PnictogenIII Dications Supported by BZIMPY Ligands DOI Creative Commons
Michael A. Land, William P. Howlett, Ala’aeddeen Swidan

et al.

Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 22, 2024

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

Language: Английский

A focus on phosphinophosphination of apolar bonds by a structurally constrained P–P bonded system DOI Creative Commons

Tyler J. Hannah,

Saurabh S. Chitnis

Chemical Science, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

This article highlights recent work by Greb et al. on the phosphinophosphination of alkenes, alkynes, and carbonyls, with a focus how polarity P–P bond controls scope resulting reactivity.

Language: Английский

Citations

0

Meta-Xylene-Based Diamines with Protected Benzyl Sites: Potential NCN Pincer Ligands with Tunable Steric Profiles DOI Creative Commons

Tamina Kirsch,

Toren Hynes,

Jason D. Masuda

et al.

Molecules, Journal Year: 2025, Volume and Issue: 30(6), P. 1331 - 1331

Published: March 16, 2025

Bulky NCN aryl-diamides featuring methyl groups in the benzyl positions were synthesized with aim of creating a new class meta-xylene-based trianionic pincer ligands where common decomposition pathway metal complexes via C-H activation is prevented. Sterically demanding substituents on furthermore provide steric protection centre and can help prevent dimerization complexes. While double deprotonation formation dilithium salt was straightforward, difficulties encountered when attempting to deprotonate ipso-CH proton central aryl ring yield ligands. This stands contrast related without benzylic positions. Experimental theoretical investigations led conclusion that challenges third are likely caused by an interplay increased electron density at nitrogen atoms hindrance. Both effects originate introduction positions, which make targeted less accessible. These results further insight into impact both electronic properties ligands, may find utility coordination chemistry applications metalation be achieved direct rather than requiring triple deprotonation.

Language: Английский

Citations

0

Geometrically Constrained Bismuth Compounds DOI

Tamina Kirsch,

Saurabh S. Chitnis

Structure and bonding, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Language: Английский

Citations

0

PnictogenIII Dications Supported by BZIMPY Ligands DOI Creative Commons
Michael A. Land, William P. Howlett, Ala’aeddeen Swidan

et al.

Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 22, 2024

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

Language: Английский

Citations

0