bis-Silyl-triazenide ligands in alkaline-earth metal chemistry

Knüpfer C, Langer J, Harder S (2023)


Publication Type: Journal article

Publication year: 2023

Journal

DOI: 10.1002/zaac.202300226

Abstract

Monoanionic N,N-chelating triazenide ligands, [R-NNN-R], are compared to formamidinate or β-diketiminate ligands considerably less electron-donating and therefore potentially suitable for stabilizing electron rich metals in low oxidations states. A feature reported for silyl-substituted triazenide ligands, is their ability to eliminate N2 resulting in (R3Si)2N anions. Here we describe a series of group 1 and 2 metal complexes with the very bulky bis-silyl-triazenide ligand [tBu3Si-NNN-SitBu3]. Heteroleptic complexes could be isolated for Mg: {[(tBu3Si)2N3]MgnBu}2 or {[(tBu3Si)2N3]MgI}2, including its ether adducts. Despite bulky silyl substituents, the ligand did not stabilize heteroleptic [(tBu3Si)2N3]AeN(SiMe3)2 complexes for Ca, Sr and Ba and only homoleptic Ae[(tBu3Si)2N3]2 complexes were isolated. Thermal decomposition of these complexes did result in N2 elimination and formation of the expected amide complexes. Reduction of [(tBu3Si)2N3]MgI ⋅ (Et2O) with KC8 in Et2O led to the formation of a MgI complex with a Mg−Mg bond length of 2.902(1) Å. As only one of the Mg centres shows coordination with a Et2O ligand, this is a rare example of an asymmetric Mg−Mg bond. This MgI complex is rather unstable in benzene solution, likely due to reduction of the ligand system. Triazenide ligands are therefore not suitable for stabilization of group 2 metals in low oxidation states.

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How to cite

APA:

Knüpfer, C., Langer, J., & Harder, S. (2023). bis-Silyl-triazenide ligands in alkaline-earth metal chemistry. Zeitschrift für Anorganische und Allgemeine Chemie. https://doi.org/10.1002/zaac.202300226

MLA:

Knüpfer, Christian, Jens Langer, and Sjoerd Harder. "bis-Silyl-triazenide ligands in alkaline-earth metal chemistry." Zeitschrift für Anorganische und Allgemeine Chemie (2023).

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