2. Articole

Permanent URI for this collectionhttps://msuir.usm.md/handle/123456789/46

Browse

Author: search.filters.author.Cotovaia, AlionaSubject: search.filters.subject.X ray diffraction analysis Engineering uncontrolled terms Acid residues

Search Results

Now showing 1 - 2 of 2
  • Thumbnail Image
    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, Elena
    A 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 .
  • Thumbnail Image
    Item
    NEW COMPLEXES OF TRIS(2-AMINOETHANOLATO-O,N)COBALT(III) SULFATES: SYNTHESIS AND STRUCTURE
    (2009) Cotovaia, Aliona; Șova, Sergiu; Simonov, Iurie; Gulea, Aurelian
    The 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.