Acta Crystallographica Section E: Crystallographic Communications (Mar 2017)

Hydrogen-bonded co-crystal structure of benzoic acid and zwitterionic l-proline

  • Aaron M. Chesna,
  • Jordan M. Cox,
  • Sanjukta Basso,
  • Jason B. Benedict

DOI
https://doi.org/10.1107/S2056989017001785
Journal volume & issue
Vol. 73, no. 3
pp. 369 – 371

Abstract

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The title compound [systematic name: benzoic acid–pyrrolidin-1-ium-2-carboxylate (1/1)], C7H6O2·C5H9NO2, is an example of the application of non-centrosymmetric co-crystallization for the growth of a crystal containing a typically centrosymmetric component in a chiral space group. It co-crystallizes in the space group P212121 and contains benzoic acid and l-proline in equal proportions. The crystal structure exhibits chains of l-proline zwitterions capped by benzoic acid molecules which form a C(5)[R33(11)] hydrogen-bonded network along [100]. The crystal structure is examined and compared to that of a similar co-crystal containing l-proline zwitterions and 4-aminobenzoic acid.

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