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<title>SYNTHESIS, CHARACTERISATION AND FLUORESCENCE PROPERTIES OF SUBSTITUTED IMIDAZOLES AND BRIDGED BIS-PHENOL LIGANDS AND MAGNETIC BEHAVIOUR OF THEIR METAL COMPLEXES</title>
<link href="http://hdl.handle.net/123456789/2128" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/123456789/2128</id>
<updated>2026-04-04T18:37:28Z</updated>
<dc:date>2026-04-04T18:37:28Z</dc:date>
<entry>
<title>SYNTHESIS, CHARACTERISATION AND FLUORESCENCE PROPERTIES OF SUBSTITUTED IMIDAZOLES AND BRIDGED BIS-PHENOL LIGANDS AND MAGNETIC BEHAVIOUR OF THEIR METAL COMPLEXES</title>
<link href="http://hdl.handle.net/123456789/2129" rel="alternate"/>
<author>
<name>AKONG, Raymond Akong</name>
</author>
<id>http://hdl.handle.net/123456789/2129</id>
<updated>2024-04-26T11:18:11Z</updated>
<published>2023-07-01T00:00:00Z</published>
<summary type="text">SYNTHESIS, CHARACTERISATION AND FLUORESCENCE PROPERTIES OF SUBSTITUTED IMIDAZOLES AND BRIDGED BIS-PHENOL LIGANDS AND MAGNETIC BEHAVIOUR OF THEIR METAL COMPLEXES
AKONG, Raymond Akong
Increasing release of harmful metal(II)/metal(III) into the environment has led to a search&#13;
for ligands with high sensitive and selective abilities to detect these ions. Studies on&#13;
metal(II) are known but there is need for ligands that can sense its presence at low&#13;
concentration. Also, studies on metal(III) are limited due to its poor coordination with&#13;
ligands. Information on the use of multi-donor imidazole derivatives as well as pentadentate&#13;
S-/O-bridged bis-phenol imines, with metal-chelating ability, as sensors are scarce.&#13;
Therefore, the aim of this study was to synthesise and characterise structurally diverse&#13;
imidazoles, imidazole-imines, bridged bis-imine ligands, their metal complexes, and&#13;
investigate the magnetic and sensing properties of these materials.&#13;
Nitro- and bis-imidazoles were prepared by one-pot reaction of appropriate aldehyde, 1,2-&#13;
dicarbonyls, aniline (nitrogen-phenyl variants) and ammonium-acetate dissolved in aceticacid and refluxed at 120oC for 5 hrs. Nitrogen-methyl variants were prepared by&#13;
methylation of the nitrogen-hydrogen imidazoles, using methyl-iodide and potassium&#13;
carbonate. Imidazole-amines were prepared by catalytic hydrogenation of the nitroimidazoles for 2 hrs. Tridentate-imidazole-imines were prepared by condensation of&#13;
salicylaldehyde/ pyridine-2-carboxaldehyde with appropriate imidazole-amines, while the&#13;
pentadentate S-/O-bridged-imines were prepared by condensation of salicylaldehyde/its&#13;
derivatives with bis(2-aminophenyl)sulphide/bis(2-aminophenyl)ether. Metal complexes&#13;
were prepared by reacting the imines with cobalt acetate and copper acetate, separately. The&#13;
compounds were characterised by elemental analysis, Mass, NMR and IR spectroscopies,&#13;
X-ray crystallography and magnetic measurements. Sensing properties of the ligands were&#13;
determined using fluorescence measurements to detect metal(II) and metal(III).&#13;
Nine nitro-imidazoles (N1 – N9), seven bis-imidazoles (BI1 – BI7), nine imidazole-amines&#13;
(A1 – A9), nine nitrogen-nitrogen-oxygen imines (I1 – I9), eight pentadentate-imines (H2S1-&#13;
7 – H2O1) and forty-three metal complexes were obtained. Elemental and mass analysis of&#13;
some representatives: BI1 [C,(81.99%), H(5.13%), N(10.66%); m/z = 515.22], I9&#13;
[C(83.10%), H(4.78%), N(8.61%); m/z = 489], H2O1 [C(76.13%), H(4.88%), N(6.80%);vii&#13;
m/z = 408], Co2S52 [C(39.31%), H(1.71%), N(3.48%), S(4.03%); m/z = 1616.5] agreed with&#13;
proposed molecular formula C36H27.5N4O0.75, C34H23N3O, C26H20N2O3, and&#13;
C52H28Br8Co2N4O4S2, respectively. In pentadentate-imines, phenanthrene and naphthalene&#13;
substitutions resulted in downfield-shift of OHphenolic, while p-methyl/bromo substitution&#13;
resulted in upfield-shift. Ligands exhibited C=Nimine bands around 1591-1617 cm-1 and&#13;
OHphenol bands around 3371-3383 cm-1. In the complexes, these bands shifted to 1577-1605&#13;
cm-1 and disappeared, respectively, suggesting coordination through Nimine and Ophenol&#13;
atoms. Distorted tetrahedral/square-planar, trigonal-bipyramidal and octahedral geometries&#13;
were observed in the complexes. The magnetic susceptibility (cm3Kmol-1) for the dinuclear&#13;
Co(II) [4.09-5.20], dinuclear Cu(II) [0.82-0.86] and trinuclear Cu(II) [1.18-1.21] complexes&#13;
were larger than expected [3.75, 0.75 and 1.125, respectively], indicating orbital&#13;
contribution. Extension of π-conjugation at positions 4 and 5 of the imidazole resulted in&#13;
higher quantum-yields (4-10 folds), while substitution at the nitrogen-hydrogen position&#13;
resulted in lower quantum-yields (4-10 folds). Among the imidazole-imines, I9 exhibited&#13;
the best selectivity for Zn2+ with Limit of Detection (LOD) 4.45 nM. Donor-acceptor&#13;
capabilities (O-H···N), in the pentadentate-imines, enabled excited state intramolecular&#13;
proton transfer behaviour and H2O1 exhibited best selectivity for Al3+ with LOD 5.48 nM.&#13;
Structures of substituted imidazoles and bridged bis-phenol imines with their cobalt(II) and&#13;
copper(II) complexes were established. Structural variation aided different magnetic&#13;
properties and excellent detection for aluminium(III) and zinc(II).
</summary>
<dc:date>2023-07-01T00:00:00Z</dc:date>
</entry>
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