IUCrJ (Sep 2017)

ζ-Glycine: insight into the mechanism of a polymorphic phase transition

  • Craig L. Bull,
  • Giles Flowitt-Hill,
  • Stefano de Gironcoli,
  • Emine Küçükbenli,
  • Simon Parsons,
  • Cong Huy Pham,
  • Helen Y. Playford,
  • Matthew G. Tucker

DOI
https://doi.org/10.1107/S205225251701096X
Journal volume & issue
Vol. 4, no. 5
pp. 569 – 574

Abstract

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Glycine is the simplest and most polymorphic amino acid, with five phases having been structurally characterized at atmospheric or high pressure. A sixth form, the elusive ζ phase, was discovered over a decade ago as a short-lived intermediate which formed as the high-pressure ∊ phase transformed to the γ form on decompression. However, its structure has remained unsolved. We now report the structure of the ζ phase, which was trapped at 100 K enabling neutron powder diffraction data to be obtained. The structure was solved using the results of a crystal structure prediction procedure based on fully ab initio energy calculations combined with a genetic algorithm for searching phase space. We show that the fate of ζ-glycine depends on its thermal history: although at room temperature it transforms back to the γ phase, warming the sample from 100 K to room temperature yielded β-glycine, the least stable of the known ambient-pressure polymorphs.

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