Reductive Hexamerization of CO Involving Cooperativity Between Magnesium(I) Reductants and [Mo(CO)6]: Synthesis of Well-Defined Magnesium Benzenehexolate Complexes**

Albert Paparo, K. Yuvaraj, Aidan J.R. Matthews, Iskander Douair, Laurent Maron, Cameron Jones

Research output: Contribution to journalArticleResearchpeer-review

14 Citations (Scopus)

Abstract

Reactions of two magnesium(I) compounds, [{(ArNacnac)Mg}2] (ArNacnac=[HC(MeCNAr)2]; Ar=mesityl (Mes) or o-xylyl (Xyl)), with CO in the presence of [Mo(CO)6] lead to the reductive hexamerization of CO, and formation of magnesium benzenehexolate complexes, [{(ArNacnac)Mg}6(C6O6)]. [Mo(CO)6] is not consumed in these reactions, but is apparently required to initiate (or catalyze) the CO hexamerizations. A range of studies were used to probe the mechanism of formation of the benzenehexolate complexes. The magnesium(I) reductive hexamerizations of CO are closely related to Liebig's reduction of CO with molten potassium (to give K6C6O6, amongst other products), originally reported in 1834. As the mechanism of that reaction is still unknown, it seems reasonable that magnesium(I) reductions of CO could prove useful homogeneous models for its elucidation, and for the study of other C−C bond forming reactions that use CO as a C1 feedstock (e.g. the Fischer–Tropsch process).

Original languageEnglish
Pages (from-to)630-634
Number of pages5
JournalAngewandte Chemie - International Edition
Volume60
Issue number2
DOIs
Publication statusPublished - 11 Jan 2021

Keywords

  • benzenehexolate
  • carbon monoxide
  • DFT calculations
  • homologation
  • magnesium

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