2014
DOI: 10.1016/j.saa.2014.04.165
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Synthesis, spectral characterization and DNA binding of Schiff-base metal complexes derived from 2-amino-3-hydroxyprobanoic acid and acetylacetone

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Cited by 45 publications
(19 citation statements)
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“…These bands confirm the presence of the free ligand in the keto form. The ligand shows also, bands at 1605, 1306, 1199 and 971 cm -1 attributed to ν (HC=N), ν (C-O), ν (C-N) and ν (N-N), respectively [25,26]. Comparison of the IR spectrum of the ligand with that of Pt(II) complex reveals that the ligand chelates Pt(II) ion in a mono-negative bidentate mode via azomethine nitrogen (C=N) and the enolized carbonyl oxygen after displacement of hydrogen ( Molecular mechanics method was used to predict rapidly the geometries of the two suggested conformers by using hyperchem series of programs [30].…”
Section: Ir Spectra Of the Ligand And Its Pt(ii) Complexmentioning
confidence: 99%
“…These bands confirm the presence of the free ligand in the keto form. The ligand shows also, bands at 1605, 1306, 1199 and 971 cm -1 attributed to ν (HC=N), ν (C-O), ν (C-N) and ν (N-N), respectively [25,26]. Comparison of the IR spectrum of the ligand with that of Pt(II) complex reveals that the ligand chelates Pt(II) ion in a mono-negative bidentate mode via azomethine nitrogen (C=N) and the enolized carbonyl oxygen after displacement of hydrogen ( Molecular mechanics method was used to predict rapidly the geometries of the two suggested conformers by using hyperchem series of programs [30].…”
Section: Ir Spectra Of the Ligand And Its Pt(ii) Complexmentioning
confidence: 99%
“…The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of [MoO 2 (Sal-Tryp)EtOH] complex are shown in Figure 4. The energy gap or E HOMO − E LUMO , an important stability index in characterizing the chemical reactivity and kinetic stability of a molecule, [51][52][53] is 0.11 au. Moreover, the 1 H NMR chemical shifts obtained for [MoO 2 (Sal-Tryp)EtOH] complex via calculation [54] have been compared to those obtained experimentally (Table S4, supporting information).…”
Section: Molecular Orbital Analysismentioning
confidence: 99%
“…The intermediate steps for all four complexes appear to represent the decomposition of the ligand to different organic moieties. 2,10 Electronic spectra and magnetic moments…”
Section: Mass Spectra Of the Complexesmentioning
confidence: 99%
“…The enol form of Schiff bases of mono-and diamines have attracted much attention because of their advantages, such as ease of synthesis and the presence of variety of coordination sites that make them invaluable in coordination chemistry. 1,2 Schiff base complexes have many applications, e.g., they are used as catalyst in oxygenation, decomposition, electro-reduction and hydrolysis reactions. 3,4 Schiff bases of β-diketones stabilize different metals in various oxidation states in many useful catalytic transformations.…”
Section: Introductionmentioning
confidence: 99%