The crystalline packing of a π-extended D3h -symmetric triptycene reveals a particular π stacking motif with an almost-eclipsed arrangement of adjacent π planes despite the steric repulsion of tert-butyl substituents. Four model compounds were analyzed by using single-crystal X-ray diffraction and theoretical calculations to study the influence of dispersion interactions of molecular parts and understand the relationship between the molecular structure and this unique packing motif.
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Kohl et al. (2015) studied this question.
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