Preparation, molecular structure, vibrational and photoluminescence study of a novel compound based chlorocadmate(II) material
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In the present work, we synthesized a new hybrid compound, (C6H10N2)2 Cd3Cl10. The crystal structure, vibrational and photoluminescence properties of the compound were studied. The structure can be described by the alternation of two different cationic-anionic layers. It consists of Cd3Cl10 dimers anions and bis Orthophenylenediammonium (C6H10N2) cations, which are connected via N-H···Cl hydrogen bonds forming a chain network. Furthermore, the 3D Hirshfild surfaces and the associated 2D fingerprint plots were investigated for intermolecular interactions in the molecule. The X ray powder is in agreement with the x ray structure. The Infrared Spectrum recorded in the 4000-400 cm-1 frequency region was compared with those found for homologous compounds in the literature. Solid state 13C NMR spectrum shows three signals, confirming the solid state structure determined by X-ray diffraction. Finally the characteristic exciton peaks in absorption spectra are located at 250 and 494 nm and the photoluminescence measurements showed one peak at around 2.06 eV.
In the present work, we synthesized a new hybrid compound, (C6H10N2)2 Cd3Cl10. The crystal structure, vibrational and photoluminescence properties of the compound were studied. The structure can be described by the alternation of two different cationic-anionic layers. It consists of Cd3Cl10 dimers anions and bis Orthophenylenediammonium (C6H10N2) cations, which are connected via N-H···Cl hydrogen bonds forming a chain network. Furthermore, the 3D Hirshfild surfaces and the associated 2D fingerprint plots were investigated for intermolecular interactions in the molecule. The X ray powder is in agreement with the x ray structure. The Infrared Spectrum recorded in the 4000-400 cm-1 frequency region was compared with those found for homologous compounds in the literature. Solid state 13C NMR spectrum shows three signals, confirming the solid state structure determined by X-ray diffraction. Finally the characteristic exciton peaks in absorption spectra are located at 250 and 494 nm and the photoluminescence measurements showed one peak at around 2.06 eV.
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Financial support from Faculty of Science in University of Gabes, Tunisia, Spanish Ministerio de Economía y Competitividad (MINECO-13-MAT2013-40950-R, and FPI grant BES-2011-046948 to MSM.A.) and Gobierno del Principado de Asturias (GRUPIN14-060), are acknowledged.
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