Solvent effect on the ν^c frequency of CH stretching vibration of the blue shifted F₃CH...FCD₃ complex has been studied in liquefied N₂, CO, Ar, Kr and Xe. In the case of Xe, the spectroscopic measurements have also been extended to the solid state. It was found that the ν^c position of the complex in the solutions studied lowers with respect to the value in the gas phase. In liquid Xe, characterized by the largest permittivity, this effect reaches its maximum value of ∼-14.5 cm^-1. The ν^c frequency begins to grow again just below the freezing point of Xe, where a noticeable (∼15%) increase of the density of Xe occurs. The experimental results obtained for the liquid phase have been analyzed in the framework of the Onsager-like reaction field model and Polarizable Continuum Model (PCM) implemented into a standard Gaussian 98 Program.