The uniaxial negative thermal expansion in pentacene crystals along a is a particularity in the series of the oligoacenes and is exceptionally large for a crystalline solid. Full x-ray structure analysis from 1200.3em0exto0.3em0ex4130.3em0exK reveals that the dominant thermal motion is a libration of the rigid molecules about their long axes, modifying the intermolecular angle which describes the herringbone packing within the layers. This herringbone angle increases with temperature (by 0.3^∘--0.6^∘0.3em0exper0.3em0ex1000.3em0exK) and causes an anisotropic rearrangement of the molecules within the layers, i.e., an expansion in the b direction and a distinct contraction along a. Additionally, a larger herringbone angle improves the cofacial overlap between adjacent, parallel molecules, and thus enhances the attractive van der Waals forces.
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Haas et al. (2007) studied this question.
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