Synthesis, X-ray Structure, Hirshfeld Analysis of Biologically Active Mn(II) Pincer Complexes Based on <i>s</i>-Triazine Ligands

Herein, the synthesis and antimicrobial activities of [Mn(<b><sup>Morph</sup>BPT</b>)(H<sub>2</sub>O)<sub>2</sub>NO<sub>3</sub>]NO<sub>3</sub>; (<b>1</b>) and [Mn(<b><sup>Pip</sup>BPT</b>)(H&l...

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Bibliographic Details
Main Authors: Saied M. Soliman, Hessa H. Al-Rasheed, Ayman El-Faham
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:Crystals
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Online Access:https://www.mdpi.com/2073-4352/10/10/931
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Summary:Herein, the synthesis and antimicrobial activities of [Mn(<b><sup>Morph</sup>BPT</b>)(H<sub>2</sub>O)<sub>2</sub>NO<sub>3</sub>]NO<sub>3</sub>; (<b>1</b>) and [Mn(<b><sup>Pip</sup>BPT</b>)(H<sub>2</sub>O)<sub>2</sub>NO<sub>3</sub>]NO<sub>3</sub>; (<b>2</b>) complexes of the pincer-type tridentate ligands <b><sup>Morph</sup>BPT</b>; 4-(4,6-di(1<i>H</i>-pyrazol-1-yl)-1,3,5-triazin-2-yl)morpholine and <b><sup>Pip</sup>BPT</b>; 2-(piperidin-1-yl)-4,6-di(1<i>H</i>-pyrazol-1-yl)-1,3,5-triazine are presented. Both complexes have slightly distorted octahedral coordination geometry. Their molecular packing depends on O–H···O, C–H···O hydrogen bonds and anion–π stacking contacts. Hirshfeld analysis was used to quantify the different contacts. Both complexes exhibited better anti-fungal activity than the standard Fluconazole and comparable antibacterial activity to Gentamycin against <i>Staphylococcus aureus</i> and <i>Escherichia coli</i> microbes. Moreover, complexes <b>1</b> and <b>2</b> are biologically more active than the free ligands against these microbes.
ISSN:2073-4352