Molecular polygons probe the role of intramolecular strain in the photophysics of pi-conjugated chromophores

Abstract

Pi-conjugated segments - chromophores - constitute the electronically active units of polymer materials used in organic electronics. To elucidate the effect of bending of these linear moieties on elementary electronic properties such as luminescence colour and radiative rate we introduce a series of molecular polygons. The pi-system in these molecules becomes so distorted in bichromophores (digons) that these absorb and emit light of arbitrary polarisation: any part of the chain absorbs and emits radiation with equal probability. Bending leads to a cancellation of transition dipole moment (TDM), increasing excited-state lifetime. Simultaneously, fluorescence shifts to the red as radiative transitions require mixing of the excited state with vibrational modes. However, strain can become so large that excited-state localisation on shorter units of the chain occurs, compensating TDM cancellation. Since these effects counteract, underlying correlations between shape and photophysics can only be resolved in single molecules.