The substitution of the azaheterocarboxylate ligand (2-quinoxalinecarboxylate, Qox) in the heteroleptic silver (I) coordination polymer AgBHQox was studied in the presence of the neutral ligands 2, 2-bipyridyl (bipy) and triphenylphosphine (PhP). It was found that dissociation of the starting polymer in dimethylformamide results in its dissociation, and the subsequent addition of neutral ligands leads to the complete displacement of the Qox anion from the silver coordination sphere. The resulting molecular complex Ag (bipy) [BH] (1) and polymeric complex Ag (PhP) [BH] (2) are determined by elemental analysis, IR spectroscopy, and X-ray diffraction analysis. In the structure of complex I, the boron cluster anion is coordinated along a face and an edge, forming a molecular compound. The structure of compound 2 is known: the -decaborate anion acts as a μ-bridging ligand, forming a one-dimensional polymer chain. The obtained results demonstrate that neutral ligands effectively compete with the anionic azaheterocarboxylate ligand for coordination sites on silver (I) under conditions of dissociation of the starting polymer in DMF.
T. A. Tikhonova (Wed,) studied this question.