Stable Open-Shell Phosphorane Based on a Redox-Active Amidodiphenoxide Scaffold

• Main Authors: Pistner, Allen J. (Author), Moon, Hye Won (Contributor), Silakov, Alexey (Author), Yennawar, Hemant P. (Author), Radosevich, Alexander T. (Contributor)
• Other Authors: Massachusetts Institute of Technology. Department of Chemistry (Contributor)
• Format: Article
• Language: English
• Published: American Chemical Society (ACS), 2018-07-30T18:35:04Z.
• Subjects: Article
• Online Access: Get fulltext

The synthesis and redox reactivity of pentacoordinate phosphorus compounds incorporating a redox-active ONO amidodiphenoxide scaffold [ONO = N,N-bis(3,5-di-tert-butyl-2-phenoxide)amide] are described. Dichloro- and diphenylphosphoranes, 2·Cl₂ and 2·Ph₂, respectively, are synthesized and crystallographically characterized. Cyclic voltammograms of 2·Cl₂ show only a single irreversible oxidation (E{subscript pa] = +0.83 V vs Cp₂Fe0/+), while the diphenyl analogue 2·Ph2 is reversibly oxidized at lower applied potential (E[subscript 1/2] = +0.47 V vs Cp2Fe[superscript 0/+]). Chemical oxidation of 2·Ph₂ with AgBF₄ produces the corresponding radical cation [2·Ph₂]•+, where electron paramagnetic resonance spectroscopy and density functional theory calculations reveal that the unpaired spin density is largely ligand-based and is highly delocalized throughout the ONO framework of the paramagnetic species. The solid-state structures indicate only minor geometrical changes between the neutral 2·Ph₂ and oxidized [2·Ph₂]•+ species, consistent with fast self-exchange electron transfer, as observed by NMR line-broadening experiments.
National Science Foundation (U.S.) (Grant CHE- 1724505)