Synthesis and Reactivity of Low-Valent f-Element Iodide Complexes with Neutral Iminophosphorane Ligands

Cheisson T, Ricard L, Heinemann FW, Meyer K, Auffrant A, Nocton G (2018)


Publication Type: Journal article

Publication year: 2018

Journal

Book Volume: 57

Pages Range: 9230-9240

Journal Issue: 15

DOI: 10.1021/acs.inorgchem.8b01259

Abstract

The coordination and reactivity of simple iodide salts of low-valent f elements [YbI2, SmI2, TmI2, and UI3(THF)4, where THF = tetrahydrofuran] with iminophosphorane (R3P=NR′) ligands are reported. The studied chelates were observed to adapt their geometry and effectively bind divalent ytterbium and samarium centers, as well as the trivalent uranium cation. The reactivity of the ytterbium adducts with benzophenone was found to be dependent on the steric demand of the supporting iminophosphorane ligand. In particular, a rare example of a stable charge-separated ketyl radical species is reported with ytterbium. Additionally, divalent thulium was observed to induce a reductive coupling at the ligand's central pyridine ring.

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APA:

Cheisson, T., Ricard, L., Heinemann, F.W., Meyer, K., Auffrant, A., & Nocton, G. (2018). Synthesis and Reactivity of Low-Valent f-Element Iodide Complexes with Neutral Iminophosphorane Ligands. Inorganic Chemistry, 57(15), 9230-9240. https://doi.org/10.1021/acs.inorgchem.8b01259

MLA:

Cheisson, Thibault, et al. "Synthesis and Reactivity of Low-Valent f-Element Iodide Complexes with Neutral Iminophosphorane Ligands." Inorganic Chemistry 57.15 (2018): 9230-9240.

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