Počet záznamů: 1  

Synthesis, thermal, spectral, and biological properties of zinc(II) 4-aminobenzoate complexes

  1. 1.
    0476288 - UMCH-V 2018 RIV HU eng J - Článek v odborném periodiku
    Homzová, K. - Györyová, K. - Hudecová, D. - Koman, M. - Melník, M. - Kovářová, Jana
    Synthesis, thermal, spectral, and biological properties of zinc(II) 4-aminobenzoate complexes.
    Journal of Thermal Analysis and Calorimetry. Roč. 129, č. 2 (2017), s. 1065-1082. ISSN 1388-6150
    Institucionální podpora: RVO:61389013
    Klíčová slova: zinc(II) 4-aminobenzoate * thermal * spectral
    Kód oboru RIV: CD - Makromolekulární chemie
    Obor OECD: Polymer science
    Impakt faktor: 2.209, rok: 2017

    New zinc(II) 4-aminobenzoate complex compounds with general formula [Zn(4-NH2benz)2L2]·nH2O, where 4-NH2benz = 4-aminobenzoate, L = nicotinamide (nad), isonicotinamide (inad), N-methylnicotinamide (mnad), thiourea (tu), urea (u), theophylline (tph), and caffeine (caf) were synthesised and characterised by elemental analysis, thermal analysis, and IR spectroscopy. The thermal behaviour of prepared compounds was studied by TG/DTG and DTA methods in argon atmosphere. During the thermal decomposition, organic ligand, carbon monoxide, carbon dioxide, and aniline were evolved. The final solid product of the thermal decomposition was zinc oxide. The volatile gaseous products were proved by mass spectrometry. Solid intermediate product and the final product of thermal decomposition were identified by IR spectroscopy and X-ray powder diffraction method. It was solved crystal structure of polymeric [Zn(4-NH2benz)2], where the coordination environment around zinc(II) atom is an unsymmetrical distorted trigonal bipyramidal with chromophore ZnO3N2. The antimicrobial activity of zinc(II) carboxylate compounds was tested against various strains of bacteria, yeasts, and filamentous fungi (S. aureus, E. coli, C. albicans, R. oryzae, A. alternata, M. gypseum). The presence of zinc in complexes led to the increase their antimicrobial activity in comparison with free 4-aminobenzoic acid and ligands.
    Trvalý link: http://hdl.handle.net/11104/0273083