Abstract
The synthesis, crystal structure, and characterization of a new organic–inorganic hybrid material with [C5H8N3]2ClSbCl4·H2O formula are described. The crystal structure refinement shows that this compound crystallizes in the monoclinic space group P21/m with the following unit cell dimensions: a = 5.6710(10) Å, b = 18.6279(2) Å, c = 9.0179(10) Å, β = 90.4480(10)°, V = 952.61(2) Å3, and Z = 2. The atomic arrangement of the title compound can be described by the three-dimensional network. The cohesion of compound entities is ensured by hydrogen bonding (N–H…Cl, OW–H…Cl, N–H…N, and C–H…Cl) and π–π interactions. The 13C CP-MAS-NMR spectrum shows five isotropic resonances, confirming the existence of five non-equivalent carbon atoms. This result is in good agreement with the X-ray single-crystal study. The infrared spectrum of this compound reported from 4,000 to 400 cm−1 confirmed the presence of the principal bands assigned to the internal modes of the organic cation.
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This work was supported by the Tunisian Ministry of H. E. Sc. R.
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Aloui, Z., Essid, M., Abid, S. et al. Synthesis, spectroscopic characterization, and X-ray structure analysis of bis(2-amino-4-methylpyrimidin-1-ium) chloride tetrachloroantimonate(III) monohydrate [C5H8N3]2ClSbCl4·H2O. Monatsh Chem 146, 1465–1471 (2015). https://doi.org/10.1007/s00706-015-1422-y
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DOI: https://doi.org/10.1007/s00706-015-1422-y