Manganese Schiff Base Complexes Research Articles

Synthesis, Structural Characterization, Reactivity and Bioactivity Studies of Some Binuclear Salen Type Schiff Base Complexes of Manganese(III)

Four new phenoxy bridged binuclear Salen type Schiff base complexes of manganese(III), [MnLX]2 with tetradentate Schiff base, H2L [H2L = N,N′-O-phenylene bis(salicylaldimine)] containing anionic co-ligands, X (X = benzoate, p-hydroxy benzoate, p-aminobenzoate, 3,5-dinitrobenzoate) have been synthesized from manganese(II) acetate, Schiff base (H2L) and the corresponding co-ligands in methanol medium. Schiff base ligand (H2L) was obtained in situ by condensation of salicylaldehyde and o-phenylenediamine in aqueous methanol. Elemental analyses, FT-IR, molar conductance, UV-visible spectroscopic studies and magnetic moment measurements at room temperature were used to characterize the binuclear Schiff base complexes. The IR spectra of [MnLX]2 (X = benzoate, p-hydroxy benzoate, p-aminobenzoate, 3,5-dinitrobenzoate) complexes showed the characteristic absorptions due to coordinated azomethine nitrogen and phenolic oxygen atoms of the Schiff base. In addition, IR spectra of the compounds also suggest coordination of the co-ligands namely benzoate, p-hydroxy benzoate, p-aminobenzoate, 3,5-dinitrobenzoate in the respective complexes. A consistent presence of a band at ca. 755 cm-1 in all the binuclear complexes arises due to (Mn-O-Mn) moiety originated from interactions of phenoxy oxygen and manganese atoms, resulted in dimeric structure of the compounds. The magnetic moment values ranging from 4.74-4.91 B.M. per manganese centre for the complexes suggest presence of Mn(III) ion in the complexes. The overall coordination geometry around the manganese centres is distorted octahedral. Redox behaviour of the synthesized complexes was ascertained from cyclic voltametric studies. The Schiff base complexes, [Mn(L)X]2 (X = p-aminobenzoate, 3,5-dinitrobenzoate) have demonstrated their catalytic potentials in oxidizing selective organic substrates namely cyclohexene and styrene by hydrogen peroxide as oxidant. The oxidized products were characterized as trans-cyclohexane 1,2-diol and styrene epoxide, respectively. Complex 4 demonstrated a considerable level of effectiveness against a wide variety of pathogenic microorganisms.

Small Molecule Interactions with Biomacromolecules: DNA Binding Interactions of a Manganese(III) Schiff Base Complex with Potential Anticancer Activities.

A manganese(III) complex, [MnIII(L)(SCN)(enH)](NO3)·H2O (1•H2O) (H2L = 2-((E)-(2-((E)-2-hydroxy-3-methoxybenzylidene-amino)-ethyl-imino)methyl)-6-methoxyphenol), has been synthesized and characterized by single-crystal X-ray diffraction analysis. The interaction of 1•H2O with DNA was studied by monitoring the decrease in absorbance of the complex at λ = 324 nm with the increase in DNA concentration, providing an opportunity to determine the binding constant of the 1•H2O-ct-DNA complex as 5.63 × 103 M-1. Similarly, fluorescence titration was carried out by adding ct-DNA gradually and monitoring the increase in emission intensity at 453 nm on excitation at λex = 324 nm. A linear form of the Benesi-Hildebrand equation yields a binding constant of 4.40 × 103 M-1 at 25 °C, establishing the self-consistency of our results obtained from absorption and fluorescence titrations. The competitive displacement reactions of dyes like ethidium bromide, Hoechst, and DAPI (4',6-diamidine-2'-phenylindole dihydrochloride) from dye-ct-DNA conjugates by 1•H2O were analyzed, and the corresponding KSV values are 1.05 × 104, 1.25 × 104, and 1.35 × 104 M-1 and the Kapp values are 2.16 × 103, 8.34 × 103, and 9.0 × 103 M-1, from which it is difficult to infer the preference of groove binding over intercalation by these DNA trackers. However, the molecular docking experiments and viscosity measurement clearly indicate the preference for minor groove binding over intercalation, involving a change in Gibbs free energy of -8.56 kcal/mol. The 1•H2O complex was then evaluated for its anticancer potential in breast cancer MCF-7 cells, which severely abrogates the growth of the cells in both 2D and 3D mammospheres, indicating its promising application as an anticancer drug through a minor groove binding interaction with ct-DNA.

Corrosion inhibition of Schiff base and their metal complexes with [Mn (II), Co (II) and Zn (II)]: Experimental and quantum chemical studies

The synthesis, characterization, and examination of anti-corrosion performance of 2-furaldehyde semicarbazone Schiff base (FSC) complexes of cobalt (II), zinc (II), and manganese (II) on XC38 carbon steel immersed in 1 M HCl solution are performed using experimental investigations and quantum chemical simulation approaches. The theoretical approach used were DFT calculations and MC simulation. The inhibition effect was also studied by electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PDP). Electrochemical testing results show that these chemical compounds are particularly powerful inhibitors, which FSC-Mn provides a considerable inhibition of 91.48%at 500 ppm. The results also demonstrate that the inhibition effect of the four inhibitors increased with increasing inhibitor concentration, revealing that these compounds adsorb significantly to the steel surface. The scanning electron microscopy (SEM) analyses indicated that FSC and its complexes adsorbed onto the surface of XC38 carbon steel by forming a barrier between the inhibitors and the vacant d-orbital of iron. Quantum investigations were consistent with experimental findings on the four inhibitors’ capacity to prevent XC38 carbon steel from corroding in 1 M HCl, which were also proven effective as cathodic and anodic type inhibitors, displacing water molecules from mild steel, and producing heterogeneous coatings on the XC38 carbon steel surface to defend against corrosion.

Two Novel Schiff Base Manganese Complexes as Bifunctional Electrocatalysts for CO2 Reduction and Water Oxidation.

One mononuclear Mn(III) complex [MnIIIL(H2O)(MeCN)](ClO4) (1) and one hetero-binuclear complex [(CuIILMnII(H2O)3)(CuIIL)2](ClO4)2·CH3OH (2) have been synthesized with the Schiff base ligand (H2L = N,N'-bis(3-methoxysalicylidene)-1,2-phenylenediamine). Single crystal X-ray structural analysis manifests that the Mn(III) ion in 1 has an octahedral coordination structure, whereas the Mn(II) ion in 2 possesses a trigonal bipyramidal configuration and the Cu(II) ion in 2 is four-coordinated with a square-planar geometry. Electrochimerical catalytic investigation demonstrates that the two complexes can electrochemically catalyze water oxidation and CO2 reduction simultaneously. The coordination environments of the Mn(III), Mn(II), and Cu(II) ions in 1 and 2 were provided by the Schiff base ligand (L) and labile solvent molecules. The coordinately unsaturated environment of the Cu(II) center in 2 can perfectly facilitate the catalytic performance of 2. Complexes 1 and 2 display that the over potentials for water oxidation are 728 mV and 216 mV, faradaic efficiencies (FEs) are 88% and 92%, respectively, as well as the turnover frequency (TOF) values for the catalytic reduction of CO2 to CO are 0.38 s-1 at -1.65 V and 15.97 s-1 at -1.60 V, respectively. Complex 2 shows much better catalytic performance for both water oxidation and CO2 reduction than that of complex 1, which could be owing to a structural reason which is attributed to the synergistic catalytic action of the neighboring Mn(III) and Cu(II) active sites in 2. Complexes 1 and 2 are the first two compounds coordinated with Schiff base ligand for both water oxidation and CO2 reduction. The finding in this work can offer significant inspiration for the future development of electrocatalysis in this area.

Manganese Schiff Base Complexes, Crystallographic Studies, Anticancer Activities, and Molecular Docking

Choice of ligands is significant to successful synthesis of metal complexes (coordination compounds). This study reports the use of Schiff base as the right ligand to control the poor bioavailability and neurodegenerative toxicity challenges of manganese ion. In line with this study, document analysis was used as the methodological approach to evaluate the significance of Schiff base ligands in easing these manganese’s challenges and aligning the resultant coordination compounds (manganese Schiff base complexes) as therapeutic agents in anticancer studies. Report also involves crystallographic studies where single crystal X-ray crystallography was used as a chemical characterization technique. In addition, molecular docking studies, MOE2008, and AutoDock software were used to reveal the mode of interaction between the Schiff base and the manganese(II) and (III) ions, as well as scrutinizing the biological efficacy of the manganese(II) and manganese(III) Schiff bases coordination compounds as anticancer agents against some anticancer cell lines. Conclusion drawn was that manganese(II) and manganese(III) Schiff bases coordination compounds gave more active and potent activities than the corresponding Schiff bases. As a result, challenges of neurodegenerative toxicity and poor bioavailability of manganese ion were overcome, and the chelation therapy was fulfilled. Results from single crystal X-ray crystallography confirmed the successful synthesis of manganese(II) and manganese(III) Schiff bases coordination compounds and revealed the mechanism of reaction, while the molecular docking buttressed the biological activities of the Schiff base ligand and manganese Schiff base coordination compounds by portraying the structure activity relationship (SAR) between either Schiff base or the manganese Schiff base coordination compounds and the virtual cancer cell line (receptor protein), where hits were obtained for lead optimizations.

Synthesis, crystal structure, quantum chemical calculations, electrochemistry and electro-catalytical properties as cytochrome P-450 model of tetradentate Mn(III)-Schiff base complex

The tetradentate Schiff base ligand has been obtained from condensation with mixing ethylenediamine and 2 mmoles of 5-methoxy-2-hydroxybenzaldehyde in absolute ethanol H2L. To the ethanolic solution was added manganese(II)acetatetetrahydrated and lithium chloride (LiCl) to obtain the tetradentate manganese(III) Schiff base complex [Mn(III)(Cl)L]. Theprepared compounds have been characterized by several spectroscopic techniques such as elemental analyses, FT-IR, UV–vis., 1H NMR and HRMS. In this paper, the X-ray diffraction (XRD) and the computational studies (DFT) of the ligand(H2L) with its manganese(III)-Schiff base complex [Mn(III)(Cl)L] are described and confirmed the given molecularstructures. The crystallographic studies have been utilized toelucidate the kinetics, selectivity and stereochemistry of thetransferred oxygen atomsto the substrate molecules when the considered complex is used as catalyst accordingthecytochrome P450 model. In addition, the density functional theory (DFT) calculation with B3LYP/6-31G(d,p) level isperformed to obtain the optimized geometries and electronic properties of the prepared compounds. The global reactivityparameters have also been calculated using the energies of frontier molecular orbitals suggesting that the ligand H2L is morestable than its Mn(III) complex. This may be due to the presence of hydrogen bonds in the ligand and the weaker energies ofcoordination bonds in the complex. The electrochemical behaviour of Mn(III)(Cl)L has been studied by cyclic voltammetryin acetonitrile solutions at room temperature. The resulting cyclic voltammogram shows Mn(III)/Mn(II) couple at E1/2= -0.62V with glassy carbon (GC) electrode. This redox couple is involved in the electrocatalytic cycle where themanganese(III) cation is successively mono-electronated until the formation of superoxo intermediates and then the oxospecies, respectively. These oxo forms, generated in situ, transfer their oxygen atoms to the substrate giving the oxidizedproduct. So, the chemical and electrochemical reactions, implicated in this electrocatalytical process, obey to the biomimeticoxidation reactions as those of monooxygenase enzymes (Cytochrome P450).

Manganese(ii) Schiff-base-mediated reversible deactivation controlled radical polymerization of vinyl acetate

The manganese Schiff-base complexes were applied in the OMRP of vinyl acetate.

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.

Manganese Schiff Base Complexes and their Biological Catalytic Applications

Manganese Schiff Base Complexes and their Biological Catalytic Applications

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.

Synthesis of Mn3O4 nanozymes from structurally characterized phenoxazinone synthase models based on manganese(iii) Schiff base complexes.

Three mononuclear and one hexanuclear manganese(iii) complexes, [Mn(L)(H2O)2]·Cl (1), [Mn(L)(H2O)2]·Br (2), [Mn(L)(H2O)2]·NO3 (3), and [Mn6(L)6(NCS)6] (4), have been synthesized using a Schiff-base ligand, namely (E)-2-((3-(2-hydroxyethylamino)propylimino)methyl)phenol (H2L), and structurally characterized by the usual physicochemical techniques such as UV-Vis, FT-IR, ESI-MS, EPR and single crystal XRD. The structure of complex 4 is unique among all four complexes as the sixth coordination position of manganese is fulfilled by the oxygen atom of a neighbouring unit by covalent interaction. The phenoxazinone synthase like activity of all four complexes has been thoroughly investigated using three different substrates, o-aminophenol (OAP), 2-amino-4-methylphenol (MAP) and 3-amino-4-hydroxybenzoic acid (CAP). All complexes were found to be active towards catalysis and complex 4 showed the highest activity. The EPR study reveals that the oxidative dimerization of the substrates occurred through metal centered redox participation rather than a radical formation pathway. The experimental observations have been supported by DFT calculations to put forward the most probable mechanistic pathways operating in the catalytic cycle. Moreover, Mn3O4 nanoparticles (NPs) having two different morphologies have been synthesized using complexes 1 and complex 4 simply by calcination, respectively, with the aim to prepare nanozymes. These two synthesized NPs were also able to show phenoxazinone synthase like activity and thus complexes 1 and 4 can be claimed as precursors of nanozymes.

Voltammetric analysis of cocaine hydrochloride at carbon paste electrode chemically modified with N,N’-ethylene-bis-(salicylideneiminato) manganese(II) Schiff base complex

This article describes a method that uses a carbon paste chemically modified with N,N’-ethylene-bis-(salicylideneiminato) manganese(II) to detect cocaine hydrochloride by linear sweep voltammetry (LSV) in aqueous medium containing 0.1 mol L−1 KCl as supporting electrolyte. The potential scans were run from 0.4 to 0.9 V (vs Ag/AgCl), at 100 Mv s−1. The carbon paste chemically modified with the [Mn(salen)] complex had to be heated at 60 °C for paste agglutination. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were conducted to assess the thermal stability of the [Mn(salen)] complex, which remained stable up to 300 °C. Scanning electron microscopy (SEM) and energy dispersive spectrometry (EDS) analyses showed that the [Mn(salen)] complex was evenly and homogeneously distributed on the chemically modified electrode surface. The possible mechanism of electronic exchange between cocaine hydrochloride and the electrode surface was proposed: cocaine hydrochloride reduction at the working electrode surface produced the radical •C–OH due to reduction of the carbonyl group (C=O) stabilized by interaction of its free electron with orbital d electrons present in the manganese(II) Schiff base complex. Cathodic activity was verified at 0.8 V (vs Ag/AgCl). Cocaine hydrochloride detection presented linear dependence from 1 to 100 μmol L−1 with linear correlation coefficient of 0.9995 ± 0.0006, average amperometric sensitivity of 0.3367 μmol L−1, limit of detection (LOD) of 0.9349 μmol L−1, and limit of quantification (LOQ) of 3.11 μmol L−1. Notably, the [Mn(salen)] complex used in herein presented higher amperometric sensitivity than the complexes published so far, which is an important contribution to the development of techniques for cocaine detection.

Catalytic application of new manganese Schiff-base complex immobilized on chitosan-coated magnetic nanoparticles for one-pot synthesis of 3-iminoaryl-imidazo[1,2-a]pyridines

In this paper, new chitosan (CS) coated magnetic iron oxide nanoparticles (MNPs) supported manganese Schiff-base complex was designed, synthesized and screened as an efficient, reusable nanocatalyst by the three-component reaction of various aldehyde derivatives with trimethylsilyl cyanide and 2-aminopyridine for the synthesis of 3-iminoaryl-imidazo[1,2-a]pyridine (IAIP) derivatives. Fourier transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), vibrating sample magnetometry (VSM) and inductively coupled plasma atomic emission spectroscopy (ICP-AES) have been used to characterize the nanocatalyst before reaction. For the first time, earlier than immobilizing of manganese complex, the chitosan-coated Fe3O4 nanoparticles prepared through covalent bond formation between CS and chlorosilane-modified MNPs which were treated with triethylamine. It is a promising nanocatalyst providing high yield, short reaction times, and excellent turnover number. The recycle studies show a significant loss of activity after recycling six times.

Construction of a new double phenoxo bridged asymmetric manganese(III) Schiff base complex: Observation of ferromagnetic interaction within the dimer and antiferromagnetic interaction between dimers

A dimeric phenoxo bridged manganese(III) complex, [Mn2L2(OH2)(CH3OH)](ClO4)2 [H2L = N,N′-bis((2-hydroxy-1-phenyl)ethylidene)ethane-1,2-diamine] has been synthesized and characterized. The structure has been confirmed by single crystal X-ray crystallography. The χMT value at room temperature is slightly higher than that expected for two non-interacting species with S = 2 (g = 2), that corresponds to two high spin manganese(III) centers. That χMT value increases gradually with lowering temperature to reach a maximum and then an abrupt decrease of χMT value is observed at lower temperature. A ferromagnetic interaction (J = 1.44 cm−1) between the manganese(III) centers within the dimer is counter balanced by the presence of zero-field splitting (ZFS, D = −2.03 cm−1) at very low temperature and possibly also by antiferromagnetic interaction between dimers (zJ = -0.06 cm−1). In order to investigate the single-molecule magnet (SMM) nature of the complex, alternating current (ac) magnetic measurements were carried out from 2 to 7 K under a 3.5 Oe ac field between 1 and 1000 Hz.

Synthesis, characterization of manganese(II) Schiff base complex and its electrocatalytic sensing of hydroquinone

Synthesis, characterization of manganese(II) Schiff base complex and its electrocatalytic sensing of hydroquinone

A manganese-salen complex as dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes

A manganese Schiff base complex with N,N′-1,2-phenylenediamine-bis(salicyladimine) was synthesized and characterized by X-ray crystallography. This complex was administered intragastrically to alloxan-diabetic mice 3 weeks. In vivo tests showed that the complex significantly lowered serum glucose levels in alloxan-diabetic mice at doses of 77 mg V kg−1. Meanwhile, this complex was investigated as dipeptidyl peptidase IV (DPP-IV) inhibitor for the treatment of type 2 diabetes. The compound exhibit moderate inhibition against DPP-IV and possessed an IC50 value of 30 μM. Lineweaver–Burk transformation of the inhibition kinetics data demonstrated that it was a noncompetitive inhibitor of DPP-IV and Ki value was 136.3 μM. Moreover, molecular modeling studies suggested that the complex could fit well within the active-site cleft of DPP-IV. An acute toxicity study showed that animals treated intragastically with complex 1 at a dose of 5.0 g/kg did not show any significantly abnormal signs. These preliminary results suggest that the manganese Schiff base complex can induce a hypoglycemic effect in alloxan-diabetic mice.

Synthesis, structural features, antibacterial behaviour and theoretical investigation of two new manganese(III) Schiff base complexes

Two discrete manganese(III) coordination compounds, [Mn(L)(OCN)]2 (1) and [Mn(L′)(H2O)2][dnba]·DMF·H2O (2) bearing in situ generated Schiff base ligands H2L [H2L = N,N′-o-phenylenebis(salicylaldimine)] or H2L′ [H2L′ = N,N′-bis(salicylidene)ethylenediamine], were easily prepared by treating Mn(CH3COO)2·4H2O with salicylaldehyde and o-phenylenediamine (for 1) or ethylenediamine (for 2), and in the presence of supporting cyanate ligands or 3,5-dinitrobenzoate (dnba) counter anions, respectively. The obtained products were isolated as air-stable crystalline solids and were fully characterized by spectroscopic methods, single-crystal X-ray diffraction, topological analysis, as well as theoretical methods. The X-ray diffraction of the compound 1 reveals that the structure is dimeric with phenolic oxygen atom acting as bridge between two symmetrically equivalent Mn(III) atoms. The structure of 2 contains mononuclear cationic [Mn(L′)(H2O)2] units along with a 3,5-dinitrobenzoate anion and crystallization DMF molecule. Structural analysis indicates a distorted octahedral geometry for both complexes. Intermolecular hydrogen bonding and π–π stacking interactions are present in the lattice and play an important role in cohesion of the structures. Topological analysis of the compound 2 reveals a binodal 3,4-connected underlying 2D net with the 3,4L13 topology. Noncovalent interactions were investigated in terms of energies and geometries using theoretical calculations. Fluorescence and antibacterial properties of 1 and 2 were also investigated and discussed.

A manganese Schiff base complex immobilized on copper–ferrite magnetic nanoparticles as an efficient and recyclable nanocatalyst for selective oxidation of alcohols

A magnetically recoverable nanocatalyst was synthesized by covalent binding of a Schiff base ligand, namely N,N′-bis(Salicylidene)-1,3-diaminopropane-2-ol (H2salpn), onto the surface of silica-coated magnetic CuFe2O4 nanoparticles, followed by complexation with MnCl2. The resulting core–shell nanoparticles were characterized by spectroscopic and microscopic methods, including FTIR, XRD, VSM, TGA elemental analysis, TEM, and SEM. The Mn content was determined by ICP analysis. The nanoparticles were investigated as a catalyst for the selective oxidation of alcohols to the corresponding carbonyl compounds with tertiary-butyl hydrogen peroxide. The catalyst can be magnetically separated for reuse, with no noticeable loss of activity in subsequent reaction cycles. FTIR, VSM, and leaching experiments after three successive cycles confirmed that the catalyst was strongly anchored to the magnetic nanoparticles. A suitable mechanism for the reaction is proposed.

Voltammertic determination of 4-nitrophenol by N,N'-bis(salicylaldimine)-benzene-1,2-diamine manganese(II) Schiff base complex modified GCE

Nitrophenols are serious environmental pollutant, which are extensively used in the production of pesticides, dyes and pharmaceuticals. Among the nitrophenols, in particular 4-nitrophenol (4-NP), as a toxic derivative of parathion insecticide, is considered as priority hazardous waste and toxic pollutant. 4-NP is a deadly pollutant causing slow photosynthetic reactions, carcinogenicity and other related serious side effects towards human and aquatic life. In terms of environmental protection and food security, it is much more important to develop an effective analytical method for the determination of 4-NP in aqueous solutions. Till date various techniques have been reported for the determination of 4-NP, such as spectrophotometry, fluorescence, HPLC, capillary electrophoresis and electrochemical methods. Due to some advantages the electrochemical methods have received more attention. The Mn(II) Schiff base complex was electrochemically polymerized and modified the GCE. The poly manganese(II) Schiff base complex is deposited on the surface of GCE and it was utilized for the determination of 4-NP. The modified GCE exhibits an anodic peak at 0.44 V and the anodic peak current is 14.06 μA. The bare GCE shows the oxidation peak at 0.40 but the peak current is 3.98 μA which is lower than modified GCE. These results clearly reveals that Mn(II) Schiff base complex modified GCE can be used as electrocatalytic sensor for the determination of 4-NP in real samples.

Catecholase activity of a manganese Schiff base complex functionalized over SBA-15 in aqueous heterogeneous medium

A novel manganese(III)-Schiff base complex anchored SBA-15 based heterogeneous catalyst SBA-15-SB-Mn was synthesized and characterized by various physicochemical techniques. The catalyst was found to exhibit excellent green catalysis for the aerial oxidation of 3,5-di-tert-butyl catechol (3,5-DTBC) to the corresponding 3,5-di-tert-butylcatechol-1,2-benzoquinone (3,5-DTBQ) with 83.17% conversion (TON = 515) within 1 h at room temperature and relevant to catechol oxidase behavior.