Treatment of two equivalents of the triphosphenium zwitterion L with sources of Ni0 and Pd0 form the mononuclear η2-diphosphoniodiphosphene complexes 1 and 2. The reaction between L and [FeCp(CO)2]2 results in the binuclear μ-η1:η1-diphosphoniodiphosphene iron complex 3, which features an alternative bonding motif of the diphosphoniodiphosphene unit. The formation of these species has been confirmed by spectroscopic methods and single-crystal X-ray diffraction analysis, and their electronic structures have been elucidated using computational methods.

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Keywords diphosphene, insertion, oligophosphorus, phosphorus, triphosphenium
Persistent URL dx.doi.org/10.1002/chem.201805711
Journal Chemistry - A European Journal
Citation
Kosnik, S.C. (Stephanie C.), Binder, J.F. (Justin F.), Nascimento, M.C. (Maxemilian C.), Swidan, A. (Ala'aeddeen), & Macdonald, C.L.B. (2018). Diphosphoniodiphosphene Formation by Transition Metal Insertion into a Triphosphenium Zwitterion. Chemistry - A European Journal. doi:10.1002/chem.201805711