2. Articole
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Item EFFECT OF THE NATURE OF THE ANION ON THE COMPOSITION AND STRUCTURE OF COBALT COMPLEX WITH MONOETHANOLAMINE(2013) Cotovaia, Aliona; Șova, Sergiu; Melnic, Elena; Simonov, Iurie; Gulea, Aurelian; Pahonțu, ElenaA number of products formed in reactions of cobalt(II) salts with monoethanolamine (HEtm) in a neutral medium were synthesized and studied. X-Ray diffraction study showed that the nitrate and acetate form the dimers [Co(HEtm)3][Co(Etm)3](NO3)3 and [Co(HEtm)3][Co(Etm)3](CH3COO)3 · 8H2O, respectively. In chloride solutions, cobalt is partially oxidized to give the trinuclear complex [CoII{Co III(Etm)3}2]Cl3 · H 2Etm · 2H2O. The reaction of the chelate [Co(Etm)3] · 3H2O with nitric acid is accompanied by complete protonation of the coordinated aminoethanolate ions, and the reaction with formic acid involves complete replacement of the coordinated ligand by acid residue anions and water molecules to give the coordination polymer {Co2(μ-HCOO)4(H2O)4} n .Item NEW COMPLEXES OF TRIS(2-AMINOETHANOLATO-O,N)COBALT(III) SULFATES: SYNTHESIS AND STRUCTURE(2009) Cotovaia, Aliona; Șova, Sergiu; Simonov, Iurie; Gulea, AurelianThe reaction of [Co(Etm)3] • 3H2O (I) with sulfuric acid affords [Co(HEtm)3]2(SO4) 3 • 4H2O (II). The change in the synthesis procedure (the direction interaction of cobalt(II) sulfate with β-aminoethanol (HEtm)) makes it possible to isolate [Co(HEtm)3](SO 4)(HSO4) • H2O (III) and {[Co(HEtm) 3][Co(Etm)3]}2(SO4)3 • 7.75H2O (IV). The X-ray diffraction analyses of compounds II-IV show that all of them are of the ionic type. In compounds II and III, the ionic structure consists of the [Co(HEtm)3]3+ cations and sulfate anions in a ratio of 2: 3 and 1: 2, respectively. The basic difference in compounds II and III is the different degrees of deprotonation of the acid residues. In complex II, two anions SO 4 2- are doubly deprotonated. In complex III, of the four anions found in the independent part of the unit cell of the sulfate anion two anions are monodeprotonated. In structure IV, two crystallographically independent complexes [Co(HEtm) 3]3+ and [Co(Etm)3] are joined into a dimer through the O-H⋯O hydrogen bonding.Item 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, IurieCompounds 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.