Quadruply hydrogen-bonded building block from hydrazide-quinolinone motif and gelation ability of its analogous oxalic monoester-monoamide derivative

Org Lett. 2007 Nov 22;9(24):4991-4. doi: 10.1021/ol702194z. Epub 2007 Oct 23.

Abstract

NMR and STM studies revealed that the hydrazide-quinolinone-based building block 5 exhibited a monomer-dimer-polymer equilibrium, while its acyclic analogue 6, due to conformational flexibility, exhibited a more complicated mode of aggregation and formed a gel in dichloromethane/hexane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemical synthesis*
  • Amides / chemistry
  • Esters / chemical synthesis*
  • Esters / chemistry
  • Gels / chemical synthesis
  • Gels / chemistry
  • Hydrogen Bonding
  • Magnetic Resonance Spectroscopy / methods
  • Microscopy, Scanning Tunneling / methods
  • Molecular Structure
  • Particle Size
  • Quinolones / chemistry*

Substances

  • Amides
  • Esters
  • Gels
  • Quinolones