Pnictogen <sup>III</sup> Dications Supported by BZIMPY Ligands

Two homologous series of pnictogen(III) dications, stabilized by 2,6-bis(benzimidazole-2-yl)pyridine ligands have been prepared. Both series contain Pn<sup>III</sup>-X moieties (Pn = P, As, Sb, Bi; X = Cl or Ph) and have been fully characterized using spectroscopic methods including X-ray crystallography. The Lewis acidity of these compounds has also been probed by computational methods; the results suggest that the dictations are strong Lewis acids, with the PnCl<sup>2+</sup> compounds being more acidic than the PnPh<sup>2+</sup> compounds, and with Lewis acidity increasing from P to Bi, in both series. The PhP<sup>2+</sup>-containing compound was also found to be a versatile P<sup>III</sup> transfer reagent, leading to new synthetic routes for various PhP-containing compounds. The redox chemistry of all compounds has also been probed using cyclic voltammetry and chemical reductions. In some cases the resulting Pn<sup>I</sup> moieties could be trapped using diazabutadienes.

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Publication Details

Journal
Chemistry - A European Journal
Published
2024-10-22
DOI
https://doi.org/10.1002/chem.202403243
Citations
4
Primary Topic
Synthesis and characterization of novel inorganic/organometallic compounds
Type
article
Field-Weighted Citation Impact
0.63

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article

Pnictogen III Dications Supported by BZIMPY Ligands

Ala’aeddeen Swidan, Michael A. Land, Charles L. B. Macdonald, Katherine N. Robertson et al.
4 citations
Chemistry - A European Journal
Synthesis and characterization of novel inorganic/organometallic compounds
0.63
article

Pnictogen III Dications Supported by BZIMPY Ligands

Ala’aeddeen Swidan, Michael A. Land, Charles L. B. Macdonald, Katherine N. Robertson, William P. Howlett, Ksenia Varga
article en
4 citations

Abstract

Two homologous series of pnictogen(III) dications, stabilized by 2,6-bis(benzimidazole-2-yl)pyridine ligands have been prepared. Both series contain Pn<sup>III</sup>-X moieties (Pn = P, As, Sb, Bi; X = Cl or Ph) and have been fully characterized using spectroscopic methods including X-ray crystallography. The Lewis acidity of these compounds has also been probed by computational methods; the results suggest that the dictations are strong Lewis acids, with the PnCl<sup>2+</sup> compounds being more acidic than the PnPh<sup>2+</sup> compounds, and with Lewis acidity increasing from P to Bi, in both series. The PhP<sup>2+</sup>-containing compound was also found to be a versatile P<sup>III</sup> transfer reagent, leading to new synthetic routes for various PhP-containing compounds. The redox chemistry of all compounds has also been probed using cyclic voltammetry and chemical reductions. In some cases the resulting Pn<sup>I</sup> moieties could be trapped using diazabutadienes.

Chemistry - A European JournalVol. 31(1)
Dalhousie University (CA), Saint Mary's University (CA), Carleton University (CA), University of Windsor (CA)
Alliance de recherche numérique du Canada, Natural Sciences and Engineering Research Council of Canada
Clean water and sanitation
Openalex Percentile: Top 36%
Synthesis and characterization of novel inorganic/organometallic compounds
0.63
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Pnictogen <sup>III</sup> Dications Supported by BZIMPY Ligands — Ala’aeddeen Swidan, Michael A. Land, et al. · Chemistry - A European Journal (2024) | TGRS Research Map | TGRS