2016
DOI: 10.1007/s13738-016-0978-8
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Crystal structure, DFT study, antimicrobial properties and DNA cleavage potential and thermal behavior of some new mercury complexes

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Cited by 6 publications
(4 citation statements)
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“…The bond lengths of Hg−I are 2.6534(7) and 2.6658(7) Å, which are longer than those observed in related complexes. 52,53 Unlike CP 1, each of the two adjacent ligands with opposite helicity in CP 2 is connected by Hg(II) ions to form a 1D heterochiral polymer (-P-Hg-M-) via a self-discrimination process (Figure 3b). In the extended structure, each 1D heterochiral chain is connected to the adjacent chains via π•••π stacking interactions between the benzene and pyridine rings, forming a 2D network parallel to the bc plane (Figure 3c).…”
Section: Materials and Physical Measurementsmentioning
confidence: 99%
“…The bond lengths of Hg−I are 2.6534(7) and 2.6658(7) Å, which are longer than those observed in related complexes. 52,53 Unlike CP 1, each of the two adjacent ligands with opposite helicity in CP 2 is connected by Hg(II) ions to form a 1D heterochiral polymer (-P-Hg-M-) via a self-discrimination process (Figure 3b). In the extended structure, each 1D heterochiral chain is connected to the adjacent chains via π•••π stacking interactions between the benzene and pyridine rings, forming a 2D network parallel to the bc plane (Figure 3c).…”
Section: Materials and Physical Measurementsmentioning
confidence: 99%
“…Because of these interesting biological properties of cadmium complexes and according to our previously performed studies on N 2 and N 3 donor Schiff bases, in the present work, we report synthesis of a novel bidentate imidazolidine Schiff base ligand by the condensation of N′ ‐(2‐aminoethyl)‐ethane‐1,2‐diamine and 2‐bromobenzaldehyde to form 4‐coordinated cadmium(II) complexes. The compounds were identified using various spectral techniques, such as Fourier transform infrared (FT‐IR), UV‐visible (Vis), proton and carbon nuclear magnetic resonance ( 1 H and 13 C NMR), and conductivity measurements.…”
Section: Introductionmentioning
confidence: 96%
“…These compounds from flavonoids make them display antibacterial [23], anti-inflammatory [24], antifungal [25], anticancer [26], and many other pharmacological activities. The chalcone with α, β unsaturated carbonyl group, and chromanone moiety may increase the pharmaceutical efficiency since chromanone has good biological activity such as antioxidant, anti-leishmanial [27][28], antimicrobial [29]. The antivascular activity of chalcones several tubulin-binding agents that inhibit tubulin assemblies, such as colchicine and vincristine, have recently been demonstrated to also disrupt tumor vasculature [29].…”
Section: Introductionmentioning
confidence: 99%
“…The chalcone with α, β unsaturated carbonyl group, and chromanone moiety may increase the pharmaceutical efficiency since chromanone has good biological activity such as antioxidant, anti-leishmanial [27][28], antimicrobial [29]. The antivascular activity of chalcones several tubulin-binding agents that inhibit tubulin assemblies, such as colchicine and vincristine, have recently been demonstrated to also disrupt tumor vasculature [29]. Presumably, these agents are capable of rapidly changing the shape of endothelial cells, thereby disrupting the endothelial cell layer surrounding blood vessels and exposing underlying basement membranes [30].…”
Section: Introductionmentioning
confidence: 99%