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

摘要

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 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 P-31 {H-1} and H-1 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.