Synthesis, Characterization and Antibacterial Studies of N-(Benzothiazol-2-yl)-4-chlorobenzenesulphonamide and Its Neodymium(III) and Thallium(III) Complexes

N-(Benzothiazol-2-yl)-4-chlorobenzenesulphonamide (NBTCS) was synthesized by condensation reaction of 4-chlorobenzenesulphonyl chloride and 2-aminobenzothiazole in acetone under reflux. Neodymium(III) and thallium(III) complexes of the ligand were also synthesized. Both ligand and metal complexes were characterized using UV-Vis, IR, 1H- and 13C-NMR spectroscopies, elemental analysis and molar conductance measurement. IR studies revealed that the ligand is tridentate and coordinates to the metal ions through nitrogen and oxygen atoms of the sulphonamide group and nitrogen atom attached to benzothiazole ring. The neodymium(III) complex displays a coordination number of eight while thallium(III) complex displays a coordination number of six. The ligand and its complexes were screened in vitro for their antibacterial activities against Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa using the agar well diffusion technique. The synthesized compounds were found to be more active against the microorganisms screened relative to ciprofloxacin, gentamicin and co-trimoxazole.

The similarity of the structure between sulphonamide and p-aminobenzoic acid (PABA), a molecule found in bacteria used in folic acid synthesis, is the basis for the inhibitory activity of sulpha drugs on dihydrofolate biosynthesis [1,6,16]. Sulpha drugs are associated with antibiotic resistance and allergies [17,18]. The work done by Yun et al. 2012 gave insight into sulpha drug resistance [1]. They revealed that the binding sites of PABA and sulpha drugs overlap, but those of sulpha drugs extend beyond the pocket in which PABA binds. Mutations associated with drug resistance cluster around this extended region of the PABA pocket. This explains how they can prevent the drugs from binding without seriously affecting the binding of PABA. Several modifications have been made on the general structure of sulphonamides, resulting in new compounds with varying pharmacological activities and reduced side effect [2]. The work done by Lawrence et al. 2010 have shown that the best therapeutic results were obtained from the compounds in which one hydrogen atom of the SO 2 NH 2 group was replaced by heterocyclic ring [19]. Previous studies by Obasi et al. have led to discovery of ligands and complexes with varying activities against multi-resistant bacterial strains isolated under clinical conditions and cultured species using agar-well diffusion method [20][21][22]. Metal complexes of sulpha drugs have been reported with appreciable biological activities [23][24][25][26][27][28]. Recently, there have been several reports on neodymium(III) and thallium(III) complexes [29][30][31][32][33][34][35][36][37]. Mimouni et al., 2014 [38] have synthesized, characterized, and studied the antibacterial, antifungal and antitubercular activities of thallium complexes of monensin and lasalocid. Their study revealed that remarkable bioactivity against different pathogens were achieved and confirmed that the compounds could very likely be used without great risk of toxicity in diverse pharmaceutical applications. In addition, the crystal structures of thallium salt of Grisorixin and antibiotic 6016 thallium salt have been reported [39,40]. In view of the need for a new generation of antibiotics that would cause fewer side effects, we designed a new class of inhibitors namely: N-(benzothiazol-2-yl)-4-chlorobenzenesulphonamide (NBTCS) and its neodymium(III), and thallium(III) complexes. Their in vitro antibacterial activities against Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa were also investigated. folate synthesis. As such, the microorganism will be starved of folate and die. The similarity of the structure between sulphonamide and p-aminobenzoic acid (PABA), a molecule found in bacteria used in folic acid synthesis, is the basis for the inhibitory activity of sulpha drugs on dihydrofolate biosynthesis [1,6,16]. Sulpha drugs are associated with antibiotic resistance and allergies [17,18]. The work done by Yun et al. 2012 gave insight into sulpha drug resistance [1]. They revealed that the binding sites of PABA and sulpha drugs overlap, but those of sulpha drugs extend beyond the pocket in which PABA binds. Mutations associated with drug resistance cluster around this extended region of the PABA pocket. This explains how they can prevent the drugs from binding without seriously affecting the binding of PABA. Several modifications have been made on the general structure of sulphonamides, resulting in new compounds with varying pharmacological activities and reduced side effect [2]. The work done by Lawrence et al. 2010 have shown that the best therapeutic results were obtained from the compounds in which one hydrogen atom of the SO2NH2 group was replaced by heterocyclic ring [19]. Previous studies by Obasi et al. have led to discovery of ligands and complexes with varying activities against multi-resistant bacterial strains isolated under clinical conditions and cultured species using agar-well diffusion method [20][21][22]. Metal complexes of sulpha drugs have been reported with appreciable biological activities [23][24][25][26][27][28]. Recently, there have been several reports on neodymium(III) and thallium(III) complexes [29][30][31][32][33][34][35][36][37]. Mimouni et al., 2014 [38] have synthesized, characterized, and studied the antibacterial, antifungal and antitubercular activities of thallium complexes of monensin and lasalocid. Their study revealed that remarkable bioactivity against different pathogens were achieved and confirmed that the compounds could very likely be used without great risk of toxicity in diverse pharmaceutical applications. In addition, the crystal structures of thallium salt of Grisorixin and antibiotic 6016 thallium salt have been reported [39,40]. In view of the need for a new generation of antibiotics that would cause fewer side effects, we designed a new class of inhibitors namely: N-(benzothiazol-2-yl)-4-chlorobenzenesulphonamide (NBTCS) and its neodymium(III), and thallium(III) complexes. Their in vitro antibacterial activities against Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa were also investigated.

Results and Discussion
The reaction of 2-aminobenzothiazole with 4-chlorobenzenesulphonylchloride yielded N-(benzothiazol-2-yl)-4-chlorobenzenesulphonamide (NBTCS) as shown in Scheme 1. The reaction of Nd(NO3)3·5H2O and C6H9O6Tl with NBTCS yielded [Nd(NBTCS)2(H2O)2]NO3 and [Tl(NBTCS)2]CH3COO, respectively. The ligand and complexes are air stable and have high melting points. They are soluble in ethanol, methanol, acetic acid and DMSO. The analytical data of NBTCS and its complexes are shown in Table 1. The elemental analysis of the NBTCS and its complexes show that the amount of carbon, hydrogen, nitrogen and sulphur (CHNS) are close to the experimentally determined values. The values of molar conductance of the complexes in DMSO at room temperature were found to be 72 Ω −1 ·cm 2 ·mol −1 and 88 Ω −1 ·cm 2 ·mol −1 for the Nd(III) and Tl(III) complexes, respectively. These values indicate 1:1 electrolytic nature of the complexes [41]. The ligand was found to be non-electrolyte with a molar conductance value of 15.6 Ω −1 ·cm 2 ·mol −1 .

Results and Discussion
The reaction of 2-aminobenzothiazole with 4-chlorobenzenesulphonylchloride yielded  Table 1. The elemental analysis of the NBTCS and its complexes show that the amount of carbon, hydrogen, nitrogen and sulphur (CHNS) are close to the experimentally determined values. The values of molar conductance of the complexes in DMSO at room temperature were found to be 72 Ω −1 ·cm 2 ·mol −1 and 88 Ω −1 ·cm 2 ·mol −1 for the Nd(III) and Tl(III) complexes, respectively. These values indicate 1:1 electrolytic nature of the complexes [41]. The ligand was found to be non-electrolyte with a molar conductance value of 15.6 Ω −1 ·cm 2 ·mol −1 .

Electronic Spectra
Electronic absorption spectra of the ligand and complexes in ethanol were recorded in the range 200-700 nm and the results are presented in Table 2. The electronic absorption spectra of the compounds show absorption bands between 230 and 282 nm, assigned to π-π* transitions. The band at 305 nm is attributed to n-π* transition from conjugation between the lone pair of electrons on p-orbital of nitrogen atom and conjugated π-bond of the benzene ring [42]. In the complexes, blue shifts were observed in the π-π* transition which could be as a result of removal of lone pair of electron on the electronegative atoms of the ligand upon coordination [43]. The Nd(III) complex did not contribute appreciably to the electronic spectra since for lanthanide ions f-f transitions are Larporte-forbidden and weak in nature.

Infrared Spectra
The IR spectral data of NBTCS and its complexes are displayed in Table 3. The N-H stretching vibration for NBTCS was observed as a broad band at 3407 cm −1 , this can be seen in Figure 2. However, in Nd(III) and Tl(III) complexes, this band disappeared. This suggests that the N-H was deprotonated prior to complexation. The IR spectrum of Nd(III) complex as shown in Figure 3 has a broad band at 3399 cm −1 , assignable to water of hydration from the metal salt. This was further confirmed by the presence of a sharp peak at 778 cm −1 due to O-H bending vibrations. The peak observed around 3046 cm −1 in the Tl(III) complex was assigned to aromatic C-H stretching vibration. The peaks at 1545 and 1465 cm −1 in the ligand were assigned to C=N stretching vibration of benzothiazole ring. In the Nd(III) complex, these shifted to 1589 and 1410 cm −1 while in the Tl(III) complex a single peak at 1548 cm −1 was obtained. This suggest that the C=N of benzothiazole was involved in the coordination [21,29]. This was further supported by emergence of M-N bands between 392 and 420 cm −1 . The medium peaks observed between 1154 and 1120 cm −1 in the compounds were assigned to SO2 stretching vibration. The observed Scheme 1. Synthesis of N-(benzothiazol-2-yl)-4-chlorobenzenesulphonamide.

Electronic Spectra
Electronic absorption spectra of the ligand and complexes in ethanol were recorded in the range 200-700 nm and the results are presented in Table 2. The electronic absorption spectra of the compounds show absorption bands between 230 and 282 nm, assigned to π-π* transitions. The band at 305 nm is attributed to n-π* transition from conjugation between the lone pair of electrons on p-orbital of nitrogen atom and conjugated π-bond of the benzene ring [42]. In the complexes, blue shifts were observed in the π-π* transition which could be as a result of removal of lone pair of electron on the electronegative atoms of the ligand upon coordination [43]. The Nd(III) complex did not contribute appreciably to the electronic spectra since for lanthanide ions f-f transitions are Larporte-forbidden and weak in nature.

Infrared Spectra
The IR spectral data of NBTCS and its complexes are displayed in Table 3. The N-H stretching vibration for NBTCS was observed as a broad band at 3407 cm −1 , this can be seen in Figure 2. However, in Nd(III) and Tl(III) complexes, this band disappeared. This suggests that the N-H was deprotonated prior to complexation. The IR spectrum of Nd(III) complex as shown in Figure 3 has a broad band at 3399 cm −1 , assignable to water of hydration from the metal salt. This was further confirmed by the presence of a sharp peak at 778 cm −1 due to O-H bending vibrations. The peak observed around 3046 cm −1 in the Tl(III) complex was assigned to aromatic C-H stretching vibration. The peaks at 1545 and 1465 cm −1 in the ligand were assigned to C=N stretching vibration of benzothiazole ring. In the Nd(III) complex, these shifted to 1589 and 1410 cm −1 while in the Tl(III) complex a single peak at 1548 cm −1 was obtained. This suggest that the C=N of benzothiazole was involved in the coordination [21,29]. This was further supported by emergence of M-N bands between 392 and 420 cm −1 . The medium peaks observed between 1154 and 1120 cm −1 in the compounds were assigned to SO 2 stretching vibration. The observed decrease in wavenumber of the complexes up to 34 cm −1 suggests coordination through SO 2 group. Similar observation has been made in the literature [44]. The Nd(III) complex showed new band at 1349 cm −1 due to ionic nitrate [45]. A medium band assigned to M-O stretch was observed in the Nd(III) complex at 621 cm −1 . The medium bands at 953, 827, 750 and 845 cm −1 in the compounds were assigned to C-H bending vibration of substituted benzene ring [46]. The spectra of the compounds are in the Supplementary Materials. Table 3. Infrared spectral data for NBTCS and its complexes. decrease in wavenumber of the complexes up to 34 cm −1 suggests coordination through SO2 group. Similar observation has been made in the literature [44]. The Nd(III) complex showed new band at 1349 cm −1 due to ionic nitrate [45]. A medium band assigned to M-O stretch was observed in the Nd(III) complex at 621 cm −1 . The medium bands at 953, 827, 750 and 845 cm −1 in the compounds were assigned to C-H bending vibration of substituted benzene ring [46]. The spectra of the compounds are in the Supplementary Materials. Table 3. Infrared spectral data for NBTCS and its complexes.

1 H-NMR and 13 C-NMR Spectra
In the ligand, the peaks obtained in the range 7.20-7.90 ppm are assigned to phenyl and benzothiazole protons. This appeared as a complex multiplet hence separate assignment could not be made. A single peak at 9.35 ppm is also assigned to benzothiazole protons. However, in the complexes, the peaks are clearly separated. In  decrease in wavenumber of the complexes up to 34 cm −1 suggests coordination through SO2 group. Similar observation has been made in the literature [44]. The Nd(III) complex showed new band at 1349 cm −1 due to ionic nitrate [45]. A medium band assigned to M-O stretch was observed in the Nd(III) complex at 621 cm −1 . The medium bands at 953, 827, 750 and 845 cm −1 in the compounds were assigned to C-H bending vibration of substituted benzene ring [46]. The spectra of the compounds are in the Supplementary Materials. Table 3. Infrared spectral data for NBTCS and its complexes.

1 H-NMR and 13 C-NMR Spectra
In the ligand, the peaks obtained in the range 7.20-7.90 ppm are assigned to phenyl and benzothiazole protons. This appeared as a complex multiplet hence separate assignment could not be made. A single peak at 9.35 ppm is also assigned to benzothiazole protons. However, in the complexes, the peaks are clearly separated. In

1 H-NMR and 13 C-NMR Spectra
In the ligand, the peaks obtained in the range 7.20-7.90 ppm are assigned to phenyl and benzothiazole protons. This appeared as a complex multiplet hence separate assignment could not be made. A single peak at 9.35 ppm is also assigned to benzothiazole protons. However, in the complexes, the peaks are clearly separated. In [Nd(NBTCS) 2 [21,22,29,44,47]. The chemical shift due to the N-H proton is observed at 13.30 ppm for the ligand but disappeared in the metal complexes indicating its replacement by metal ions. In Tl(III) complex, peaks at 3.34 ppm (3H, s) are assigned to CH 3 protons of acetate [22]. The spectra of all the compounds showed a multiplet centered at 2.50 ppm due to DMSO [46]. Figure 4 gives the structure of the ligand showing carbon numbering. 13 C-NMR spectrum of the ligand as shown in Figure 5 has a peak at 115.80 ppm attributed to benzothiazole ring carbon (C1). Peaks assigned to benzothiazole ring carbon (C2) appear at 126.70 ppm. Peaks at 139.0 and 140.0 ppm are assigned to benzothiazole ring carbon (C3) and (C4) respectively. Peak at 170.10 ppm is attributed to benzothiazole ring carbon (C5). Peaks at 132.10 and 143.60 ppm are assigned to phenyl ring carbon (C6) and (C9) respectively. The increase in chemical shift of C6 and C9 are due to increase in the electronegativity of the atoms attached to them. C9 shows a higher value than C6 because chlorine which is attached to it is more electronegative than sulphur which is attached to C6. Peaks assignable to phenyl ring carbon (C7) and (C8) are observed at 130.30 and 130.60 ppm respectively. Similar observations have been made in literature [21,22,29,44]. The 13 C-NMR of the complexes show none of the peaks except for the solvent peak at 40.0 ppm. The spectra of the compounds are in the Supplementary Materials. literature [21,22,29,44,47]. The chemical shift due to the N-H proton is observed at 13.30 ppm for the ligand but disappeared in the metal complexes indicating its replacement by metal ions. In Tl(III) complex, peaks at 3.34 ppm (3H, s) are assigned to CH3 protons of acetate [22]. The spectra of all the compounds showed a multiplet centered at 2.50 ppm due to DMSO [46]. Figure 4 gives the structure of the ligand showing carbon numbering. 13 C-NMR spectrum of the ligand as shown in Figure 5 has a peak at 115.80 ppm attributed to benzothiazole ring carbon (C1). Peaks assigned to benzothiazole ring carbon (C2) appear at 126.70 ppm. Peaks at 139.0 and 140.0 ppm are assigned to benzothiazole ring carbon (C3) and (C4) respectively. Peak at 170.10 ppm is attributed to benzothiazole ring carbon (C5). Peaks at 132.10 and 143.60 ppm are assigned to phenyl ring carbon (C6) and (C9) respectively. The increase in chemical shift of C6 and C9 are due to increase in the electronegativity of the atoms attached to them. C9 shows a higher value than C6 because chlorine which is attached to it is more electronegative than sulphur which is attached to C6. Peaks assignable to phenyl ring carbon (C7) and (C8) are observed at 130.30 and 130.60 ppm respectively. Similar observations have been made in literature [21,22,29,44]. The 13   Based on the spectral results, coordination numbers of eight and six were proposed for Nd(III) and Tl(III) complexes, respectively, as shown in Figure 6.  literature [21,22,29,44,47]. The chemical shift due to the N-H proton is observed at 13.30 ppm for the ligand but disappeared in the metal complexes indicating its replacement by metal ions. In Tl(III) complex, peaks at 3.34 ppm (3H, s) are assigned to CH3 protons of acetate [22]. The spectra of all the compounds showed a multiplet centered at 2.50 ppm due to DMSO [46]. Figure 4 gives the structure of the ligand showing carbon numbering. 13 C-NMR spectrum of the ligand as shown in Figure 5 has a peak at 115.80 ppm attributed to benzothiazole ring carbon (C1). Peaks assigned to benzothiazole ring carbon (C2) appear at 126.70 ppm. Peaks at 139.0 and 140.0 ppm are assigned to benzothiazole ring carbon (C3) and (C4) respectively. Peak at 170.10 ppm is attributed to benzothiazole ring carbon (C5). Peaks at 132.10 and 143.60 ppm are assigned to phenyl ring carbon (C6) and (C9) respectively. The increase in chemical shift of C6 and C9 are due to increase in the electronegativity of the atoms attached to them. C9 shows a higher value than C6 because chlorine which is attached to it is more electronegative than sulphur which is attached to C6. Peaks assignable to phenyl ring carbon (C7) and (C8) are observed at 130.30 and 130.60 ppm respectively. Similar observations have been made in literature [21,22,29,44]. The 13   Based on the spectral results, coordination numbers of eight and six were proposed for Nd(III) and Tl(III) complexes, respectively, as shown in Figure 6. Based on the spectral results, coordination numbers of eight and six were proposed for Nd(III) and Tl(III) complexes, respectively, as shown in Figure 6.

Antibacterial Activity
The ligand and its complexes were screened in vitro for their antibacterial activity against multiresistant bacterial strains isolated under clinical conditions namely: Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa. The antibacterial activities of the compounds were determined using the agar well diffusion method [48]. The inhibitory zone diameter (IZD) and minimum inhibition concentration (MIC) in μg/mL of the compounds were determined. Co-trimoxazole, ciprofloxacin and gentamicin were used as positive control. The structure of these drugs are shown in Figures 7-9 respectively. Gentamicin belongs to aminoglycosides and their mechanism of action is by inhibition of protein synthesis by preventing the synthesis of nucleic acids (DNA replication or RNA synthesis), thereby blocking transcription. Ciprofloxacin belongs to quinolones and inhibit bacteria growth by preventing DNA synthesis before mitosis [49]. Co-trimoxazole is a sulphonamide, known to prevent the growth of microorganisms by inhibiting folic acid production. Co-trimoxazole contains a fixed combination of sulphamethoxazole and trimethoprim.

Antibacterial Activity
The ligand and its complexes were screened in vitro for their antibacterial activity against multi-resistant bacterial strains isolated under clinical conditions namely: Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa. The antibacterial activities of the compounds were determined using the agar well diffusion method [48]. The inhibitory zone diameter (IZD) and minimum inhibition concentration (MIC) in µg/mL of the compounds were determined. Co-trimoxazole, ciprofloxacin and gentamicin were used as positive control. The structure of these drugs are shown in Figures 7-9 respectively. Gentamicin belongs to aminoglycosides and their mechanism of action is by inhibition of protein synthesis by preventing the synthesis of nucleic acids (DNA replication or RNA synthesis), thereby blocking transcription. Ciprofloxacin belongs to quinolones and inhibit bacteria growth by preventing DNA synthesis before mitosis [49]. Co-trimoxazole is a sulphonamide, known to prevent the growth of microorganisms by inhibiting folic acid production. Co-trimoxazole contains a fixed combination of sulphamethoxazole and trimethoprim.

Antibacterial Activity
The ligand and its complexes were screened in vitro for their antibacterial activity against multiresistant bacterial strains isolated under clinical conditions namely: Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa. The antibacterial activities of the compounds were determined using the agar well diffusion method [48]. The inhibitory zone diameter (IZD) and minimum inhibition concentration (MIC) in μg/mL of the compounds were determined. Co-trimoxazole, ciprofloxacin and gentamicin were used as positive control. The structure of these drugs are shown in Figures 7-9 respectively. Gentamicin belongs to aminoglycosides and their mechanism of action is by inhibition of protein synthesis by preventing the synthesis of nucleic acids (DNA replication or RNA synthesis), thereby blocking transcription. Ciprofloxacin belongs to quinolones and inhibit bacteria growth by preventing DNA synthesis before mitosis [49]. Co-trimoxazole is a sulphonamide, known to prevent the growth of microorganisms by inhibiting folic acid production. Co-trimoxazole contains a fixed combination of sulphamethoxazole and trimethoprim.

Antibacterial Activity
The ligand and its complexes were screened in vitro for their antibacterial activity against multiresistant bacterial strains isolated under clinical conditions namely: Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa. The antibacterial activities of the compounds were determined using the agar well diffusion method [48]. The inhibitory zone diameter (IZD) and minimum inhibition concentration (MIC) in μg/mL of the compounds were determined. Co-trimoxazole, ciprofloxacin and gentamicin were used as positive control. The structure of these drugs are shown in Figures 7-9 respectively. Gentamicin belongs to aminoglycosides and their mechanism of action is by inhibition of protein synthesis by preventing the synthesis of nucleic acids (DNA replication or RNA synthesis), thereby blocking transcription. Ciprofloxacin belongs to quinolones and inhibit bacteria growth by preventing DNA synthesis before mitosis [49]. Co-trimoxazole is a sulphonamide, known to prevent the growth of microorganisms by inhibiting folic acid production. Co-trimoxazole contains a fixed combination of sulphamethoxazole and trimethoprim.    Figure 9. Structure of gentamicin.
The result of the IZD (Table 4) shows that the metal complexes exhibit higher antibacterial activity against the microorganisms relative to the ligand. It was also observed that the ligand did not inhibit the growth of S. aureus and P. aeruginosa. Likewise, the thallium complex had no effect on P. aeruginosa. The increase in antibacterial activity of the metal chelates might be due to the effect of the metal ion on the normal cell process. Chelation reduces the polarity of the metal ion because of partial sharing of its positive charge with donor groups and the π-electron delocalization over the whole chelate ring. Such chelation could enhance the lipophilic character of the central metal atom, which subsequently favours its permeation through the lipid layers of the cell membrane [50]. From the MIC values (Table 5), it is observed that the synthesized compounds are more active against Escherichia coli strains 6 and 13 relative to the standard drugs, since the lower the MIC value, the more effective the antibacterial activity of the drug. However, Ciprofloxacin has a higher antibacterial activity against S. aureus and Proteus species compared to the compounds. It can also be inferred from Table 5 that the synthesized compounds have better antibacterial activity against the microorganisms screened relative to Gentamicin and Co-trimoxazole.   The result of the IZD (Table 4) shows that the metal complexes exhibit higher antibacterial activity against the microorganisms relative to the ligand. It was also observed that the ligand did not inhibit the growth of S. aureus and P. aeruginosa. Likewise, the thallium complex had no effect on P. aeruginosa. The increase in antibacterial activity of the metal chelates might be due to the effect of the metal ion on the normal cell process. Chelation reduces the polarity of the metal ion because of partial sharing of its positive charge with donor groups and the π-electron delocalization over the whole chelate ring. Such chelation could enhance the lipophilic character of the central metal atom, which subsequently favours its permeation through the lipid layers of the cell membrane [50]. From the MIC values (Table 5), it is observed that the synthesized compounds are more active against Escherichia coli strains 6 and 13 relative to the standard drugs, since the lower the MIC value, the more effective the antibacterial activity of the drug. However, Ciprofloxacin has a higher antibacterial activity against S. aureus and Proteus species compared to the compounds. It can also be inferred from Table 5 that the synthesized compounds have better antibacterial activity against the microorganisms screened relative to Gentamicin and Co-trimoxazole.

Materials
All the reagents and solvents used were of analytical grade and were used as supplied unless otherwise stated. The melting point of the ligand and the complexes were determined using a Gallenkamp melting point apparatus (Weiss Technik, Loughborough, UK) and were uncorrected. Electronic spectra (in ethanol) were recorded on a UV-2500PC series spectrophotometer (SHIMADZU, Tokyo, Japan). The FTIR spectra were performed using FTIR-8400S Spectrophotometer (SHIMADZU), in the range 4500-200 cm −1 using KBr. The 1 H-and 13 C-NMR of the ligand were recorded on Bruker Spectrospin 250(Bruker, Billerica, MA, USA) using DMSO while the elemental analysis was done using Euro EA 3000 Dual CHNS Analyzer (Eurovector S.P.A, Zurich, Switzerland) both at the Department of Chemistry, University of Mauritius.

Antibacterial Activity
The inhibitory activity of the ligand and its metal complexes were carried out on the following microorganisms: Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa. The bacteria strains used were isolated from clinical conditions. The method used was the agar well-diffusion Technique [46]. Mueller-Hinton agar plates were inoculated with 0.1 mL of 3 h broth culture of the test microorganisms. Using a cork borer, wells (7 mm in diameter and 2.5 mm deep) were bored into the inoculated agar. Fresh solutions (1000 µg/mL) of all the synthesized compounds were prepared in DMSO and 50 µL of each compound was delivered into the wells. Wells containing 1000 µg/mL of ciprofloxacin, gentamicin and co-trimoxazole in DMSO were used as positive controls. The plates were incubated at 37 • C for 24 h and assessment of antibacterial activity was based on the measurement of the diameter of inhibition zone (IZD) around the wells.
The minimum inhibitory concentrations (MIC) of the test compounds were determined using the same method. Two-fold serial dilutions of test compound were made in DMSO. The final concentration of the compounds ranged from 250 to 0.625 µg/mL. Inoculated plates were incubated at 37 • C for 24 h and observed for presence of visible growth. The minimum inhibition concentration was determined as the value of the lowest concentration that completely suppressed the growth of the microorganisms.

Conclusions
NBTCS and its neodymium(III) and thallium(III) complexes were synthesized. Based on the UV, IR and NMR spectral studies and elemental analysis, a coordination number of eight was proposed for neodymium(III) complex and six for thallium(III) complex. The antibacterial activity revealed that the synthesized compounds have better antibacterial activity against the microorganisms screened relative to gentamicin and co-trimoxazole. The low MIC values observed for NBTCS and its complexes indicate the potency of these compounds as antibacterial agents. This serves as a marker in drug design, hence these compounds should be screened for in vivo antibacterial activity and the lethal dose (LD 50 ) determined.