Fluorescence Anisotropy Decay of Molecular Rotors with Acene Rotators in Viscous Solution.

Herein, we report the use of fluorescence anisotropy decay for measuring the rotation of six shape-persistent molecular rotors with central naphthalene (), anthracene (, , and ), tetracene (), and pentacene () rotators axially linked by triple bonds to bulky trialkylsilyl groups of different sizes. Steady-state and time-resolved polarization measurements carried out in mineral oil confirmed that the vibrationally resolved lowest-energy absorption bands are characterized by a transition dipole moment oriented along the short acene axes, in the direction of the alkyne linkers. Fluorescence lifetimes increased significantly with increasing acene size and moderately with a decrease in the size of the trialkylsilyl group. The fluorescence anisotropy decay for all compounds in mineral oil with a viscosity of ca. 21.6 cP at 40 °C was completed within the fluorescence lifetime, so that the rotational time constants could be obtained via their rotational correlation times, which increased with silyl protecting group size rather than acene size, indicating that polarization decay is determined by tumbling of the molecular rotor about the long acene axis. These results suggest that monitoring the rotational motion of bis(silylethynyl)acenes in restricted media should be possible for media with viscosity values on the order of 21.6 cP or greater.