Mixing and matching N,N- and N,O-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO
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Updated: Jun 23, 2025

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
Published on: December 29, 2016
Andrea O'Reilly1, Matthew D Haynes2, Zoë R Turner2
1School of Chemical and Physical Sciences, Victoria University of Wellington, PO Box 600, Wellington 6012, New Zealand. martyn.coles@vuw.ac.nz.
Abstract:
Reduction of [Mg(NON)]2 ([NON]2- = [O(SiMe2NDipp)2]2-, Dipp = 2,6-iPr2C6H3) affords Mg(I) species containing NON- and NNO-ligands ([NNO]2- = [N(Dipp)SiMe2N(Dipp)SiMe2O]2-). The products of reactions with iPrNCNiPr and CO are consistent with the presence of reducing Mg(I) centres. Extraction with THF affords [K(THF)2]2[(NNO)Mg-Mg(NNO)] with a structurally characterised Mg-Mg bond that was examined using density functional theory.
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