Mono- and polynuclear ferrocenylthiosemicarbazones: Synthesis, characterisation and antimicrobial evaluation

Baartzes, Nadia, Stringer, Tameryn ORCID: https://orcid.org/0000-0002-4439-131X, Okombo, John, Seldon, Ronnett, Warner, Digby F., de Kock, Carmen, Smith, Peter J. and Smith, Gregory S. (2016) Mono- and polynuclear ferrocenylthiosemicarbazones: Synthesis, characterisation and antimicrobial evaluation. Journal of Organometallic Chemistry, 819. pp. 166-172. ISSN 0022-328X

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Abstract

A series of mono- and polynuclear ferrocenylthiosemicarbazone complexes were prepared via nucleophilic substitution reactions of various amine scaffolds with a ferrocenyl dithiocarbamate. The dithiocarbamate was prepared via a Schiff base condensation reaction. The compounds were characterised using various spectroscopic and analytical techniques including Nuclear Magnetic Resonance (NMR) and Infrared (IR) spectroscopy, mass spectrometry and elemental analysis. The ferrocenyl dithiocarbamate and thiosemicarbazone compounds were screened for their preliminary antimicrobial activity against the H37Rv strain of Mycobacterium tuberculosis and the chloroquine-sensitive (CQS) NF54 strain of Plasmodium falciparum. Against M. tuberculosis, the compounds displayed moderate to low activity. The mononuclear and octanuclear complexes were the most active, exhibiting similar MIC values. All compounds displayed moderate activity in the antiplasmodial screening. The mononuclear and trinuclear complexes exhibited enhanced activity compared to the complexes with higher nuclearity.

Item Type: Article
Uncontrolled Keywords: sdg 3 - good health and well-being ,/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being
Faculty \ School: Faculty of Science > School of Chemistry
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Depositing User: LivePure Connector
Date Deposited: 19 Jul 2022 13:30
Last Modified: 12 Aug 2022 05:32
URI: https://ueaeprints.uea.ac.uk/id/eprint/86607
DOI: 10.1016/j.jorganchem.2016.06.032

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