Issue 14, 2016

Assessing the reactivity of sodium alkyl-magnesiates towards quinoxaline: single electron transfer (SET) vs. nucleophilic alkylation processes

Abstract

By exploring the reactivity of sodium butyl-magnesiate Image ID:c5dt04044b-t1.gif (1) supported by the bulky chelating silyl(bisamido) ligand {Ph2Si(NAr*)2}2− (Ar* = 2,6-iPr2-C6H3) towards Quinoxaline (Qx), the ability of this bimetallic system to effectively promote SET processes has been disclosed. Thus 1 executes the single-electron reduction of Qx affording complex Image ID:c5dt04044b-t2.gif (2) whose structure in the solid state contains two quinaxolyl radical anions Qx˙ stabilised within a dimeric magnesiate framework. Combining multinuclear NMR and EPR measurements with DFT calculations, new insights into the constitution of 2 in solution and its magnetic behaviour have been gained. Further evidence on the SET reactivity of 1 was found when it was reacted with nitroxyl radical TEMPO which furnished contacted ion pair sodium magnesiate [(Ph2Si(NAr*)2)Mg(TEMPO)Na(THF)3] (4) where both metals are connected by an alkoxide bridge, resulting from reduction of TEMPO. The role that the different ligands present in 1 can play in these new SET reactions has also been assessed. Using an amination approach, the Bu group in 1 can be replaced by the more basic amide TMP allowing the isolation of Image ID:c5dt04044b-t3.gif (3) which was characterised by multinuclear NMR and X-ray crystallography. 1H NMR monitoring of the reaction of 3 with Qx showed its conversion to 2, leaving the hydrogen atoms of the heterocycle untouched. Contrastingly, using sodium homoalkyl magnesiate [NaMg(CH2SiMe3)3] (5) led to the chemoselective C2 alkylation of this heterocycle, suggesting that the presence of the steric stabiliser {Ph2Si(NAr*)2}2− on the mixed-metal reagent is required in order to facilitate the Qx reduction.

Graphical abstract: Assessing the reactivity of sodium alkyl-magnesiates towards quinoxaline: single electron transfer (SET) vs. nucleophilic alkylation processes

Supplementary files

Article information

Article type
Paper
Submitted
15 Oct 2015
Accepted
18 Nov 2015
First published
20 Nov 2015

Dalton Trans., 2016,45, 6175-6182

Assessing the reactivity of sodium alkyl-magnesiates towards quinoxaline: single electron transfer (SET) vs. nucleophilic alkylation processes

Z. Livingstone, A. Hernán-Gómez, S. E. Baillie, D. R. Armstrong, L. M. Carrella, W. Clegg, R. W. Harrington, A. R. Kennedy, E. Rentschler and E. Hevia, Dalton Trans., 2016, 45, 6175 DOI: 10.1039/C5DT04044B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements