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International Journal of Inorganic Chemistry
Volume 2012 (2012), Article ID 791219, 11 pages
Polydentate Schiff Base Ligands and Their La(III) Complexes: Synthesis, Characterization, Antibacterial, Thermal, and Electrochemical Properties
1Chemistry Department, Osmaniye Korkut Ata University, 80100 Osmaniye, Turkey
2Chemistry Department, K.Maras Sütcü Imam University, 46100 K.Maras, Turkey
3Biology Department, K.Maras Sütcü Imam University, 46100 K.Maras, Turkey
Received 3 November 2011; Revised 27 December 2011; Accepted 14 January 2012
Academic Editor: Maurizio Peruzzini
Copyright © 2012 Ali E. Şabik et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
We synthesized the Schiff base ligands H2L1–H2L4 and their La(III) complexes and characterized them by the analytical and spectroscopic methods. We investigated their electrochemical and antimicrobial activity properties. The electrochemical properties of the ligands H2L1–H2L4 and their La(III) complexes were studied at the different scan rates (100 and 200 mV), different pH ranges (), and in the different solvents. The electrooxidation of the Schiff base ligands involves a reversible transfer of two electrons and two protons in solutions of pH up to 5.5, in agreement with the one-step two-electron mechanism. In solutions of pH higher than 5.5, the process of electrooxidation reaction of the Schiff base ligands and their La(III) complexes follows an ECi mechanism. The antimicrobial activities of the ligands and their complexes were studied. The thermal properties of the metal complexes were studied under nitrogen atmosphere in the range of temperature 20–1000°C.
Schiff bases were firstly synthesized by H. Schiff. Condensation of primary amines with carbonyl compounds yields Schiff bases [1, 2]. Schiff bases have been amongst the most widely studied coordination compounds and are becoming increasingly important as biochemical, analytical, and antimicrobial reagents . Schiff bases derived from a large number of carbonyl compounds and amines have been used [4, 5]. The transition metal complexes having oxygen and nitrogen donor Schiff bases possess unusual configuration, structural liability, and are sensitive to the molecular environment . Lanthanides or lanthanos form a largest series of periodic table. It is 4f inner transition series. Lanthanide (III) ions, because of their size, are the best ions form stable complexes with high coordination number [7, 8]. The number of Schiff base complexes of the lanthanide elements is similarly limited to a few reports .
A large number of compounds of the type M(N2O2), M(N2S2), M(N2), and M(N4) (using the binding atom representation) have been synthesized and characterized. These type complexes have been investigated because of their catalytic activity in oxygenation reactions , carrying out, for instance, the selective oxidation of organic substrates, such as olefins, alcohols, alkanes, and aldehydes, under mild conditions. This property may be very attractive , since the oxidation products can provide important starting materials for the production of fine chemicals and polymers [12, 13]. In addition, the oxidation of organic substrates mediated by high valent ruthenium oxo species evokes much interest in the modeling of cytochrome P-450 . Several researches have proposed that the redox potential in Schiff base complexes is directly related to many of the biologically relevant chemical characteristics of the entire complex, for example, dioxygen binding ability and nucleophilicity . Thus, there has been a strong interest in determining thermodynamically meaningful redox potentials of copper Schiff base complexes and in understanding the relationship between these potentials and the detailed structure of the Schiff base ligand . Numerous electrochemical studies have been made for a fairly large number of acyclic and macrocyclic copper (II) complexes derived from Schiff bases. These investigations revealed that the redox properties of copper (II) complexes are markedly influenced by structural and electronic factors .
In this study, we synthesized four Schiff base ligands and their La(III) complexes and characterized by the analytical and spectroscopic methods. The ligands and their metal complexes show the reversible, quasireversible, and irreversible electrochemical processes. The Schiff base ligands and their La(III) complexes have the antimicrobial activity.
2.1. Reagents and Materials
All chemicals used in this study were obtained commercially and used without purification. The metal salt La(NO3)3·6H2O and organic solvents were purchased from commercial sources and used as received, unless noted otherwise. 2,4-Diaminobenzene sulphonic acid, 2,5-diaminobenzene sulphonic acid, 3,5-diaminobenzoic acid, 2,4-dihydroxybenzaldehyde, and 2-hydroxy-3-methoxybenzaldehyde and ([CH3(CH2)3]4NBF4) were obtained from Fluka.
2.2. Physical Measurements
Elemental analyses (C, H, N) were performed using a LECO CHNS 932. Infrared spectra were obtained using KBr dics (4000–400 cm−1) on a Perkin Elmer Spectrum 100 FT-IR. Far spectra of the complexes were recorded on a Perkin Elmer spectrum 400 FT-IR/FT-FAR. The electronic spectra in the 200–900 nm range were obtained on a Perkin Elmer Lambda 45 spectrophotometer. Molar conductivities of the Schiff base ligands and their transition metal complexes were determined in DMF (~10−3 M) at room temperature using a Jenway Model 4070 conductivity meter. Mass spectra of the ligands were recorded on a LC/MS APCI AGILENT 1100 MSD mass spectrophotometer. 1H and 13C NMR spectra were taken on a Varian XL 200 NMR instrument. TMS was used as internal standart deuterated dimethyl sulfoxide as solvent.
Cyclic voltammograms were recorded on an Iviumstat Electrochemical workstation equipped with a low current module (BAS PA-1) recorder. The electrochemical cell was equipped with a BAS glassy carbon working electrode (area 4.6 mm2), a platinum coil auxiliary electrode, and an Ag+/AgCl reference electrode filled with tetrabutylammonium tetrafluoroborate (0.1 M) in DMSO and DMF solvents and adjusted to 0.00 V versus SCE. Cyclic voltammetric measurements were made at room temperature in an undivided cell (BAS model C-3 cell stand) with a platinum counterelectrode and an Ag+/AgCl reference electrode (BAS). All potentials are reported with respect to Ag+/AgCl. The solutions were deoxygenated by bubbling dry nitrogen through the solution for 30 min prior to the experiments, and, during the experiments, the flow was maintained over the solution. Digital simulations were performed using DigiSim 3.0 for windows (BAS, Inc.). Experimental cyclic voltammograms used for the fitting process had the background subtracted and were corrected electronically for ohmic drop.
2.3. Preparation of Schiff Base Ligands (H2L1–H2L4)
All the Schiff base ligands were prepared according to the fallowing method. The amine derivatives (2,4-diaminobenzene sulphonic acid (1 mmol) to prepare H2L1 and H2L3; 3,5-diaminobenzoic acid (1 mmol) to prepare HL2; 2,5-diaminobenzenesulfonic acid (1 mmol) to prepare H2L4) in the EtOH solution (50 mL) were mixed and then added to the carbonyl compounds (o-vanillin (2 mmol) to prepare H2L1, H2L2, and H2L4; 2,4-dihydroxybenzaldehyde (2 mmol) to prepare H2L3) and refluxed for 12 h at 80°C. After the reaction mixture was allowed to cool to room temperature, the solvent was evaporated and the solid residue was recrystallized from EtOH and dried under vacuum desiccator.
2.4. Preparation of Schiff Base Complexes
To solution of Schiff base ligand (H2L1–H2L4) (1 mmol) dissolved in absolute EtOH (20 mL) was added a solution of [La(NO3)3·6H2O] (1 mmol) in the EtOH (20 mL) [2 : 1 molar ratio (M : L) for H2L1, H2L3, and H2L4, 1 : 1 molar ratio (M : L) for H2L2] was added. The mixture was stirred for 20 hours at 80°C. The final complex precipitated out from the solution was filtered off, washed with cold ethanol, and dried in a vacuum desiccator.
3. Preparation of Microbial Culture
The Schiff base ligands and their metal complexes were evaluated for their in vitro antibacterial activity against the B. megaterium, B. cereus, S. aureus, M. luteus, and E. faecalis (as Gram-positive bacteria) and P. aeruginosa, E. coli, and C. albicans (as Gram-negative bacteria) by agar-well diffusion. Bacterium was inoculated into nutrient broth (Difco), incubated for 24 h and the fungi studied inoculated in malt extract broth (Difco) for 48 h. In the agar-well diffusion method, Mueller Hinton Agar (Oxoid) for bacterium and in Malt Extract Broth (Difco) sterilized in a flask, cooled to 45–50°C, and were distributed (20 mL) to sterilized petri dishes after injecting 0.01 mL cultures of bacterium prepared as mentioned above and allowed to solidify. The dilution plate method was used to enumerate microorganisms (105 bacterium mL−1) and fungi (103-104 mL−1) for 24 h . By using a sterilized cork borer (7 mm diameter), wells were dug in the culture plates. Compounds dissolved in DMSO were added (0.2 mL) to these wells. The petri dishes were left at 4°C for 2 h, and then the plates were incubated at 30°C for bacterium (18–24 h) and at 25°C for fungi (72 h). At the end of the period, inhibition zones formed on the medium were evaluated as millimeters (mm). The control samples were only absorbed in DMSO. Blank tests showed that DMSO solvent did not affect the antimicrobial activity of the compounds.
4. Results and Discussion
In this study, the ligands N,N′-bis[(3-metoxysalicylidene)]-2,4-diaminobenzene sulphonic acid (H2L1), N,N′-bis[(3-metoxysalicylidene)]-3,5-diaminobenzene carbonic acid (H2L2), N,N′-bis[(4-hidroxysalicylidene)]-2,4-diaminobenzene sulphonic acid (H2L3) N,N′-bis[(3-metoxysalicylidene)]-2,5-diaminobenzene sulphonic acid (H2L4) were synthesized and characterized by the analytical and spectroscopic methods. Condensation of the aldehydes with primary amines readily gives the corresponding imines, which were easily identified by their IR, 1H-, and 13C-NMR spectra. Replacement of the carbonyl by the imine results in (i) lowering of the energy of the (C=O) stretch in the IR spectrum and (ii) a shift to higher field of the CH=N proton signal in the 1H-NMR spectrums. The imines prepared in this way are formed in nearly quantitive yields and are of high purity. All compounds are stable at room temperature in the solid state. Analytical data and some physical properties of the Schiff base ligands and their metal complexes are given in Table 1.
All the ligands and their complexes are soluble in common organic solvents, such as CHCl3, EtOH, MeOH, DMF, and DMSO because of –OH, –CH=N–, SO3H, and COOH groups. The –SO3H and –COOH groups in the ligands provide great advantages of the solubility properties. These groups provide solubility also in the water. La(III) complexes of the ligands H2L1–H2L4 were synthesized and investigated by the some analytical and spectroscopic methods. A little water added secure solubility of the ligands when some problems occur at solubility. The proposed structures of the ligands were shown in Figure 1.
The infrared spectral data of the ligands (H2L1–H2L4) and their metal complexes are given in Table 2. Ligands have carboxyl, azomethine, and phenolic C–OH groups. In the infrared spectra of ligands H2L1 and H2L4, the strong vibration at 3402 and 3099 cm−1 can be attributed to the (O–H) group. In the complexes, these bands were shifted to the lower regions. For the free ligands, the board bands in the 2800–2700 cm−1 range are assigned to the OH group vibration (ortho position) associated intramolecularly with the nitrogen atom of the CH=N group .
In the complexes, these bands disappear as a result of proton substitution by cation coordination to the oxygen atoms of the ligands. In the spectra of the ligands, the strong bands observed in the 1659–1611 cm−1 range were assigned to the azomethine group vibration and its shift indicates that, in complexes, coordination of ligands in complexes is through azo methinic nitrogen atom. The bands assigned to benzene ring vibration compared well, with those of monosubstituted derivatives of benzene, several other modes associated with C–H out of plane deformation appear in the region [764–754 cm−1]. Some new medium to weak bands were also observed in the range (496 to 470 cm−1) in case of complexes ligands have no absorption. These new medium to weak bands are assigned as (Ln–N) modes observed for various lanthanide (III) nitrate complexes. Bands in the far infrared spectra, in the region 278–255 cm−1, can be assigned to (Ln–N) vibration in the new complexes . This situation was shown in Figure 2.
It has been found that the separation of () and () is greater in bidentate (about 30–40 cm−1) than in monodentate (about 10 cm−1) nitrate complexes. The separation of () and () frequencies is greater for bidentate nitrate anions (about 80–100 cm−1) as compared to monodentate nitrate anions (about 10–80 cm−1) complex containing ionic nitrate groups show only one band in this region assignable to (). The occurrence of two absorptions at 1540–1501 cm−1 and 1380–1287 cm−1 region is attributed to and modes which suggest that nitrate anions in the complexes under study are covalently bonded and are present inside the coordination sphere. If () difference is taken as an approximate measure of covalence of nitrate groups, a value of [~200 cm−1] for the complexes under study suggests a strong covalency nature of nitrate in the complexes. Lever separation rule  states that bidentate coordination of nitrate anion involves a greater distortion from D3h symmetry than unidentate coordination. In case of spectra of complexes, under study, it has been found that the separation of () is good enough and is in the order [~200 cm−1]. This shows that, according to Lever separation rule, nitrate ion may be considered as covalently bonded to metal ions in bidentate fashion. Infrared absorption frequencies (cm−1) of nitrate groups of lanthanide (III) complexes of Schiff base ligands are listed in Table 3.
Electronic spectra were measured in EtOH, and the spectroscopic data are given in Table 2. Electronic spectral studies of lanthanide (III) metal complexes are significant and are important tool for the measurement of covalency in complexes. The line-like spectra of lanthanide (III) metal compound appearing in the UV-visible and near IR regions arise from electronic transitions within the 4f levels which are normal forbidden [22, 23] but may become allowed after removal of degeneracy of 4f orbitals by external crystal field [24, 25]. Lanthanum (III) complexes have no significant absorption in visible region. The shift of hypersensitive bands has been utilized to calculate the nephelauxetic effect (), Sinha’s covalency parameter (%) (metal ligand covalency percentage), and the covalency factor () along with covalency angular overlap parameter (); these parameters have been calculated using the following expressions :
The electronic spectral studies of the lanthanide (III) metal complexes yield positive value for () and (%) which suggest that the bonding between metal and ligand is covalent in the complexes. The values of parameter of bonding () and angular overlap parameter () are also found to be positive indicating covalent bonding complexes.
In the spectrum of the ligands, the bands observed in the range 345–305 nm were assigned to and transitions. The bands in the 405–345 nm range may be assigned to the transitions. In the electronic spectra of the La(III) complexes, the bands in the 465–405 nm may be assigned to (LaIII) → (L) (symmetric) and (LaIII) → (L) (asymmetric) MLCT transition.
The magnetic moments of the lanthanide (III) complexes are consistent with the presence of unpaired 4f electrons and close to the values for the free metal ions reported by Van Vleck and Frank . These observations suggest that the 4f electrons of the lanthanide (III) do not take part in bond formation in these species. The lanthanide (III) Schiff base complexes have the diamagnetic nature.
Molar conductivities were measured for freshly prepared solutions in DMF and after standing for two weeks. The conductivities increased very slightly with time in DMF for all the complexes. The coordination moieties present can not be replaced by the solvent molecules. The values of these conductances are in the range 13.2–18.5 Ω−1 cm2 mol−1 in DMF and are in accordance with those reported for weak electrolytes in this solvent . This is indicative that these complexes dissociate very slightly in this solvent.
Additional structural information can be deduced from the 1H- and 13C-NMR spectra. The 1H- and 13C-chemical shifts for the Schiff base ligands are given in Table 4.
In the 1H-NMR spectrum, signal belong to phenolic OH groups seen at between 10.2–10.4 (HL1), 9.0–9.8 (H2L2), 10.0–11.2 (H2L3), and 10.2–10.4 (H2L4) ppm as a broad singlet. The singlets belong to azomethine group seen 8.6 (H2L1), 8.8 (H2L3), and 8.9 (H2L4) ppm. The multiplets belong to aromatic ring seen as a broad band at 6.2–8.0 ppm. Furthermore, the signals relative to methoxy group seen at 3.6–4.0 (H2L1), 3.8 (H2L2), and 3.8–4.0 (H2L4) as a sharp signal. In the 13C-NMR, the signal of carbon atom belongs to azomethine group seen at 150.0–154.0 (HL1), 166.0–168.0 (HL2), 164.0–166.0 (H2L3), and 150.0–152.0 (H2L4). The signals related to the carbon atoms at the aromatic ring are seen at 118.0–124.0 (H2L1), 118.0–154.0 (H2L2), 104.0–136.0 (H2L3), and 118.0–124.0 (H2L4) ppm.
The Schiff base ligands and their metal complexes were evaluated for their in vitro antibacterial activity against the B. megaterium, B. cereus, S. aureus, M. luteus, and E. faecalis (as Gram-positive bacteria) and P. aeruginosa, E. coli, and C. albicans (as Gram-negative bacteria) by agar-well diffusion. The results of antibacterial activities are given in Table 5.
The ligands and all the complexes showed prominent activity against all the bacteria B. megaterium, B. cereus, S. aureus, M. luteus, and E. faecalis (as Gram-positive bacteria) and P. aeruginosa, E. coli, and C. Albicans (as Gram-negative bacteria). All the complexes are found to be more active compared to the parent Schiff base. This is because, on chelation , the charge on the metal ion is reduced to a minimum increasing the lipophilicity of the complexes. This leads to the breakdown of the permeability barrier of the bacterial cell and thus retards the normal cell processes. Among the complexes formed from La(III) metal salt, La2(L1)(NO3)4(H2O)4 complex showed maximum inhibition. Also comparing the anionic species, nitrate complexes were found to inhibit bacterial growth most effectively. Antifungal studies against the fungus, E. coli, showed that both ligands and all the complexes exhibited almost hundred percent inhibitions.
The thermal studies of all the complexes were performed under nitrogen atmosphere in the temperature range of 20–1000°C. The thermal curves of the La2(L1)(NO3)4(H2O)4 (a) and La2(L4)(NO3)4(H2O)4 (b) complexes are given in Figures 4(a) and 4(b).
All complexes have the coordinated water molecules. As seen from Figures 4(a) and 4(b) and the figures of the other complexes, in the first step, the coordinated water molecules were eliminated at the first step in the 100–150°C temperature range. In the second step, the NO3 − ion(s) coordinated to La(III) loss in the 250–310°C temperature range. In the last step, the organic fragments of the complexes decompose to La2O3 metal oxide.
4.1. Cyclic Voltammetry
DMSO and DMF solutions of the ligands and their La(III) complexes have been used to study the redox properties with the help of cyclic voltammetry. Obtained data from the electrochemical studies are given in Table 6.
The cyclic voltammograms have been recorded at a wide range of scan rates from 100 to 200 mVs−1 and investigated in the potential range +2.0 to −2.0 V and in pH = 2–12 with phosphate buffer. A representative voltammograms are shown in Figures 5(a)–5(c).
The one-electron stoichiometry of this electron transfer process is established by comparing the current height with known one electron redox processes under identical conditions. The reversible character of the La(II) → La(III) oxidation is evident from the peak-to-peak separation of 60–70 mV and almost equal anodic () and cathodic peak currents (). All the complexes display irreversible ligand-based one-electron reductions on the cathodic side (Table 6). Interestingly, La(L2)(NO3)(H2O), La2(L3)(NO3)4(H2O)4, and La2(L4)(NO3)4(H2O)4 display two closely spaced MLCT bands in the electronic absorption spectra, whereas La2(L1)(NO3)4(H2O)4 displays only one MLCT band (Table 2). The MLCT transitions involve excitation of metal electrons to the orbitals of ligand which are also involved in electrochemical reductions. The MLCT band positions and the electrode potentials associated with the metal ion oxidation and ligand reduction are correlated and reflect the relative energies of the metal and ligand levels . As mentioned before, the difference in the molecular structures of La2(L1)(NO3)4(H2O)4, La2(L3)(NO3)4(H2O)4, and La2(L4)(NO3)4(H2O)4 is the central chelate ring size formed by the imine-N and phenolic-O atoms of the ligands. Possibly for La(L2)(NO3)(H2O) with six-membered central chelate ring, there is a small but detectable energy difference between two lowest energy acceptor levels. The observations of two MLCT bands and two ligand-based reductions for La2(L3)(NO3)4(H2O)4 and La2(L4)(NO3)4(H2O)4 and single MLCT band and single ligand-based reduction are consistent with such a situation. The La(II) → La(III) oxidation potentials for La2(L3)(NO3)4(H2O)4 and La2(L4)(NO3)4(H2O)4 are within 20 mV (Table 6). Such a situation may also be another consequence of the difference in the central chelate ring size in these complexes. The cathodic and anodic peak currents are essentially identical for all the complexes. The one-electron stoichiometry of this response is confirmed by comparing the current heights with known one-electron redox processes under identical experimental conditions . The trend in the values reflects the influence of the electronic nature of the substituents (R) at the para position of the O-coordinating deprotonated carboxy and sulphoxy functionality present in the ligands. For the most electron-releasing substituent (R = OH, OCH3), the oxidation of the metal ion occurs at the lowest potential, and, for the most electron withdrawing substituent (R = COOH, SO3H), it occurs at the highest potential.
The influence of pH on the cyclic voltammograms at a glassy carbon electrode in M ligands and their complexes solutions, mVs−1, is shown in Figures 5(a)–5(c). It is observed that the profile of the curves is the same in the pH range studied, indicating that the electrooxidation of the ligands follows the same reaction mechanism. However, with the increase of pH, the anodic and cathodic peak potentials are shifted toward less positive values. The shift of to less positive values indicates an increase in the nucleophilicity of the organic compound  and that its antioxidant activity is thermodynamically favored with the pH increase.
It is important to note that the dependence of with pH is attenuated when the pH changes from 7.4 to 8.5. This behavior can be explained by the increase of the concentration of the ligands in solution. In the oxidation of the ligands H2L1, H2L2 and H2L4, only two protons are involved (Figure 6), while, in the oxidation of the ligand H2L3, four protons are involved. In the solutions of pH higher than 8.5, the reduction peak was not observed (data not shown), which indicates that the products of oxidation of the Schiff base ligands and their metal complexes became unstable and an irreversible homogeneous chemical reaction occurs. For this reason, we limited our studies to the pH range 2.0–8.5.
In summary, we have synthesized new lanthanum complexes from the Schiff base ligands with La(III) and characterized by conventional methods. The structures of the ligands are drawn in Figure 1. Various attempts such as crystallization using mixtures of solvents, low-temperature crystallization were unsuccessful to obtain a single crystal suitable for X-ray crystallography. Promising results are obtained when screened for antibacterial and antifungal activities. The effect of pH in the complex solutions was investigated and determined that affect the redox properties of the ligands and their metal complexes.
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