongation of the triphosphacyclopentadienyl ring P–P bond.

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