Abstract
Cationic nickel(II) complexes containing chelating O,O′-donor maltolate or ethyl maltolate ligands in conjunction with bidentate bisphosphine ligands Ph2P(CH2) n PPh2 were prepared by a one-pot reaction starting from nickel(II) acetate, bisphosphine, maltol (or ethyl maltol), and trimethylamine, and isolated as their tetraphenylborate salts. An X-ray structure determination of [Ni(maltolate)(Ph2PCH2CH2PPh2)]BPh4 shows that the maltolate ligand binds asymmetrically to the (slightly distorted) square-planar nickel(II) center. The simplicity of the synthetic method was extended to the synthesis of the known platinum(II) maltolate complex [Pt(maltolate)(PPh3)2]BPh4 which was obtained in high purity.
Acknowledgments
We thank the University of Waikato for financial support of this work, Julia Lin and Bevan Jarman for NMR spectra, and Dr Tania Groutso (University of Auckland) for collection of the X-ray data set.