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Neutron diffraction of tri(3,5- tert -butylphenyl)methane at 20 K reveals an intermolecular C–H···H–C distance of only 1.566(5) Å, which is the shortest reported to date. The compound crystallizes as a C 3 -symmetric dimer in an unusual head-to-head fashion. Quantum chemical computations of the solid state at the HSE-3c level of theory reproduce the structure and the close contact well (1.555 Å at 0 K) and emphasize the significance of packing effects; the gas-phase dimer structure at the same level shows a 1.634 Å C–H···H–C distance. Intermolecular London dispersion interactions between contacting tert -butyl substituents surrounding the central contact deliver the decisive energetic contributions to enable this remarkable bonding situation.
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Rösel et al. (2017) studied this question.
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