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The kinetics of the high temperature (isotropic ? mesophase) and low temperature (mesophase ? crystalline) transition of PBFP atTm andT(1), respectively, and its local dynamics were studied by differential scanning calorimetry (DSC) at variable heating and cooling rate and by dielectric relaxation spectroscopy (DRS). While on heating no substantial effect of the rate on both transition temperatures was found,T(1) andTm showed a strong dependence on the cooling rate. The high temperature transition revealed thermally activated behaviour with an activation energy ofEa = 400 kJ/mol, whereas the transition atT(1) showed the typical signature of supercooling. This finding is consistent with the picture that the isotropic/mesophase transition atTm is controlled by long-range, strongly hindered, chain diffusion that leads to the long-range orientational mesomorphic order. In contrast, the low temperature transition, the enthalpy of which is far larger and the temperature of which depending linearly on the cooling rate, indicates a kinetical control by nucleation as characteristic for a (2D ? 3D) crystallization process.Complementary information about the molecular dynamics in the various phases was obtained by DRS that revealed three relaxation processes, which were assigned to the dynamic glass transition (a), local motions of CF3-groups in the glassy state (ß -process) and cooperative fluctuations of side-groups both in the mesophase and crystalline state (? -process). Interestingly, both the Arrhenius-type ß- and ? -relaxation are characterised by a non-zero activation entropy, which indicates the cooperative nature of the underlying molecular dynamics. [ABSTRACT FROM AUTHOR]