| Literature DB >> 20961129 |
Filip Meersman1, Barbara Geukens, Michael Wübbenhorst, Jan Leys, Simone Napolitano, Yaroslav Filinchuk, Guy Van Assche, Bruno Van Mele, Erik Nies.
Abstract
N-Isopropylpropionamide (NiPPA), which can self-associate via hydrogen bonds, was found to undergo a solid-solid transition as identified by DSC and X-ray diffraction. Below the melting temperature of 51 °C NIPPA adopts a plastic crystalline state with a tetragonal unit cell until it transforms into an ordered crystal with a monoclinic structure at temperatures ≤10 °C. Dielectric spectroscopy was used to characterize the dynamics of the system, determining the activation parameters for the plastic to crystalline phase transition. The activation enthalpy is relatively high, as expected for a system that involves hydrogen bonds. However, most of the activation energy as the plastic phase assumes a more crystalline state is due to the activation entropy, suggesting that the increased cooperativity observed in the relaxation processes is due to a steric locking of the molecules.Entities:
Year: 2010 PMID: 20961129 DOI: 10.1021/jp105008k
Source DB: PubMed Journal: J Phys Chem B ISSN: 1520-5207 Impact factor: 2.991