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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Ansmann, Nils (VerfasserIn) , Münch, Joshua (VerfasserIn) , Schorpp, Marcel (VerfasserIn) , Greb, Lutz (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 6 December 2023
In: Angewandte Chemie. International edition
Year: 2023, Jahrgang: 62, Heft: 50, Pages: 1-6
ISSN:1521-3773
DOI:10.1002/anie.202313636
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/anie.202313636
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.202313636
Volltext
Verfasserangaben:Nils Ansmann, Joshua Münch, Marcel Schorpp, and Lutz Greb
Beschreibung
Zusammenfassung: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.
Beschreibung:Gesehen am 30.01.2024
Beschreibung:Online Resource
ISSN:1521-3773
DOI:10.1002/anie.202313636