New hydrophobic L-amino acid salts: maleates of L-leucine, L-isoleucine and L-norvaline

Acta Crystallogr C Struct Chem. 2015 Jul;71(Pt 7):584-92. doi: 10.1107/S2053229615010888. Epub 2015 Jun 18.

Abstract

Crystals of maleates of three amino acids with hydrophobic side chains [L-leucenium hydrogen maleate, C6H14NO2(+)·C4H3O4(-), (I), L-isoleucenium hydrogen maleate hemihydrate, C6H14NO2(+)·C4H3O4(-)·0.5H2O, (II), and L-norvalinium hydrogen maleate-L-norvaline (1/1), C5H11NO2(+)·C4H3O4(-)·C5H12NO2, (III)], were obtained. The new structures contain C2(2)(12) chains, or variants thereof, that are a common feature in the crystal structures of amino acid maleates. The L-leucenium salt is remarkable due to a large number of symmetrically non-equivalent units (Z' = 3). The L-isoleucenium salt is a hydrate despite the fact that L-isoleucine is a nonpolar hydrophobic amino acid (previously known amino acid maleates formed hydrates only with lysine and histidine, which are polar and hydrophilic). The L-norvalinium salt provides the first example where the dimeric cation L-Nva...L-NvaH(+) was observed. All three compounds have layered noncentrosymmetric structures. Preliminary tests have shown the presence of the second harmonic generation (SGH) effect for all three compounds.

Keywords: SHG effect; crystal structure; l-amino acids; l-isoleucine; l-leucine; l-norvaline; l-norvaline–l-norvalinium dimer; maleate; noncentrosymmetric layered structures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemistry
  • Crystallography, X-Ray
  • Histidine / chemistry*
  • Hydrogen Bonding
  • Hydrophobic and Hydrophilic Interactions
  • Isoleucine / chemistry*
  • Leucine / chemistry*
  • Lysine / chemistry*
  • Maleates / chemistry*
  • Molecular Structure
  • Valine / analogs & derivatives*
  • Valine / chemistry

Substances

  • Amino Acids
  • Maleates
  • Isoleucine
  • Histidine
  • norvaline
  • Leucine
  • Valine
  • Lysine