摘要
The use of tetramethylpropanediammonium (2+) or hexaamminecobalt (III) as counter cations allowed the preparation of monomeric or dimeric uranyl bis(dimethylmalonato) complexes, respectively, which were characterised by solid-state 13C NMR and X-ray crystallography. These two structures are different from the monomeric and dimeric structures we reported earlier with unsubstituted malonate as ligand [4].