Cocrystallization of adamantane-1,3-dicarboxylic acid and 4,4'-bipyridine

Acta Crystallogr C. 2008 Feb;64(Pt 2):o41-3. doi: 10.1107/S0108270107058672. Epub 2008 Jan 12.

Abstract

The cocrystallization of adamantane-1,3-dicarboxylic acid (adc) and 4,4'-bipyridine (4,4'-bpy) yields a unique 1:1 cocrystal, C(12)H(16)O(4).C(10)H(8)N(2), in the C2/c space group, with half of each molecule in the asymmetric unit. The mid-point of the central C-C bond of the 4,4'-bpy molecule rests on a center of inversion, while the adc molecule straddles a twofold rotation axis that passes through two of the adamantyl C atoms. The constituents of this cocrystal are joined by hydrogen bonds, the stronger of which are O-H...N hydrogen bonds [O...N = 2.6801 (17) A] and the weaker of which are C-H...O hydrogen bonds [C...O = 3.367 (2) A]. Alternate adc and 4,4'-bpy molecules engage in these hydrogen bonds to form zigzag chains. In turn, these chains are linked through pi-pi interactions along the c axis to generate two-dimensional layers. These layers are neatly packed into a stable crystalline three-dimensional form via weak C-H...O hydrogen bonds [C...O = 3.2744 (19) A] and van der Waals attractions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adamantane / analogs & derivatives*
  • Adamantane / chemistry
  • Crystallization
  • Dicarboxylic Acids / chemistry*
  • Hydrogen Bonding
  • Molecular Structure
  • Pyridines / chemistry*

Substances

  • 1,3-adamantanedicarboxylic acid
  • Dicarboxylic Acids
  • Pyridines
  • Adamantane
  • 4,4'-bipyridyl