Abstract
Exciton interactions in molecular aggregates play a crucial role in tailoring the optical behaviour of π-conjugated materials. Though vital for optoelectronic applications, ideal Greek cross-dipole (α=90°) stacking of chromophores remains elusive. We report a novel Greek cross (+) assembly of 1,7-dibromoperylene-3,4,9,10-tetracarboxylic tetrabutylester (PTE-Br2 ) which exhibits null exciton coupling mediated monomer-like optical characteristics in the crystalline state. In contrast, nonzero exciton coupling in X-type (α=70.2°, PTE-Br0 ) and J-type (α=0°, θ=48.4°, PTE-Br4 ) assemblies have perturbed optical properties. Additionally, the semi-classical Marcus theory of charge-transfer rates predicts a selective hole transport phenomenon in the orthogonally stacked PTE-Br2 . Precise rotation angle dependent optoelectronic properties in crystalline PTE-Br2 can have consequences in the rational design of novel π-conjugated materials for photonic and molecular electronic applications.
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