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International Journal of Inorganic Chemistry
Volume 2011 (2011), Article ID 274073, 7 pages
http://dx.doi.org/10.1155/2011/274073
Research Article

Synthesis and Characterization of Bis(4-methylbenzylammonium) Tetrachloridocadmate(II)

1Laboratoire de Chimie des Matériaux, Faculté des Sciences de Bizerte, Zarzouna 7021, Tunisia
2Department of Chemistry, Youngstown State University, One University Plaza, Youngstown, OH 44555-3663, USA
3Laboratoire de Chimie Organometallique de Surface (LCOMS), Ecole Supérieure de Chimie Physique Electronique, 69622 Villeurbanne Cedex, France

Received 11 November 2011; Accepted 13 December 2011

Academic Editor: Alexander Steiner

Copyright © 2011 R. Kefi 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

The crystal structure of the new inorganic-organic hybrid compound [4-CH3C6H4CH2NH3]2[CdCl4] has been determined by single crystal X-ray diffraction. The compound crystallizes in the orthorhombic space group Pnma with lattice parameters , ,  Å, ,  Å3, and . The framework of the title compound is built upon layers parallel to (010) made up from corner-sharing CdCl6 octahedra. 4-Methylbenzylammonium cations are situated between the layers and connect them via an N–HCl hydrogen bonding network. The Cd atom is located on an inversion centre, and the coordination environment is described as distorted octahedral. Solid state 13C CP-MAS NMR spectroscopy is in agreement with the X-ray structure. DFT calculations allow the attribution of the carbon peaks to the independent crystallographic sites. Thermal analysis and infrared spectroscopy were also used to characterize the complex.

1. Introduction

In recent years, a great effort has been devoted to the self-assembly of organic and inorganic molecules in the solid state, because it allows to design new solids with specific properties, such as electronic, optical, thermal, and catalytic [1, 2]. Among these materials, chlorocadmate compounds have been of special interest for their structural flexibility. Complexes with Cd(II) centers have been at the center of growing interest due to their variable frameworks, and their potential photoluminescent and nonlinear optical (NLO) properties [3, 4]. They can occur as simple tetrahedral anions CdX42− or form the backbone of chain polymers. This is due to the fact that the Cd2+ ion, being a d10 transition metal ion, exhibits a great variety of coordination numbers and geometries, depending on crystal packing and hydrogen bonding, as well as halide dimensions [510]. A wide variety of stoichiometries that belong to this class of compounds makes the crystal chemistry of chlorocadmates extremely diverse and complex. Common features of all these compounds are the invariable presence of octahedral (CdCl6) units in the anhydrous species. A network of hydrogen bonding, involving organic cations, generally connects the inorganic anions together and stabilizes the whole crystal structure [1114]. Therefore, the Cd(II) salt is suitable for the assembly of coordination frameworks.

As a part of our ongoing investigations in molecular salts containing metal-chlorido complexes [15, 16], we present here the crystal structure of one such compound, [4-CH3C6H4CH2NH3]2[CdCl4].

2. Experimental

2.1. Chemical Preparation

4-Methybenzylamine (2 mmol, 0.242 g) and CdCl2 (1 mmol, 0.183 g) were dissolved in dilute HCl (10 mL, 1 M), and the resultant solution was slowly evaporated at room temperature. A crystal of the title compound, which remained stable under normal conditions of temperature and humidity, was isolated after several days and subjected to X-ray diffraction analysis (yield 56%). Element analysis calculated: C 38.51, H 4.81, N 5.61%; found: C 38.46, H 4.67, N 5.78%.

2.2. Investigation Techniques

The characterization of these salts was carried out using X-ray diffraction, solid state NMR spectroscopy, DFT calculations, infrared spectroscopy, and thermal analysis (differential thermal analysis, DTA, and thermal gravimetric analysis, TGA).

2.2.1. X-Ray Diffraction

A single crystal was carefully selected under a microscope in order to perform its structural analysis by X-ray diffraction. The intensity data were collected on a Bruker AXS SMART APEX CCD diffractometer using the omega scan technique with MoKα radiation (λ = 0.7107 Å). The structure was solved with direct methods using SHELXS-97 [17] and refined with full-matrix least-squares techniques using SHELXTL-6.14 [18]. The drawings were made with Diamond [19]. Crystal data and experimental parameters used for the intensity data collection are summarized in Table 1.

tab1
Table 1: Cristallographic data and refinement details of the title compound.

Crystals of the title compound were also analyzed at lower temperature (100 K). At this temperature the diffraction patterns exhibit pronounced “streaks” of intensity between rows of well defined Bragg peaks, indicating modulation of the structure and disorder of molecular entities with repeating patterns that are not a multiple of the basic unit cell as defined by the main Bragg peaks. Integration of only the Bragg peaks under omission of the streaks confirmed this. The average structure thus obtained shows substantial disorder of some of the chlorine atoms, with ratios refining to an 82 : 18 ratio. It can be imagined that the positions of the Cl atoms in neighboring layers of Cd and Cl are in some way related, but not in a way that repeats itself within the dimensions given by the unit cells, thus causing the non-Bragg like behavior at 100 K. No attempts were made to completely analyze the non-Bragg low temperature phase of the compound.

2.2.2. NMR Spectroscopy

The 13C NMR spectrum was recorded on a solid-state high-resolution Bruker DSX-300 spectrometer operating at 75.49 MHz with a classical 4 mm probehead allowing spinning rates up to 10 kHz. The chemical shifts are given relative to tetramethylsilane (external reference, precision 0.5 ppm). The spectrum was recorded by use of cross-polarization (CP) from protons (contact time 5 ms) and MAS. Before recording the spectrum, it was checked that there was a sufficient delay between the scans allowing a full relaxation of the protons. DFT calculations were undertaken in order to assign the NMR resonances to the different nonequivalent C atoms of the unit cell. These calculations were made at the B3LYP/6-31+G* level using the GAUSSIAN98 program [20].

2.2.3. IR Spectroscopy

The spectrum was recorded in the range 4000–400 cm−1 with a “Perkin-Elmer FTIR” spectrophotometer 1000 using a sample dispersed in spectroscopically pure KBr pressed into a pellet.

2.2.4. Thermal Analysis

Thermal analysis was performed using the “multimodule 92 Setaram” analyzer operated between room temperature and 773 K with an average heating rate of 5 K min−1.

3. Results and Discussion

3.1. X-Ray Diffraction Study

The main geometrical features of the different chemical entities of the organic-inorganic hybrid compound [4-CH3C6H4CH2NH3]2[CdCl4] are reported in Tables 2, 3, and 4.

tab2
Table 2: Selected bond lengths (Å) in [4-CH3C6H4CH2NH3]2[CdCl4].
tab3
Table 3: Selected bond angles (°) in [4-CH3C6H4CH2NH3]2[CdCl4].
tab4
Table 4: Hydrogen-bond geometry (Å, °) in [4-CH3C6H4CH2NH3]2[CdCl4].

The asymmetric unit of the title compound (Figure 1) contains one 4-methylbenzylammonium and one half of a CdCl2(Cl1/2)4 fragment. Packing of [4-CH3C6H4CH2NH3]2[CdCl4] viewed along the b-axis (Figure 2) shows a layer of corner sharing [CdCl6] octahedra. The minimum Cd–Cd distance within a layer is 5.362(1) Å. In the structure, three symmetry independent chlorine atoms are observed (Cl1, Cl2, and Cl3), and only Cl1 and Cl3 form a bridge between two cadmium centers. In this way, the chlorine atoms form a distorted octahedron around each cadmium atom (Figure 3), giving the overall stoichiometry for the anions of [CdCl2(Cl1/2)4]2−. The Cd atom is located on an inversion centre. Table 2 shows that the symmetric bridging Cd–Cl distances are long, varying between 2.663(1) and 2.709(1) Å, while the terminal Cd–Cl distances are close to 2.502(1) Å, which is typical of six coordinated Cd(II) [18]. The Cl–Cd–Cl bond angles average exactly 90.0° and range between 84.62 (5)° for Cl3–Cd1–Cl1 and 92.92 (3) for Cl2–Cd1–Cl3 (Table 3), again confirming the close to symmetric octahedral nature of the CdCl6 building units.

274073.fig.001
Figure 1: Asymmetric unit of [4-CH3C6H4CH2NH3]2[CdCl4] with atom labels and 50% probability displacement ellipsoids for non-H atoms.
274073.fig.002
Figure 2: Projection of [4-CH3C6H4CH2NH3]2[CdCl4] structure in the plane (a, c). The dotted lines indicate hydrogen bonds. A polyhedral representation is given for [CdCl6].
274073.fig.003
Figure 3: Coordination geometry of Cd(II) ions in [4-CH3C6H4CH2NH3]2[CdCl4]. Symmetry codes: (i) x, −y + 1/2, z; (ii) x, y, z − 1; (iii) x − 1/2, y, −z + 1/2.

In this structure, the 4-methylbenzylammonium cationic group compensates the negative charge of a half [CdCl2(Cl1/2)4]2− anion leading to neutrality for the structure as a whole. Figure 4 shows CdCl6 octahedra and the 4-methylbenzylammonium cations connected via hydrogen bonds N1–H1CCl1, N1–H1DCl3vi, N1–H1DCl1vi, and N1–H1ECl3iii, one of which is bifurcated N1–H1D(Cl3vi, Cl1vi) (symmetry codes in Table 4). Only the bridging chlorine atoms Cl1 and Cl3 of the CdCl6 octahedron participate in hydrogen bonding, while all hydrogen atoms that are attached to N1 are involved in hydrogen bondings. No π-π stacking interactions between neighboring aromatic rings or C–H⋯π interactions towards them are observed. The interlayer space is large enough to allow for only minimal distortions of the cation. The angles and atom distances of the cation have their usual values as reported for the related compound with the same cation, bis(4-methylbenzylammonium) tetrachlorozincate [21]. It is worth noting that as cadmium is found in the second period of the transition metals, it has more variable coordination numbers and geometries than zinc. This explains the difference of the architectures between the cadmium and zinc salts. Indeed, for the title compound, the CdCl6 octahedra are sharing their common vertex of chlorine, while, in the Zn(II) salt [21], the ZnCl4 tetrahedra are linked by hydrogen bonds.

274073.fig.004
Figure 4: Projection of [4-CH3C6H4CH2NH3]2[CdCl4] structure along the -axis. The dotted lines indicate hydrogen bonds. A polyhedral representation is given for [CdCl6].
3.1.1. NMR Spectroscopy

The 13C CP-MAS NMR spectrum of the title compound is shown on Figure 5. It displays two well-defined peaks in the resonance region of the aliphatic carbon atoms, at 22.2 and 44.3 ppm, showing that the asymmetric unit cell should contain only one organic molecule, which is in good agreement with the X-ray results (Figure 1). Theoretical calculations were then undertaken in order to assign the NMR resonances to the different crystallographically inequivalent carbon atoms of the unit cell. These calculations were made at the B3LYP/6-31+G* level. The different atoms were labeled as depicted below:

274073.fig.008

274073.fig.005
Figure 5: Experimental and simulated 13C CP-MAS NMR spectra of the studied compound.

Three different calculations were made on the organic cation, and, in all cases, the theoretical chemical shifts were subtracted from those of the reference (tetramethylsilane) calculated at the same level of theory:(1)calculation of the NMR chemical shifts (with the GIAO method) by taking the positions of atoms obtained by X-ray diffraction;(2)optimization of the positions of the protons in the above molecule and calculation of the NMR chemical shifts in this semioptimized geometry. Indeed, X-ray diffraction leads always to underestimated X–H bond lengths, due to the fact that it is sensitive to the electronic cloud and does not see the nuclei;(3)full optimization of all atoms and calculation of NMR chemical shifts. This calculation, compared to the above one, will give indications on the steric hindrance around the organic cation and on the positions where it is the strongest.

The results are listed in Table 5 which shows that there is a good agreement between the experimental and theoretical values calculated after optimization of the position of the protons, allowing unambiguously the attribution of the different NMR signals to the carbon atoms of the structure.

tab5
Table 5: Calculated and experimental 13C chemical shifts in the studied compound.
3.1.2. IR Spectroscopy

The IR spectrum of crystalline [4-CH3C6H4CH2NH3]2[CdCl4] is shown in Figure 6. The most representative and characteristic vibrational modes of this compound can be compared to those of similar complexes [22]. Some aspects of the performed assignments are briefly commented as follows.(i)In the high-frequency region, the broad band between 3600 and 2500 cm−1 corresponds to the valence vibrations of CH and NH groups [23].(ii)The observed bands in the 1620−1200 cm−1 region can be attributed to the bending vibrations of NH groups and to the valence vibrations of C=C and CN groups [24].(iii)The bands between 1000 and 700 cm−1 are assigned to out of plane bending modes γ(Cary-H) and γ(Cary-C) [25].

274073.fig.006
Figure 6: IR absorption spectrum of [4-CH3C6H4CH2NH3]2[CdCl4].
3.1.3. Thermal Analysis

Simultaneous TGA-DTA curves of the bis(4-methylbenzylammonium) tetrachlorido-cadmate(II) are given in Figure 7. The DTA curve shows that this compound undergoes a series of endothermic transformations in a wide temperature range (560–773 K). The most important one appears at about 565 K. It corresponds to the melting point, which is in good agreement with the result obtained by the capillarity tube method. The important weight loss observed in this temperature region is attributed to the degradation of the organic entity. A black residue is obtained at the end of the experiment.

274073.fig.007
Figure 7: DTA and TGA curves of [4-CH3C6H4CH2NH3]2[CdCl4] at rising temperature.

Additional Material
Crystallographic data for the title compound have been deposited at the Cambridge Crystallographic Data Center as supplementary publication (CCDC 852580). These data can be obtained free of charge at http://www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Center, 12, Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223/336 033; mailto: deposit@ccdc.cam.ac.uk).

4. Summary

The title compound was prepared as single crystals at room temperature and characterized by physicochemical methods. On the structural level, the atomic arrangement of this material consists of a network of [CdCl2(Cl1/2)4]2− anions and 4-methylbenzylammonium cations connected by N−HCl hydrogen bonding interactions. The number of 13C CP-MAS-NMR components is in full agreement with the ones of crystallographically independent sites. Upon heating, this salt melts and the organic entities degrade.

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