• Media type: E-Article
  • Title: Structure of Amido Pyridinium Betaines: Persistent Intermolecular C−H⋅⋅⋅N Hydrogen Bonding in Solution
  • Contributor: Thatcher, Robert J.; Johnson, David G.; Slattery, John M.; Douthwaite, Richard E.
  • imprint: Wiley, 2016
  • Published in: Chemistry – A European Journal
  • Language: English
  • DOI: 10.1002/chem.201503884
  • ISSN: 0947-6539; 1521-3765
  • Keywords: General Chemistry ; Catalysis ; Organic Chemistry
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title><jats:p>A hydrogen bond of the type C−H⋅⋅⋅X (X=O or N) is known to influence the structure and function of chemical and biological systems in solution. C−H⋅⋅⋅O hydrogen bonding in solution has been extensively studied, both experimentally and computationally, whereas the equivalent thermodynamic parameters have not been enumerated experimentally for C−H⋅⋅⋅N hydrogen bonds. This is, in part, due to the lack of systems that exhibit persistent C−H⋅⋅⋅N hydrogen bonds in solution. Herein, a class of molecule based on a biologically active norharman motif that exhibits unsupported intermolecular C−H⋅⋅⋅N hydrogen bonds in solution has been described. A pairwise interaction leads to dimerisation to give bond strengths of about 7 kJ mol<jats:sup>−1</jats:sup> per hydrogen bond, which is similar to chemically and biologically relevant C−H⋅⋅⋅O hydrogen bonding. The experimental data is supported by computational work, which provides additional insight into the hydrogen bonding by consideration of electrostatic and orbital interactions and allowed a comparison between calculated and extrapolated NMR chemical shifts.</jats:p>