Benjamin, Sophie and Krämer, Tobias and Levason, William and Light, Mark E and Macgregor, Stuart A. and Reid, Gillian (2016) [Pd4(μ3‑SbMe3)4(SbMe3)4]: A Pd(0) Tetrahedron with μ3‑Bridging Trimethylantimony Ligands. Journal of the American Chemical Society, 138 (22). A-D. ISSN 0002-7863
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Abstract
The palladium(II) chlorostibine complex [PdCl2(SbMe2Cl)2]2 has a dimeric structure in the solid state, stabilized by hyper-coordination at the Lewis amphoteric Sb centers. Reaction with 8 equiv of MeLi forms [Pd4(μ3-SbMe3)4(SbMe3)4], whose structure comprises a tetrahedral Pd(0) core with four terminal SbMe3 ligands and four μ3-SbMe3 ligands, one capping each triangular Pd3 face. Density functional theory calculations, supported by energy decomposition analysis and the natural orbitals for chemical valence scheme, highlight significant donor and acceptor orbital contributions to the bonding between both the terminal and the bridging SbMe3 ligands and the Pd4 core.
Item Type: | Article |
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Keywords: | Pd4(μ3‑SbMe3)4(SbMe3)4; Pd(0); Tetrahedron; μ3‑Bridging Trimethylantimony Ligands; |
Academic Unit: | Faculty of Science and Engineering > Computer Science Faculty of Science and Engineering > Research Institutes > Hamilton Institute |
Item ID: | 15491 |
Identification Number: | https://doi.org/10.1021/jacs.6b04060 |
Depositing User: | Tobias Kraemer |
Date Deposited: | 14 Feb 2022 16:49 |
Journal or Publication Title: | Journal of the American Chemical Society |
Publisher: | American Chemical Society |
Refereed: | Yes |
URI: | |
Use Licence: | This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available here |
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