Bis(amidophenolate)-supported pnictoranides: Lewis acid-induced electromerism in a bismuth complex

Abstract

The synthesis of the complete series of 10-Pn-4 bis(amidophenolate)-supported pnictoranide anions is reported. Coordination of these anions to the cyclopentadienyliron(II) dicarbonyl fragment, [CpFe(CO)2]+, delivers the corresponding 10-Pn-5 complexes for P, As and Sb, while in the case of Bi an electron redistribution takes place, and the corresponding 12-Bi-5 compound is isolated. This case of Lewis acid-induced electromerism has been experimentally confirmed through X-ray diffraction analyses as well as IR, UV-Vis and Mössbauer spectroscopy. Effective Oxidation State analysis of the Fe-complexes assigns an oxidation state +3 to all Pn, while it predicts the Fe-atom to be reduced to Fe(0) in the Bi-derivative. The mixture of the Bi(6p) orbital with the π-system of the bis(amidophenolate) ligand and the efficient electronic donation from this orbital to the Fe-center explain this situation.

Graphical abstract: Bis(amidophenolate)-supported pnictoranides: Lewis acid-induced electromerism in a bismuth complex

Supplementary files

Article information

Article type
Edge Article
Submitted
09 May 2025
Accepted
28 Jun 2025
First published
08 Jul 2025
This article is Open Access

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

Chem. Sci., 2025, Advance Article

Bis(amidophenolate)-supported pnictoranides: Lewis acid-induced electromerism in a bismuth complex

S. B. H. Karnbrock, J. F. Köster, I. Becker, C. Golz, F. Meyer, M. Gimferrer and M. Alcarazo, Chem. Sci., 2025, Advance Article , DOI: 10.1039/D5SC03374H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements