• Media type: E-Article
  • Title: (μ-Dihydrogen pyrazine-2,3,5,6-tetracarboxylato-κ6O2,N1,O6;O3,N4,O5)bis(diaqualithium) monohydrate
  • Contributor: Starosta, Wojciech; Leciejewicz, Janusz
  • imprint: International Union of Crystallography (IUCr), 2014
  • Published in: Acta Crystallographica Section E Structure Reports Online
  • Language: Not determined
  • DOI: 10.1107/s1600536814007223
  • ISSN: 1600-5368
  • Keywords: Condensed Matter Physics ; General Materials Science ; General Chemistry
  • Origination:
  • Footnote:
  • Description: <jats:p>The structure of the title compound, [Li<jats:sub>2</jats:sub>(C<jats:sub>8</jats:sub>H<jats:sub>2</jats:sub>N<jats:sub>2</jats:sub>O<jats:sub>8</jats:sub>)(H<jats:sub>2</jats:sub>O)<jats:sub>4</jats:sub>]·H<jats:sub>2</jats:sub>O, is composed of dinuclear molecules in which the ligand bridges two symmetry-related Li<jats:sup>I</jats:sup>ions, each coordinated also by two water O atoms, in an<jats:italic>O</jats:italic>,<jats:italic>N</jats:italic>,<jats:italic>O</jats:italic>′-manner. The Li and N atoms occupy special positions on twofold rotation axes, whereas a crystal water molecule is located at the intersection of three twofold rotation axes. The Li<jats:sup>I</jats:sup>cation shows a distorted trigonal–bipyramidal coordination. Two carboxylate groups remain protonated and form short interligand hydrogen bonds. The molecules are held together by a network of hydrogen bonds in which the coordinating and solvation water molecules act as donors and carboxylate O atoms as acceptors, forming a three-dimensional architecture.</jats:p>
  • Access State: Open Access