Abstract
We have investigated the influence of molecular arrangement on the transfer rates of photoexcitations along supramolecular assemblies of hydrogen-bonded oligo- p-phenylenevinylene (OPV) molecules for two different packing geometries. For well-defined, helical stacks of monofunctional OPVs fast (≈50 ps) photoluminescence depolarization and excitation transfer to dopants was observed, in agreement with semi-coherent exciton diffusion. For disordered assemblies of bifunctional OPVs incorporating a spacer to link adjacent molecules, depolarization and energy transfer dynamics occur on a longer time scale (≈nanosecond). This strongly suggests that such spacers need to be tuned carefully as they may otherwise interfere with the π-stacking thereby reducing the intermolecular electronic coupling.
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