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

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

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 100K 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 100K to room temperature yielded β-glycine, the least stable of the known ambient-pressure polymorphs.

Original languageEnglish
Pages (from-to)569-574
Number of pages6
JournalIUCrJ
Volume4
DOIs
StatePublished - 2017

Funding

The following funding is acknowledged: Science and Technology Facilities Council/ISIS (award No. RB1520301); Engineering and Physical Sciences Research Council (award No. DTA); SISSA, CINECA and PRACE (award No. 2011050736); H2020 European Research Council (award No. 676531).

FundersFunder number
Science and Technology Facilities Council/ISIS
Horizon 2020 Framework Programme676531

    Keywords

    • amino acids
    • crystal structure prediction
    • crystallization under non-ambient conditions
    • neutron diffraction
    • phase transitions
    • polymorphism

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