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Hydrothermal synthesis,thermal decomposition and optical properties of Fe2F5(H2O)(Htaz)(taz)(Hdma)
Authors:Mouna Smida  Jérome Lhôste  Mohamed Dammak  Santiago Garcia-Granda
Institution:1. Laboratoire de Chimie Inorganique, Faculté des Sciences de Sfax, Université de Sfax, BP 1171, Sfax 3000, Tunisia;2. Département de Chimie Physique Analytique et Chimie Organique et Inorganique, Université d’Oviedo, CINN, 33006 Oviedo, Spain;3. IMMM-UMR 6283 CNRS, LUNAM, Faculté des Sciences et Techniques, Université du Maine, Avenue Olivier Messiaen, 72085 Le Mans Cedex 9, France
Abstract:Crystal structure of Fe2F5(H2O)(Htaz)(taz)(Hdma) which crystallizes in the triclinic system space group P1¯ with unit cell parameters a = 8.8392(5) Å, b = 9.1948(5) Å, c = 9.5877(5) Å, α = 82.070(3)°, β = 63.699(3)°, γ = 89.202(3)°, Z = 2, and V = 690.91(7) Å3, was synthesized under hydrothermal conditions at 393 K for 72 h, by a mixture of FeF2/FeF3, 1,2,4-triazole molecule (Htaz), and hydrofluoric acid solution (HF 4%) in dimethylformamide solvent (DMF). The main feature of this material is the coexistence of two oxidation states for iron atoms (Fe2+, Fe3+) in the unit cell, which associate by opposite fluorine corners of FeF5N and FeF2N4 octahedra, and/or triazole molecule which originates the 2D produces material. The structure determination, performed from single crystal X-ray diffraction data, lead to the R1/WR2 reliability factors 0.031/0.087. Thermal stability studies (TG/DTG/DTA) show that the decomposition provides in the temperature range 473–773 K and no mass loss was detected before 473 K. Mass spectrometry (MS) has been used. The optical absorption of the solid was measured at the corresponding λmax using UV–vis diffuse-reflectance spectrum.
Keywords:Corresponding author  Tel  : +216 95 231 854/+216 28 742 375    Thermal analysis  Mass spectrometry  UV–vis
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