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Structure and phase transitions in chloroantimonate(V) crystals: [(C2H5)3NH]SbCl6 and [(C2H5)3NH]SbCl6·1/2[(C2H5)3NH]Cl.
Autorzy
Rok wydania
2002
Czasopismo
Journal of Physics and Chemistry of Solids
Numer woluminu
63
Strony
507-518
DOI
10.1016/S0022-3697(01)00189-5
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
New triethylammonium salts: [(C2H5)3NH]SbCl6 (TCA) and [(C2H5)3NH]SbCl6·1/2[(C2H5)3NH]Cl (TCAT) have been synthesized. The compounds crystallise in monoclinic symmetry: space groups P21/n and P21/c, for TCA at 293 K and TCAT at 100 K, respectively. The crystal structure of [(C2H5)3NH]SbCl6 consists of discrete ionic pairs—triethylammonium cations and hexachloroantimonate anions—linked via the bifurcated N–H⋯Cl hydrogen bonds. The crystal structure of [(C2H5)3NH]SbCl6·1/2[(C2H5)3NH]Cl is composed of three symmetrically independent triethylammonium cations, chlorine anion and two symmetrically independent hexachloroantimonate anions. TCA undergoes a structural phase transition at 336 K (on heating) into the orthorhombic C222 space group, whereas TCAT reveals a structural phase transition at 332 K. The phase transitions are of the first order type. TCA shows a ferroelastic domain structure below 336 K. Differential scanning calorimetry, dilatometric, dielectric dispersion and Raman scattering measurements have been used to study the phase transition mechanisms in these triethylammonium salts.
Adres publiczny
https://doi.org/10.1016/S0022-3697(01)00189-5
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