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Accessing Stable Magnesium Acyl Compounds: Reductive Cleavage of Esters by Magnesium(I) Dimers
Author(s) -
Boutland Aaron J.,
Lamsfus Carlos A.,
Maitland Brant,
Maron Laurent,
Stasch Andreas,
Jones Cameron
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201703061
Subject(s) - magnesium , umpolung , alkoxide , chemistry , electrophile , carbene , reactivity (psychology) , nucleophile , medicinal chemistry , stereochemistry , crystal structure , cleavage (geology) , reagent , crystallography , catalysis , organic chemistry , medicine , alternative medicine , geotechnical engineering , pathology , fracture (geology) , engineering
The first examples of magnesium acyls, [(Nacnac)Mg{μ‐C(Ph)O}(μ‐OR)Mg(Nacnac)] (R=Me, t Bu or Ph; Nacnac=[HC(MeCNAr) 2 ] − ; Ar=C 6 H 2 Me 3 ‐2,4,6 ( Mes Nacnac), C 6 H 3 Et 2 ‐2,6 ( Dep Nacnac), C 6 H 3 i Pr 2 ‐2,6 ( Dip Nacnac)), have been prepared by reductive cleavage of a series of esters using dimeric magnesium(I) reducing agents, [{(Nacnac)Mg} 2 ]. Crystallographic studies reveal the complexes to be dimeric, being bridged by both phenyl‐acyl and alkoxide/aryloxide fragments. The crystal structures, combined with results of spectroscopic and computational studies suggest that the nature of the acyl ligands within these complexes should be viewed as lying somewhere between anionic umpolung acyl and oxo‐carbene. However, reactions of the acyl complexes with a variety of organic electrophiles did not provide evidence of umpolung acyl reactivity. A number of attempts to prepare alkoxide free magnesium acyls were carried out, and while these were unsuccessful, they did lead to unusual products, the crystallographic and spectroscopic details of which are discussed.