Neutral and anionic square planar palladium(0) complexes stabilized by a silicon Z-type ligand

Anionic [Pd(0)−X]− ate complex were proposed as key intermediates in Pd-catalyzed cross-coupling for decades, but their isolation remained elusive. Herein, a chelating Lewis acidic bis(amidophenolato)silane is introduced as a strong Z-type ligand which enables the characterization of the first anion...

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Main Authors: Ansmann, Nils (Author) , Münch, Joshua (Author) , Schorpp, Marcel (Author) , Greb, Lutz (Author)
Format: Article (Journal)
Language:English
Published: 6 December 2023
In: Angewandte Chemie. International edition
Year: 2023, Volume: 62, Issue: 50, Pages: 1-6
ISSN:1521-3773
DOI:10.1002/anie.202313636
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/anie.202313636
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.202313636
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Author Notes:Nils Ansmann, Joshua Münch, Marcel Schorpp, and Lutz Greb
Description
Summary:Anionic [Pd(0)−X]− ate complex were proposed as key intermediates in Pd-catalyzed cross-coupling for decades, but their isolation remained elusive. Herein, a chelating Lewis acidic bis(amidophenolato)silane is introduced as a strong Z-type ligand which enables the characterization of the first anionic [Pd(0)−X]− ate complex. Intriguingly, these compounds and the neutral L−Pd(0) analogs exhibit a square planar coordination that is highly unusual for a d10 metal. Theoretical methods scrutinize the interaction between the Lewis acidic Si(IV) center and the late transition metal, while reactivity studies shed light on the potential role of anionic additives in oxidative addition reactions.
Item Description:Gesehen am 30.01.2024
Physical Description:Online Resource
ISSN:1521-3773
DOI:10.1002/anie.202313636