Browsing by Author "Gdanec, M."

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    SYNTHESIS AND STRUCTURE OF {M-OXALATO-BIS[ETHYLENEDIAMINETETRAACETATO- BISMUTHATO(III)]}PENTAAMMINETHIOCYANATOCOBALT(III) DODECAHYDRATE, [CO(NH3)5NCS]2[(EDTA)BI(M-C2O4)BI(EDTA)] • 12H2O
    (2000) Stăvilă, Vitalie; Gdanec, M.; Șova, Sergiu; Simonov, Iurie; Gulea, Aurelian; Vignacourt, Jean-Pierre
    A heterometallic complex of cobalt(III) and bismuth(III), [Co(NH3)5NCS]2[(Edta)Bi(μ-C2O4)Bi(Edta)] · 12H2O, was synthesized and studied by X-ray diffraction analysis. The crystals are monoclinic, a = 12.792(3) Å, b = 9.792(2) Å, c = 22.945(5) Å, β = 92.92(3)°, P(calcd) = 1.970 g/cm3, space group P21/c, Z = 4. The complex has an isle structure composed of [(Edta)Bi(μ-C2O4)Bi(Edta)]4- and [Co(NH3)5NCS]2+ complex ions and molecules of crystallization water. The Edta4- ligand functions as a hexadentate chelating (2N + 40) agent, while the oxalate ion acts as a bridging ligand. The thiocyanate ion is coordinated to cobalt(III) through the N atom, while the cation interacts with the anion via the Bi-S contact (3.571 Å). Hence, the coordination polyhedron of Bi can be regarded as a tricapped trigonal prism. It was shown that thermolysis of the complex proceeds in several stages, viz., the deaquation, deamination, and pyrolysis of its ligands.
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    SYNTHESIS AND STUDY OF HETEROMETALLIC CO–BI COMPOUNDS BASED ON ETHYLENEDIAMINETETRAACETIC ACID. CRYSTAL AND MOLECULAR STRUCTURES OF [CO(DH)2(O -NH2C6H4CH3)2]2[BI2(M-EDTA)2(H2O)2] • 10H2O (DH2 IS DIMETHYLGLYOXIME)
    (2002) Stăvilă, Vitalie; Gulea, Aurelian; Șova, Sergiu; Gdanec, M.; Simonov, Iurie
    Compounds of the [Co(DH)2A2](BiEdta)·6H 2O type (where DH is the monodeprotonated dimethylglyoxime -ON=C(CH3)-(CH3)C=NOH; A is the o-, m-, or p-toluidine; and Edta is the ethylenediaminetetraacetate(4-) ion) were synthesized and studied. The composition and structures of the complexes were determined from their UV and 1H NMR spectra and from X-ray diffraction data. The isomer [Co(DH)2(o-NH2C 6H4CH3)2]2[Bi 2(μ-Edta)2(H2O)2]·10H 2O was structurally characterized using X-ray diffraction analysis. The crystals are triclinic: a = 12.153(2) Å, b = 12.824(3) Å, c = 16.215(3) Å, α = 67.73(3)°, β = 86.18(3)°, γ = 66.96(3)°, space group P1̄ , ρ(calcd) = 1.719 g/cm3, Z = 4. The structure is composed of complex binuclear [Bi2(μ-Edta) 2(H2O)2]2- anions, [Co(DH) 2(o-NH2C6H4CH3) 2]+ cations, and molecules of crystallization water. The Edta4- anion chelates with the Bi atom in a hexadentate manner (N2O4); the fifth O atom functions as a bridging ligand. The bismuth coordination polyhedron can be regarded as a strongly distorted antiprism. In the octahedral cation, the Co(III) atom coordinates four N atoms of two DH ligands (average Co-N 1.897 Å) and two N atoms of two o-toluidine molecules (Co-N 2.023 Å). Thermolysis of the complexes studied was found to proceed in several successive steps, namely, the deaquation, deamination, and pyrolysis of the ligands.