Magnitudes and chemical consequences of R(3)N(+)-C-H...O[double bond]C hydrogen bonding

J Am Chem Soc. 2002 Jun 19;124(24):7163-9. doi: 10.1021/ja012417q.

Abstract

The magnitude of the stabilizing interaction between an aliphatic C[bond]H bond attached to an ammonium nitrogen and a carbonyl oxygen was evaluated by ab initio calculations at the MP2/6-311++G** level of theory. Attractive R(3)N(+)-C-H...O[double bond]C interactions play an important role in supramolecular recognition and various types of stereoselective catalysis. Our calculations show that R(3)N(+)-C-H...O[double bond]C is the strongest hydrogen bond of the C-H...O type known to date. Such hydrogen bonds remain as stabilizing interactions even in water for amide acceptors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetates / chemistry*
  • Dimethylformamide / chemistry*
  • Hydrogen Bonding
  • Models, Molecular
  • Molecular Conformation
  • Quantum Theory
  • Quaternary Ammonium Compounds / chemistry*

Substances

  • Acetates
  • Quaternary Ammonium Compounds
  • Dimethylformamide
  • methyl acetate