2. Articole

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Author: search.filters.author.Șova, SergiuSubject: search.filters.subject.crystal structure

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    SYNTHESIS, CHARACTERIZATION, CRYSTAL STRUCTURE AND ANTIMICROBIAL ACTIVITY OF COPPER(II) COMPLEXES WITH THE SCHIFF BASE DERIVED FROM 2-HYDROXY-4-METHOXYBENZALDEHYDE
    (2015) Pahonțu, Elena; Ilieș, Diana Carolina; Șova, Sergiu; Paraschivescu, Codruța; Badea, Mihaela; Gulea, Aurelian; Roșu, Tudor
    A novel Schiff base, ethyl 4-[(E)-(2-hydroxy-4-methoxyphenyl)methyleneamino] benzoate (HL), was prepared and structurally characterized on the basis of elemental analyses, 1H NMR, 13C NMR, UV-Vis and IR spectral data. Six new copper(II) complexes, [Cu(L)(NO3)(H2O)2] (1), [Cu(L)2] (2), [Cu(L)(OAc)] (3), [Cu2 (L)2Cl2(H2O)4] (4), [Cu(L)(ClO4)(H2O)] (5) and [Cu2(L2S)(ClO4)(H2O)]ClO4·H2O (6) have been synthesized. The characterization of the newly formed compounds was done by IR, UV-Vis, EPR, FAB mass spectroscopy, elemental and thermal analysis, magnetic susceptibility measurements and molar electric conductivity. The crystal structures of Schiff base and the complex [Cu2(L2S)(ClO4)(H2O)]ClO4·H2O (6) have been determined by single crystal X-ray diffraction studies. Both copper atoms display a distorted octahedral coordination type [O4NS]. This coordination is ensured by three phenol oxygen, two of which being related to the μ-oxo-bridge, the nitrogen atoms of the azomethine group and the sulfur atoms that come from the polydentate ligand. The in vitro antimicrobial activity against Escherichia coli ATCC 25922, Salmonella enteritidis, Staphylococcus aureus ATCC 25923, Enterococcus and Candida albicans strains was studied and compared with that of free ligand. The complexes 1, 2, 5 showed a better antimicrobial activity than the Schiff base against the tested microorganisms
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    NEW CRYSTAL FORMS OF TRIS(2-AMINOETHANOLATO-O,N)COBALT(III): STRUCTURES AND PROPERTIES
    (2006) Cotovaia, Aliona; Șova, Sergiu; Simonov, Iurie; Roșu, Tudor; Sandu, Ion; Gulea, Aurelian
    Crystal forms of cobalt(III) tris(2-aminoethanolate) hydrates, i.e., red cubic crystals of the composition fac-[Co(NH2CH2CH 2O)3] • 5.44H2O (fac-I • 5.44H 2O) and blue prismatic crystals of the composition mer-[Co(NH 2CH2CH2O)3] • 3H2O (mer-I • 3H2O) were studied by the 59Co, 13C NMR and X-ray diffraction methods. It was found that mer-[Co(NH2CH2CH2O)3] • 3H 2O (mer-I • 3H2O) is a new pseudopolymorphic modification of fac-[Co(NH2CH2CH2O) 3] • 3H2O (fac-I • 3H2O), while fac-I • 3H2O represents a new polymorphic modification of the complex mer-[Co(NH2CH2CH2O)3] • 3H2O (mer-I • 3H2O) described previously. The comparative analysis of the spectra revealed dynamic equilibrium between these geometric isomers; the fac-isomer is stable in aqueous solutions.
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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.