• Views 1,846
• Citations 0
• ePub 36
• PDF 948
`International Journal of Inorganic ChemistryVolume 2013 (2013), Article ID 281270, 9 pageshttp://dx.doi.org/10.1155/2013/281270`
Research Article

Synthesis and Characterization of Heteronuclear Copper(II)-Lanthanide(III) Complexes of N,N′-1,3-Propylenebis(Salicylaldiminato) Where Lanthanide(III) = Gd or Eu

Department of Chemistry, Manipur University, Imphal 795 003, India

Received 10 December 2012; Revised 6 April 2013; Accepted 15 April 2013

Copyright © 2013 Longjam Jaideva Singh and Rajkumar Hemakumar Singh. 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

Three complexes, namely, [Cu(salbn)] (1), [Cu(salbn)Gd(NO3)3·H2O] (2), and [Cu(salbn)Eu(NO3)3·H2O] (3) where salbn = N,N′-1,3-propylenebis (salicylaldiminato) have been synthesized and characterized by elemental analyses, ICP-AES, IR, UV, NMR, MS, EDX, powder XRD, and EPR spectroscopies. The EDX results suggest the presence of two different metal ions in heteronuclear complexes (2) and (3). The ligand(salbn), complex (1), and complex (3) crystallize in triclinic system while complex (2) crystallizes in monoclinic system. The EPR studies suggest that [Cu(salbn)] complex is tetragonally coordinated monomeric copper(II) complex with unpaired electron in the orbital and spectral features that are the characteristics of axial symmetry while complex (2) in DMF solution at liquid nitrogen temperature exhibits an anisotropic broad signal around g ~ 2.03 which may suggest a weak magnetic spin-exchange interaction between Gd(III) and Cu(II) ions. The fluorescence intensity of Eu(III) decreased markedly in the complex (3).

1. Introduction

The spectroscopic and unique properties of copper(II)-lanthanide(III) complexes have become a subject of intense research interest with coordination chemists because of their wide arrays of applications in electroluminescent devices, biomedicine, MRI, magneto magnets, and many more [15]. The coordination chemistry of lanthanide(III) ions is also increasing day by day, owing to the relevance of these compounds in basic and applied research in various fields to chemistry, material science, life science, and so forth [68]. Lanthanide complexes possessing higher stability are especially important in two different fields of research where inert complexes are potentially useful, namely, for the design of Gd(III) contrast agents for NMR imaging and for the separation of the lanthanides as a set of metals [9]. Most of the heteronuclear copper(II)-lanthanide(III) complexes have been synthesized with heterodonor ligands of N and O which are coordinated to copper and lanthanide atoms. The structural chemistry of the lanthanides is interesting as they have a strong tendency to form complexes with higher coordination numbers up to twelve. Because of their large size and their tendency to form ionic bonds rather than covalent bonds, lanthanide(III) ions may form complexes having higher coordination numbers with monodentate, simple bidentate or polydentate ligands possessing small chains [10]. The structural versatility arises from the lack of strong crystal efforts for the 4f electronic configurations as well as from the large ionic radii of these lanthanide metal ions, which change markedly with atomic number or oxidation number of the lanthanides. The chemistry of lanthanides with N,N/N,O donor ligands and their thermal properties has been intensively investigated [11]. Vey recently, Akine made a review on design of novel ion recognition systems based on salen (H2 salen = N,N′-disalicylideneethylenediamine) or related ligands [12]. These ligands are versatile and important compounds that have been widely used in coordination chemistry. In general, salen-type ligands coordinate to a transition or typical metals as a doubly form in a tetradentate fashion [13]. Heteronuclear copper(II)-lanthanide(III) complexes have attracted increasing interest because of their different coordination capabilities. Thus, heteronuclear copper(II)-lanthanide(III) compounds have commonly been synthesized with heterodonor ligands of N and O which are good building blocks for the formation of different lanthanide coordination compounds [1416].

In view of the above observations, it seemed interesting to synthesize heteronuclear copper(II)-lanthanide(III) complexes from heterodonor ligands like N,N′-1,3-propylenebis(salicylaldiminato), salbn in order to investigate the spectroscopic and their magnetic properties. In this paper, the synthesis and characterization of [Cu(salbn)] (1), [Cu(salbn)Gd(NO3)3H2O] (2) and [Cu(salbn)Eu(NO3)3H2O] (3) complexes from heterodonor ligand; that is, N,N′-1,3-propylenebis(salicylaldiminato) have been described.

2. Experimental

2.1. Materials and Methods

The commercially available AR grade chemicals were used without further purification. The solvents were used as either AR or spectroscopic grade. Gadolinium nitrate pentahydrate [Gd(NO3)35H2O] was obtained from Sigma Aldrich, europium nitrate pentahydrate [Eu(NO3)35H2O] from Fluka, and copper acetate monohydrate, Salicylaldehyde (C7H6O2), and 1,3-diaminopropane from Merck (India).

2.2. Physical Measurements

FT-IR spectra were recorded on a Shimadzu FT-IR 8400S model spectrometer in the range of 4000–400 cm−1 using KBr disks. Electronic spectra of the ligand and complexes were recorded at room temperature on a Perkin Elmer UV-Vis Lambda 35 spectrophotometer. The fluorescence spectra were recorded by a Perkin Elmer LS55 fluorescence spectrophotometer. The elemental analyses (C, H, N) were performed on a Perkin Elmer 2400 series II analytical instrument. Lanthanid(III) metals were estimated from Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) by using ARCOS Spectrometer (Germany). MS spectra were recorded on MS Waters ZQ-4000. Energy-dispersive X-ray spectroscopy (EDX) spectra were recorded on JEOL and JEM-7600F models. The powder X-ray diffraction pattern was recorded on PAN analytical Philips diffractometer with Cu-kα radiation of wavelength 1.54056 Å operating at a voltage of 40 kV and a current of 20 mA. The 2θ range used was from 5° to 65° at a step of 0.02°. The peak positions of the various complexes were obtained by fitting Lorentzian function. The peak positions so obtained were used to index the pattern and compute the cell parameters using the programme DICVOL and P-INDEX. Thermogravimetric analyses (TGA/DTA) of the compounds were carried out in the temperature from 40°C to 900°C with Perkin Elmer STA 6000. The experimental conditions were platinum crucible, nitrogen atmosphere with 20 mL/min flow rate, and a heating rate 5°C/min. Magnetic moment at room temperature () was measured using Sherwood Scientific susceptibility balance (MSB). EPR experiments were conducted on a VARIAN-E-112 spectrometer X-band frequency (9.5 GHz) with sensitivity of 5 × 1010 ΔH spins using tetracyanoethylene (TCNE). 1H NMR and 13C NMR spectra were recorded on FT-NMR spectrometer BRUKER AVANCE II 400 in CDCl3 solution, using TMS as the internal standard chemical shifts, and were reported in δ units downfield from TMS.

2.3. Synthesis of Ligand and Complexes

The ligand N,N′-1,3-propylenebis(salicylaldiminato) was prepared by employing the procedure [17], but we use 1,3-diaminopropane instead of 1,4-diaminobutane. The ligand (salbn) was used for the synthesis of following copper(II) and heteronuclear copper(II)-lanthanide(III) complexes.

[Cu(salbn)] (1) was synthesized by adding the methanolic solution of copper acetate (0.01 mole) to the methanolic solution of the yellow ligand (0.01 mole) under constant stirring. The reaction mixture was subsequently allowed to stir and refluxed for 5 hours giving green precipitate. After cooling, the green precipitate was filtered and washed with methanol and finally dried in air. [Cu(salbn)] complex is found to be soluble in DMF, chloroform, and ethanol solvents.

[Cu(salbn)Ln(NO3)3H2O] where Ln = Gd or Eu was synthesized by slowly adding a methanolic solution of Ln(III) nitrate salts to a solution of [Cu(salbn)] dissolved in hot chloroform under constant stirring. The reaction mixture was subsequently allowed to stir and refluxed for 5 hours giving dark green precipitate. Then the volume of the dark green precipitate solution was reduced to half of the initial volume and recrystallized in hot chloroform-methanol mixture. The dark green precipitate so obtained was filtered and finally dried in air. [Cu(salbn)Gd(NO3)3H2O] (2) and [Cu(salbn)Eu(NO3)3H2O] (3) complexes were soluble in chloroform, DMF, methanol, and ethanol solvents. The following reaction scheme (Scheme 1) affords the synthesis of [Cu(salbn)] and [Cu(salbn)Ln(NO3)3H2O] where Ln Gd or Eu complexes from the ligand(salbn).

Scheme 1: Reaction scheme showing the synthesis of [Cu(salbn)] and [Cu(salbn)Ln(NO3)3H2O] (where Ln = Gd or Eu) complexes from the ligand(salbn).

3. Results and Discussion

3.1. Characterization of the Complexes

Some analytical data of the ligand(salbn), [Cu(salbn)], and [Cu(salbn)Ln(NO3)3H2O] where Ln = Gd or Eu are tabulated in Table 1 which are in close agreement with theoretical and experimental values. All the complexes are soluble in chloroform, DMF, ethanol, and methanol.

Table 1: Analytical data, magnetic moment, and electronic spectral data of ligand(salbn), [Cu(salbn)], and [Cu(salbn)Ln(NO3)3H2O)] complexes where Ln = Eu or Gd.
3.2. X-Ray Diffraction Studies

Since single crystal of the complexes could not be obtained, the exact crystal structure could not be determined. In order to provide a typical idea about the single phasic nature of the complexes, we have carried out powder X-ray diffraction pattern for the ligand, [Cu(salbn)] (1), [Cu(salbn)Gd(NO3)3H2O] (2), and [Cu(salbn)Eu(NO3)3H2O] (3) complexes as shown in Figure 1. Lattice parameters of the XRD spectra were determined using a set of DICVOL and P-INDEX programs [18].

Figure 1: XRD patterns of ligand and complexes (1), (2), and (3).

The lattice parameters, volume, and figure of merit of ligand, complex (1), complex (2), and complex (3) are tabulated in Table 2. The ligand(salbn), complex (1), and complex (3) crystallize in triclinic system while complex (2) crystallizes in monoclinic system.

Table 2: Lattice parameter, volume, and figure of merit of ligand(salbn), complex (1), complex (2), and complex (3).
3.3. Electronic Spectral Study

The electronic spectra of the free ligand(salbn) exhibits two charge transfer (CT) bands at 257 and 310 nm attributed to ππ* and n → π* transitions within the ligand. In the spectrum of the complex, the CT band at 257 nm remains intact, in agreement with the ππ* transition of the ligand. Another band at ca. 342 nm is observed in the spectrum of complex (1). The band at 310 nm observed in the spectrum of free ligand is red shifted to 342 nm in the form of ligand to metal charge transfer transition (LMCT). Unlike the spectrum of the free ligand, broadband at ca. 597 nm is observed in the spectrum of complex (1) (see SFigure 1 in Supplementary Material available online at http://dx.doi.org/10.1155/2013/281270). The d-d transition at ca. 597 nm may be attributed to structurally well characterised square-planar copper(II) complexes [19]. The electronic spectrum of complex (1) in DMF exhibits a higher energy band at 597 nm, which has been shifted to lower energy at ca. 615 nm (SFigure 2) for the complex (2) seems to be due to a distortion of geometry occurring at the copper centre. Other f-f transitions, which are expected to appear, may be concealed by d-d, charge-transfer, or intraligand transitions. The electronic spectra taken in DMF have the higher absorbance and shifted to longer wavelength compared to the spectra taken in ethanol (EtOH) and methanol (MeOH) of complex (2) (SFigure 2).

3.4. Infrared Spectral Study

A strong sharp absorption band around 1638 cm−1 in the spectrum of the ligand may be assigned to the C=N stretching. In the complex, this band is shifted to 1627 cm−1 upon complexation with the metal, which may be attributed to the coordination of the imine nitrogen to the metal centre [2023]. The ligand shows band at 3539 cm−1 due to O–H stretching from phenolic group which disappears in the complexes (1), (2), and (3), indicating the deprotonation of the ligand upon complexation [5]. The strong phenolic C–O absorption band at 1212 cm−1 observed in the spectrum of ligand shifts to lower frequency at 1017 cm−1, supporting the coordination of the deprotonated phenolic oxygen atoms to the metal centres in the complexes [22]. A broadband at ca. 3300–3450 cm−1 indicates that coordinated water is present in the heteronuclear Cu(II)-Ln(III) complexes which is also supported by thermal data. The IR spectra of the complexes (2) and (3) show weak bands at 860 and 897 cm−1 for and at 550 cm−1 for of coordinated water [21]. The ligand coordination to the metal centre is substantiated by a band appearing at 470 cm−1 which is mainly attributed to in the complexes.

The spectra of the heteronuclear copper(II)-lanthanide(III) complexes (2) (SFigure 3) and (3) exhibit characteristic vibrational frequencies of coordinated nitrate group, which is supported by two bands observed at ca. 1485 and 1301 cm−1 [24]. The medium band at 1030 cm−1 due to the υ2 vibration of the nitrate group () stands as additional evidence for the presence of coordinated nitrate group. The difference in wavenumbers between the two highest frequency bands () of nitrate () is about 184 cm−1, indicating the nature of bidentate nitrate bridging [2126].

3.5. NMR and Mass Spectral Studies

1H and 13C NMR spectra have been used to extract information regarding the coordination mode of the ligand(salbn) with the metal ion (SFigures  4 and  5). The 1H NMR (400 MHz, CDCl3) spectra of ligand within a range of 0 to +15 ppm have δ 8.31 (s, 2H, N=CH), 7.29 and 6.86 (t each, 2 : 2 H, aromatic CH), 7.21 and 6.96 (d each, J 7.2 and 8.4 Hz, 2 : 2 H, aromatic CH), 5.31 (s, 2H, OH of salbn), 3.65 (s, 4H, methylene, α to –N=CH–), and 2.06 (s, 2H, methylene, to –N=CH–), and 13C NMR (100 MHz, CDCl3) has δ 31.70(methylene, α to –N=CH–), 56.81(methylene, to –N=CH–), 116.97, 116.68, 118.75, 131.34, and 132.30 (aromatic CH), 161.13(–HC=N–), and 165.48(–C–OH).

In the 1H NMR spectrum of the free ligand no broad peak was observed due to free amine proton in the region 5.0–8.0 ppm indicating that both –NH2 functions of the 1,3-diamine have undergone condensation with the carbonyl functional group of salicylaldehyde to give the Schiff base ligand [27, 28]. The 13C NMR spectra of the ligand (SFigure 6) were recorded in CDCl3 solution and revealed the presence of expected number of signals corresponding to different types of carbon atoms present in the ligand. In the free ligand, the aromatic carbons appear in the range 116–165 ppm. For the ligand, the azomethine carbon of the phenolic moiety appears at 161–165 ppm. Large chemical shift values for the carbon atoms attached to the azomethine nitrogen and phenolic oxygen suggest coordination of these atoms. The tetradentate nature of the ligand is confirmed from the spectral studies of 1H NMR and 13C NMR.

The FAB mass spectra of complex, [Cu(salbn)] with ligand (SFigures 7 and  8), play an important role in confirming the monomeric Cu(II) complex. The molecular ion peak of [Cu(salbn)] complex was observed at m/z 344, which is equivalent to its molecular weight and that of ligand(salbn) was observed at m/z 282 which is also equivalent to its molecular weight. The other peaks like 336, 344, 346, 368, 369, 382, and 384 in [Cu(salbn)] complex correspond to various fragments. The stoichiometry of metal to ligand in the ratio 1 : 2 was supported by the observed molecular ion peaks in spectrum of complex (1). These observations confirm the stoichiometric composition of the complex formation. This is also supported by the FAB mass spectra of the other complexes [17]. The data of mass spectra was found in complete agreement with that of obtained via elemental analysis.

3.6. Energy-Dispersive X-Ray Spectroscopy Study

The composition of the heteronuclear copper(II)-lanthanide(III) complexes that is, complexes, (2) and (3), was defined by energy-dispersive X-ray spectrometer (EDX) analysis as shown in Figures 2 and 3, respectively. The analysis of the EDX spectra indicates the presence of two kinds of different metals ions in heteronuclear complexes (2) and (3). Thus, from the EDX analysis, it can be proved that complexes (2) and (3) are heterobinuclear complex [29].

Figure 2: Energy-dispersive X-ray spectrum of heteronuclear Cu(II)-Gd(III) complex (2).
Figure 3: Energy-dispersive X-ray spectrum of heteronuclear Cu(II)-Eu(III) complex (3).
3.7. Thermal Analysis of the Complexes

The thermogravimetric studies show that all lanthanide(III) nitrate complexes undergo a series of weight loss starting from 40 to 820°C range (SFigure 9). TG curve of complex (2) shows the three steps of decomposition. The first weight loss corresponds to coordinated one water molecule at around 241°C vide IR while the second weight loss correspond to decomposition of ligand and anion in temperature around 330°C with a significant sharp endothermic peak. Finally the third step corresponds to decomposition in the Ln2O3 oxides in temperature around 680°C. The residue obtained after heating up to 820°C to constant weight is very close to those expected for the lanthanide(III) oxides [5, 29, 30].

3.8. VSM Study

The magnetic hysteresis loop of the complex (3) taken at room temperature is shown in Figure 4. Saturation magnetization is not observed as the applied magnetic field is raised, and hence there is no coercivity and remanence in the hysteresis loop of complex (3) [31].

Figure 4: VSM hysteresis loop curve of complex (3) at room temperature.
3.9. Fluorescence Study

In order to investigate the effect of an adjacent metal ion on fluorescence of Eu(III), fluorescence spectra of complex (3) were recorded. The complex (3) showed no significant fluorescence in the range of 550–750 nm by the maximum excitation wavelength, while [Eu(NO3)35H2O] gave the well-known five typical fluorescence bands at ~592, ~618, ~649, ~685, and ~698 nm when excitation monitored at 395 nm corresponding to characteristic emission transitions 5D07FJ (, 1, 2, 3, 4) [32, 33]. This significant decrease in fluorescence intensity may be due to the energy transfer from the excited Eu(III) to the adjacent Cu(II) complex moiety (intramolecular energy transfer), followed by the radiationless energy loss through the Cu(II) complex moiety [34].

3.10. Magnetic Moment and EPR Studies of the Complex

The magnetic susceptibility measurement of the [Cu(salbn)] complex showed a magnetic moment value of 1.73 B.M (Table 1) corresponding to one unpaired electron, indicating that the Cu(II) complex is mononuclear. The heteronuclear copper(II)-lanthanide(III) complexes (2) and (3) under study showed a magnetic moment, value at room temperature of 8.06 and 3.84 B.M (Table 1), respectively. The magnetic moments observed are compared with the theoretical spin orbital coupling values (the Hund’s values) and the values calculated from Van Vleck formula of the respective lanthanide ion. These values agree well with each other for the copper(II)-lanthanide(III) complexes [35].

The solid and DMF solution EPR spectra of [Cu(salbn)] complex were recorded at 300 K and liquid nitrogen temperature by using tetracyanoethylene () as reference. According to and calculation expression (), four hyperfine splitting lines can be expected. Indeed four weak peaks are observed giving parameters and which is a normal axial symmetric EPR spectrum as shown in Figure 5. This is typical of tetragonally coordinated monomeric copper(II) complex with unpaired electron in the orbital and spectral features which are the characteristics of axial symmetry [36]. The and values are >2.0023 indicating that the complexes are largely covalent [37].

Figure 5: EPR spectrum of [Cu(salbn)] complex in DMF at liquid nitrogen temperature.

EPR spectra of complex (2) were recorded at X-band in the solid and solution state at room temperature and liquid nitrogen temperature. The room temperature polycrystalline powder EPR spectrum of complex (2) shows a unique quasi-isotropic broad signal centred at (Figure 6) but shows no clear characteristic peak in the region [17, 38]. Little information is obtained from the room temperature polycrystalline powder EPR spectrum. The EPR spectrum of liquid nitrogen temperature in DMF solution of complex (2) exhibits an anisotropic broad signal around which may suggest a weak magnetic spin-exchange interaction between Gd(III) and Cu(II) ions [39] as shown in Figure 7.

Figure 6: Powder EPR spectrum of complex (2) at 300 K.
Figure 7: EPR spectrum of complex (2) in DMF at liquid nitrogen temperature.

In the EPR spectrum of complex (2) in DMF solution at liquid nitrogen temperature, the fine structure exhibits the seven expected transitions around 2380, 2680, 3000, 3220, 3300, 3480, and 4000 G which may be generated by zero field splitting [17, 40]. This spectrum corresponds to the superposition of the signals of the copper(II) and gadolinium(III) ions. These results suggest that the copper(II) () and gadolinium(III) () spins are coupled to yield the total spin states (low lying excited state) and (ground state) which is a weak interaction between copper(II) and gadonium(III) ions [41].

4. Conclusions

Three complexes, namely, [Cu(salbn)] (1), [Cu(salbn)Gd(NO3)3H2O] (2), and [Cu(salbn)Eu(NO3)3H2O] (3) where salbn N,N′-1,3-propylenebis (salicylaldiminato) have been synthesized and characterized. The EDX results suggest the presence of two different metal ions in heteronuclear complexes (2) and (3). The ligand(salbn), complex (1), and complex (3) crystallize in triclinic system while complex (2) crystallizes in monoclinic system. The EPR studies suggest that [Cu(salbn)] complex is tetragonally coordinated monomeric copper(II) complex with unpaired electron in the orbital and spectral features that are the characteristics of axial symmetry while complex (2) in DMF solution at liquid nitrogen temperature exhibits an anisotropic broad signal around which may suggest a weak magnetic spin—exchange interaction between Gd(III) and Cu(II) ions. The fluorescence intensity of Eu(III) decreased markedly in the complex (3).

Acknowledgments

One of the authors L. Jaideva Singh thanks CSIR, New Delhi for providing financial assistance under Senior Research Fellowship Scheme. All authors thank SAIF, Bombay, for measuring the EPR, EDX, VSM, and ICP-AES data, and SAIF NEHU, for measurement of NMR and MS spectra.

References

1. Q. Y. Chen, Q. H. Luo, L. M. Zheng, Z. L. Wang, and J. T. Chen, “A study on the novel d-f heterodinuclear Gd(III)—Ni(II) cryptate: synthesis, crystal structure, and magnetic behavior,” Inorganic Chemistry, vol. 41, no. 3, pp. 605–609, 2002.
2. S. Prasad, R. K. Agarwal, and A. Kumar, “Synthesis, characterization and biological evaluation of a novel series of mixed ligand complexes of lanthanides(III) with 4[N-(Furfural)amino]antipyrine semicarbazone as primary ligand and diphenyl sulfoxide as secondary ligand,” Journal of the Iranian Chemical Society, vol. 8, no. 3, pp. 825–839, 2011.
3. J. R. Morrow and K. O. A. Chin, “Synthesis and dynamic properties of kinetically inert lanthanide compounds: lanthanum(III) and europium(III) complexes of 1,4,7,10-tetrakis(2-hydroxyethyl)-1,4,7,10-tetraazacyclododecane,” Inorganic Chemistry, vol. 32, no. 15, pp. 3357–3361, 1993.
4. J. Rocha, L. D. Carlos, F. A. A. Paz, and D. Ananias, “Luminescent multifunctional lanthanides-based metal-organic frameworks,” Chemical Society Reviews, vol. 40, no. 2, pp. 926–940, 2011.
5. A. L. El-Ansary and N. S. Abdel-Kadara, “Synthesis, characterization of La(III), Nd(III), and Er(III) complexes with Schiff bases derived from benzopyran-4-one and their fluorescence study,” International Journal of Inorganic Chemistry, Article ID 901415, pp. 1–13, 2012.
6. P. A. Vigato and S. Tamburini, “The challenge of cyclic and acyclic schiff bases and related derivatives,” Coordination Chemistry Reviews, vol. 248, no. 17–20, pp. 1717–2128, 2004.
7. C. Benelli and D. Gatteschi, “Magnetism of lanthanides in molecular materials with transition-metal ions and organic radicals,” Chemical Reviews, vol. 102, no. 6, pp. 2369–2387, 2002.
8. A. Døssing, “Luminescence from lanthanide(3+) ions in solution,” European Journal of Inorganic Chemistry, no. 8, pp. 1425–1434, 2005.
9. H. J. Weinmann, R. C. Brasch, W. R. Press, and G. E. Wesbey, “Characteristics of gadolinium-DTPA complex: a potential NMR contrast agent,” American Journal of Roentgenology, vol. 142, no. 3, pp. 619–624, 1984.
10. V. Alexander, “Design and synthesis of macrocyclic ligands and their complexes of lanthanides and actinides,” Chemical Reviews, vol. 95, no. 2, pp. 273–342, 1995.
11. C. Papadopoulos, N. Kantiranis, S. Vecchio, and M. Lalia-Kantouri, “Lanthanide complexes of 3-methoxy-salicylaldehyde: thermal and kinetic investigation by simultaneous TG/DTG-DTA coupled with MS,” Journal of Thermal Analysis and Calorimetry, vol. 99, no. 3, pp. 931–938, 2010.
12. S. Akine, “Novel ion recognition systems based on cyclic and acyclic oligo(salen)-type ligands,” Journal of Inclusion Phenomena and Macrocyclic, vol. 72, pp. 25–54, 2012.
13. C. S. Marvel, S. A. Aspey, and E. A. Dudley, “Quadridentate and sexadentate chelates. Some preliminary studies in their preparation and thermal stability,” Journal of the American Chemical Society, vol. 78, no. 19, pp. 4905–4909, 1956.
14. Y. Liang, R. Cao, W. Su, M. Hong, and W. Zhang, “Syntheses, structures, and magnetic properties of two gadolinium (III)—Copper (II) coordination polymers by a hydrothermal reaction,” Angewandte Chemie-International Edition, vol. 39, no. 18, pp. 3304–3307, 2000.
15. Y. Liang, M. Hong, W. Su, R. Cao, and W. Zhang, “Preparations, structures, and magnetic properties of a series of novel copper(II)-lanthanide(III) coordination polymers via hydrothermal reaction,” Inorganic Chemistry, vol. 40, no. 18, pp. 4574–4582, 2001.
16. J. P. Costes, J. M. Clemente, F. Dahan, F. Nicod`eme, and M. Verelst, “Unprecedented ferromagnetic interaction in homobinuclear erbium and gadolinium complexes: structural and magnetic studies,” Angewandte Chemie-International Edition, vol. 41, no. 2, pp. 323–325, 2002.
17. T. M. Rajendiran, R. Kannappan, R. Mahalakshmi, R. Venkatasan, and P. S. Rao, “A novel discrete dinuclear copper(II)-gadolinium(III) complex derived from Schiff base ligand,” Transition Metal Chemistry, vol. 28, pp. 644–649, 2003.
18. L. J. Singh, R. K. H. Singh, and R. Chitra, “Synthesis, spectroscopic, powder X-ray diffraction and DNA binding studies on copper(II) complexes of 4, ${4}^{\prime }$-diaminodiphenyl sulfone,” Journal of the Iranian Chemical Society, vol. 9, pp. 441–448, 2012.
19. A. B. P. Lever, Inorganic Electronic Spectroscopy, Elsevier, Amsterdam, The Netherlands, 2nd edition, 1984.
20. M. Dolaz, M. Tümer, and M. Diǧrak, “Synthesis, characterization and stability constants of polynuclear metal complexes,” Transition Metal Chemistry, vol. 29, no. 5, pp. 528–536, 2004.
21. K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds: Theory and Applications in Inorganic Chemistry, Part-A, John Willey and Sons, New York, NY, USA, 5th edition, 1997.
22. Z. L. You and H. L. Zhu, “Syntheses, crystal structures, and antibacterial activities of four schiff base complexes of copper and zinc,” Zeitschrift fur Anorganische und Allgemeine Chemie, vol. 630, no. 15, pp. 2754–2760, 2004.
23. R. C. Mourya, R. Varma, and P. Shukla, “Synthesis of nitrato complexes of lanthanum(III) with schiff bases derived from 4-antipyrinecarboxaldehyde and aromatic amines,” Journals of the Indian Chemical Society, vol. 74, no. 9, pp. 789–790, 1997.
24. B. M. Gatehouse, S. E. Livingstone, and R. S. Nyholm, “Infrared spectra of some nitrato and other oxy-anion co-ordination complexes,” Journal of Inorganic and Nuclear Chemistry, vol. 8, pp. 75–78, 1958.
25. Y. T. Li, C. W. Yan, and J. Zhang, “Synthesis, characterization, and magnetic properties of copper(II)-lanthanide(III) heterobinuclear complexes bridged by N,N′-oxamidobis(3,5-dibromobenzoato)cuprate(II),” Crystal Growth and Design, vol. 3, no. 4, pp. 481–485, 2003.
26. A. P. Hunter, A. M. J. Lees, and A. W. G. Platt, “Synthesis, structures and mass spectrometry of lanthanide nitrate complexes with tricyclohexylphosphine oxide,” Polyhedron, vol. 26, no. 17, pp. 4865–4876, 2007.
27. W. Kemp, Organic Spectroscopy, Macmillan Press, 3rd edition, 1991.
28. A. Ray, D. Sadhukhan, G. M. Rosair, C. J. Gómez-García, and S. Mitra, “An unprecedented CuII-Schiff base complex existing as two different trinuclear units with strong antiferromagnetic couplings,” Polyhedron, vol. 28, no. 16, pp. 3542–3550, 2009.
29. H. D. Wang, Y. Chen, Y. T. Li, and X. C. Zeng, “Synthesis, characterization, and thermal decomposition of oxamido heterobinuclear Cu(II)-Ln(III) complexes,” Thermochimica Acta, vol. 412, no. 1-2, pp. 97–105, 2004.
30. R. K. Agarwal and S. K. Gupta, “Magneto, spectral and thermal investigations of lanthanide (III) complexes of 5, 6-benzoquinoline,” Polish Journal of Chemistry, vol. 61, p. 341, 1987.
31. A. A. Dakhel and M. El-Hilo, “Ferromagnetic nanocrystalline Gd-doped ZnO powder synthesized by coprecipitation,” Journal of Applied Physics, vol. 107, no. 12, Article ID 123905, 6 pages, 2010.
32. M. Sakamoto, K. Yamamoto, A. Matsumoto, Y. Nishida, and H. Okawa, “Effect of some d-transition metal complexes of salen-type ligands and acetylacetone on fluorescence of europium(III) and terbium(III),” Bulletin of the Chemical Society of Japan, vol. 67, pp. 2707–2711, 1994.
33. M. Sakamoto, T. Ishikawa, Y. Nishida et al., “V(IV) O & Ln(III) complexes (Ln = La, Eu or Gd) of the compartmental ligand N, N′-bis(3-hydroxysalicylidene)ethylenediamine,” Journal of Alloys and Compounds, vol. 238, pp. 23–27, 1996.
34. M. Sakamoto, Y. Kitakami, H. Sakiyama et al., “Synthesis and properties of copper (II)-lanthanide(III) complexes of N,N′-bis(3-formyl-5-methylsalicylidene)-1,3-propanediamine,” Polyhedron, vol. 16, no. 19, pp. 3345–3351, 1997.
35. V. M. Naik and N. B. Mallur, “Synthesis and characterisation of lanthanide(III) nitrate complexes with tetradentate O N O donor hydrazone derived from 2-benzimidazoyl mercaptoaceto hydrazide and o-hydroxyl aromatic aldehyde,” E-Journal of Chemistry, vol. 8, pp. 1900–1910, 2011.
36. A. Bencini and D. Gatteschi, EPR of Exchange Coupled Systems, Springer, Berlin, Germany, 1990.
37. D. Kivelson and R. Nieman, “ESR studies on the bonding in copper complexes,” Journal of Chemical Physics, vol. 35, pp. 149–155, 1961.
38. C. Benelli, A. Caneschi, D. Gatteschi, O. Guillou, and L. Pardi, “Synthesis, crystal structure, and magnetic properties of tetranuclear complexes containing exchange-coupled Ln2Cu2 (Ln = Gd, Dy) species,” Inorganic Chemistry, vol. 29, no. 9, pp. 1750–1755, 1990.
39. A. Bencini, C. Benelli, A. Caneschi, R. L. Carlin, A. Dei, and D. Gatteschi, “Crystal and molecular structure of and magnetic coupling in two complexes containing gadolinium(III) and copper(II) ions,” Journal of the American Chemical Society, vol. 107, no. 26, pp. 8128–8136, 1985.
40. A. Bencini, C. Benelli, A. Caneschi, A. Dei, and D. Gatteschi, “Crystal and molecular structure and magnetic properties of a trinuclear complex containing exchange-coupled GdCu2 species,” Inorganic Chemistry, vol. 25, no. 4, pp. 572–575, 1986.
41. K. Kambe, “On the paramagnetic susceptibilities of some polynuclear complex salts,” Journal of the Physical Society of Japan, vol. 5, no. 1, pp. 48–51, 1950.