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

и другие.

Chemistry - A European Journal, Год журнала: 2024, Номер unknown

Опубликована: Окт. 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.

Язык: 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, Год журнала: 2025, Номер unknown

Опубликована: Янв. 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.

Язык: Английский

Процитировано

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

и другие.

Molecules, Год журнала: 2025, Номер 30(6), С. 1331 - 1331

Опубликована: Март 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.

Язык: Английский

Процитировано

0

Geometrically Constrained Bismuth Compounds DOI

Tamina Kirsch,

Saurabh S. Chitnis

Structure and bonding, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

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

и другие.

Chemistry - A European Journal, Год журнала: 2024, Номер unknown

Опубликована: Окт. 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.

Язык: Английский

Процитировано

0