The thermal behavior of propylammonium chloride (PAC) has been investigated by parallel beam X-ray powder diffraction in the 303-463 K thermal range. A polymorphic transition has been observed at 403 K, whereas the melting process starts at 438 K. The low-temperature (LT) polymorph is tetragonal, P4/n or P4/nmm, and a = 6.2429(2) angstrom, c = 7.3830(3) angstrom, and Z = 2. Thermal expansion is isotropic as the N center dot center dot center dot Cl interactions have components along the three crystallographic axes. At the transition temperature, a high-temperature (HT) polymorph was observed, with candidate space groups P23, Pm (3) over bar, P432, P (4) over bar 3m, and Pm (3) over barm and cell parameter a = 11.715(3) angstrom, consistent with Z = 12. This phase has features reminiscent of those of plastic phases of molecular crystals. The structural properties of a PAC/water mixture at ambient conditions were also studied by using an integrated approach, which combines X-ray diffraction measurements and molecular dynamics simulations carried out with the SPC/E and TIP5P water models. By using a Cl-water Lennard-Jones parameter previously refined for a similar system, a very good agreement between the theoretical and experimental diffraction patterns was obtained, especially in the case of the TIP5P simulation. A complex structural behavior has been highlighted, in which cations and anions do not possess a completely dosed hydration shell of their own, but rather "solvent-shared ion pairs" are formed, where one or more water molecules act as a bridge between the chloride and Propylammonium ions.

Crystal Polymorphism of Propylammonium Chloride and Structural Properties of Its Mixture with Water

GONTRANI, LORENZO;CAMINITI, RUGGERO
2011-01-01

Abstract

The thermal behavior of propylammonium chloride (PAC) has been investigated by parallel beam X-ray powder diffraction in the 303-463 K thermal range. A polymorphic transition has been observed at 403 K, whereas the melting process starts at 438 K. The low-temperature (LT) polymorph is tetragonal, P4/n or P4/nmm, and a = 6.2429(2) angstrom, c = 7.3830(3) angstrom, and Z = 2. Thermal expansion is isotropic as the N center dot center dot center dot Cl interactions have components along the three crystallographic axes. At the transition temperature, a high-temperature (HT) polymorph was observed, with candidate space groups P23, Pm (3) over bar, P432, P (4) over bar 3m, and Pm (3) over barm and cell parameter a = 11.715(3) angstrom, consistent with Z = 12. This phase has features reminiscent of those of plastic phases of molecular crystals. The structural properties of a PAC/water mixture at ambient conditions were also studied by using an integrated approach, which combines X-ray diffraction measurements and molecular dynamics simulations carried out with the SPC/E and TIP5P water models. By using a Cl-water Lennard-Jones parameter previously refined for a similar system, a very good agreement between the theoretical and experimental diffraction patterns was obtained, especially in the case of the TIP5P simulation. A complex structural behavior has been highlighted, in which cations and anions do not possess a completely dosed hydration shell of their own, but rather "solvent-shared ion pairs" are formed, where one or more water molecules act as a bridge between the chloride and Propylammonium ions.
2011
thermal behavior; complexes; x ray diffraction; force field; rietveld refinement; powder diffraction; reliability; potentials; molecular dynamics; ionic liquids
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/89405
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