Reactions of as eries of magnesium(I) compounds with ethylene, in the presenceo fa nN-heterocyclic carbene (NHC), have been explored. Treating [{(Mes Nacnac)Mg} 2 ] (Mes Nacnac = [HC(MeCNMes) 2 ] À ,M es = mesityl) with an excess of ethylene in the presence of two equivalents of :C{(MeNCMe) 2 }(TMC) leads to the formal reductivec oupling of ethylene, and formationo ft he 1,2-dimagnesiobutane complex, [{(Mes Nacnac)(TMC)Mg} 2 (m-C 4 H 8)].I nc ontrast, when the reactioni sr epeated in the presence of three equivalents of TMC, am ixture of the b-diketiminato magnesium ethyl, [(Mes Nacnac)(TMC)MgEt],a nd the NHC coordinated magnesium diamide, [(Mes Nacnac-H)Mg(TMC) 2 ], results. Four related products,[ (Ar Nacnac)(TMC)MgEt] (Ar = 2,6-dimethylphenyl (Xyl) or 2,6-diisopropylphenyl (Dip)) and [(Ar Nacnac-H)Mg-(TMC) 2 ](Ar = Xyl or Dip), were similarly synthesised and crystallographically characterized. Computational studies have been employed to investigate the mechanisms of the two observed reaction types, whicha ppear dependent on the substitution pattern of the magnesium(I) compound, and the stoichiometrice quivalents of TMC used in the reactions.