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Synthesis, crystal structure and Hirshfeld analysis of a novel supramolecular compound [Co(tsc)<sub>3</sub>]<sub>2</sub>[Co(cit)<sub>2</sub>](NO<sub>3</sub>)<sub>4</sub>·4H<sub>2</sub>O

Guzal NuralievaNational University of Uzbekistan named after Mirzo Ulugbek 4 University St Tashkent 100174 UzbekistanOydinoy UmirzakovaNational University of Uzbekistan named after Mirzo Ulugbek 4 University St Tashkent 100174 UzbekistanBаtirbаy TоrаmbеtоvNational University of Uzbekistan named after Mirzo Ulugbek 4 University St Tashkent 100174 UzbekistanAbdusamat RasulovTermez University of Economics and Service, 41B Farovon St, Termiz, 190111, UzbekistanJamshid AshurovInstitute of Bioorganic Chemistry, Academy of Sciences of Uzbekistan, M. Ulugbek St, 83, Tashkent, 100125, UzbekistanShakhnoza KadirovaNational University of Uzbekistan named after Mirzo Ulugbek 4 University St Tashkent 100174 Uzbekistan
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Abstract

A new cobalt complex, bis[tris(aminothiourea)cobalt(III)] bis[2-(carboxymethyl)-2-hydroxybutanedioato]cobalt(II) tetranitrate tetrahydrate, [Co(CH 5 N 3 S) 3 ][Co(C 6 H 6 O 7 ) 2 ] 0.5 (NO 3 ) 2 ·2H 2 O, designated as [Co(tsc) 3 ] 2 [Co(cit) 2 ](NO 3 ) 4 ·4H 2 O, was synthesized. Two crystallographically independent cobalt centers are present. In the first, the central metal atom is chelated by three thiosemicarbazide ligands in a bidentate fashion whereas the second, positioned on a crystallographic inversion center, is hexacoordinated by two citrate anions in a distorted octahedral geometry. Additionally, two water molecules and two nitrate anions are present in the asymmetric unit. Hirshfeld surface analysis revealed that the presence of numerous donor and acceptor groups in the complex, which facilitate hydrogen-bonding interactions that contribute significantly to the overall cohesion of the crystal structure.

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