Abstract
The cationic complexes, [TpRNi(bpym)]+ {TpR = tris(3,5-diphenylpyrazolyl)borate, R = Ph2 1; tris(3-phenyl-5-methylpyrazolyl)borate, R = Ph,Me 2} were synthesized by reacting [TpRNiBr] (R = Ph2; Ph,Me) with bipyrimidine followed by subsequent addition of KPF6 in CH2Cl2. The green solids have been characterized by IR, UV–Vis and 1H NMR spectroscopy. Crystallographic studies of [TpPh,MeNi(bpym)]PF6 reveal a five-coordinate square pyramidal nickel centre with a κ3-coordinated TpPh,Me ligand and a chelating bipyrimidine ligand. Cyclic voltammetric studies show irreversible reduction with the degree of reversibility dependent on the type of TpR ligand.
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Acknowledgments
We gratefully acknowledge the Thailand Research Fund (Grant No. RMU5080029) and the National Research Office of Thailand for funding this research (Grant no. WU51106). The School of Chemistry, University of Bristol is thanked for elemental analysis and MS services.
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Harding, D.J., Harding, P., Kivnang, J. et al. Cationic tris(pyrazolyl)borate bipyrimidine complexes. Transition Met Chem 35, 521–526 (2010). https://doi.org/10.1007/s11243-010-9358-x
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DOI: https://doi.org/10.1007/s11243-010-9358-x