Abstract:SrCI2 · 1/2 H2O. konnte mit Hilfe von Hochtemperatur‐Guinier‐ und Hochtemperatur‐Raman‐Messungen nachgewiesen und durch Entwässerung Höherer Hydrate des Strontiumchlorids bei 165°C unter einem Wasserdampfpartialdruck von 1 bar dargestellt werden. Der Verlauf der Entwässerung des SrCI2 · 6 H2O und SrCI2 · 2H2O wird diskutiert. Die Röntgenpulverdaten sowie die IR‐ und Raman‐Spektren des SrCl2 · 1/2 H2O und des SrCI2 · H2O werden mitgeteilt. SrCI2 · H2O Kristallisiert orthorhombisch im BaCl2 · H2O‐Typ (Raumgruppe… Show more
“…The first signal corresponds to the dehydration of SrCl 2 ⋅ 6 H 2 O, however, since only the loss of half a water molecule per molar unit is observed the precursor powder of formal “SrCl 2 ⋅ 6 H 2 O” has been drained to form a roughly equimolar mixture of SrCl 2 ⋅ H 2 O and SrCl 2 as could be proven later by PXRD measurements. The second signal can be assigned to “Sr[ReO 4 ] 2 ⋅ H 2 O”, which in fact was a mixture of Sr[ReO 4 ] 2 ⋅ H 2 O and Sr[ReO 4 ] 2 ⋅ 2 H 2 O, as indicated by a loss of more than one, but less than two water molecules per molar unit [13–15] …”
Section: Resultsmentioning
confidence: 99%
“…An exothermal signal at 625 °C in the DSC curve can not be assigned clearly to a particular process, but may be a recrystallization event or a phase transformation. However, the melting point of SrCl 2 [13–15] and the expected melting point of possibly formed Sr 4 OCl 6 [17] both range at higher temperatures. Alternatively, the lower melting point of the reaction mixture could be caused by the formation of dys‐ or peritectica.…”
Section: Resultsmentioning
confidence: 99%
“…This means that equimolar mixtures of Sr [ O, as indicated by a loss of more than one, but less than two water molecules per molar unit. [13][14][15] Upon further heating no additional signal is observed until 584 °C, revealing that the complete dehydration process of the reaction mixture has already taken place with the previous events. The endothermic signal at 584 °C without any correlating mass loss in the thermogravimetric curve (TG) indicates a possible melting process or a phase transition.…”
Hygroscopic single crystals of a new hexagonal high‐temperature modification of Sr[ReO4]2 were prepared from a melt of Sr[ReO4]2 ⋅ H2O and SrCl2 ⋅ 6 H2O. The structure analysis of the obtained crystals by X‐ray diffraction revealed that the title compound crystallizes in the ThCd[MoO4]3‐type structure with the hexagonal space group P63/m and the lattice parameters a=1023.81(7) pm and c=646.92(4) pm (c/a=0.632) for Z=2 in its quenchable high‐temperature form. Two crystallographically independent Sr2+ cations are coordinated by oxygen atoms forming either octahedra or tricapped trigonal prisms, whereas the Re7+ cations are found in the centers of discrete tetrahedral meta‐perrhenate units [ReO4]−. Temperature‐dependent in‐situ PXRD studies of dry powder samples of Sr[ReO4]2 exhibited its thermal dimorphy with a phase‐transition temperature at 500–550 °C from literature‐known m‐Sr[ReO4]2 into the newly discovered h‐Sr[ReO4]2 (hexagonal).
“…The first signal corresponds to the dehydration of SrCl 2 ⋅ 6 H 2 O, however, since only the loss of half a water molecule per molar unit is observed the precursor powder of formal “SrCl 2 ⋅ 6 H 2 O” has been drained to form a roughly equimolar mixture of SrCl 2 ⋅ H 2 O and SrCl 2 as could be proven later by PXRD measurements. The second signal can be assigned to “Sr[ReO 4 ] 2 ⋅ H 2 O”, which in fact was a mixture of Sr[ReO 4 ] 2 ⋅ H 2 O and Sr[ReO 4 ] 2 ⋅ 2 H 2 O, as indicated by a loss of more than one, but less than two water molecules per molar unit [13–15] …”
Section: Resultsmentioning
confidence: 99%
“…An exothermal signal at 625 °C in the DSC curve can not be assigned clearly to a particular process, but may be a recrystallization event or a phase transformation. However, the melting point of SrCl 2 [13–15] and the expected melting point of possibly formed Sr 4 OCl 6 [17] both range at higher temperatures. Alternatively, the lower melting point of the reaction mixture could be caused by the formation of dys‐ or peritectica.…”
Section: Resultsmentioning
confidence: 99%
“…This means that equimolar mixtures of Sr [ O, as indicated by a loss of more than one, but less than two water molecules per molar unit. [13][14][15] Upon further heating no additional signal is observed until 584 °C, revealing that the complete dehydration process of the reaction mixture has already taken place with the previous events. The endothermic signal at 584 °C without any correlating mass loss in the thermogravimetric curve (TG) indicates a possible melting process or a phase transition.…”
Hygroscopic single crystals of a new hexagonal high‐temperature modification of Sr[ReO4]2 were prepared from a melt of Sr[ReO4]2 ⋅ H2O and SrCl2 ⋅ 6 H2O. The structure analysis of the obtained crystals by X‐ray diffraction revealed that the title compound crystallizes in the ThCd[MoO4]3‐type structure with the hexagonal space group P63/m and the lattice parameters a=1023.81(7) pm and c=646.92(4) pm (c/a=0.632) for Z=2 in its quenchable high‐temperature form. Two crystallographically independent Sr2+ cations are coordinated by oxygen atoms forming either octahedra or tricapped trigonal prisms, whereas the Re7+ cations are found in the centers of discrete tetrahedral meta‐perrhenate units [ReO4]−. Temperature‐dependent in‐situ PXRD studies of dry powder samples of Sr[ReO4]2 exhibited its thermal dimorphy with a phase‐transition temperature at 500–550 °C from literature‐known m‐Sr[ReO4]2 into the newly discovered h‐Sr[ReO4]2 (hexagonal).
The crystal structures of isomorphous SrCI, and BaCI, hemihydrates were solved by powder diffraction method. Strontium and barium atoms are coordinated either by nine chloride atoms or by seven chloride and two oxygen atoms.
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