Mn Schiff Base Complexes Research Articles

Novel Bromo and methoxy substituted Schiff base complexes of Mn(II), Fe(III), and Cr(III) for anticancer, antimicrobial, docking, and ADMET studies

In this study, four new Mn(II), Fe(III), and Cr(III) complexes with two Schiff base ligands namely, 4-bromo-2-[(E)-{[4-(2-hydroxyethyl)phenyl]imino}methyl]phenol (HL1) and 2-[(E)-{[4-(2-hydroxyethyl)phenyl]imino}methyl]-4-methoxy phenol (HL2) have been synthesized and characterized. Different analytical and spectral methods have been used to characterize the ligands and their complexes. General formulas of [M(L)Cl2(H2O)2] for FeL1, CrL1 and CrL2, and [M(L)Cl(H2O)3] for MnL2 were proposed. HOMO and LUMO energies, as well as the electrical characteristics, have been calculated using DFT/B3LYP calculations with Gaussian 09 program. The optimized lowest energy configurations of the complexes are proven. The disc diffusion technique was used to test the pharmacological activities' antibacterial efficacy against diverse bacterial and fungus species. The MTT technique was used to assess the in vitro cytotoxicity of the ligands and their metal complexes on the Hep-G2 human liver carcinoma cell line and the MCF-7 human breast cancer cell line. All compounds displayed better activity compared to the free ligands. MnL2 complex showed predominant activity when compared to the other complexes with an IC50 value of 2.6 ± 0.11 μg/ml against Hep-G2, and against MCF-7 the IC50 value was 3.0 ± 0.2 μg/ml which is less than the standard drug cisplatin (4.0 μg/ml). UV–vis electronic spectrum and gel electrophoresis techniques have been used to investigate the compounds’ affinity to bind and cleavage CT-DNA. The interaction’s binding constants, or Kb, have been identified, and it was discovered that the new complexes' binding affinities are in the order of FeL1 > MnL2 > CrL2 > CrL1, and the binding mechanism has been suggested. To assess the kind of binding and binding affinity of the investigated drugs with human DNA, a molecular docking study was carried out (PDB:1bna). The acquired results supported the intercalation binding mechanism proposed in the experimental part and revealed that complexes may be inserted into the DNA molecule to stop DNA replication. According to ADMET data, the synthesized compounds have a high bioavailability profile and their physicochemical and pharmacological features remained within Lipinski's RO5 predicted limitations.

Synthesis and Characterization of Cobalt(II) and Manganese(II) Schiff Base Complexes: Metal Effect on the Binding Affinity with β-Casein

In this study, two metal Schiff base complexes (cobalt(II) and manganese(II), were synthesized and characterized by 1H-NMR and FT-IR analyses. The in vitro binding behavior of this complexes with β-Casein (β-CN) was investigated by using biophysical techniques. For evaluation the thermodynamics parameters of interaction between Schiff base complexes and β-CN,the fluorescence data at different temperatures were done. The results showed that the intrinsic fluorescence of the β-CN was quenched by increasing the complexes through the dynamic quenching mechanism. Also, these complexes demonstrated a considrable binding affinity to β-CN and the process is mainly entropy driven. Fluorescence resonance energy transfer was used in order to estimating the distance between donor (β-CN) and acceptor (complex). Results demonstrated that the sequence of tendency of the complexes to β-CN was as follows: Mn-Schiff base complex > Co-Schiff base complex. All these experimental results propose that β-CN might act as carrier protein for Co(II) and Mn (II) complexes to deliver it to the target molecules.

In Methanolic Solvent Synthesis of New MnII, CoII, NiII and CuII Schiff Base of Aromatic β Amino Acids: Spectroscopic, Thermal, Molecular Docking and Antimicrobial Studies

In this article, four new Schiff base complexes of Mn(II), Co(II), Ni(II) and Cu(II) complexes have been synthesized with two different compositions as [M(L)2Cl2] · nH2O and [M(L)2(H2O)2]Cl2 · nH2O [where L1 = benzoin-o-amino benzoic acid (aromatic β amino acid) and L2 = benzoin bromo-o-amino benzoic acid (aromatic β amino acid); M = MnII, CoII, NiII and CuII; n = 1, 2 and 4]. These Schiff base complexes were discussed by many tool of analyses like elemental analysis, magnetic susceptibility, molar conductance, mass spectra, infrared spectra "IR," proton nuclear magnetic resonance "1H-NMR," electronic spectral and thermogravimetric analysis (TG/DTG). These complexes have an electrolytic nature within range of 78–174 Ω1 cm–1 mol –1 based on conductance measurements. Magnetic moment and electronic spectral results deduced that the geometry of Mn2+, Co2+ and Ni2+ and Cu2+ complexes has an octahedral configuration. The number of coordinated and uncoordinated water molecules for the synthesized complexes were calculated based on the thermal analysis technique. The kinetic thermodynamic data were estimated by using commonly integral equations of Horowitz-Metzger (HM) and Coats-Redfern (CR). In vitro the antimicrobial activity of both free L1 and L2 ligands in comparable with their metal complexes were evaluated. This study was strengthen by molecular docking against three protein receptors, which attributing to selected organisms already used in vitro study.

A manganese(iii) Schiff base complex immobilized on silica-coated magnetic nanoparticles showing enhanced electrochemical catalytic performance toward sulfide and alkene oxidation.

In this study, a novel Mn(iii)–Schiff base complex was synthesized and characterized. The structure of this complex was determined to be a deformed octahedral coordination sphere by single-crystal X-ray diffraction analysis. The Mn(iii)–Schiff base complex was supported on silica-coated iron magnetic nanoparticles via axial coordination by one-step complex anchoring to produce a heterogenized nanocatalyst. After this, the complex was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), and powder X-ray diffraction (XRD). Moreover, atomic absorption spectroscopy was used to determine the amount of the loaded metal. The heterogenized nanocatalyst effectively catalyzed the oxidation of a broad range of sulfides and alkenes with H2O2 in the presence of a glassy carbon electrode, applying voltage to the reaction mixture. The results showed that the application of a potential to the reaction mixture could significantly decrease the reaction time when compared with the case of similar chemical oxidation reactions. In addition, an excellent value of turnover frequency (17 750 h−1) was achieved for the electrochemical oxidation of styrene. Moreover, the nanocatalyst showed good recoverability without significant loss of its activity within six successive runs in the electrochemical oxidation of methyl phenyl sulfide and cyclooctene. The electrochemical properties and stability of Fe3O4@SiO2-[MnL(OAc)] were investigated by cyclic voltammetry measurements and chronoamperometry technique.

Insights into Second-Sphere Effects on Redox Potentials, Spectroscopic Properties, and Superoxide Dismutase Activity of Manganese Complexes with Schiff-Base Ligands.

Six Mn-Schiff base complexes, [Mn(X-salpn)]0/+ (salpn = 1,3-bis(sal-ic-ylidenamino)propane, X = H [1], 5-Cl [2], 2,5-F2 [3], 3,5-Cl2 [4], 5-NO2 [5], 3,5-(NO2)2 [6]), were synthesized and characterized in solution, and second-sphere effects on their electrochemical and spectroscopic properties were analyzed. The six complexes catalyze the dismutation of superoxide with catalytic rate constants in the range 0.65 to 1.54 × 106 M–1 s–1 obtained through the nitro blue tetrazolium photoreduction inhibition superoxide dismutases assay, in aqueous medium of pH 7.8. In solution, these compounds possess two labile solvent molecules in the axial positions favoring coordination of the highly nucleophilic O2•– to the metal center. Even complex 5, [Mn(5-(NO2)salpn) (OAc) (H2O)], with an axial acetate in the solid state, behaves as a 1:1 electrolyte in methanolic solution. Electron paramagnetic resonance and UV–vis monitoring of the reaction of [Mn(X-salpn)]0/+ with KO2 demonstrates that in diluted solutions these complexes behave as catalysts supporting several additions of excess O2•–, but at high complex concentrations (≥0.75 mM) catalyst self-inhibition occurs by the formation of a catalytically inactive dimer. The correlation of spectroscopic, electrochemical, and kinetics data suggest that second-sphere effects control the oxidation states of Mn involved in the O2•– dismutation cycle catalyzed by complexes 1–6 and modulate the strength of the Mn-substrate adduct for electron-transfer through an inner-sphere mechanism.

Mn-Schiff base complex supported on magnetic nanoparticles: Synthesis, crystal structure, electrochemical properties and catalytic activities for oxidation of olefins and sulfides

A novel, magnetically recoverable Mn-Schiff base catalyst has been prepared by the adsorption on silica-coated magnetic nanoparticles. X-ray crystallography studies reveal that the Mn-complex adopt a distorted octahedral six-coordinate configuration formed by the tetradentate Schiff base ligand and two oxygen atoms of acetate anion. The heterogeneous catalyst was characterized by powder X-ray diffraction, transmission electron microscopy, scanning electron microscopy, vibrating sample magnetometer, thermo-gravimetric analysis, the energy-dispersive X-ray spectroscopy and FTIR spectroscopy. The catalyst loading on the magnetic support was determined by atomic absorption spectroscopy. Highly chemoselective oxidation of sulfides with excellent yield to the corresponding sulfoxides, and epoxidation of olefins in ethanol at room temperature were efficiently enhanced under the influence of the magnetically separable catalyst. The separation and recycling of the catalyst is simple, effective, and economic in this clean oxidation method. The electrochemical properties of the Mn-complex were investigated.

Synthesis, characterization, and catalytic application of Cr and Mn Schiff base complexes immobilized on modified nanoporous MCM-41

Immobilization of chromium and manganese Schiff base complexes by postgrafting of ligand then metal salts on the walls of mesoporous MCM-41 functionalized with (3-aminopropyl)triethoxysilane is described. Characterization of the resulting heterogeneous catalysts by Fourier-transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), transmission electron microscopy (TEM), X-ray diffraction (XRD) analysis, and Brunauer–Emmett–Teller (BET) techniques indicated successful grafting of these two complexes inside the nanochannels of MCM-41. The complexes were found to be efficient, selective catalysts for oxidation of various sulfides to sulfoxides and oxidative coupling of thiols to corresponding disulfides using H2O2 as oxidant at room temperature. The recycling results of these heterogeneous catalysts showed good recyclability without significant loss of activity or selectivity in successive runs, indicating that the Cr and Mn Schiff base complexes supported on nanoporous MCM-41 remained intact and the coordination environments were not altered during the reaction.

Synthesis, spectroscopic, coordination and biological activities of some transition metal complexes containing ONO tridentate Schiff base ligand

The main target of this paper is to get an interesting data for the preparation and characterizations of metal oxide (MO) nanoparticles using H2L Schiff base complexes as precursors through the thermal decomposition procedure. Five Schiff base complexes of Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) metal ions were synthesized from 2-[(2-hydroxy-naphthalen-1-ylmethylene)-amino]-benzoic acid new adduct (H2L). Theses complexes were characterized using infrared, electronic, mass and 1H NMR spectroscopic techniques. The elemental analysis data was confirmed that the stoichiometry of (metal:H2L) is 1:1 molar ratio. The molar conductance indicates that all of complexes are non electrolytic. The general chemical formulas of these complexes is [M(L)(NH3)]·nH2O. All complexes are tetrahedral geometry. The thermal decomposition behavior of H2L hydrated and anhydrous complexes has been discussed using thermogravimetric analysis (TG/DTG) and differential thermal analyses (DTA) under nitrogen atmosphere. The crystalline phases of the reaction products were checked using X-ray diffractometer (XRD) and scanning electron microscopy (SEM).

New Dinuclear Schiff Base Complexes of Mn(II) Derived from Amino Acids

Inthis study we describe the synthesis and characterization of four and six coordinated compounds of Mn(II)with Schiff bases derived from vanillin with amino acids (glycine, L-serine, L-tyrosine, and L-phenylalanine).These complexeswere characterized by many physicochemical methods such as elemental analysis(CHN),magnetic susceptibility, molar conductance as well as spectral studies such as IR and UV-Visible .The analytical data showed that the complexes having the formulas[Mn(VA)(H2O)]2,[Mn2(VA)(CH3COO)(H2O)2],whereA-=serineortyrosine[Mn2(Vg)(CH3COO)(H2O)3],[Mn2(VA*H2)2(H2O)2(NO3)2](NO3)2and Na2[Mn2(VA*)2(H2O)2(NO3)2] , A* = all the amino acids .The ligands behave as Tetradentate coordinating through the atomsNOOO, or tridentate NOO; where V= vanillin, A=amino acids (glycine and phenylalanine) that suggested tetrahedral and octahedral geometry.

Structural, spectral, thermal and biological studies on (E)-2-(1-(4-hydroxyphenyl)ethylidene)-N-(pyridin-2-yl)hydrazinecarbothioamide and its metal complexes

Schiff base complexes of Mn(II), Co(II), Ni(II), Cu(II), Cd(II), Hg(II) and U(VI)O2 with (E)-2-(1-(4-hydroxyphenyl)ethylidene)-N-(pyridin-2-yl)hydrazinecarbothioamide (H2PHAT) were synthesized and characterized by different physicochemical methods, elemental analysis, (UV–vis, IR and 1H NMR spectra) and thermal analysis (TG and DTG) techniques. Spectral data showed that H2PHAT behaves as a NS bidentate ligand through both thione sulphur or thiol sulphur and the nitrogen of the pyridine ring or azomethine nitrogen, NSN tridentate ligand through both thione sulphur or thiol sulphur, the nitrogen of the pyridine ring and azomethine nitrogen. ESR spectrum data for Cu(II) solid complex confirms the square planar state is the most fitted one for the coordinated structure. The kinetic parameters were determined for each thermal degradation stage of the complexes using Coats–Redfern and Horowitz–Metzger methods. From modeling studies, the bond length, bond angle, HOMO, LUMO and dipole moment had been calculated to confirm the geometry of the ligand and their investigated complexes.The biological activity was tested against DNA showing that Cd(II), U(VI)O2, Ni(II) and Mn(II) complexes had powerful and complete degradation effect. Also, the ligand and its complexes were screened against Bacillus thuringiensis as Gram-positive bacteria and Pseudomonas aeuroginosa as Gram-negative bacteria using the inhibitory zone diameter.

Synthesis, characterisation and catalase-like activity of silica-coated magnetite nanoparticles modified by a Schiff base Mn complex

Silica-coated magnetite nanoparticles (Mn-L1-NPs), modified by a Mn complex of N, N′-bis(3-formyl-5-methylsalicylidene)ethylenediimine (L1), have been synthesised and characterised by Fourier transform infrared spectroscopy, scanning electron microscope, X-ray photoelectron spectroscopy, atomic absorption spectroscopy and thermogravimetric analysis techniques. The catalase-like activity of Mn-L1-NPs was evaluated by its ability to catalytically decompose hydrogen peroxide in aqueous solution. The results indicated that the nanoparticles have higher catalase-like activity.

Spectrophotometric Study on the Binding of Two Water Soluble Schiff Base Complexes of Mn (III) with ct-DNA

In this work, binding of two water soluble Schiff base complexes: Bis sodium (5-sulfosalicylaldehyde) o-phenylendiiminato) Manganese (III) acetate (Salophen complex) and Bis sodium (5-sulfosalicylaldehyde) 1, 2 ethylendiiminato) Manganese (III) acetate (Salen complex) with calf thymus (ct) DNA were investigated by using different spectroscopic and electrometric techniques including UV-vis, Circular dichroism (CD) and fluorescence spectroscopy, viscommetry and cyclic voltammetry (CV). Both complexes have shown a hyperchromic and a small bathochromic shift in the visible region spectra. A competitive binding study showed that the enhanced emission intensity of ethidium bromide (EB) in the presence of DNA was quenched by the addition of the two Schiff base complexes indicating that they displace EB from its binding site in DNA. Moreover structural changes in the CD spectra and an increase in the CV spectra with addition of DNA were observed. The results show that both complexes bind to DNA. The binding constants have been calculated using fluorescence data for two complexes also K(b) was calculated with fluorescence Scatchard plot for Salophen. Ultimately, the experimental results show that the dominant interactions are electrostatic while binding mode is surface binding then followed by hydrophobic interactions in grooves in high concentration of complexes.

Template synthesis and spectral characterization of some Schiff base complexes derived from quinoxaline-2-carboxaldehyde and L-histidine

New Schiff base complexes of Mn(II), Fe(III), Co(II), Ni(II), Cu(II), and Zn(II) were synthesized by template condensation of quinoxaline-2-carboxaldehyde, L-histidine, and the metal compound, and were characterized by elemental analysis, fourier transform infrared spectroscopy, electronic spectra, conductance measurements, magnetic susceptibility measurements, ESR spectra, and thermal analysis. In all the complexes, the Schiff base coordinates through azomethine nitrogen, quinoxaline nitrogen, and carboxylato oxygen. The physicochemical and spectroscopic measurements reveal square planar geometry for the copper(II) complex, tetrahedral geometry for the manganese(II), cobalt(II), and zinc(II) complexes, and octahedral geometry for the iron(III) and nickel(II) complexes.

Hydroxylation of Benzene to Phenol by Molecular Oxygen over an Organic–Inorganic Hybrid Catalyst: Schiff Base Manganese Complex Attached to Molybdovanadophosphoric Heteropolyacid

The organic–inorganic hybrid catalyst L-Mn-PMoV was prepared simply by combining a schiff base Mn complex (L-Mn, L: N,N′-disalicylidene-1, 6-hexanediamine) with the Keggin-structured molybdovanadophosphoric heteropolyacid (PMoV). The proposed composition and structure of the catalyst were evidenced by TG, elemental analysis, FT-IR, and UV–Vis characterizations. Its catalytic performance was evaluated in the direct hydroxylation of benzene to phenol by molecular oxygen with ascorbic acid as the reducing agent. Various reaction parameters were changed to attain the optimal conditions. The hybrid catalyst has a formula [{Mn(C20H22N2O2)(Cl)}2(H4PMo11VO40)], with the two terminal oxygen atoms in the PMoV Keggin structure coordinately linked to the two Mn(III) ions in two L-Mn units, respectively. It exhibits a remarkably enhanced yield to phenol compared to the pure PMoV due to the synergy effect between the Schiff-base manganese complex and PMoV.

Synthesis, spectral, crystallography and thermal investigations of novel Schiff base complexes of manganese (III) derived from heterocyclic β-diketone with aromatic and aliphatic diamine

The Schiff base tetradentate ligands N,N-bis-(3,5-dimethyl-1-p-tolyl-1H-pyrazol-4-ylmethylene)-ethane-1,2-diamine (H(2)L(1)), N,N-bis-(3,5-dimethyl-1-p-sulfonyl-1H-pyrazol-4-ylmethylene)-ethane-1,2-diamine (H(2)L(2)), N,N-bis-(3,5-dimethyl-1-p-tolyl-1H-pyrazol-4-ylmethylene)-benzene-1,2-diamine (H(2)L(3)) and N,N-bis-(3,5-dimethyl-1-p-sulfonyl-1H-pyrazol-4-ylmethylene)-benzene-1,2-diamine (H(2)L(4)) were prepared from the reaction between 5-oxo-3-methyl-1-p-tolyl-1H-pyrazole-4-carbaldehyde or 4-(4-formyl-5-oxo-3-methyl-pyrazol-1-yl)-benzenesulfonic acid and o-phenylenediamine or ethylenediamine. And these are characterized by elemental analysis, FT-IR, (1)H NMR and GC-MS. The corresponding Schiff base complexes of Mn(III) were prepared by condensation of [Mn(3)(mu(3)-O)(OAc)(6)(H(2)O)(3)].3H(2)O with ligands H(2)L(1), H(2)L(2), H(2)L(3) and H(2)L(4). All these complexes have been characterized by elemental analysis, magnetic susceptibility, X-ray crystallography, conductometry measurement, FT-IR, electronic spectra and mass (FAB) spectrometry. Thermal behaviour of the complexes has been studied by TGA, DTA and DSC. Electronic spectra and magnetic susceptibility measurements indicate octahedral stereochemistry of manganese (III) complexes, while non-electrolytic behaviour complexes indicate the absence of counter ion.

Alumina-supported metal(II) Schiff base complexes as heterogeneous catalysts in the high-regioselective cleavage of epoxides to halohydrins by using elemental halogen

A highly regioselective method for the synthesis of β-iodohydrins and β-bromohydrins through direct ring opening of epoxides with elemental halogen in the presence of alumina-supported Schiff base complexes of Mn(II), Co(II), Ni(II) and Cu(II) as new catalysts is described. This method is regioselective under mild conditions in various aprotic solvents with high yields, even when sensitive functional groups are present. The catalysts are easily recovered and can be reused several times.

Synthesis, characterization and catalytic property of tetradentate Schiff-base complexes for the epoxidation of styrene

A series of Schiff-base complexes has been synthesized by the condensation of 1,2-diaminocyclohexane with salicylaldehyde, 2-pyridinecarboxaldehyde, and 2-hydroxy-1-naphthaldehyde, followed by the metallation with manganese ( 1, 2, 3a), cobalt ( 3b), copper ( 3c) and iron ( 3d) salts. These Schiff-base ligands L 1 – L 3 and complexes 1, 2, 3a– d were then characterized by IR, 1H NMR, 13C NMR, UV–vis spectra, and DSC measurement. Schiff-base Mn complex ( 3a) resulting from N, N′-bis(2-hydroxy-1-naphthalidene)cyclohexanediamine ( L 3 ) ligand was considerably active for the catalytic epoxidation of styrene under mild conditions, in which the highest yield of styrene oxide reached 91.2 mol%, notably higher than those achieved from simple salt catalysts Mn(Ac) 2·4H 2O and MnSO 4·H 2O. However, another two salen–Mn complexes 1 and 2 derived from ligands N, N′-bis(salicylidene)cyclohexanediamine ( L 1 ) and N, N′-bis(2-pyridine carboxalidene)cyclohexanediamine ( L 2 ) exhibited relatively poor activity under identical experimental conditions.

Olefin epoxidation catalysed by Schiff-base complexes of Mn and Ni in heterogenised-homogeneous systems

M(salen) complexes (M=Mn(III), Ni(II); salen=bis-(salicyldene)ethylenediamine) have been encapsulated in zeolite Y and characterised. Mn(salen) + complex was also anchored in montmorillonite clay and characterised. Epoxidation of olefins, viz. cyclohexene, cyclooctene and 1-hexene with terminal oxidants (NaOCl, KHSO 5) was carried out with the anchored catalyst complexes and found that the epoxidation of linear olefin (1-hexene) is selectively facile than cyclic olefins. Experimental results are compared with those reported for M(salen) complexes catalysed olefin epoxidation in homogeneous and heterogenised-homogeneous catalytic conditions.

Synthesis, Structure, and Magnetic Properties of Mn(salpn)N(3,) a Helical Polymer, and Fe(salpn)N(3), a Ferromagnetically Coupled Dimer (salpnH(2) = N,N'-bis(Salicylidene)-1,3-diaminopropane).

The preparation, crystal structures, and variable temperature magnetic susceptibility data are presented for two azido-bridged Schiff base complexes of Mn(III) and Fe(III). Mn(salpn)N(3) (1), where salpn is the dianion of N,N'-bis(salicylidene)-1,3-diaminopropane, crystallizes in the orthorhombic system, space group Pna2(1), with a = 11.947(2) Å, b = 11.818(2) Å, c = 11.227(5) Å, and Z = 4. Fe(salpn)N(3) (2) crystallizes in the monoclinic system, space group P2(1)/c, with a = 10.199(7) Å, b = 14.081(6) Å, c = 12.017(3) Å, beta = 105.19(3) degrees, and Z = 4. In 1, salpn coordinates in the equatorial mode, with two azide ions coordinating in axial positions. The azide ions act as "end-to-end" (&mgr;-(1,3)) bridges, leading to an infinite helical chain propagating along the crystallographic c axis. In striking contrast, 2 has a dimeric structure in which the Schiff base adopts a cis-octahedral coordination mode. The dimer is held together by two "head-on" (&mgr;-(1,1)) bridging azide ions. The polymeric compound, 1, is weakly antiferromagnetic (J = -4.03 cm(-)(1), H(ex) = -2J summation operatorS(i)()S(i)()(+1)), while 2 is weakly ferromagnetic (J = 0.76 cm(-)(1), H(ex) = -2JS(1)S(2)).

The thermal stability and temperature dependence of the electrical conductivity of Mn(II), Fe(III), Co(II), Ni(II), and Cu(II) indazole Schiff base complexes

The thermal stabilities of the indazole Schiff base complexes of Mn(II), Fe(III), Co(II), Ni(II), and Cu(II) were studied. The stabilities are discussed in terms of structure and type of metal ions. The activation energies E α of the different processes were evaluated and discussed in accordance with the structure of the complexes. The electrical properties of the metal complexes were also investigated with reference to the types of metal ion and organic ligand.