2021
DOI: 10.4236/ojapps.2021.111001
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Metal Complexes with 8-Hydroxyquinoline: Synthesis and <i>In Vitro</i> Antimicrobial Activity

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Cited by 18 publications
(9 citation statements)
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“…The peak at 1567 cm 743 cm -1 [43]. The absorption band in capped HNTs spectra are similar to the uncapped ones; however, there is the appearance of a peak at 567 cm -1 , which is attributed to the metal(II)-nitrogen bond (Co-Inhibitor complex) [20]. The appearance of this peak is an indication of the formation of the metal-inhibitor complex on HNTs.…”
Section: Ftir Analysismentioning
confidence: 82%
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“…The peak at 1567 cm 743 cm -1 [43]. The absorption band in capped HNTs spectra are similar to the uncapped ones; however, there is the appearance of a peak at 567 cm -1 , which is attributed to the metal(II)-nitrogen bond (Co-Inhibitor complex) [20]. The appearance of this peak is an indication of the formation of the metal-inhibitor complex on HNTs.…”
Section: Ftir Analysismentioning
confidence: 82%
“…5a, we can see two primary UV spectra at pH 2. The spectra for uncapped HNTs represent two main absorption peaks at 234 and 308 nm, demonstrating p-p* and n-p* transition in the quinoline ring [20]. The absorption spectra of capped HNTs represent three main absorption peaks at 237, 310, and 370 nm.…”
Section: Uv-vis Spectroscopic Analysis For Release Studiesmentioning
confidence: 95%
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“…Significant Tf binding of In(III) in blood serum is likely, while GaQ 3 interacts less with this protein. The complex band was shifted only in serum samples; the presence of HQ – Fe(II)/(III) or Cu(II) complexes can be excluded on the basis of the obtained spectra [ 49 , 50 ]. Formation of HQ – Mg(II) complex is not feasible even at physiological Mg(II) ion levels (0.7–1.0 mM) based on the available stability constants [ 51 ].…”
Section: Resultsmentioning
confidence: 99%