Synthesis, Spectroscopy, Thermal Analysis, Electrochemistry and Superoxide Scavenging Activity of a New Bimetallic Copper(II) Complex

A new bimetallic copper(II) complex has been synthesized with ligand obtained by the condensation of salicylaldehyde and the amine derived from reduction of nitration product of benzil. e ligand was characterized by H NMR and mass spectra, and the binuclear Copper(II) complex was characterized by vibrational and electronic spectra, EPR spectra, and magnetic moment measurement.ermogravimetric analysis study and electrochemical study of the complex were also done.e complex was found to show superoxide dismutase activity.


Introduction
Copper is a biologically important metal found in a number of enzymes such as-superoxide dismutase, tyrosinase, Bhydroxylases, monoaminooxidase, and ascorbic acid oxidase [1][2][3].Complexes of copper in oxidation state +2 were found to show signi�cant antioxidant and anti-free radical activity also [4,5].Bimetallic copper complexes are potential models for a number of important biological systems containing couple sites [6] and have been studied extensively [7][8][9][10][11][12].Bimetallic complexes of copper with Schiff bases have been shown to be useful chemical probe of DNA and have found its importance in various biochemical and biomedical applications [13,14].Synthesis of a new copper(II) complex with multidentate Schiff base ligand also contributes in the development of coordination chemistry [15][16][17].
Superoxide dismutase (SOD) is an enzyme which protects cells from the toxic effect of superoxide [18].e three main types of SOD are-Cu-Zn-SOD, Mn-SOD, and Fe-SOD of which the �rst one is found in mammals [19].De�ciency or imbalance of SOD in human body leads to many diseases and disorders such as diabetes, ischemia, cataract, Parkinson's disease, and cancers [20,21].Such disorders could be treated by supplementation of antioxidant enzymes but administration of these enzymes through oral or intraperitoneal routes is severely restricted due to their rapid degradation and short lifetime in biological systems [22].Small metal complexes having good superoxide scavenging activity should be good candidate in this respect.
A good number of copper complexes have been reported to mimic SOD activity which includes copper(II) complexes with Schiff base ligands derived from various aldehydes and ketones [23], imidazole bridged copper(II) complexes [24], planar copper(II) complex on addition of a base such as Nmethyl imidazole or pyridine [25], curcumin complexes of copper(II) [26], and so forth.It is also reported that the copper(II) complexes with Schiff base ligands of salicylaldehyde semicarbazone have SOD activity which could be tuned by heterocyclic bases pyridine and N-methyl imidazole [27].ere are recent reports on copper complexes with SOD activity having pyridine and pyrimidine derivatives [28][29][30].
In this paper, we report the synthesis of a new ligand by the condensation of salicylaldehyde and the amine derived from reduction of nitration product of benzil.e ligand was characterized by 1 H NMR and mass spectra.Binuclear copper (II) complex of the ligand was synthesized, and its FTIR spectra, electronic spectra, EPR spectra, thermogravimetric (TGA) analysis study, and electrochemical study results are reported.

Experimental
All the chemicals and solvents used for the synthesis are reagent grade.Benzil, ethylenediamine, and salicylaldehyde were purchased from Merck.e FTIR spectra were recorded using KBr discs on a Perkin-Elmer spectrum RXI FTIR system.e NMR spectra were recorded in Bruker Ultra shield 300 spectrophotometer.e electronic spectra in the range 200-1000 nm were obtained in acetonitrile on a UV-1800 SHIMADZU spectrophotometer.ermogravimetric measurements were carried out on a METTLER TOLEDO TGA/DSC instrument.Magnetic moment measurements were recorded at room temperature by the Gouys method using Cambridge Magnetic Balance.CHI 600B Electrochemical Analyzer (USA) with a three electrode cell assembly was used for electrochemical studies.e electrodes were cleaned as per reported procedure [31].e SOD activity of the copper complex has been studied by the method of NBT reduction using KO 2 − • as the source of superoxide radical [32].

Synthesis and Characterization of Schiff Base Ligand (L).
1 g benzil was taken in 10 mL of 1 : 1 conc.HNO 3 : H 2 SO 4 mixture and re�uxed for 6 hours.A yellow product was obtained which was �ltered and washed many times with distilled water.Aer drying, 0.5 g of the product was dissolved in 10 mL methanol.A freshly prepared solution of SnCl 2 was added to this solution drop wise till the color became dark brown.e solvent was evaporated and the product was washed many times with distilled water and dried.e product was then dissolved in methanol and made basic by adding NaOCH 3 .Salicylaldehyde was added dropwise under stirring till the dark brown color of the solution became light brown.e solvent was evaporated under vacuum and product was washed many times with distilled water and dried.e product was further washed with n-hexane to remove any unreacted aldehyde present.e synthetic path for the ligand has been shown in Scheme 1).

Synthesis of the
Complex.0.1 mol of L was dissolved in 10 mL of methanol, and 0.2 mol of Cu-acetate was added in small portions with continuous stirring followed by further stirring for 3 hours.Dark green product was obtained which was �ltered and washed with distilled water.e compound was recrystallized from CH 3 CN.

Characterisation of the Bimetallic Copper(II) Complex
3.1.1.UV/Visible and FTIR Spectroscopy.e uv/visible spectra of L showed two well-de�ned peaks at 213 nm and 323 nm, due to  −  * and  −  * , respectively, together with a shoulder at 400 nm. Figure 2 shows the electronic spectra of the copper(II) complex in DMSO.When L formed complex with Cu(II), the peaks at 213 nm and 323 nm disappeared and the shoulder became a well-de�ned peak at 380 nm.Binding to Cu(II) ion redistributed the electron densities of L and hence the �rst two peaks disappeared.e 380 nm peak should be due to ligand to metal charge transfer.Another peak at 700 nm was observed due to d → d transition originating at Cu(II).FTIR spectra for the complex synthesized showed peaks at 2861 cm −1 ( C-H of C 6 H 5 ); 772.8 cm −1 , 718.9 cm −1 (C-H out of plan vibration for C 6 H 5 ); 1616.5 cm −1 ( C=O ); 1538.1 cm −1 ( C=N ); 1391 cm −1 ( C-N ); 1349.3 cm −1 ( C-N ); 3430.9 cm −1 ( O-H coordinated H 2 O).e stretching frequency due to  C=O has decreased to 1616.5 cm −1 in the complex from 1680 cm −1 in the ligand.is indicates possibility of formation of H bonding between coordinated water molecule and the carbonyl groups.

Magnetic Moment
Measurements.e magnetic moment value was measured to be 2.199 BM which was much higher than the single electron value of 1.74 BM. is magnetic moment value can be explained by considering that the complex formed is a bimetallic Cu(II) one.Because of exchanged couple phenomena, the observed magnetic moment is smaller than the total magnetic moment due to two single Cu(II) ions, that is, 1.74 BM × 2 = 3.48 BM.

EPR Studies of the Complex
. e X-band EPR spectra of the complex was recorded as the polycrystalline samples at room temperature (Figure 3).e  iso value and geometric parameter G, that is, the measurement of exchange interaction between the copper centers were evaluated by using the following expression [31]: = (  − 2.0023) e calculated value of  tensor parameter was   = 2.24 and  ⟂ = 2.11.Hence   >  ⟂ > 2.0023 which reveals that  2−2 is the ground state [30].e value of G was calculated to be 2.207 which means G is less than 4 indicating effective interaction between the copper centers [32].

ermogravimetric Analysis. ermogravimetric (TG)
weight loss curves and the corresponding differential thermogravimetric (DTG) curves for the complex are shown in Figure 4. e complex showed two well-de�ned steps at 160 ○ C and 290 ○ C together with another steps at 350 ○ C. e loss in weight in the �rst step is 4.02% which should be due to the two co-ordinated water molecules (calculated weight loss was 4.28%).e second, and third weight losses are 65.95% and 6.58%, respectively, totaling 72.53%.is large weight drop can be explained by considering that the residue is a 1 : 1 mixture of Cu 2 O and CuO (calculated weight loss 72.51%).
Based on various spectroscopic and magnetic studies together with the TG analysis results, the structure of the complex has been con�rmed to the one shown in Scheme 2. e plot of cathodic and anodic currents versus square root of scan rate was found to be linear.is linearity in redox currents against square root of scan rate indicates the redox process is diffusion controlled.Double potential step chronocoulometry was done for the complex in DMSO.e plot of charge (Q) versus square root of time ( 1/2 ) was gradual, and no sharp decrease was observed.is con�rms that the complex was not adsorbed onto the electrode surface, and the redox process is diffusion controlled.

Superoxide Dismutase (SOD) Activity of the Complex.
e SOD activity of the copper complex has been studied by the method of NBT reduction using KO 2 − • as the source of superoxide radical [32].e blue color developed due to the formation of dye was measured immediately at 560 nm against an appropriate blank.One unit of SOD activity (IC 50 value) was de�ned as the test substance required for 50% inhibition of NBT reduction by the superoxide anion [27].A linear relation was obtained between the concentration of the copper complex and the inhibition of the superoxide ion.e 100% of superoxide activity corresponds to an assay performed in the absence of complex.In order to determine the concentration of the complex required to yield 50% inhibition of the reaction, we plotted the percentage of inhibition against the metal complex concentration.A linear relation was obtained between the concentration of the copper complex and the inhibition of the superoxide ion and from this plot IC 50 value could be determined.e obtained value was 0.150 mM which was lower than the IC 50 value reported [25,27].e IC 50 value of the native enzyme is 0.72 M.

Conclusions
A new Schiff base ligand system obtained from benzil by �rstly introducing nitro groups which were reduced to amine and secondly allowing condensation between the amine and salicylaldehyde has been synthesized and characterized.e ligand binds to two Cu(II) ions giving a new bimetallic Cu(II) complex which shows efficient superoxide dismutase activity.
Figure 5  shows the cyclic voltammogram of Cu(II)⋅L⋅2H 2 O in CH 3 CN using platinum disc as working electrode and Ag-AgCl as the reference.e cyclic voltammetric pro�le is of quasi reversible one with the redox potential value +0.105 V ±0.005 V with peak potential difference Δ = 0.228 V. is redox potential is due to Cu(II)/Cu(I) redox couple.e ratio of cathodic to anodic current is found to be 0.949.e redox potential value was further con�rmed by square wave voltammogram (not shown).Observation of only one redox couple in the cyclic voltammogram or square wave voltammogram con�rms that both the Cu(II) ions are in identical coordination environment.