Issue 5, 2018

Paramagnetic ionic plastic crystals containing the octamethylferrocenium cation: counteranion dependence of phase transitions and crystal structures

Abstract

In recent years, ionic plastic crystals have attracted much attention. Many metallocenium salts exhibit plastic phases, but factors affecting their phase transitions are yet to be elucidated. To investigate these factors, we synthesized octamethylferrocenium salts with various counteranions [Fe(C5Me4H)2]X ([1]X; X = B(CN)4, C(CN)3, N(CN)2, FSA (= (SO2F)2N), FeCl4, GaCl4 and CPFSA (= CF2(SO2CF2)2N)) and elucidated their crystal structures and phase behavior. Correlations between the crystal structures and phase sequences, and the shapes and volumes of the anions are discussed. Except for [1][CPFSA], these salts exhibit phase transitions to plastic phases at or above room temperature (TC = 298–386 K), and the plastic phases exhibit either NaCl- or anti-NiAs-type structures. X-ray crystal structure analyses of these salts at 100 K revealed that they have structures in which cations and anions are alternately arranged, with the exception of [1][CPFSA]. [1][CPFSA] exhibits a structure in which anions and cations are separately stacked to form columns. [1][N(CN)2] exhibits a polar crystal structure that undergoes a monotropic phase transition to a centrosymmetric structure. The magnetic susceptibilities of room-temperature plastic crystals [1][GaCl4] and [1][FeCl4] were investigated; the latter exhibits a small ferromagnetic interaction at low temperatures.

Graphical abstract: Paramagnetic ionic plastic crystals containing the octamethylferrocenium cation: counteranion dependence of phase transitions and crystal structures

Supplementary files

Article information

Article type
Paper
Submitted
29 رجب 1438
Accepted
27 شعبان 1438
First published
27 شعبان 1438

Phys. Chem. Chem. Phys., 2018,20, 3019-3028

Paramagnetic ionic plastic crystals containing the octamethylferrocenium cation: counteranion dependence of phase transitions and crystal structures

T. Mochida, M. Ishida, T. Tominaga, K. Takahashi, T. Sakurai and H. Ohta, Phys. Chem. Chem. Phys., 2018, 20, 3019 DOI: 10.1039/C7CP02746J

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