Abstract
The reaction of gold(III) neutral complexes AuBr(CN)2(N–N) {N–N = 2,2′-bipyridine (bpy), 5,5′-dimethyl-2,2′-bipyridine (Me2bpy), 1,10-phenanthroline (phen)} with a stoichiometric amount of K[AuCl4] · 2H2O in nitromethane at room temperature led to the formation of 1:1 electrolytes which were characterized by NMR and IR spectroscopy, conductivity measurements, elemental analyses and X-ray diffraction. Both the anions and the cations of these salts are singly charged square-planar Au(III) complexes and the cations have general formula [AuCl2(N–N)]+. A hypothesis on the possible reaction mechanisms is presented to give an explanation for the formation of the reaction products.
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Abbreviations
- Bpy:
-
2,2′-Bipyridine
- Me2bpy:
-
5,5′-Dimethyl-2,2′-bipyridine
- phen:
-
1,10-Phenanthroline
- DMF:
-
Dimethylformamide
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We gratefully thank the Ca’ Foscari University of Venice for financial support (Ateneo fund 2006).
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Pitteri, B., Bortoluzzi, M. & Bertolasi, V. Chelate polypyridine ligand rearrangement in Au(III) complexes. Transition Met Chem 33, 649–654 (2008). https://doi.org/10.1007/s11243-008-9092-9
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DOI: https://doi.org/10.1007/s11243-008-9092-9