Comprehensive measurements of the pressure- and temperature-dependent dc-transport are combined with dielectric spectroscopy and structural considerations in order to elucidate the charge and anion orderings in the quasi-one-dimensional charge-transfer salts (TMTTF) 2 X with non-centrosymmetric anions X = BF 4 , ClO 4 and ReO 4 . Upon applying hydrostatic pressure, the charge-order transition is suppressed in all three compounds, whereas the influence on the anion order clearly depends on the particular compound. A review of the structural properties paves the way for understanding the effect of the anions in their methyl cavities on the ordering. By determining the complex dielectric constant ϵ ^ ( ω , T ) in different directions we obtain valuable information on the contribution of the anions to the dielectric properties. For (TMTTF) 2 ClO 4 and (TMTTF) 2 ReO 4 , ϵ b ′ exhibits an activated behavior of the relaxation time with activation energies similar to the gap measured in transport, indicating that the relaxation dynamics are determined by free charge carriers.
