d10s2 Post-Transition Metal Anions: Identifying and Analyzing Their Dual-Mode Lewis Basicity
Source abstract
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
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
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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