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    [Pd4(μ3‑SbMe3)4(SbMe3)4]: A Pd(0) Tetrahedron with μ3‑Bridging Trimethylantimony Ligands


    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
    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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