Dynamics of polar low mass molecules encapsulated in the δ-cocrystal of syndiotactic polystyrene

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Abstract

The 8-cocrystal of syndiotactic polystyrene (sPS) can capsulate various small guest molecules in the cavity of the crystalline region. We examined the rotational motion of isolated polar guest molecule, benzonitrile (BN), caged in the crystalline cavities by dielectric spectroscopy and the results were compared with the previously reported data of sPS / methyl ethyl ketone (MEK) system. The relaxation of BN in the crystalline region was specifed from the comparison with the dielectric data of atactic-PS / BN system in which only the amorphous phase exists. The rotational relaxation time of BN in the crystalline cavity was 6 orders of magnitude longer, and the activation energy of BN was twice larger than those of MEK. These results suggest that spatial restriction due to the small cavity size strongly retards the rotational dynamics of the larger guest molecule, BN. Two-site model could successfully describe the temperature dependence of the dielectric intensity for sPS / BN system, revealing that there exist two stable states of BN molecules with energy difference of 7.42 kJmol1 in the crystalline cavity. © 2014 The Society of rheology, Japan.

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Kobayashi, H., Urakawa, O., Kaneko, F., & Inoue, T. (2014). Dynamics of polar low mass molecules encapsulated in the δ-cocrystal of syndiotactic polystyrene. Nihon Reoroji Gakkaishi, 42(1), 19–23. https://doi.org/10.1678/rheology.42.19

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