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Updated: Feb 12, 2026

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
Published on: May 28, 2014
Synthesis and non-conventional structure of square-planar Pd(ii) and Pt(ii) complexes with an N,C,N-chelated
Monika Kořenková1, Martin Hejda, Petr Štěpnička
1Department of General and Inorganic Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentská 573, CZ-532 10, Pardubice, Czech Republic. libor.dostal@upce.cz.
Abstract:
The N,C,N-chelated stibinidene, ArSb (Ar = C6H3-2,6-(CH[double bond, length as m-dash]NtBu)2), reacts with Pt(ii) compounds [PtCl2L2] resulting in the formation of 1 : 1 complexes, cis-[PtCl2L(ArSb)] (L = Me2S (1), dmso (2)). In contrast, attempts to synthesize similar Pd(ii) complexes failed, resulting only in the formation of elemental palladium. To increase the stability of the ArSb complexes, in particular those containing Pd(ii), the simple auxiliary ligands were replaced with C,N-chelating ones, which led to a set of four compounds of the type [RMCl(ArSb)], where R = C6H4-2-(CH2NMe2) or Fe(η5-C5H4)(η5-C5H3-2-(CH2NMe2)) and M = Pd (3, 5) or Pt (4, 6). Compounds 1-6 were characterized by 1H and 13C{1H} NMR spectroscopy and single-crystal X-ray diffraction analysis, and in the case of ferrocene derivatives 5 and 6, also by cyclic voltammetry. Compounds 2-6 were shown to form rotamers in solution due to the side-on coordination of the ArSb ligand and a hindered rotation around the Sb-Pd(Pt) bond. This process was investigated by 1H-VT-NMR spectroscopy and by DFT computations.
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