Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes

Reduction of the magnesium(ii) diamide [Mg(TripNON)] (TripNON = 4,5-bis(2,4,6-triisopropylanilido)-2,7-diethyl-9,9-dimethyl-xanthene) with 5% w/w K/KI leads to a good yield of a dianionic dimagnesium(i) species, as its potassium salt, [{K(TripNON)Mg}2]. An X-ray crystallographic analysis shows the m...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2024-01, Vol.60 (8), p.1016-1019
Hauptverfasser: Mondal, Rahul, Evans, Matthew J, Nguyen, Dat T, Thayalan Rajeshkumar, Maron, Laurent, Jones, Cameron
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creator Mondal, Rahul
Evans, Matthew J
Nguyen, Dat T
Thayalan Rajeshkumar
Maron, Laurent
Jones, Cameron
description Reduction of the magnesium(ii) diamide [Mg(TripNON)] (TripNON = 4,5-bis(2,4,6-triisopropylanilido)-2,7-diethyl-9,9-dimethyl-xanthene) with 5% w/w K/KI leads to a good yield of a dianionic dimagnesium(i) species, as its potassium salt, [{K(TripNON)Mg}2]. An X-ray crystallographic analysis shows the molecule to contain a very long Mg–Mg bond (3.137(2) Å). The formation of [{K(TripNON)Mg}2] contrasts with a previously reported reduction of a magnesium(ii) complex incorporating a bulkier diamide ligand, which instead afforded a magnesium–dinitrogen complex. In the current study, [{K(TripNON)Mg}2] has been shown to be a viable reagent for the reductive activation of CO, H2 and N2O.
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Chemical reduction
Chemical Sciences
Crystallography
Magnesium
Nitrogen compounds
Potassium salts
Reagents
title Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes
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