International Journal of Inorganic ChemistryVolume 2013 (2013), Article ID 524179, 6 pageshttp://dx.doi.org/10.1155/2013/524179

Research Article

Syntheses and Characterization of the Coordination Compounds of N-(2-hydroxymethylphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one

Dinesh Kumar,¹ Amit Kumar,² and Durga Dass³

¹Department of Chemistry, National Institute of Technology, Haryana, Kurukshetra 136119, India²Department of Chemistry, Haryana College of Technology & Management, Haryana, Kaithal 136027, India³Department of Chemistry, Shri Krishan Institute of Engineering & Technology, Haryana, Kurukshetra 136118, India

Received 26 December 2012; Accepted 7 February 2013

Academic Editor: Hakan Arslan

Copyright © 2013 Dinesh Kumar 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.

Abstract.

A dry benzene solution of the Schiff base N-(2-hydroxymethylphenyl)-3′-carboxy-2′-hydroxybenzylideneimine upon reacting with mercaptoacetic acid undergoes cyclization and forms N-(2-hydroxymethylphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one, LH₃ (I). A MeOH solution of I reacts with Co(II), Ni(II), Cd(II), Zr(OH)₂(IV), and UO₂(VI) ions and forms the monomeric coordination compounds, [M(LH)(MeOH)₃] [where M = Co(II), Ni(II)], [M′(LH)(MeOH)] [here M′ = Cd(II), UO₂(VI)] and [Zr(OH)₂(LH)(MeOH)]. The coordination compounds have been characterized on the bases of elemental analyses, molar conductance, molecular weight, spectral (IR, NMR, and reflectance) studies, and magnetic susceptibility measurements. I behaves as a dibasic tridentate OOS donor ligand in these compounds. The compounds are nonelectrolytes ( = 3.8–8.9 mho cm² mol⁻¹) in DMF. A tetrahedral structure for [Cd(LH)(MeOH)] and an octahedral structure for the remaining compounds are suggested.

1. Introduction

The chemistry of thiazolidin-4-ones is very well documented in the literature and has been studied extensively due to their versatile biological properties [1]. Thiazolidin-4-ones, a saturated form of thiazole with carbonyl group on fourth carbon [2], have biological activities like those that are antipsychotic [3], antitubercular [4], antibacterial [5], anticonvulsant [6], antifungal [7], amoebicidal [8], antioxidant [9], antibiotic [10], and so forth.

Literature survey shows that much has been reported on the syntheses and characterization [11] of a variety of thiazolidin-4-ones, but very less is known about their coordination compounds [12–14].

Metal complexes play an important role in plant and animal life due to their physicochemical and biological properties. Metal ions are involved in specific interactions with antibiotics, proteins, nucleic acids, and other biomolecules [15]. Most of the drugs have improved pharmacological properties in the form of their metal complexes. Transition metal ions play a very important role in the pharmacological action of metal-based drugs and these drugs are more effective against infectious microbes than the uncomplexed drugs [16].

These facts motivate us to explore the coordination behavior of a newly synthesized thiazolidin-4-one with some transition metal ions.

In this paper, we describe the syntheses and characterization of N-(2-hydroxymethylphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one, LH₃ (I) and its coordination compounds with Co(II), Ni(II), Cd(II), Zr(OH)₂(IV), and UO₂(VI) ions. The structure of Schiff base and thiazolidin-4-one, LH₃ (I) is shown in Figure 1.

Figure 1

2. Experimental

2.1. Materials

o-Aminobenzylalcohol [Aldrich]; nickel(II) acetate tetrahydrate, cadmium(II) acetate dihydrate, dioxouranium(VI) acetate tetrahydrate (Sarabhai); cobalt(II) acetate tetrahydrate, hexadecaaquaoctahydroxotetrazirconium(IV) chloride (BDH); methanol, ethanol, mercaptoacetic acid, dry benzene, and sodium bicarbonate (Ranbaxy) were used as supplied for the syntheses. 3-Formylsalicylic acid [17] and hexadecaaquaoctahydroxotetrazirconium(IV) acetate [18] were synthesized by the following reported procedures.

2.2. Analyses and Physical Measurements

The organic skeleton of the respective coordination compounds was decomposed by the slow heating of ~0.1 g of the latter, with conc. HNO₃. The residue was dissolved in a minimum amount of conc. HCl and the corresponding metal ions were estimated as follows: the Ni(II) contents of the respective coordination compound were estimated by complexometric titration method against standardized EDTA solution using murexide as an indicator. The Co(II) and Cd(II) contents in the respective coordination compounds were estimated by the complexometric titration method against standardized EDTA solution using xylenol orange as an indicator. The uranium content in [UO₂(LH)(MeOH)] was estimated gravimetrically as U₃O₈ after decomposing the compound with a few drops of conc. HNO₃ and then igniting the residue. The zirconium contents were estimated gravimetrically as ZrO₂ after decomposing the corresponding compound with a few drops of conc. HNO₃ and then igniting the residue. The C, H, and N contents of LH₃ and its coordination compounds were determined by CHN Eager analyzer model-300. The S and Cl contents were estimated gravimetrically as BaSO₄ and AgCl, respectively. The molecular weight measurements were carried out by the Rast method using diphenyl as the solvent [19]. The molar conductances of the coordination compounds were measured in DMF with the help of a Toshniwal conductivity bridge (CL01-02A) and a dip-type cell calibrated with KCl solutions. The IR spectra were recorded in KBr pellets (4000–400 cm⁻¹) on a Beckman 20 spectrophotometer. The reflectance spectra were recorded on a Beckmann DU spectrophotometer attached with a reflectance arrangement. The magnetic susceptibility measurements were carried out at room temperature, using Hg[Co(NCS)₄] as the standard [20]. The diamagnetic corrections were computed using Pascal’s constants. The magnetic susceptibilities were corrected for temperature-independent paramagnetism term (TIP) [20] using a value of units for Ni(II) and Co(II) ions.

2.3. Synthesis of the N-(2-hydroxymethylphenyl)-3′-carboxy-2′-hydroxybenzylide-neimine (Schiff Base)

A MeOH solution (30 mL) of o-aminobenzylalcohol (1.23 g, 10 mmol) was added to a MeOH solution (30 mL) of 3-formylsalicylic acid (1.66 g, 10 mmol) and the mixture was then refluxed for 1 h. The precipitates formed were suction filtered, washed with MeOH, and dried in vacuo at room temperature over silica gel for 24 h. Yield = 58%. The elemental analyses of the compound gave the satisfactory results.

2.4. Synthesis of N-(2-hydroxymethylphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one (I)

A dry benzene solution of the Schiff base (2.71 g, 10 mmol) and mercaptoacetic acid (0.92 g, 10 mmol) were refluxed for 12 h in a water bath. The mixture was cooled to room temperature and then was washed with 10% sodium bicarbonate solution. The benzene layer was separated using a separating funnel. The partial evaporation of the benzene layer gave a solid product, which was filtered, washed with petroleum ether and recrystallized from petroleum ether. The compounds were dried as mentioned above. Yield = 14%. Anal: (I, C₁₇H₁₅NO₅S) (obsd: C, 58.91%; H, 4.37%; N, 4.12%; S, 9.11%. calc.: C, 59.13%; H, 4.35%; N, 4.06%; S, 9.28%); IR bands (KBr): 2860 cm⁻¹ [(O–H)(intramolecular H-bonding)], 1710 cm⁻¹ [(C=O)(thiazolidinone ring)], 1675 cm⁻¹ [(C=O)(carboxylic)], 1570 cm⁻¹ [(C–N)(thiazolidinone ring)], 1520 cm⁻¹ [(C–O)(phenolic)], 1225 cm⁻¹ [(C–O)(alcoholic)], and 830 cm⁻¹ [(C–S)(thiazolidinone ring)].

2.5. Syntheses of Coordination Compounds of I

A MeOH solution (30–50 mL) of the appropriate metal salt (10 mmol) was added to a MeOH solution (50 mL) of I (3.45 g, 10 mmol) and the mixture was then refluxed for 3-4 h. The solid products formed were suction filtered, washed with MeOH and recrystallized from MeOH and were then dried as mentioned above. Yield = 50–75%.

3. Results and Discussion

A dry benzene solution of the Schiff base reacts with mercaptoacetic acid and forms N-(2-hydroxymethylphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one, LH₃ (I). The reaction of I with appropriate metal salt in 1 : 1 molar ratio in MeOH produces the coordination compounds, [M(LH)(MeOH)₃] [where M = Co(II), Ni(II)], [M′(LH)(MeOH)] [where M′ = Cd(II), UO₂(VI)], and [Zr(OH)₂(LH)(MeOH)]. The formations of I from the Schiff base and the coordination compounds of I take place according to Schemes 1 and 2.

Scheme 1: Preparative scheme of LH₃ (I).

Scheme 2: Preparative scheme of coordination compounds of LH₃ (I).

The coordination compounds are air-stable at room temperature. They are insoluble in H₂O, partially soluble in MeOH, EtOH, and completely soluble in DMSO and DMF. Their molar conductance measurements = 3.8–8.9 mho cm² mol⁻¹) in DMF indicate their nonelectrolytic nature. The analytical data of I and its coordination compounds are presented in Table 1.

Table 1: Analytical, molar conductance (), and molecular weight data of I and its coordination compounds.

Compound
Mol. formula
(mho cm²Mol⁻¹)
Mol. wt obsd (calcd)
Obsd (calcd)%

M
C
H
N
S

LH₃ (I)
C₁₇H₁₅NO₅S
—
345a (345.0)
—
58.91(59.13)
4.37(4.35)
4.12(4.06)
9.11(9.28)

Co(LH)(MeOH)₃
CoC₂₀H₂₅NO₈S
4.8
511.6b (497.9)
11.64(11.83)
48.37(48.20)
5.10(5.02)
2.74(2.81)
6.32(6.43)

Ni(LH)(MeOH)₃
NiC₂₀H₂₅NO₈S
3.8
481.3b (497.7)
11.56(11.79)
48.17(48.22)
5.17(5.02)
2.72(2.81)
6.28(6.43)

Cd(LH)(MeOH)
CdC₁₈H₁₇NO₆S
7.7
511.2b (487.4)
23.17(23.06)
44.50(44.32)
3.53(3.49)
2.72(2.87)
6.49(6.56)

Zr(OH)₂(LH)(MeOH)
ZrC₁₈H₁₉NO₈S
8.9
517.2b (500.2)
18.06(18.23)
43.34(43.18)
3.74(3.80)
2.85(2.80)
6.32(6.40)

UO₂(LH)(MeOH)
UC₁₈H₁₇NO₈S
6.8
659.5 b (645.0)
36.67(36.90)
33.24(33.49)
2.45(2.64)
2.05(2.17)
4.85(4.96)

aMass spectral data. bRast method data.

3.1. Infrared Spectral Studies

The infrared spectra of I and its coordination compounds were recorded in KBr and the prominent peaks (in cm⁻¹) are shown in Table 2. The Schiff base exhibits the (C=N)(azomethine) stretch at 1640 cm⁻¹. This band disappears in I and a new band appears at 1570 cm⁻¹ due to the (C–N)(thiazolidinone ring) stretch [21] indicating the conversion of the Schiff base into I. The formation of I is further supported by the appearance of a new band at 830 cm⁻¹ due to the (C–S)(thiazolidinone ring) stretch [22]. A negative shift of 15–35 cm⁻¹ of the (C–S)(thiazolidinone ring) stretch in the coordination compounds indicates the involvement of the S atom of the thiazolidinone moiety in coordination [14]. I shows the (C=O)(thiazolidinone ring) stretch [23] at 1710 cm⁻¹. This band remains unchanged in the coordination compounds indicating the noninvolvement of O atom in the coordination. The (C–O)(alcoholic) stretch [24] of I occurs at 1225 cm⁻¹ which remains unchanged in the complexes. I exhibits a strong band at 2860 cm⁻¹ due to the intramolecular H-bonded OH group of phenolic and/or carboxylic acid moieties [25]. This band disappears in the coordination compounds indicating the breakdown of H-bonding and subsequent deprotonation of the OH group followed by the involvement of phenolic and carboxylic acid O atoms in coordination. The presence of a broadband at ~3400  cm⁻¹ due to (O–H)(MeOH) and the decrease of (C–O)(MeOH) stretch from 1034 cm⁻¹ to lower energy by 45–60 cm⁻¹ in the coordination compounds of I indicate the involvement of the O atom of MeOH in coordination [26]. The appearance of two new bands between 1560–1572 cm⁻¹, (COO) and 1337–1358 cm⁻¹, (COO) stretches indicates the presence of the coordinated carboxylate group in the coordination compounds. The energy difference (Δ = 213–225 cm⁻¹) between these stretches is >210 cm⁻¹ which indicates the monodentate nature of the carboxylate moiety [27]. The (C–O) stretch of I occurs at 1520 cm⁻¹. This band shifts to higher energy by 6–10 cm⁻¹ in the coordination compounds indicating the involvement of phenolic O atom of 3-formylsalicylic acid moiety in coordination [26]. The absence of a band between 835–955 cm⁻¹ due to the (Zr=O) stretch [28] in the present Zr(OH)₂(IV) compound suggests its formulation as [Zr(OH)₂(LH)(MeOH)] and not as [ZrO(H₂O)(LH)(MeOH)] [29]. The presence of a broadband at 3440 cm⁻¹ due to (OH) stretch and the appearance of a new medium intense band at 1135 cm⁻¹ due to the (Zr–OH) bending mode [29] also support the proposed structure of the present Zr(OH)₂(IV) compound. [UO₂(LH)(MeOH)] exhibits the (O=U=O) stretch at 898 cm⁻¹ and this band occurs in the usual range (870–950 cm⁻¹) observed for the majority of trans-UO₂(VI) compounds [30]. The force constant and U–O bond length in the present dioxouranium(VI) compound are 6.70 mdyn/Å and 1.74 Å, respectively. These values are in the expected range (6.58–7.03 mdyn/Å and 1.60–1.92 Å) reported for the majority of UO₂(VI) compounds [29]. The new nonligand bands in the present coordination compounds in the low-frequency region are assigned to the (M–O) (550–570 cm⁻¹) and the (M–S) (345–375 cm⁻¹) and these bands [31] are in the expected order of increasing energy: (M–S) < (M–O).

Table 2: IR, reflectance spectral data (cm⁻¹), and magnetic moments of the coordination compounds of I.

Compound
(COO)
(COO)
(C–O)(phenolic)
(C–S)
(C–O)(MeOH)

Mag. moment (B. M.)

LH₃ (I)
—
—
1520
830
—
—
Diamagnetic

Co(LH)(MeOH)₃
1572
1358
1530
795
986
8700, 13000, 18550
4.75

Ni(LH)(MeOH)₃
1572
1352
1526
805
989
8980, 15980, 24900
3.14

Cd(LH)(MeOH)
1560
1347
1530
810
984
—
Diamagnetic

Zr(OH)₂(LH)(MeOH)
1562
1337
1530
815
974
—
Diamagnetic

UO₂(LH)(MeOH)
1567
1349
1529
810
980
—
Diamagnetic

3.2. NMR Spectral Studies

The NMR spectra of I and its coordination compounds were recorded in DMSO-. The chemical shifts () are expressed in ppm downfield from TMS. The prominent resonance signals of these compounds were compared with the reported peaks [32]. I exhibits a singlet at 17.5 ppm due to the carboxylic proton, a sharp singlet at 13.60 ppm due to phenolic proton, a singlet at 2.35 ppm due to alcoholic proton, multiplets due to methylene protons at 4.70–4.79 ppm, and multiplets between 7.34 and 7.50 ppm due to the aromatic protons. The occurrence of the resonance signal at the same frequency ( 2.35 ppm) due to alcoholic proton (CH₂OH) indicates the noninvolvement of the alcoholic group in coordination. The absence of the signal at 17.5 ppm due to the COOH proton in the coordination compounds indicates the deprotonation of the COOH group, followed by the involvement of its O atom in coordination. The absence of the resonance signal at 13.60 ppm due to the phenolic proton in the coordination compounds indicates the deprotonation of the phenolic OH group followed by its involvement in coordination [26]. The appearance of resonance signals at 2.81–2.85 ppm due to alcoholic proton and at 3.0–3.1 ppm due to methyl protons in the coordination compounds supports the presence of MeOH in these compounds.

3.3. Reflectance Spectral Studies

The presence of three bands at 8700, 13000, and 18550 cm⁻¹ due to →, → , and → transitions, respectively, suggests an octahedral arrangement of I around Co(II) ions in [Co(LH)(MeOH)₃] [33]. The value of / (2.13) lies in the range 2.00–2.80, reported for most of the octahedral Co(II) compounds [33]. The spectral parameters [33–35] for [Co(LH)(MeOH)₃] are  cm⁻¹,  cm⁻¹, , , and CFSE = −93.57 kJ mol⁻¹. Reduction of Racah parameter from 971 cm⁻¹ (free ion value) to 729 cm⁻¹ and the value (25%) indicate the covalent nature of the compound and strong field nature of I [20]. [Ni(LH)(MeOH)₃] shows three bands at 8980, 15980, and 24900 cm⁻¹ due to → , → , and → transitions, respectively, in an octahedral symmetry [33]. The value of / is 1.78 which lies in the usual range (1.60–1.82), reported for the majority of octahedral Ni(II) compounds. The spectral parameters [34, 35] for [Ni(LH)(MeOH)₃] are  cm⁻¹,  cm⁻¹, , , and CFSE = −128.75 kJ mole⁻¹. The reduction of the Racah parameter from the free ion value (1030 cm⁻¹) to 843 cm⁻¹ and the value (18%) are indicative of the presence of covalent nature of the compound and the strong field nature of the tridentate ligand (I) [20]. For a given ligand and given stereochemistry, the covalent character of the corresponding Co(II) and Ni(II) coordination compounds is comparable since Co(II) and Ni(II) occupy the adjacent positions in the nephelauxetic metal ion series (i.e., Co(II) ~ Ni(II)) [20]. In the present Co(II) and Ni(II) coordination compounds, the values are quite comparable: [Co(LH)(MeOH)₃]: 25%; [Ni(LH)(MeOH)₃]: 18%. For a given ligand and given stereochemistry, the spectrochemical series of metal ions on the basis of increasing 10 values is Ni(II) < Co(II). Our calculated 10 values indicate that the 10 values are in the expected order: Ni(II) < Co(II). The greater negative CFSE value (−128.75 kJ mol⁻¹) for [Ni(LH)(MeOH)₃] in comparison to that of [Co(LH)(MeOH)₃] (CFSE = −93.57 kJ mol⁻¹) is as expected [35].

3.4. Magnetic Measurements

The room temperature magnetic moments of the coordination compounds of I are presented in Table 2. The magnetic moments of [Co(LH)(MeOH)₃] and [Ni(LH)(MeOH)₃] are 4.75 and 3.14 B.M., respectively. These values are indicative of the magnetically dilute high-spin octahedral coordination compounds of Co(II) and Ni(II) ions [36]. The coordination compounds of other ions are diamagnetic.

Thus, on the basis of analytical data, valence requirements, molecular weight, spectral and the magnetic studies, it is proposed that I behaves as a dibasic tridentate OOS donor ligand in the tetrahedral compound, [Cd (LH)(MeOH)] (II) and in the octahedral compounds, [M(LH)(MeOH)₃] [where M = Co(II), Ni(II)] (III), [Zr(OH)₂(LH)(MeOH)] (IV) and for [UO₂(LH)(MeOH)] (V), as shown in Figure 2.

Figure 2

References

M. Abhinit, M. Ghodke, and N. A. Pratima, “Exploring potential of 4-thiazolidinone: a brief review,” International Journal of Pharmacy and Pharmaceutical Sciences, no. 1, pp. 47–64, 2009.

D. A. Horton, G. T. Bourne, and M. L. Smyth, “The combinatorial synthesis of bicyclic privileged structures or privileged substructures,” Chemical Reviews, vol. 103, no. 3, pp. 893–930, 2003.

N. J. Hrib, J. G. Jurcak, and J. G. Bregna, “3[4-[1-(6-Fluorobenzo[b]thiophen-3-yl)-4-piperazinyl]butyl]-2,5,5-trimethyl-4-thiazolidinone: a new atypical antipsychotic agent for the treatment of schizophrenia,” Journal of Medicinal Chemistry, vol. 35, no. 14, pp. 2712–2715, 1992.

A. Solanki and K. Kishore, “Synthesis and antitubercular activity of some 4-thiazolidinones,” Asian Journal of Chemistry, vol. 6, no. 3, p. 177, 1994.

B. P. Choudhari and V. V. Mulwad, “Synthesis of 1-(6-methylbenzofuran-2-yl)-3-aryl/[4-(β-substitutedethoxy)phenyl]propenones as marked anti-microbial agents,” Indian Journal of Chemistry, vol. 44, p. 1074, 2005.

N. J. Gaikwad and S. B. Agrawal, “Substituted 4-thiazolidinones as anticonvulsants VII,” Indian Drugs, vol. 34, no. 9, pp. 542–543, 1997.

P. V. Patel and K. R. Desai, “Synthesis and anti-bacterial activity of new isoxazolines derivatives of 3,5-diaryl isoxazolines,” Oriental Journal of Chemistry, vol. 18, no. 3, p. 311, 2002.

N. C. Desai, B. R. Parekh, and K. A. Thaker, “Preparation of some important medicinal compounds. Thiosemicarbazones, thiadiazolines, 4-thiazolidinones and 5-arylidine derivatives as antibacterial and tuberculostatic agents,” Journal of the Indian Chemical Society, vol. 64, no. 8, pp. 491–493, 1987.

T. Kato, T. Ozaki, K. Tamura, Y. Suzuki, M. Akima, and N. Ohi, “Novel calcium antagonists with both calcium overload inhibition and antioxidant activity. 2. Structure-activity relationships of thiazolidinone derivatives,” Journal of Medicinal Chemistry, vol. 42, no. 16, pp. 3134–3146, 1999.

V. S. Ingle, A. R. Sawale, R. D. Ingle, and R. A. Mane, “Synthesis of new 4-thiazolidinones bearing potentially active heteryl moities,” Indian Journal of Chemistry B, vol. 40, no. 2, pp. 124–128, 2001.

S. B. Junne, S. S. Wadje, M. M. V. Baig, and Y. B. Vibhute, “Novel heterocyclic schiff bases, 4-thiazolidinones and 2-azetidinones possessing antibacterial and antifungal activity,” International Journal of Chemical Sciences, vol. 5, p. 2093, 2007.

D. Kumar and A. Kumar, “Syntheses, magnetic and spectral studies on the coordination compounds of the polystyrene anchored thiazolidin-4-one,” E-Journal of Chemistry, vol. 9, no. 4, pp. 2532–2539, 2012.

A. M. Rehab Al-Hasani, M. M. Sinan Al-byatti, and M. S. Sarab Al Azawi, “Synthesis, structural and biological studies of /3-(1, 3- benzothiazol-2-yl) - /4H- spiro[indole2,3-[1,3]thiazolidine]- 2,/4(1H) dion with Cr (III), Mn (II), Co (II), Ni (II), Cu (II), and Zn (II) ions,” Engineering & Technology Journal, vol. 29, no. 15, pp. 3067–3078, 2011.

D. Kumar, A. Kumar, and J. Sharma, “Physico-chemical studies on the coordination compounds of thiazolidin-4-one,” Journal of Chemistry, vol. 2013, Article ID 870325, 7 pages, 2013.

J. R. Anacona and I. Rodriguez, “Synthesis and antibacterial activity of cephalexin metal complexes,” Journal of Coordination Chemistry, vol. 57, no. 15, pp. 1263–1269, 2004.

J. R. Anacona and J. Estacio, “Synthesis and antibacterial activity of cefixime metal complexes,” Transition Metal Chemistry, vol. 31, no. 2, pp. 227–231, 2006.

J. C. Duff and E. J. Bills, “The solubility of picric acid in mixed solvents. Part II. Benzene-alcohol mixtures,” Journal Ofthe Chemical Society, pp. 881–884, 1932.

A. Syamal and D. Kumar, “Syntheses of new zirconium (IV) complexes with the tridentate Schiff bases derived from o-aminophenol and salicylaldehydes or 2-hydroxy-1-naphthaldehyde,” Indian Journal of Chemistry A, vol. 24, p. 62, 1985.

F. G. Mann and B. C. Saunders, Practical Organic Chemistry, Longmans, London, UK, 1961.

R. L. Dutta and A. Syamal, Elements of Magnetochemistry, Affiliated East-West Press, New Delhi, India, 2nd edition, 1993.

P. V. Patel and K. R. Desai, “Synthesis and anti-bacterial activity of new isoxazolines derivatives of 3,5-diaryl isoxazolines,” Oriental Journal of Chemistry, vol. 18, no. 3, p. 311, 2002.

D. C. Dash, A. Mahapatra, R. K. Mahapatra, S. Ghosh, and P. Naik, “Synthesis and characterization of dioxouranium(VI), thorium(IV), oxozirconium(IV) and oxovanadium(IV) complexes with 1,11-dihydroxy-1,4,5,7,8,11-hexaaza-2,3,9,10-tetramethyl-1,3,8,10-decatetraene-6- thione and their derivatives with chloroacetic acid,” Indian Journal of Chemistry, vol. 47A, pp. 1009–1013, 2008.

R. U. Roy and K. R. Desai, “Anticancer evaluation of azetidinone and thiazolidinone derivatives of quinolone,” International Journal of Chemical Sciences, vol. 3, no. 3, p. 529, 2005.

A. Syamal and O. P. Singhal, “New dioxouranium(VI)complexes with tridentate dibasic schiff bases containing ONO donor sets,” Transition Metal Chemistry, vol. 4, no. 3, pp. 179–182, 1979.

A. Syamal and D. Kumar, “New zirconium (IV) complexes with the ons donor triden tate schiff bases derived from salicyaldehyde or substituted salicylal dehydes and 2-aminobih anethiol,” Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry, vol. 14, no. 3, p. 325, 1984.

D. Kumar, A. Syamal, A. Gupta, M. Rani, and P. K. Gupta, “Role of pH on the formation of the coordination compounds with the schiff base derived from 3-formylsalicylic acid and 4-amino-2,3-dimethyl-l-phenyl-3-pyrazolin-5-one,” Journal of the Indian Chemical Society, vol. 87, no. 10, pp. 1185–1197, 2010.

J. R. Anacona and C. Toledo, “Synthesis and antibacterial activity of metal complexes of ciprofloxacin,” Transition Metal Chemistry, vol. 26, no. 1-2, pp. 228–231, 2001.

D. Kumar, A. Syamal, A. Kumar, P. K. Gupta, and D. Dass, “Syntheses and characterization of coordination compounds of N-(2-mercaptoethyl)-4-(3′-carboxy-2′-hydroxyphenyl)-2-azetidinone,” Journal of the Indian Chemical Society, vol. 87, no. 4, pp. 417–423, 2010.

D. Kumar, A. Syamal, and L. K. Sharma, “Synthesis and characterization of polystyrene-anchored monobasic bidentate schiff base and its complexes with bi-, tri-, tetra- and hexavalent metal ions,” Journal of Coordination Chemistry, vol. 61, no. 11, pp. 1788–1796, 2008.

D. Kumar, P. K. Gupta, A. Kumar, D. Dass, and A. Syamal, “Syntheses, spectroscopic, and magnetic properties of polystyrene-anchored coordination compounds of tridentate ONO donor schiff base,” Journal of Coordination Chemistry, vol. 64, no. 4, pp. 590–599, 2011.

M. R. Charasia, “Cu(II), Ni(II) and Co(II) complexes of N-phenyl-benzothiazolyl thiocarbamide,” Journal of Inorganic and Nuclear Chemistry, vol. 37, no. 6, pp. 1547–1548, 1975.

J. K. Nag, S. Pal, and C. Sinha, “Synthesis and characterization of cobalt(II), nickel(II), copper(II), palladium(II) and dioxouranium(VI) complexes of the antipyrine schiff base of 3-formylsalicylic acid,” Transition Metal Chemistry, vol. 30, no. 5, pp. 523–526, 2005.

A. B. P. Lever, Inorganic Electronic Spectroscopy, Elsevier, Amsterdam, The Netherlands, 2nd edition, 1984.

A. Syamal, D. Kumar, A. K. Singh, et al., “Syntheses and characterization of a chelating resin containing ONO donor tridentate Schiff Base and its coordination compounds with copper (II). nickel(II), cobalt(II), iron(III), zinc(II), cadmium(II), manganese(II), molybdenum(VI), zirconium(IV) and uranium(VI),” Indian Journal of Chemistry, vol. 41, no. 7, pp. 1385–1390, 2002.

J. E. Huheey, Inorganic Chemistry, Principles of Structure and Reactivity, Harper and Row Publishers, New York, NY, USA, 3rd edition, 1983.

F. A. Cotton, G. Wilkinson, C. A. Murillo, and M. Bochmann, Advanced Inorganic Chemistry, John Wiley, New York, NY, USA, 6th edition, 1999.