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Coordination Compounds of Transition Metals with Rhodanine-3-Acetic Acid

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Abstract

Seven compounds are synthesized by the reactions of the transition metals with rhodanine-3-acetic acid and studied by X-ray structure analysis. The compositions of the compounds can be presented by the formulas: [Co(Rda)2(H2O)4] (I), [Ni(Rda)2(H2O)4] (II), [Zn(Rda)2(H2O)4] (III), [Zn(5,5'-Rda-Rda)(Dmf)2(H2O)2]n (IV), [Co(Rda)2(bipy)(H2O)2]n (V), [Cd(Rda)2(Bpe)]n (VI), and [Co(Gly)3]⋅H2O (VII), where 5,5'-Rda-RdaН2 is the new ligand (condensation product of two RdaН molecules), bipy is 4,4-bipyridine, Bpe is bis(4-pyridyl)ethane, and Gly is glycine (CIF files CCDC nos. 2070334–2070339 for IVI, respectively). Compounds IIII and VII are mononuclear molecular complexes, and compounds IVVI are 1D coordination polymers. In complexes IIII, Rda coordinates via one oxygen atom of the carboxyl group as the monodeprotonated monodentate ligand, whereas in compound VII this ligand undergoes decomposition due to the solvothermal synthesis to form glycine molecules. Polymer IV is formed by the new ligand (5,5'-Rda-Rda)2– that coordinates as the bis(deprotonated) bidentate-bridging ligand, and molecules of the bis(pyridine) class (bipy and Bpе) act as bridging neutral ligands in compounds V and VI. In compound V, Rda coordinates as in complexes IIII, whereas in polymer VI two crystallographically independent Rda ligands coordinate via different modes: one ligand coordinates via the bidentate-chelating mode to one cadmium atom, and another coordinates via the tridentate-chelating mode to two metal atoms.

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Funding

This work was carried out in terms of state assignments (projects nos. 20.80009.5007.15 and 20.80009.5007.28) of the National Agency for Research and Development of Republic of Moldova.

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Correspondence to P. Bourosh.

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Translated by E. Yablonskaya

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Vitiu, A., Coropceanu, E. & Bourosh, P. Coordination Compounds of Transition Metals with Rhodanine-3-Acetic Acid. Russ J Coord Chem 47, 717–729 (2021). https://doi.org/10.1134/S1070328421110063

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  • DOI: https://doi.org/10.1134/S1070328421110063

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