학술논문

Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes.
Document Type
Article
Source
Chemical Communications. 1/25/2024, Vol. 60 Issue 8, p1016-1019. 4p.
Subject
*MAGNESIUM compounds
*NITROGEN
*POTASSIUM salts
*MAGNESIUM
*DIAMIDES
*MAGNESIUM diboride
Language
ISSN
1359-7345
Abstract
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. [ABSTRACT FROM AUTHOR]