Abstract
The synthesis and characterization of cadmium(II) and calcium(II) complexes with N,O-bidentate ligands derived from pyrazinecarboxylic acid (3-hydroxy-2-quinoxalinecarboxylic acid HL1, pyrazine-2-carboxylic acid HL2) are reported. Obtained compounds [Cd(L1)2(H2O)2](H2O)2 (1), [Cd(L2)2]n (2) and [Ca(L2)2(H2O)4] (3) were studied by elemental analyses, IR, Raman spectroscopy and thermogravimetric methods (TG, DTG, DSC). In addition, the molecular structure of complex 1 has been determined by X-ray single crystal diffraction. Thermal analysis reveals a decomposition process of 1, 3 complexes in multiple stages. The data obtained from TG and DSC curves for 1, 3 confirm not only the presence but also the nature of water (crystallization and coordination) and the stoichiometry of the studied metal complexes. The results of thermal studies are in good agreement with their crystal structures. Thermal behavior of complex 2 indicates a single complete decomposition process of the sample. In addition, complex 2 as a coordination polymer is the most stable all of them and the thermal stability of the obtained complexes can be ordered in the following sequence: 1 < 3 ≪ 2.
Introduction
Recently, our research group has embarked on a comparative study of coordination chemistry of calcium and cadmium model complexes with N,O-biologically important ligands to find differences and similarities related to their thermal stability and molecular structures [1, 2]. The similarities presented by Ca(II) and Cd(II) ions (they show similarity in their radius 0,95 and 1,00 Å) favor the exchange of the metals in the biological system. Therefore, a comparison of coordination chemistry of calcium and cadmium model complexes ought to provide a solid-based example of how toxic metal ion substitution may perturb the structure of the calcium compound with the same or derivative ligand. As an extension of this study, we report here the synthesis, spectroscopic analysis, X-ray crystallography and thermal behavior of cadmium(II) complex with 3-hydroxy-2-quinoxalinecarboxylate (L1). We have not found the crystal structure of [Cd(L1)2(H2O)2](H2O)2 in the literature. Furthermore, the study included the comparison of spectroscopic data and thermal stability of Cd(II) (2) and Ca(II) (3) complexes with pyrazine-2-carboxylate. Compounds 2 and 3 were first reported by Liu [3] and Ptasiewicz-Bąk with coworkers [4], respectively. Liu [3] synthesized [Cd(L2)2]n in a hydrothermal method using cadmium(II) nitrate, pyrazine-2-carboxylate, NaOH, and water (20% yield). Complex 3 was isolated from the reaction of pyrazine-2-carboxylic acid (HL2) and calcium oxide.
In this article, we report an alternative, non-hydrothermal preparation which has afforded 2 and 3 in high yield. Bearing in mind that the coordination ability of the carboxylate ligands toward metal ions frequently depends on hydrothermal or non-hydrothermal methods used to prepare the complexes [1, 5–8], we investigated the crystal structure of obtained compounds with X-ray crystallography. By comparing the crystallographic data, it can be seen that the crystal structure of the obtained complexes look similar to those reported in the literature [3, 4]. However, up to now, the spectroscopic data (IR, Raman) and thermal properties of the two complexes have not been found in the literature.
Both of the ligands have a recognized biological function in the body metabolism. 3-hydroxy-2-quinoxalinecarboxylic acid (HL1) was found to antagonize the 22Na+ efflux produced in 22Na+-preloaded brain slices by N-methyl-d-aspartate and kainate [9]. Pyrazine-2-carboxylic acid (HL2) is the active form which is encoded by the pncA gene for activity against Mycobacterium tuberculosis [10]. In addition, the in vitro antibacterial screening of the free acid and its metal complexes has been carried out against Escherichia coli, Salmonella typhi and Vibrio cholera [11]. Moreover, carboxylates [12–14] are versatile ligands which offer a great variety of coordination modes (Scheme 1) and this makes them interesting in the construction of molecular architectures.
Possible coordination modes of the 3-oxo-4H-quinoxaline-2-carboxylate and pyrazine-2-carboxylate
Citation: Journal of Thermal Analysis and Calorimetry J Therm Anal Calorim 108, 3; 10.1007/s10973-011-2137-x
Experimental procedure
Reagents and physical measurement
All reagents (pyrazine-2-carboxylic acid, 3-hydroxy-2-quinoxalinecarboxylic acid, the metal salts) were purchased from Aldrich, Merck Chemical and used as received. Ethanol was purchased from Linegal Chemicals and water was deionised.
Elemental analyses (C, N, H) were performed on Model 240 Perkin-Elmer CHN Analyzer. Elemental analysis of Cd2+ was carried out using ICP-MS method (ELAN DRCII, PerkinElemer). A sample of the compound was dissolved in a solution of 2% HNO3 and diluted. Calibration solution available from PerkinElemer (1000 mg L−1, 2% HNO3 [7440–43–9]). ESI–MS spectra was carried out with a micrOTOF-QII instrument (Bruker). IR spectra were recorded with Nicolet 380 FTIR spectrophotometer in the region 4000–400 cm−1 using the diffusive reflection method. Fourier transforms Raman scattering measurements (FT-RS) were performed at room temperature with a PerkinElemer RamanStation™ 400F spectrometer, resolution 4 cm−1. The incident radiation (λ = 785 nm) came from a diode laser. The thermal decompositions of ~10 mg of the prepared complexes were measured under the static air atmosphere with Mettler-Toledo Star TG/SDTA 851e thermal analyzer at a heating rate of 5 K min−1. For all complexes in the temperature range of 298–1273 K alumina open crucibles were used. DSC analysis was carried out using DSC Mettler-Toledo instrument in standard closed sample pans, static air atmosphere, and heating rate of 5 K min−1. The thermoanalytical curves were obtained using STARe System METTLER-TOLEDO software. The powder X-ray diffraction (XRD) patterns of the products of decomposition were recorded by DRON-2 using CuKα radiation (λ = 1.54178 Å) over 2θ angle range 8–65°.
Syntheses of the complexes
Preparation of [Cd(L1)2(H2O)2](H2O)2 (1)
A solution of Cd(NO3)2 · 4H2O (0.5 mmol) in deionised water (5 mL) was slowly added to a solution of 3-hydroxy-2-quinoxaliniecarboxylic acid (HL1) (1 mmol), in ethanol (15 mL). The molar ratio M:L was 1:2. The mixture was heated (~323 K) and stirred for 7 h, then left standing at room temperature. Passive evaporation of green solution resulted in yellow crystals of the complex suitable for X-ray investigation. The product was filtered and dried under vacuum. The crystals were collected in 45% yield. Anal. Calc. for C18H18N4O10Cd: C, 38.40, N, 9.98, H, 3.00, Cd, 19.96. Found: C, 38.42, N, 9.96, H, 3.22, Cd, 19.98%. ESI–MS (positive ion mode, acetonitrile): m/z (%) [Cd(L1)2(CH3CN)2]Na]+ = 613 (100), [Cd(L1)2(H2O)2]Na]+ = 551 (40), [Cd(L1)2(H2O)2](H2O)2H]+ = 565 (30), [Cd(L1)2(H2O)2](H2O)2 K]+ = 603 (25). The complex was readily soluble in dimethylformamide.
Preparation of [Cd(L2)2]n (2) and [Ca(L2)2(H2O)4] (3)
The Cd(II) and Ca(II) crystals of complexes with pyrazine-2-carboxylate (L2) suitable for X-ray investigation and thermal analyses were prepared according to the following procedure: a solution of pyrazine-2-carboxylic acid (HL2) (2 mmol) in redistilled water (15 mL) heated to 343 K was stirred, while CaCO3 or Cd(NO3)2 · 4H2O (1 mmol) in 40 mL redistilled water was added drop wise to the solution. After 3 h, the resulting mixture was cooled to room temperature. The solution was filtered to remove any undissolved material and left to crystallize at room temperature. After 3 days, the colorless crystals were collected by vacuum filtration, washed with mother liquid and dried in a vacuum box. The products were collected in 53 and 86% yield, respectively. Anal. Calc. for: C10H6N4O4Cd: C, 33.49, N, 15.62, H, 1.69. Found: C, 33.50, N, 15.75, H, 1.64%. Anal. Calc. for: C10H14N4O8Ca: C, 33.52, N, 15.64, H, 3.94. Found: C, 33.59, N, 15.62, H, 3.95%. The complexes were insoluble in most polar and non-polar solvents.
Crystal structure determination
Diffraction intensity data for single crystal of new cadmium complex were collected at room temperature on a KappaCCD (Nonius) diffractometer with graphite-monochromated MoKα radiation (λ = 0.71073 Å). Corrections for Lorentz, polarization and absorption effects [15, 16] were applied. The structure was solved by direct methods using SIR-92 program package [17] and refined using a full-matrix least square procedure on F2 using SHELIXL-97 [18]. Anisotropic displacement parameters for all non-hydrogen atoms and isotropic temperature factors for hydrogen atoms were introduced. In the structure the hydrogen atoms connected to carbon atoms were included in calculated positions from the geometry of molecules, whereas hydrogen atoms of water molecules were included from the difference maps and were refined with isotropic thermal parameters. Further details of the structure analysis are given in Table 1. The figures were made using DIAMOND software [19]. CCDC 830735 contains the supplementary crystallographic data for complex 1. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html, or from the Cambridge Crystallographic data Centre (CCDC), 12 Union Road, Cambridge CB2 1 EZ, UK; fax: (+44) 1223 366 033; email: deposit@ccdc.cam.ac.uk.
Crystal data and structure refinement for 1
| [Cd(L1)2(H2O)2](H2O)2 | |
| Empirical formula | Cd C18 H18 N4 O10 |
| Formula weight | 562.63 |
| T/K | 293(2) |
| Wavelength/Å | 0.71073 |
| Crystal system, space group | Triclinic, P |
| Unit cell dimension | |
| a/Å = 6.8300(4) | α/° = 76.229(4) |
| b/Å = 8.0310(4) | β/° = 76.450(3) |
| c/Å = 9.6620(5) | γ/° = 77.480(4) |
| V/Å3 | 493.09(5) |
| Z, Dcalc/mg m−3 | 1, 1.895 |
| Absorption coefficient/mm−1 | 1.177 |
| F(000) | 282 |
| Crystal size/mm | 0.19 × 0.13 × 10 |
| θ/° | 2.65–27.38 |
| Index ranges | −8 ≤ h ≤ 8, −10 ≤ k ≤ 10, −11 ≤ l ≤ 12 |
| Reflections collected/unique | 6,872/2,155 [Rint = 0.0582] |
| Max. and min. transmission | 0.8914 and 0.8074 |
| Refinement method | Full-matrix least-squares on F2 |
| Data/restraints/parameters | 2216/6/167 |
| Goodness-of-fit (GOF) on F2 | 1.077 |
| Final R indices [I > 2σ(I)] | R 1 = 0.0290, wR2 = 0.0726 |
| R indices (all data) | R 1 = 0.0304, wR2 = 0.0733 |
| Extinction coefficient | 0.023(4) |
| Largest differences in peak and hole/eÅ−3 | 0.455 and −0.879 |
Results and discussion
3-Hydroxy-2-quinoxalinecarboxylate due to the labile hydrogen atom of OH-group in α-position to the basic pyrimidine N atom forms enol-keto tautomers (Scheme 2).
Enol a keto b tautomers of 3-hydroxy-2-quinoxalinecarboxylate
Citation: Journal of Thermal Analysis and Calorimetry J Therm Anal Calorim 108, 3; 10.1007/s10973-011-2137-x
The molecular and crystal structure of cadmium complex [Cd(L1)2(H2O)2](H2O)2 (1)
The asymmetric unit of title compound, [Cd(C9H5N2O3)2(H2O)2](H2O)2, consists of octahedrally coordinated Cd2+ ions, with the 3-oxo-3,4-dihydroquinoxaline-2-carboxylate ligands acting in a bidentate manner (Cd–O(1) = 2.2644(16) Å and Cd–N(1) = 2.3513(18) Å), a water molecule coordinated axially (apical) via the O(4) atom (Cd–O(4) = 2.3219(19) Å) and additional water of crystallization molecule. The Diamond drawing of the Cd(II) complex with atom numbering is shown in Fig. 1. Selected geometrical data for the compound are given in Table 1. On the basis of the observed valence angles (Table 2) the shape of coordination polyhedron can be described as distorted octahedron {CdO4N2}. The octahedron around the Cd2+ atom, which lies on an inversion center, is slightly flattened in the equatorial direction. The ligand exhibits enol-to-keto tautomerization by H-atom transfer from the hydroxyl group at position 3 to the N atom at position 4 of the quinoxaline ring of the ligand. The chelate ring defined by atoms Cd(1)/O(1)/C(11)/C(2)/N(1) is approximately planar, with a maximum out-of-plane deviation of 0.116 Å for Cd. This plane makes a small angle of 3.69(13) with the planar quinoxaline ring (atoms N(1)/C(2)/C(3)/N(4)/C(10)/C(9)). The geometry of the quinoxaline ring corresponds to tautomeric protonation at N(4) (O(3)–C(3) = 1.226(3) Å and C(3)–N(4) = 1.363(3) Å) [20]. The O(1)–C(11) bond distance of the carboxylate group (1.254(3) Å) is longer than O(2)–C(11) (1.240(3) Å), due to the coordination of atom O(1) to Cd2+. Packing analysis reveals that the complex has a very interesting coordination network (Fig. 2). The complex molecules are linked through an intermolecular N–H···O hydrogen bond (N(4)···O(3) = 2.804(3) Å) formed between the quinoxaline NH group and a carbonyl O atom, and by five O–H···O hydrogen bonds formed between a O atoms of ligand and water molecules (Table 3). In addition, there is a intermolecular O–H···O hydrogen bond (2.819(3) Å) formed between a two water molecules (Table 3).
Molecular structure of [Cd(L1)2(H2O)2](H2O)2 (1) mono
Citation: Journal of Thermal Analysis and Calorimetry J Therm Anal Calorim 108, 3; 10.1007/s10973-011-2137-x
Selected bond lengths/Å and valence angles/° for 1
| Bond lengths/Å | Valence angels/° | ||
|---|---|---|---|
| Cd–O(1)i | 2.2644(16) | O(1)i–Cd–O(1) | 180.00 |
| Cd–O(1) | 2.2644(16) | O(1)i–Cd–O(4) | 95.91(7) |
| Cd–O(4) | 2.3219(19) | O(1)–Cd–O(4) | 84.09(7) |
| Cd–O(4)i | 2.3219(19) | O(1)i–Cd–O(4)i | 84.09(7) |
| Cd–N(1)i | 2.3513(18) | O(1)–Cd–O(4)i | 95.91(7) |
| Cd–N(1) | 2.3513(18) | O(1)–Cd–O(4)i | 180.0 |
| O(1)i–Cd–N(1)i | 71.36(6) | ||
| O(1)–Cd–N(1)i | 108.64(6) | ||
| O(1)–Cd–N(1)i | 92.76(7) | ||
| O(1)i–Cd–N(1)i | 87.24(7) | ||
| O(1)i–Cd–N(1) | 108.64(6) | ||
| O(1)–Cd–N(1) | 71.36(6) | ||
| O(4)–Cd–N(1) | 87.24(7) | ||
| O(4)i–Cd–N(1) | 92.76(7) | ||
| N(1)i–Cd–N(1) | 180.0 | ||
Symmetry transformations used to generate equivalent atoms: (i) −x + 1, −y, −z + 1
Crystal packing of cadmium(II) complex (1) showing the water molecules placement (view [1 0 0])
Citation: Journal of Thermal Analysis and Calorimetry J Therm Anal Calorim 108, 3; 10.1007/s10973-011-2137-x
Hydrogen bonds lengths/Å and valence angles/° for 1
| D–H···A | d(D–H) | d(H···A) | d(D···A) | ∢(DHA) |
|---|---|---|---|---|
| O(4)–H(4A)···O(2)i | 0.861(19) | 2.02(3) | 2.842(3) | 158(5) |
| O(4)–H(4A)···O(3)i | 0.861(19) | 2.50(4) | 3.004(3) | 118(4) |
| O(4)–H(4B)···O(5) | 0.900(19) | 1.96(3) | 2.819(3) | 158(5) |
| O(5)–H(5A)···O(2) | 0.904(19) | 2.18(2) | 3.074(3) | 168(5) |
| O(5)–H(5B)···O(2)ii | 0.904(19) | 2.07(2) | 2.966(3) | 171(5) |
| N(4)–H(4)···O(3)iii | 0.89(5) | 1.91(5) | 2.804(3) | 174(4) |
Symmetry transformations used to generate equivalent atoms: (i) x + 1, y, z; (ii) −x, −y + 1, −z + 1; (iii) −x, −y, −z
Infrared and Raman spectra
The most important IR (Raman) frequencies attributed to the vibrations of free acids and complexes 1–3 are reported in Table 4. The IR spectrum of both free acids, 3-hydroxy-2-quinoxalinecarboxylic acid (HL1) and pyrazine-2-carboxylic acid (HL2) show a strong band centered at 1755 cm−1 (1763) and 1714 cm−1 (1709), respectively assigned to stretching vibration of the non-ionized carboxyl groups which are absent in the spectrum of the complexes, confirming that the carboxylic groups are deprotonated. Furthermore, the infrared spectrum of [Cd(L1)2(H2O)2](H2O)2 display an intense stretch at 1678 (1685) cm−1 corresponding to ν(C=O)ketone stretching vibration [21] and the in-plane δ(NH) band (at: 1616 cm−1) suggesting the protonation of pyrazine nitrogen atom, and indicates the coordination of keto tautomers, 3-oxo-4H-quinoxaline-2-caroxylate (L1) to Cd(II) ion. This is in agreement with the results of the X-ray analysis (Fig. 1). The new broad absorption band of medium intensity in the spectra in the region 3000–3500 cm−1 of 1 and 3 indicates hydrogen bonds involving water molecules coordinated to metals ions or molecules of lattice water. In addition, infrared spectroscopy confirms a bidentate fashion of coordination of L1 and L2 ligands to the metal ion via the carboxylate group and nitrogen atom from the pyrazine ring (Table 4). The calculated values of Δ(νasym(–COO−))−(νsym(–COO−)) for 1 (276 (275)), 2 (313, 328 (294)), and 3 (238 (231)) indicate the presence of carboxylate groups coordinated to metal ions in unidentate mode [22, 23], which is in agreement with the crystal structures of 1, 2, and 3. Moreover, the IR data confirm that the carboxylate of the ligand 2, adopts two types of coordination modes: bridging and unidentate.
The most characteristic bands in the IR (Raman) spectra for 3-hydroxy-2-quinoxalinecarboxylic acid (HL1), pyrazine-2-carboxylic acid (HL2), and its complexes/cm−1
| Assignments | HL1 | [Cd(L1)2(H2O)2](H2O)2 | HL2 | [Cd(L2)2]n | [Ca(L2)2(H2O)4] |
|---|---|---|---|---|---|
| – | 3364 vb | – | – | 3400–3100 vb |
| ν(O···HN) | 3138–2950 vb | 3000–2800 vb | – | – | – |
| ν(COOH) | 1755 (1763) | – | 1714 (1709) | – | – |
| νas, νs(COO−) | – | 1648, 1372 Δ = 276 | – | 1613, 1300; 1285 Δ = 313, 328 | 1610, 1372 Δ = 238 |
| (1660, 1385 Δ = 275) | (1581; 1287 Δ = 294) | (1613, 1382 Δ = 231) | |||
| Pyrazine ring vibration | 1596, 1493, 1417 (1593, 1420) | 1587, 1492, 1398 (1584,1400) | 1571, 1484, 1394 (1591, 1396) | 1573, 1470, 1408 | 1577, 1472, 1414 (1581, 1474, 1414) |
| (1472, 1410, 1574) | |||||
| ν(C=O)ketone | 1684 (1690) | 1678 (1685) | – | – | – |
| δ(C–O) | 1053 (1100) | 1046 (1109) | 1049 (1054) | 1040 (1044) | 1049 (1058) |
| δ NH | 1608 (1606) | 1604 (1601) | – | – | – |
vb very broad
Thermal analysis and structure correlation
Plausible tentative thermal degradation patterns proposed for the metal complexes under air are presented in Fig. 3. The thermal data of three compounds are collected in Table 5 and the result concerning thermal decomposition are presented as follows:
Thermoanalytical curves (TG/DTG and DSC) of the compounds [Cd(L1)2(H2O)2](H2O)2 (a), [Cd(L2)2]n (b), [Ca(L2)2(H2O)4] (c)
Citation: Journal of Thermal Analysis and Calorimetry J Therm Anal Calorim 108, 3; 10.1007/s10973-011-2137-x
Thermoanalytical results (TG/DTG, DSC) of cadmium(II) and calcium(II) complexes
| Complex | Stage | TG results | DTG (DSC) results | Peak nature | Mass/% | Loss | Residue | |
|---|---|---|---|---|---|---|---|---|
| T range/K | T max. peaks/K | Calc. | Found | |||||
| [Cd(L1)2(H2O)2](H2O)2 | I | 333–383 | 350 (361) | Endo | 6.4 | 5.2 | 2 H2O (crystallisation water) | |
| II | 383–593 | 519 (515, 537) | Endo | 30.6 | 31.8 | 2 H2O, 0.71 L fragments of two quinoxaline rings | ||
| III | 593–863 | 629 (636) | Exo | 19.5 | 20.1 | 0.58 L next parts of ligands | ||
| IV | 863–1093 | 808, 838 (744, 757) | Exo | 17.8 | 17.9 | 0.54 L fragments of ligands containing donor atoms | ||
| Σ | 74.3 | 75.0 | ||||||
| 25.7 | 25.0 | CdO | ||||||
| [Cd(L2)2]n | I | 623–793 | 689, 754 (696, 723) | Exo | 64.1 | 63.9 | Organic ligands | |
| 35.9 | 36.1 | CdO | ||||||
| [Ca(L2)2(H2O)4] | I | 373–423 | 390 (393) | Endo | 20.1 | 19.2 | 4 H2O | |
| II | 423–743 | 695 (705) | Exo | 22.4 | 22.2 | 0.65 L fragments of pyrazine rings | ||
| III | 743–1,083 | 1021 | Exo | 29.6 | 28.8 | 0.86 L next fragments of rings | ||
| IV | 1083–1273 | 12.3 | 12.1 | CO2 | ||||
| Σ | 84.4 | 82.3 | ||||||
| 15.6 | 17.7 | CaO | ||||||
Thermal analysis of 1
The thermal stability of 1, as determined from TG/DTG curves (Fig. 3a) is up to 333 K. 1 loses two uncoordinated water molecules in temperature range 333–383 K. Thermogravimetry shows 5.2% mass loss at such a low temperature which indicates the nature of water molecules, namely lattice water. The next stage, between 383 and 593 K involves both the loss of two coordinated water molecules and the fragments of two quinoxaline rings. This process is accompanied by endothermic effect (doublet max. 515 and 537 K on DSC curve). The discussed two mass loss steps of the molecules of water (lattice and coordination water) are in good agreement with the crystal structures of 1 (Fig. 2). The third experimental mass loss of about 21.0% may be attributed to the loss of fragments of pyrazine rings without donor atoms (19.5%). The final step occurs in the temperature range 863–1093 K and represents detachment of donor atoms connected with central ion. Thus, according to X-ray data (Fig. 1), the Cd atom is six-coordinate with two nitrogen atoms of two pyrazine rings and four oxygen atoms, two of carboxylate group of ligands and two of the water molecules, which gives CdN2O4 chromophore. At the end of last stage, 25% cadmium oxide remains as final residue, calculated 25.7%. The final solid product was identified on the basis of powder XRD studies [24].
Thermal analysis of 2
A thermal behavior of complex 2 indicates a process with maximum at 693 K which is followed by a single complete decomposition process of sample (Fig. 3b). This process is accompanied by a strong endothermic effect. The experimental mass loss of 63.9% is in good agreement with those calculated of 64.2%. Liu [3] described Cd(II) complex as a two-dimensional coordination polymer in which each central atom is six-coordinated with CdN2O4 chromophore (Scheme 3a). The two types of mean lengths bonds: 2.2415 and 2.353 Å support the data from DSC curve (double peaks of 696 and 723 K). The total mass loss occurring up to 793 K is in agreement with the formation of CdO as a final residue (found 36.1, calculated 35.8%). It was confirmed from the XRD patterns [24].
The structures of the pyrazine-2-carboxylate complexes: a [Cd(L2)2]n [3], b [Ca(L2)2(H2O)4] [4]
Citation: Journal of Thermal Analysis and Calorimetry J Therm Anal Calorim 108, 3; 10.1007/s10973-011-2137-x
Thermal analysis of 3
The TG curve of 3 shows that the four-stage mass loss occurs in the temperature range of 373–1273 K (Fig. 3c). The first mass loss starts at about 373 K and is about 19.2% and corresponds to the release of all the H2O molecules (calculated 20.1%). According to X-ray results [4] and Scheme 3b, the complex exists as a monomeric molecule in which the central ion has a distorted dodecahedral coordination, formed by four water molecules, two nitrogen atoms, and two oxygen atoms from monodentate carboxylic groups of two heterocyclic ligands (Scheme 3b). Taking into consideration that the whole molecules of water in Ca(II) complex are coordination water, the thermal and X-ray data correlated very well. The consecutive stages of the decomposition observed between 423 and 1083 K represents combustion of the pyrazine rings (found 51.0, calculated 51.9%). Further degradation of the previously formed intermediate (CaCO3) occurs above 1083 K with a weak endothermic effect. On the last step the value of 12.2% calculated for the mass loss is attributed to elimination of carbon dioxide molecule. The mass of the residue obtained corresponds to CaO formation (found 17.7, calculated 15.8%). In addition, the final product was confirmed from XRD patterns [25] and identified on the basis of ICDD using XRAYAN package.
Conclusions
In conclusions, the relationship between the thermal decomposition and structures of metal complexes and the influence of the ligands on thermal behavior of obtained compounds are very important to gain some information about new materials (especially, porous coordination polymers), synthesized by combining organic ligands and metal salts [26–30].
We have successfully synthesized two cadmium and one calcium complexes [Cd(L1)2(H2O)2](H2O)2 (1), [Cd(L2)2]n (2), [Ca(L2)2(H2O)4] (3) via a new, non-hydrothermal reaction and investigated the crystal structure of obtained compounds with X-ray crystallography. By comparing the crystallographic data of 2 and 3, it can be seen that the crystal structure of the obtained complexes look similar to those reported in the literature [3, 4]. So we concentrated our effort on the spectroscopic data (IR, Raman) and thermal properties of 2 and 3 complexes, and only additionally, on X-ray study for 1. X-ray structure analysis and IR data confirm that during coordination with Cd(II) 3-hydroxy-2-quinoxalinecarboxylic acid (HL1) undergoes deprotonation and exists in the keto tautomeric form in complex 1.
Thermal analysis reveals a decomposition process of 1, 3 complexes in multiple stages. Data obtained from TG and DSC curve confirm not only the presence but also the nature of water and the stoichiometry of the studied metal complexes. The two mass loss steps of the molecules of water (crystallization and coordination water) are in good agreement with the crystal structures of 1. A thermal behavior of complex 2 indicates a single complete decomposition process of the sample. In the case of this compound, the two type of mean lengths bonds: 2.2415 and 2.353 Å support the date from DSC curve (double peaks of 696 and 723 K). In addition, complex 2 as a coordination polymer is the most stable and the thermal stability of the obtained complexes can be ordered in the following sequence: 1 < 3 ≪ 2.
The authors are grateful to Dr Wiesław Surga for his help during the thermal work. The opportunity of making an analytical measurement of cadmium ions in the Environmental Analytical Laboratory and the Raman spectra in the Structural Laboratory of the Jan Kochanowski University are also gratefully acknowledged.
References
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