journal article·2025-03-20Open access

d10s2 Post-Transition Metal Anions: Identifying and Analyzing Their Dual-Mode Lewis Basicity

Jake M. Seymour, Ekaterina Gousseva, Lewis G. Parker, Frances K. Towers Tompkins, Richard M. Fogarty, Lennart Frankemoelle, Rebecca Rowe, Coby J. Clarke, David A. Duncan, Robert G. Palgrave, Roger A. Bennett, Patricia A. Hunt, Kevin R. J. Lovelock

Abstract

High Resolution Image Download MS PowerPoint Slide Liquid-phase d 10 s 2 post-transition metal anions, such as [SnCl 3 ] −, appear in a range of applications with a focus on catalysis and material preparation. However, little is known about their electronic structure and how it relates to reactivity. Using X-ray photoelectron spectroscopy and ab initio calculations, we demonstrate that liquid-phase d 10 s 2 post-transition metal anions can act as dual-mode Lewis bases, interacting through the metal center and/or the ligands, with the interaction mode depending on the identity of the Lewis acid/electron acceptor. The Lewis basicity of the metal donor atom is controlled mainly by the metal identity; the ligand can be used for fine-tuning. Changing the metal center has a strong effect on the ligand basicity. These findings provide insight into d 10 s 2 post-transition metal anion electronic structure, which will enable better molecular-level design of catalytic systems.
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Research context

OpenAlex topics: Inorganic Chemistry and Materials · Inorganic Fluorides and Related Compounds · Crystallography and molecular interactions

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Affiliations

Department of Chemistry

University of Reading

Department of Materials

Imperial College London

School of Chemistry

University of Nottingham

Diamond Light Source

University College London

School of Chemical and Physical Sciences

Victoria University of Wellington

Funding

Royal Society · Diamond Light Source

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