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Dynamic coordination behavior of a structurally constrained, nucleophilic Sn(II) towards gold(I)

Tetradentate meso-octaalkylcalix[4]pyrroles are well-established ligands in d- and f-block chemistry. In contrast to the related porphyrins, the sp3-hybridized meso-carbon atoms linking the four pyrrole units result in highly divers coordination modes. We previously reported on the combination of th...

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Main Authors: Ruppert, Heiko (Author) , Schreyer, Till (Author) , Dietl, Martin C. (Author) , Rudolph, Matthias (Author) , Hashmi, A. Stephen K. (Author) , Greb, Lutz (Author)
Format: Article (Journal)
Language:English
Published: August 19, 2024
In: Zeitschrift für anorganische und allgemeine Chemie
Year: 2024, Volume: 650, Issue: 16, Pages: 1-6
ISSN:1521-3749
DOI:10.1002/zaac.202400081
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/zaac.202400081
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/zaac.202400081
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Author Notes:Heiko Ruppert, Till Schreyer, Martin C. Dietl, Matthias Rudolph, A. Stephen K. Hashmi, and Lutz Greb
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Summary:Tetradentate meso-octaalkylcalix[4]pyrroles are well-established ligands in d- and f-block chemistry. In contrast to the related porphyrins, the sp3-hybridized meso-carbon atoms linking the four pyrrole units result in highly divers coordination modes. We previously reported on the combination of this ligand system with Sn(II) centers yielding tetracoordinated stannate(II) anions which could be employed as electron-rich, strong σ-donor ligands in transition metal chemistry. With this work we are extending the coordination chemistry of meso-octaethylcalix[4]pyrrolato stannate(II) [1]2− onto gold(I). Synthesis of mono- and dinuclear gold complexes reveal a new dynamic binding mode involving μ2-bridging coordination of a pyrrole nitrogen atom to both Sn and Au. Single-crystal X-ray diffraction and variable temperature NMR spectroscopy combined with quantum mechanical computations and bond analysis tools shed light on the involved intermediates.
Item Description:Gesehen am 26.11.2024
Physical Description:Online Resource
ISSN:1521-3749
DOI:10.1002/zaac.202400081

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