Reverse sequence of transitions in prototypic relaxor 1,4-diazabicyclo[2.2.2]octane

Two phase transitions consecutively reduce the crystal symmetry with rising temperature in 1,4-diazabicyclo[2.2.2]octane hydrobromide, [C6H13N2](+)center dot Br-, dabcoHBr. Low-temperature prototypic hexagonal phase III, space group P (6) over bar m2, Z = 1 above 458 K transforms into orientational states of orthorhombic phase II, space group Cmc2(1), Z = 4 and above 471 K to orthorhombic phase I, space group Pca2(1), Z = 8. The reverse transitions have been attributed to entropy and enthalpy contributions of the proton disordering, disproportionation of dabcoH(+) cations into neutral dabco molecules and dabcoH(2)(2+) dications at nanodomain walls, opposite propeller versus planar dabco conformations and conversions between NH+center dot center dot center dot N and NH+center dot center dot center dot Br- hydrogen bonds in dabcoHBr phase III, the NH+center dot center dot center dot N bonded relaxor material. All of the structural-disorder features in the NH+center dot center dot center dot N bonded aggregates are essential for the short-range polarization and giant dielectric response in dabcoHBr phase III. Despite the first-order type of the phase transitions, the lattice dimensions of phases I and II remain related to the prototypical relaxor phase III.