Issue 16, 2024

Combining geometric constraint and redox non-innocence within an ambiphilic PBiP pincer ligand

Abstract

The synthesis of the first pincer ligand featuring a strictly T-shaped group 15 element and its coordination behaviour towards transition metals is described. The platform is itself derived from a trianionic redox non-innocent NNN scaffold. In addition to providing a rigid coordination environment to constrain a Bi centre in a T-shaped geometry to manipulate its frontier molecular orbital constitution, the NNN chelate displays highly covalent bonding towards the geometrically constrained Bi centre. The formation of intriguing ambiphilic Bi–M bonding interactions is demonstrated upon formation of a pincer complex as well as a multimetallic cluster. All compounds are comprehensively characterised by spectroscopic methods including X-ray Absorption Near Edge Structure (XANES) spectroscopy and complemented by DFT calculations.

Graphical abstract: Combining geometric constraint and redox non-innocence within an ambiphilic PBiP pincer ligand

Supplementary files

Article information

Article type
Edge Article
Submitted
09 Jan 2024
Accepted
16 Mar 2024
First published
18 Mar 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2024,15, 6036-6043

Combining geometric constraint and redox non-innocence within an ambiphilic PBiP pincer ligand

P. Coburger, A. G. Buzanich, F. Emmerling and J. Abbenseth, Chem. Sci., 2024, 15, 6036 DOI: 10.1039/D4SC00197D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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