Ambidentate ligands capable of variable bond angles in the coordination-driven self-assembly of discrete Pt macrocycles

J Org Chem. 2006 Aug 18;71(17):6662-5. doi: 10.1021/jo060971i.

Abstract

Flexible, ambidentate pyridyl-carboxylate based donor ligands such as sodium 3-(3-pyridyl)benzoate, sodium 4-(3-pyridyl)benzoate, and potassium 4-(3-pyridyl)ethynylbenzoate self-assemble into discrete [2 + 2] macrocyclic species instead of infinite networks when combined with a 90 degrees platinum-containing acceptor. In each case, only one isomeric ensemble is selectively formed in high yield. All products are characterized by electrospray ionization mass spectrometry (ESI-MS) and 31P{1H} and 1H NMR spectroscopy. They are the first examples of discrete supramolecules incorporating flexible, ambidentate donor ligands. Despite their potential versatility, these pyridyl-carboxylate donors adjust their bonding directionality to accommodate a rigid platinum acceptor in the formation of one discrete ensemble.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ligands
  • Macrocyclic Compounds / chemical synthesis*
  • Macrocyclic Compounds / chemistry
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Platinum Compounds / chemical synthesis*
  • Platinum Compounds / chemistry
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Ligands
  • Macrocyclic Compounds
  • Platinum Compounds