Key points are not available for this paper at this time.
Variation of the ferroelectric phase transition has been investigated for a series of isomorphous donor (D)-acceptor (A) charge-transfer complexes composed of 4,4'-dimethyltetrathiafulvalene (DMTTF) and tetrahalo-p-benzoquinones by measurements of dielectric susceptibility, X-ray diffraction, and infrared molecular vibrational spectra. The neutral-ionic phase transition of DMTTF-p-chloranil at 65 K accompanies a dielectric peak anomaly associated with the DA stack dimerization. Successive halogen replacement by bromine in the component tetrahalo-p-benzoquinone molecule expands the lattice along the DA stack of the DMTTF complex, and reduces the critical temperature steeply toward zero temperature in an analogous way to the critical behavior of quantum ferroelectrics. The 2,6-dibromo-substituted compound showing the behavior of the quantum paraelectricity is located in the immediate vicinity of the quantum critical point of this phase diagram as signified also by enhancement of the ionicity, the dielectric susceptibility, and the dynamical dimeric distortion at the lowest temperature.
Horiuchi et al. (Mon,) studied this question.